GE - Custom Search manager-regulatory-reporting-jobs

Regulatory Affairs Director Job (Salt Lake City, UT, United States)

Sat, 25 May 2013 08:00:00 GMT

Job Number:	1728939
Business:	GE Healthcare
Business Segment:	Healthcare Quality
About Us:	GE Healthcare’s Surgery business offers a range of market-leading intra-operative and interventional imaging products. Surgery's C-arm imaging products are integral in many fields including general surgery, orthopedics, neurosurgery, urology, cardiology, and GI, and for specialized procedures such as pain management. Surgery prides itself on offering imaging products with superb image quality and an unparalleled technical and clinical support team that ensures the products deliver optimum performance.
Posted Position Title:	Regulatory Affairs Director
Career Level:	Experienced
Function:	Quality
Function Segment:	Regulatory Affairs
Location:	United States
U.S. State, China or Canada Provinces:	Utah
City:	Salt Lake City
Postal Code:	84116-2862
Relocation Assistance:	Yes
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. The Regulatory Affairs Director is responsible for leading the overall Regulatory Affairs strategy and direction within the assigned area of responsibility (technical standards, laws and regulations, regulatory programs, etc). He/she may lead a team of direct reports to deliver a world-class regulatory service to the business by creating and supporting a regulatory compliant culture, and provides advice and counsel to business managers and Quality & Regulatory personnel.
Essential Responsibilities:	- Scan the external environment and work with external associations & global regulatory bodies, proactively adapt regulatory strategies, and influence change within areas of responsibility. - Establish and submit on time annual reports as required by regulatory agencies. - Submit country applications/submissions for approval to market safe and effective Medical Devices. - Determine where device design or process changes occur whether and how regulatory agencies need to be informed and provide appropriate documentation. - Interpret regulatory requirements and assure they are applied during the life-cycle of the product to meet those requirements. - Identify global regulatory trends & their implications for GE Healthcare, taking into consideration the impact on business decisions - Analyze & communicate proposed, new or changing requirements and standards, & lead teams to develop strategies, programs and processes to meet business objectives and ensure compliance with regulatory requirements - Communicate with regulatory authorities within areas of responsibility. - Evaluate performance metrics to identify program weaknesses & drive improvements in procedures or oversight. - Educate, train, advise & coach company professionals to ensure compliance with RA requirements. - Work across GEHC to ensure a consistent approach to regulations is adopted throughout the business within areas of responsibility. - Lead & support continuous improvement activities with regard to areas of responsibility. - Recruit, mentor, coach and train direct and indirect reports on activities within area of responsibility Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 2. Complete all planned Quality & Compliance training within the defined deadlines 3. Identify and report any quality or compliance concerns and take immediate corrective action as required 4. Maintain up-to-date knowledge and understanding of current regulatory requirements within area of responsibility 5. Effectively implement & manage programs and processes to meet regulatory requirements within area of responsibility
Qualifications/Requirements:	1. Bachelor’s Degree & minimum of 10 years experience in the medical device or pharmaceutical industry or medical product regulatory agencies; OR minimum of 14 years progressive regulatory affairs experience in medical device or pharmaceutical industry or medical product regulatory agencies, including knowledge & experience applying drug or device laws & regulations for product registration, adverse event reporting, & recalls. 2. At least 2 years leadership experience, including training and coaching of team members 3. Demonstrated ability to lead cross-functional, cross-business teams. 4. Demonstrated knowledge of regulatory issues and experience interfacing with local & internationals regulatory bodies, such as FDA, European competent authorities & notified bodies, Health Canada, SFDA, KFDA, MHLW, etc. 5. Ability to prioritize, plan, delegate and evaluate deliverables to established strategic goals. 6. Demonstrated experience operating in a highly regulated environment; Proven application of analytical skills in a regulatory environment 7. Strong problem solving and negotiation skills with the ability to develop and implement complex influencing and negotiating strategies that demonstrate political awareness 8. Ability to work well independently and in a team setting. 9. Excellent verbal and written communication and presentation skills with the ability to speak and write clearly and convincingly in English, tailoring communication methods to customer’s requirements. 10. Ability to influence and make recommendations at all levels of the company 11. Experience using spreadsheet and presentation software 12. Must be willing to travel up to 15% of time
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	1. Advanced degree in scientific, technology or legal disciplines. 2. Regulatory Affairs Certification (RAPS). 3. Knowledge of Quality Management Systems 4. Experience working across cultures/countries/sites 5. Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment. 6. Demonstrated ability to drive change, challenge the status quo and champion new activities, stimulating others to change and manage implementation effectively. 7. Demonstrated understanding of healthcare environment and knowledge of current competitive, commercial or political situations and their impact on GEHC regulatory strategies.

Regulatory Affairs Manager-HC Job (Waukesha, WI, United States)

Fri, 24 May 2013 05:00:00 GMT

Job Number:	1769068
Business:	GE Healthcare
Business Segment:	Healthcare Quality
About Us:
Posted Position Title:	Regulatory Affairs Manager-HC
Career Level:	Experienced
Function:	Quality
Function Segment:	Regulatory Affairs
Location:	United States
U.S. State, China or Canada Provinces:	Wisconsin
City:	Waukesha
Postal Code:	53188-1696
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. The Regulatory Affairs Manager provides subject matter expertise to ensure GEHC establishes & implements best practices within the assigned areas of responsibility including global labeling, advertising and promotion & premarket authorization (technical standards, laws and regulations, regulatory programs, etc).
Essential Responsibilities:	- Analyze and communicate regulatory trends and their implications for GE Healthcare; develop & implement effective regulatory strategies, programs and processes to meet business objectives and ensure compliance with regulatory requirements - Support effective and efficient development and maintenance of procedures, workflows and resources in support of GEHC regulatory affairs professionals in the areas of labeling, advertising and promotion and premarket authorization/clearance. - Lead and support continuous improvement activities, including such areas as regulatory procedure development and documentation, standards compliance, and metrics development and implementation. - Liaise with external regulatory bodies to guide input into regulatory strategies. - Work closely with regulatory, engineering, marketing, legal, and other professionals across the company to develop & implement company-wide programs and processes for regulatory compliance. - Collect, summarize & analyze performance metrics to identify program weaknesses & drive improvements in procedures or oversight. - Work across GEHC to ensure a consistent approach to regulations is adopted throughout the business within areas of responsibility. - Educate, train, & advise company professionals to ensure compliance with RA requirements. - As appropriate, recruit, mentor, coach & train direct and indirect reports on activities within areas of responsibility Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 2. Complete all planned Quality & Compliance training within the defined deadlines 3. Identify and report any quality or compliance concerns and take immediate corrective action as required 4. Maintain up-to-date knowledge and understanding of current regulatory requirements within area of responsibility 5. Effectively implement & manage programs and processes to meet regulatory requirements within area of responsibility
Qualifications/Requirements:	1. Bachelor’s Degree & minimum of 7 years experience in the medical device or pharmaceutical industry or with medical product regulatory agencies; OR minimum of 11 years progressive regulatory affairs experience in medical device or pharmaceutical industry or with medical product regulatory agencies, including knowledge & experience applying drug or device laws & regulations. 2. Demonstrated experience operating in a highly regulated environment; proven application of analytical skills in a regulatory environment 3. Demonstrated knowledge of regulatory issues, and experience interfacing with local & international regulatory bodies, such as FDA, European competent authorities & notified bodies, Health Canada, SFDA, KFDA, MHLW, etc. 4. Demonstrated project management skills; ability to prioritize, plan, evaluate & execute deliverables for established tactical goals 5. Demonstrated ability to lead cross-functional, cross-business teams. 6. Ability to influence and make recommendations at multiple levels of the company 7. Excellent verbal and written communication and presentation skills with the ability to speak and write clearly and convincingly in English, tailoring communication methods to customer’s requirements. 8. Experience using spreadsheet and presentation software 9. Must be willing to travel up to 15% of time. 10. Must be willing to work out of an office in Waukesha, WI
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	1. Advanced degree in scientific, technology or legal disciplines. 2. Regulatory Affairs Certification (RAPS). 3. Knowledge of Quality Management Systems (QMS). 4. Experience working across cultures/countries/sites. 5. Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment. 6. Strong problem solving and negotiation skills. 7. Demonstrated ability to work well independently & in a team setting. 8. Demonstrated ability to drive change, challenge the status quo and champion new activities, stimulating others to change and manage implementation effectively. 9. Demonstrated understanding of healthcare environment and knowledge of current competitive, commercial or political situations and their impact on GEHC regulatory strategies.

Regulatory Affairs Leader - Product Job (Waukesha, WI, United States)

Mon, 17 Jun 2013 05:00:00 GMT

Job Number:	1786405
Business:	GE Healthcare
Business Segment:	Healthcare Quality
About Us:
Posted Position Title:	Regulatory Affairs Leader - Product
Career Level:	Experienced
Function:	Quality
Function Segment:	Regulatory Affairs
Location:	United States
U.S. State, China or Canada Provinces:	Wisconsin
City:	Waukesha
Postal Code:	53188-1678
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. The Regulatory Affairs (RA) Leader – Product provides subject matter expertise. He/she works within a team of Regulatory Affairs professionals to ensure GEHC establishes best practices in the area of premarket regulatory submissions and new product development. This position will provide regulatory support for GE Healthcare’s MR products.
Essential Responsibilities:	Key responsibilities/essential functions include: - Define global regulatory strategy for assigned product lines in order to meet business objectives and provide a competitive advantage through strong product claims and timely market authorizations. - File / maintain regulatory deliverables - Actively participate as team member on all assigned new product introductions. - Create regulatory compliance / project plan using Regulatory Intelligence and in collaboration with Region RA to ensure all requirements are met for country submissions; work with relevant personnel to ensure appropriate, timely input is provided for submissions. - Create and file submissions; communicate with authorities regarding these submissions. - Assist in the planning and coordination of product testing when needed to support regulatory submissions, working in collaboration with engineering and Region RA. - Review and approve advertising and promotion material ensuring it is consistent with approved claims for regulated products. - Review changes in existing products to determine need for new/revised submissions or document reason for no submission - Educate, train, & advise company professionals to ensure compliance with regulatory requirements - Communicate changes in existing products to Region RA representatives for determination of the need for new/revised licenses or registrations. - Partner with Region RA representative for countries with license expiration requirements, to establish plan and deliverables for timely submission for renewal of license. - Identify any clinical data requirements for product licensing globally and insure the requirements are documented in the compliance plan. - Provide RA oversight to clinical studies. - Support regulatory inspections as required. - Coach or mentor other RA professionals. - Contribute to GE Healthcare efforts to influence new and changing regulations and standards through participation in commenting opportunities, trade associations, and/or standards committees. Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 2. Complete all planned Quality & Compliance training within the defined deadlines 3. Identify and report any quality or compliance concerns and take immediate corrective action as required 4. Maintain up-to-date knowledge and understanding of current regulatory requirements within area of responsibility. 5. Effectively support implementation & management of current regulatory requirements within area of responsibility. 6. Ensure assigned regulatory submissions are accurate, complete and timely.
Qualifications/Requirements:	Required Qualifications: 1. Bachelor’s Degree (or internationally recognized equivalent) & minimum of 3 years experience in the medical device or pharmaceutical industry or with medical product regulatory agencies; OR minimum of 7 years progressive regulatory affairs experience in medical device or pharmaceutical industry or with medical product regulatory agencies, including knowledge & experience applying drug or device laws & regulations for product registration 2. Ability to prioritize, plan & evaluate deliverables to established strategic goals. 3. Proven application of analytical skills in a regulatory environment 4. Excellent verbal and written communication and presentation skills with the ability to communicate business issues in English in an easy to understand manner. 5. Demonstrated knowledge & experience conducting scientific, regulatory, legal, or business research. 6. Strong problem solving and negotiation skills 7. Ability to work well independently & in a team setting. 8. Prior experience using spreadsheet and presentation software. 9. Must be willing to travel up to 10% of time.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	Preferred Qualifications: 1. Advanced degree in scientific, technology or legal disciplines. 2. Regulatory Affairs Certification (RAPS). 3. Demonstrated experience interfacing with regulatory agencies (e.g. FDA, MHLW, Health Canada, KFDA, etc.) and standards bodies such as AAMI, IEC, ISO, UL. 4. Knowledge of Quality Management Systems (QMS) 5. Experience with working across cultures/countries/sites 6. Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment. 7. Demonstrated understanding of healthcare environment and knowledge of current competitive, commercial or political situations and their impact on GEHC regulatory strategies.

Regulatory Affairs Manager – Medical Radiation Strategy Job (Waukesha, WI, United States)

Fri, 07 Jun 2013 07:59:00 GMT

Job Number:	1758958
Business:	GE Healthcare
Business Segment:	Healthcare Quality
About Us:
Posted Position Title:	Regulatory Affairs Manager – Medical Radiation Strategy
Career Level:	Experienced
Function:	Quality
Function Segment:	Regulatory Affairs
Location:	United States
U.S. State, China or Canada Provinces:	Wisconsin
City:	Waukesha
Postal Code:	53188-1696
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. The Regulatory Affairs Manager will be responsible for leading the execution and further development of GEHC’s medical radiation strategy across all radiation emitting products and associated services. The individual will work closely with regulatory, legal and business representatives as well as senior leadership in the tracking and fulfillment of GEHC’s medical radiation initiatives to deliver world class performance in the diverse landscape associated with medical radiation stakeholders.
Essential Responsibilities:	1. Scan the external environment and work with external associations & global regulatory bodies, proactively adapt regulatory strategies, and influence change within areas of responsibility. 2. Identify global regulatory trends & their implications for GE Healthcare, analyzing & communicating proposed, new or changing requirements and taking into consideration the impact on business decisions 3. Analyze & communicate proposed, new or changing requirements, & lead teams to develop strategies, programs and processes to meet business objectives and ensure compliance with regulatory requirements. 4. Evaluate performance metrics to identify program weaknesses & drive improvements in procedures or oversight. 5. As appropriate, mentor, coach & teach direct and/or indirect reports on activities within areas of responsibility. 6. Educate, train, advise & coach company professionals to ensure compliance with RA requirements. 7. Work across GEHC to ensure a consistent approach to regulations is adopted throughout the business within areas of responsibility. Including maintaining and facilitating GEHC’s Medical Radiation Strategy. 8. Lead & support continuous improvement activities with regard to areas of responsibility, including medical radiation strategy regarding new product offerings and advertising and promotion. Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position. 2. Complete all planned Quality & Compliance training within the defined deadlines. 3. Identify and report any quality or compliance concerns and take immediate corrective action as required. 4. Maintain up-to-date knowledge and understanding of current regulatory requirements within area of responsibility 5. Effectively implement & manage programs and processes to meet regulatory requirements within area of responsibility
Qualifications/Requirements:	1. Bachelor's Degree (or international equivalent) and a minimum of 7 years’ experience in the medical device or pharmaceutical industry or government / government relations; OR minimum of 11 years progressive regulatory affairs experience in medical device or pharmaceutical industry or government / government relations, including knowledge & experience applying global drug or device laws & regulations for product registration, adverse event reporting, & recalls. 2. At least 2 years leadership experience, including training and coaching of team members (If managing a team) 3. Demonstrated ability to lead cross-functional, cross-business teams. 4. Demonstrated knowledge of regulatory issues and experience interfacing with local & internationals regulatory bodies, such as FDA, European competent authorities & notified bodies, Health Canada, SFDA, KFDA, MHLW, etc. 5. Demonstrated experience interfacing with external associations to assess regulatory impact and effect regulatory change. 6. Ability to prioritize, plan, delegate and evaluate deliverables to established strategic goals. 7. Demonstrated experience operating in a highly regulated environment; Proven application of analytical skills in a regulatory environment 8. Excellent verbal and written communication and presentation skills with the ability to speak and write clearly and convincingly in English, tailoring communication methods to customer's requirements. 9. Ability to influence and make recommendations at all levels of the company 10. Prior experience using spreadsheet and presentation software 11. Must be willing to travel up to 20% of time
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	1. Advanced degree in scientific, technology or legal disciplines. 2. Regulatory Affairs Certification (RAPS). 3. Knowledge of Quality Management Systems 4. Ability to work across cultures/countries/sites 5. Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment. 6. Strong problem solving and negotiation skills with the ability to develop and implement complex influencing and negotiating strategies that demonstrate political awareness 7. Demonstrated ability to drive change, challenge the status quo and champion new activities, stimulating others to change and manage implementation effectively. 8. Demonstrated understanding of healthcare environment and knowledge of current competitive, commercial or political situations and their impact on GEHC regulatory strategies. 9. Demonstrated knowledge of global regulations and requirements related to ionizing radiation use in medicine (e.g. 21 CFR subchapter J).

Regulatory Affairs Leader - Product Job (Barrington, IL, United States)

Wed, 12 Jun 2013 07:59:00 GMT

Job Number:	1719728
Business:	GE Healthcare
Business Segment:	Healthcare Quality
About Us:
Posted Position Title:	Regulatory Affairs Leader - Product
Career Level:	Experienced
Function:	Quality
Function Segment:	Regulatory Affairs
Location:	United States
U.S. State, China or Canada Provinces:	Illinois
City:	Barrington
Postal Code:	60010-3076
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. The Regulatory Affairs (RA) Leader – Product provides subject matter expertise. He/she works within a team of Regulatory Affairs professionals to ensure GEHC establishes best practices in the area of premarket regulatory submissions and new product development.
Essential Responsibilities:	- File / maintain regulatory deliverables - Actively participate as team member on all assigned new product introductions. - Create regulatory compliance / project plan using Regulatory Intelligence and in collaboration with Region RA to ensure all requirements are met for country submissions; work with relevant personnel to ensure appropriate, timely input is provided for submissions. - Create and file submissions; communicate with authorities regarding these submissions. - If specific country testing is needed, work with Region RA, and arrange for test devices and support as needed. - Review and approve advertising and promotion material ensuring it is consistent with approved claims for regulated products. - Review changes in existing products to determine need for new/revised submissions or document reason for no submission - Educate, train, & advise company professionals to ensure compliance with regulatory requirements - Communicate changes in existing products to Region RA representatives for determination of the need for new/revised licenses or registrations. - Partner with Region RA representative for countries with license expiration requirements, to establish plan and deliverables for timely submission for renewal of license. - Identify any clinical data requirements for product licensing globally and insure the requirements are documented in the compliance plan. - Provide RA oversight to clinical studies. - Support regulatory inspections as required. - Coach or mentor other RA professionals. Quality Specific Goals: 1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position 2. Complete all planned Quality & Compliance training within the defined deadlines 3. Identify and report any quality or compliance concerns and take immediate corrective action as required 4. Maintain up-to-date knowledge and understanding of current regulatory requirements within area of responsibility. 5. Effectively support implementation & management of current regulatory requirements within area of responsibility. 6. Ensure assigned regulatory submissions are accurate, complete and timely.
Qualifications/Requirements:	1. Bachelor’s Degree (or internationally recognized equivalent) & minimum of 3 years experience in the medical device or pharmaceutical industry or with medical product regulatory agencies; OR minimum of 7 years progressive regulatory affairs experience in medical device or pharmaceutical industry or with medical product regulatory agencies, including knowledge & experience applying drug or device laws & regulations for product registration 2. Ability to prioritize, plan & evaluate deliverables to established strategic goals. 3. Proven application of analytical skills in a regulatory environment 4. Excellent verbal and written communication and presentation skills with the ability to communicate business issues in English in an easy to understand manner. 5. Demonstrated knowledge & experience conducting scientific, regulatory, legal, or business research. 6. Strong problem solving and negotiation skills 7. Ability to work well independently & in a team setting. 8. Prior experience using spreadsheet and presentation software. 9. Must be willing to travel up to 10% of time.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	1. Advanced degree in scientific, technology or legal disciplines. 2. Regulatory Affairs Certification (RAPS). 3. Demonstrated experience interfacing with regulatory agencies (e.g. FDA, MHLW, Health Canada, KFDA, etc.) and standards bodies such as AAMI, IEC, ISO, UL. 4. Knowledge of Quality Management Systems (QMS) 5. Experience with working across cultures/countries/sites 6. Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment. 7. Demonstrated understanding of healthcare environment and knowledge of current competitive, commercial or political situations and their impact on GEHC regulatory strategies.

Regulatory Reporting Manager Job (Stamford, Chicago, Connecticut, Illinois, United S)

Tue, 28 May 2013 05:00:00 GMT

Job Number:	1766687
Business:	GE Capital
Business Segment:	Capital - Treasury
About Us:	GE Treasury team is responsible for global funding, cash & foreign exchange management, and other treasury services for all of GE's worldwide operations. Almost all of GE's debt is issued through GE Capital to support its financial services businesses. We fund ourselves through the issuance of long term debt, commercial paper, CDs & bank deposits, and other debt products as well. imagination at work? GE is an Equal Opportunity Employer. GE offers a competitive salary, outstanding benefits & the professional advantages of an environment that supports your development & recognizes your achievements. GE offers an inclusive environment where employees have the opportunity to succeed and diversity is embraced as a competitive advantage in the marketplace. The passion that our people bring to their work extends to their private worlds, and GE encourages a healthy balance between the two. GE values education and is dedicate to providing the tools and training for your professional development.
Posted Position Title:	Regulatory Reporting Manager
Career Level:	Experienced
Function:	Finance
Function Segment:	Controllership
Location:	United States
U.S. State, China or Canada Provinces:	Connecticut, Illinois
City:	Stamford, Chicago
Postal Code:	06905-3417
Relocation Assistance:	Yes
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. Execute on the Regulatory Reporting strategy within the Treasury regulatory reporting team, to include identifying and communicating regulatory reporting requirements to functional teams, reviewing LE reporting submissions, ensuring accurate data and analysis, and implementing process and data improvements. Drive operational ownership to ensure consistency and compliance. Summarize analysis and communicate results. Reports to the Finance Regulatory Readiness Manager and manages direct report(s).
Essential Responsibilities:	Own collection of regulatory reporting data within focused area of Regulatory Reporting. Perform detailed validation work on the data collected by the team and address unexpected results or inconsistencies in data. Verify and perform the consolidation of Regulatory Reporting data utilizing provided tools. Summarize results of analysis and verifications to the Regulatory Reporting Manager. Interface with Capital headquarters Regulatory Reporting team members. Use interpretive and analytical skills to drive operational excellence in above areas and offer solutions to further enhance processes. Lead projects to remediate any data, process, or documentation gaps. Supervise and manage direct report(s).
Qualifications/Requirements:	Bachelor's Degree. Minimum 4 years controllership or financial planning and analysis experience. Experience with the closing and reporting process. Demonstrated leadership experience. Experience managing projects. Demonstrated oral and written communication skills and ability to work cross functionally. Proficient use of financial systems and Microsoft Office (eg. Excel, Word, PowerPoint). Eligibility Qualifications: Must submit your application for employment through gecareers.com to be considered (Internals via COS) Must be 18 years or older Must be willing to comply with pre-employment screening, including but not limited to drug testing, reference verification, and background check. Must be willing to work out of an office in Stamford, CT Must be willing to travel up to 10%, if applicable - MUST BE ABLE TO SATISFY THE REQUIREMENTS OF SECTION 19 OF THE FEDERAL DEPOSIT INSURANCE ACT. For U.S. employment opportunities, GE hires U.S. citizens, permanent residents, asylees, refugees, and temporary residents. Temporary residence does not include those with non-immigrant work authorization (F, J, H or L visas), such as students in practical training status. Exceptions to these requirements will be determined based on shortage of qualified candidates with a particular skill. GE will require proof of work authorization.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	Bachelor’s Degree in Finance or Accounting or Business Administration. Master's degree, Certified Public Accountant (CPA) or equivalent certification. Financial services industry experience. Demonstrated ability to solve complex issues related to data from multiple systems/environments. Demonstrated ability to manage multiple priorities. Experience with FED Regulatory reporting requirements.

Regulatory Affairs Manager-HC Job (Pasching, Austria)

Tue, 28 May 2013 00:00:00 GMT

Job Number:	1752610
Business:	GE Healthcare
Business Segment:	Healthcare Life Sciences
About Us:	GE Healthcare Life Sciences provides products and services used as tools for biopharmaceutical manufacturing, drug discovery and the latest in cellular technologies, thereby enabling our customers around the world to be more productive, effective and creative. Our motivation is to create better health for more people: through our five decades of supporting the biopharmaceutical industry and its research partners to become more productive, we are helping to reduce costs, increase access and improve quality in the healthcare system. We use our expertise and know-how in imaginative ways to work with our customers to provide what’s needed today and create products and solutions to enable the medical treatments of tomorrow. We add value to our customers by: Providing cutting-edge research tools that give deeper insights into cell function to enable disease diagnosis and the development of treatments. Enabling manufacturing productivity: we provide solutions for the entire bioprocess workflow (i.e. start-to-finish bioprocessing) helping our customers to develop and manufacture biopharmaceuticals more efficiently.Providing high quality support and maintenance services. We are the home of many famous brands, including Whatman, Amersham, Biacore, MicroCal, WAVE, Applied Precision and more.
Posted Position Title:	Regulatory Affairs Manager-HC
Career Level:	Experienced
Function:	Quality
Function Segment:	Regulatory Affairs
Location:	Austria
U.S. State, China or Canada Provinces:
City:	Pasching
Postal Code:	4061
Relocation Assistance:	No
Role Summary/Purpose:	The Regulatory Affairs Leader provides subject matter expertise and works with a team of regulatory affairs professionals to ensure GEHC establishes best practice within the assigned area of responsibility (regional regulatory submissions & reporting, technical standards, collection and dissemination of intelligence, influencing the global regulatory environment, etc).
Essential Responsibilities:	- Work closely with regulatory, engineering, marketing, legal, and other professionals across the company to develop & implement company-wide programs and processes for regulatory affairs compliance within areas of responsibility. - Identify regulatory trends and their implications for GE Healthcare; Develop & implement effective regulatory strategies to meet business objectives - Analyze & communicate proposed, new or changing requirements, & devise strategies for their implementation, ensuring business goals are met. - Scan the external environment and work with external associations to proactively adapt regulatory strategies and influence change within areas of responsibility. - Educate, train, & advise company professionals to ensure compliance with RA requirements. - Audit business units for compliance and consistency, and track/address trends observed that could lead to non-compliance, or risk to patient/user safety. - Collect, summarize & evaluate performance metrics to identify program weaknesses & drive improvements in procedures or oversight. - Support continuous improvement activities with regard to areas of responsibility. - Drive improvements to overall Quality Management System documentation to provide clear flow down of regulations in areas of responsibility.
Qualifications/Requirements:	1. Bachelor’s Degree & minimum of 5 years experience in the medical device or pharmaceutical industry or government / government relations; OR minimum of 10 years progressive regulatory affairs experience in medical device or pharmaceutical industry or government / government relations, including knowledge & experience applying global drug or device laws & regulations for product registration, adverse event reporting, & recalls. 2. Ability to prioritize, plan & evaluate deliverables to established strategic goals. 3. Demonstrated experience operating in a highly regulated environment; Proven application of analytical skills in a regulatory environment 4. Demonstrated knowledge & experience conducting scientific, regulatory, legal, or business research. 5. Excellent verbal and written communication and presentation skills with the ability to communicate business issues in German and in English in an easy to understand manner 6. Prior experience using spreadsheet and presentation software 7. Must be willing to travel up to 15% of time.
Additional Eligibility Qualifications:
Desired Characteristics:	1. Advanced degree in scientific, technology or legal disciplines. 2. Regulatory Affairs Certification (RAPS). 3. Demonstrated experience interfacing with regulatory agencies (e.g. FDA, MHLW, Health Canada, KFDA, etc.) and standards bodies such as AAMI, IEC, ISO, UL. 4. Knowledge of Quality Management Systems (QMS) 5. Ability to work across cultures/countries/sites 6. Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment. 7. Strong problem solving and negotiation skills 8. Ability to work well independently & in a team setting. 9. Demonstrated understanding of healthcare environment and knowledge of current competitive, commercial or political situations and their impact on GEHC regulatory strategies. 10. We offer a minimum of € 50.000/year, depending on experience and knowledge.

Regulatory Affairs Manager-HC Job (Waukesha, WI, United States)

Thu, 13 Jun 2013 05:00:00 GMT

Job Number:	1784017
Business:	GE Healthcare
Business Segment:	Healthcare Quality
About Us:
Posted Position Title:	Regulatory Affairs Manager-HC
Career Level:	Experienced
Function:	Quality
Function Segment:	Regulatory Affairs
Location:	United States
U.S. State, China or Canada Provinces:	Wisconsin
City:	Waukesha
Postal Code:	53188-1696
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. The Regulatory Affairs (RA) Manager – Product provides subject matter expertise and may directly or indirectly lead a team of experts to ensure that GEHC establishes and implements best practices in the area of Pre-Market regulatory submissions and new product development.
Essential Responsibilities:	- File and maintain regulatory deliverables, - Actively participate as team member on all assigned new product introductions. - Create regulatory compliance / project plan in collaboration with Region RA to ensure all requirements are met for country submissions; work with relevant personnel to ensure accurate, complete, timely input is provided for submissions. - Create and file submissions; communicate with authorities for these submissions. - If specific country testing is needed, work with Region RA, and arrange for test devices and support as needed. - Review and approve advertising and promotion material ensuring it is consistent with approved claims for regulated products. - Review changes in existing products to determine need for new/revised submissions or document reason for no submission - Communicate changes in existing products to Region RA for determination of the need for new/revised licenses or registrations; partner with Region RA for countries with license expiration requirements, to establish plan and deliverables for timely submission for renewal of license. - Identify any clinical data requirements for product licensing globally and insure the requirements are documented in the compliance plan; provide RA oversight to clinical studies. - May have GE Healthcare signature authority for submissions and other regulatory documents. - Support local regulatory authority / notified body inspections as required. - Identify regulatory trends and their implications for GE Healthcare; analyze & communicate proposed, new or changing requirements; communicate and track information for country. - As appropriate, recruit, mentor, coach & train direct and indirect reports on activities within areas of responsibility
Qualifications/Requirements:	1. Bachelor’s Degree & minimum of 7 years experience in the medical device or pharmaceutical industry or with medical product regulatory agencies; OR minimum of 11 years progressive regulatory affairs experience in medical device or pharmaceutical industry or with medical product regulatory agencies, including knowledge & experience applying drug or device laws & regulations. 2. Demonstrated experience operating in a highly regulated environment; proven application of analytical skills in a regulatory environment 3. Demonstrated knowledge of regulatory issues, and experience interfacing with local & international regulatory bodies, such as FDA, European competent authorities & notified bodies, Health Canada, SFDA, KFDA, MHLW, etc. 4. Demonstrated project management skills; ability to prioritize, plan, evaluate & execute deliverables for established tactical goals 5. Demonstrated ability to lead cross-functional, cross-business teams. 6. Ability to influence and make recommendations at multiple levels of the company 7. Excellent verbal and written communication and presentation skills with the ability to speak and write clearly and convincingly in English, tailoring communication methods to customer’s requirements. 8. Experience using spreadsheet and presentation software 9. Must be willing to travel up to 15% of time.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	1. Advanced degree in scientific, technology or legal disciplines. 2. Regulatory Affairs Certification (RAPS). 3. Knowledge of Quality Management Systems (QMS). 4. Experience working across cultures/countries/sites. 5. Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment. 6. Strong problem solving and negotiation skills. 7. Demonstrated ability to work well independently & in a team setting. 8. Demonstrated ability to drive change, challenge the status quo and champion new activities, stimulating others to change and manage implementation effectively. 9. Demonstrated understanding of healthcare environment and knowledge of current competitive, commercial or political situations and their impact on GEHC regulatory strategies.

Regulatory Affairs Manager - Product Job (Waukesha, WI, United States)

Thu, 13 Jun 2013 05:00:00 GMT

Job Number:	1784042
Business:	GE Healthcare
Business Segment:	Healthcare Quality
About Us:
Posted Position Title:	Regulatory Affairs Manager - Product
Career Level:	Experienced
Function:	Quality
Function Segment:	Regulatory Affairs
Location:	United States
U.S. State, China or Canada Provinces:	Wisconsin
City:	Waukesha
Postal Code:	53188-1696
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. The Regulatory Affairs (RA) Manager – Product provides subject matter expertise and may directly or indirectly lead a team of experts to ensure that GEHC establishes and implements best practices in the area of Pre-Market regulatory submissions and new product development.
Essential Responsibilities:	- File and maintain regulatory deliverables, - Actively participate as team member on all assigned new product introductions. - Create regulatory compliance / project plan in collaboration with Region RA to ensure all requirements are met for country submissions; work with relevant personnel to ensure accurate, complete, timely input is provided for submissions. - Create and file submissions; communicate with authorities for these submissions. - If specific country testing is needed, work with Region RA, and arrange for test devices and support as needed. - Review and approve advertising and promotion material ensuring it is consistent with approved claims for regulated products. - Review changes in existing products to determine need for new/revised submissions or document reason for no submission - Communicate changes in existing products to Region RA for determination of the need for new/revised licenses or registrations; partner with Region RA for countries with license expiration requirements, to establish plan and deliverables for timely submission for renewal of license. - Identify any clinical data requirements for product licensing globally and insure the requirements are documented in the compliance plan; provide RA oversight to clinical studies. - May have GE Healthcare signature authority for submissions and other regulatory documents. - Support local regulatory authority / notified body inspections as required. - Identify regulatory trends and their implications for GE Healthcare; analyze & communicate proposed, new or changing requirements; communicate and track information for country. - As appropriate, recruit, mentor, coach & train direct and indirect reports on activities within areas of responsibility
Qualifications/Requirements:	1. Bachelor’s Degree & minimum of 7 years experience in the medical device or pharmaceutical industry or with medical product regulatory agencies; OR minimum of 11 years progressive regulatory affairs experience in medical device or pharmaceutical industry or with medical product regulatory agencies, including knowledge & experience applying drug or device laws & regulations. 2. Demonstrated experience operating in a highly regulated environment; proven application of analytical skills in a regulatory environment 3. Demonstrated knowledge of regulatory issues, and experience interfacing with local & international regulatory bodies, such as FDA, European competent authorities & notified bodies, Health Canada, SFDA, KFDA, MHLW, etc. 4. Demonstrated project management skills; ability to prioritize, plan, evaluate & execute deliverables for established tactical goals 5. Demonstrated ability to lead cross-functional, cross-business teams. 6. Ability to influence and make recommendations at multiple levels of the company 7. Excellent verbal and written communication and presentation skills with the ability to speak and write clearly and convincingly in English, tailoring communication methods to customer’s requirements. 8. Experience using spreadsheet and presentation software 9. Must be willing to travel up to 15% of time.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	1. Advanced degree in scientific, technology or legal disciplines. 2. Regulatory Affairs Certification (RAPS). 3. Knowledge of Quality Management Systems (QMS). 4. Experience working across cultures/countries/sites. 5. Demonstrated experience prioritizing conflicting demands from multiple business entities in an extremely fast paced environment. 6. Strong problem solving and negotiation skills. 7. Demonstrated ability to work well independently & in a team setting. 8. Demonstrated ability to drive change, challenge the status quo and champion new activities, stimulating others to change and manage implementation effectively. 9. Demonstrated understanding of healthcare environment and knowledge of current competitive, commercial or political situations and their impact on GEHC regulatory strategies.

Regulatory Reporting Manager Job (Chicago, IL, United States)

Sun, 09 Jun 2013 07:59:00 GMT

Job Number:	1719052
Business:	GE Capital
Business Segment:	Capital - Staff
About Us:	Headquartered in Norwalk, Connecticut, GE Capital offers consumers and businesses around the globe an array of financial products and services. For over 1 million businesses, we provide real estate, equipment and inventory financing; fleet services; working capital; and funds for corporate acquisitions, refinancings and restructurings. For our 130 million consumer customers, we offer credit cards, retail sales finance programs, home, car and personal loans and credit insurance.
Posted Position Title:	Regulatory Reporting Manager
Career Level:	Experienced
Function:	Finance
Function Segment:	Controllership
Location:	United States
U.S. State, China or Canada Provinces:	Illinois
City:	Chicago
Postal Code:	60661-3671
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. Execute on the Regulatory Reporting strategy within the Capital HQ reg reporting team and provide analysis, reporting and recommendations to management. Drive operational ownership to ensure consistency and compliance. Summarize analysis and communicate results to the Regulatory Reporting Manager. Reports to the Regulatory Reporting Manager and manages direct reports.
Essential Responsibilities:	Own collection of regulatory reporting data within focused area of Regulatory Reporting. Perform detailed validation work on the data collected by the team and address unexpected results or inconsistencies in data. Verify and perform the consolidation of Regulatory Reporting data utilizing provided tools. Summarize results of analysis and verifications to the Regulatory Reporting Manager. Occasionally interface with headquarters Regulatory Reporting leadership. Use interpretive and analytical skills to drive operational excellence in above areas and offer solutions to further enhance processes. Offer solutions to further enhance processes. Supervise and manage direct report(s).
Qualifications/Requirements:	Basic Qualifications: Bachelor's Degree. Minimum 4 years controllership or financial planning and analysis experience. Experience with the closing and reporting process. Demonstrated leadership experience. Experience managing projects. Demonstrated oral and written communication skills and ability to work cross functionally. Proficient use of financial systems and Microsoft Office (eg. Excel, Word, PowerPoint). This role is eligible for a Referral bonus award that is double the current eligibility amount. All other guidelines under the WDYK program are applicable. Eligibility Qualifications: Must submit your application for employment through gecareers.com to be considered (Internals via COS) Must be able to satisfy the requirements of Section 19 of the Federal Deposit Insurance Act. Must be willing to comply with pre-employment screening, including but not limited to drug testing, reference verification, and background check. Must be willing to work out of an office in Chicago, IL Must be willing to travel up to 10% of the time
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	Bachelor’s Degree in Finance or Accounting or Business Administration. Master's degree, Certified Public Accountant (CPA) or equivalent certification. Financial services industry experience. Demonstrated ability to solve complex issues related to data from multiple systems/environments. Financial Management Program (FMP) grad or Corporate Audit Staff (CAS) grad. Demonstrated ability to manage multiple priorities.

Regulatory Reporting Lead Analyst Job (Stamford, CT, United States)

Wed, 12 Jun 2013 07:59:00 GMT

Job Number:	1761396
Business:	GE Capital
Business Segment:	Capital - Treasury
About Us:	GE Treasury team is responsible for global funding, cash & foreign exchange management, and other treasury services for all of GE's worldwide operations. Almost all of GE's debt is issued through GE Capital to support its financial services businesses. We fund ourselves through the issuance of long term debt, commercial paper, CDs & bank deposits, and other debt products as well. imagination at work? GE is an Equal Opportunity Employer. GE offers a competitive salary, outstanding benefits & the professional advantages of an environment that supports your development & recognizes your achievements. GE offers an inclusive environment where employees have the opportunity to succeed and diversity is embraced as a competitive advantage in the marketplace. The passion that our people bring to their work extends to their private worlds, and GE encourages a healthy balance between the two. GE values education and is dedicate to providing the tools and training for your professional development.
Posted Position Title:	Regulatory Reporting Lead Analyst
Career Level:	Experienced
Function:	Finance
Function Segment:	Controllership
Location:	United States
U.S. State, China or Canada Provinces:	Connecticut
City:	Stamford
Postal Code:	06905-3417
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. Provide Regulatory analysis and reporting support to management including collecting, reconciling and validating data for ~$70 B of investments and ~$40 B of short term funding. In addition, individual will be directly responsible for legal entity reporting associated with several guaranteed investment contract businesses
Essential Responsibilities:	Role Summary/Purpose Continued: Within this role they will be 1. Engaging with and providing analysis and support to Regulatory team leadership, 2. Identifying and executing process improvements and working independently on tasks. 3. Evaluating complex situations using multiple sources of data and analytical skills. Essential Functions/Responsibilities: Timely collection of Regulatory Reporting within area of focus Preparation of work papers to support regulatory reporting Perform detailed validation work on the data collected and address or escalate further any unexpected results or inconsistencies in data. Verify prepare Regulatory Reporting utilizing provided tools for assigned areas Communicate results to manager and provide visibility into details of underlying work. Drive operational excellence in above areas and offer solutions to further enhance processes. Drive the remediation of current data / process gaps Identify and implement simplification and automation opportunities Apply solid knowledge of Finance concepts and principles to Regulatory Reporting. May be responsible for providing direction to other team members Perform analytical review including variance analysis for purposes of team and management assessment of accuracy of regulatory filings. Assist with other reporting / operational controllership tasks
Qualifications/Requirements:	Bachelor's degree Minimum 2 years Controllership or Financial Planning and Analysis Experience with the closing and reporting process Proficient use of financial systems and analysis tools to include Microsoft Excel Eligibility Qualifications: Must submit your application for employment through gecareers.com to be considered (Internals via COS) Must be 18 years or older Must be willing to comply with pre-employment screening, including but not limited to drug testing, reference verification, and background check. Must be willing to work out of an office in Stamford, CT Must be willing to travel up to 10%, if applicable - MUST BE ABLE TO SATISFY THE REQUIREMENTS OF SECTION 19 OF THE FEDERAL DEPOSIT INSURANCE ACT. For U.S. employment opportunities, GE hires U.S. citizens, permanent residents, asylees, refugees, and temporary residents. Temporary residence does not include those with non-immigrant work authorization (F, J, H or L visas), such as students in practical training status. Exceptions to these requirements will be determined based on shortage of qualified candidates with a particular skill. GE will require proof of work authorization.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	Bachelor's Degree in Accounting, Finance or Business Administration. CPA, Master’s degree, or equivalent certification. Experience with Regulatory Reporting. Financial Management Program / Corporate Audit Staff graduate. Demonstrated oral and written communication skills and ability to work cross functionally at all levels. Experience working in complex corporate environments (i.e., multiple systems, multiple products / businesses, multiple reporting environments, multiple GAAPs, multiple regulatory, legal or country jurisdictions. Demonstrated ability to manage multiple priorities

Regulatory Reporting Lead Analyst Job (Stamford, CT, United States)

Fri, 24 May 2013 05:00:00 GMT

Job Number:	1770037
Business:	GE Capital
Business Segment:	Capital - Treasury
About Us:	GE Treasury team is responsible for global funding, cash & foreign exchange management, and other treasury services for all of GE's worldwide operations. Almost all of GE's debt is issued through GE Capital to support its financial services businesses. We fund ourselves through the issuance of long term debt, commercial paper, CDs & bank deposits, and other debt products as well. imagination at work? GE is an Equal Opportunity Employer. GE offers a competitive salary, outstanding benefits & the professional advantages of an environment that supports your development & recognizes your achievements. GE offers an inclusive environment where employees have the opportunity to succeed and diversity is embraced as a competitive advantage in the marketplace. The passion that our people bring to their work extends to their private worlds, and GE encourages a healthy balance between the two. GE values education and is dedicate to providing the tools and training for your professional development.
Posted Position Title:	Regulatory Reporting Lead Analyst
Career Level:	Experienced
Function:	Finance
Function Segment:	Controllership
Location:	United States
U.S. State, China or Canada Provinces:	Connecticut
City:	Stamford
Postal Code:	06905-3417
Relocation Assistance:	Yes
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. The GE Treasury Funding Structures Analyst role is a critical part of a global controllership organization headquartered in Stamford with operations throughout North America, Europe and Asia. The role will support efforts to enhance controllership, compliance, reporting and financial management for the US legal entities
Essential Responsibilities:	Role Summary/Purpose Continued: Key part of the role will be to support the US Legal Entity Controller on multiple tasks including Regulatory reporting, analysis and supporting the Regulatory Leadership team with collecting, reconciling and validating data. Essential Functions/Responsibilities: Timely collection of Regulatory Reporting within area of focus Perform detailed validation work on the data collected and address or escalate further any unexpected results or inconsistencies in data. Verify and perform the consolidation of Regulatory Reporting data utilizing provided tools. Communicate results to manager and provide visibility into details of underlying work. Drive operational excellence in above areas and offer solutions to further enhance processes. Apply solid knowledge of Finance concepts and principles to Regulatory Reporting. Provide direction to other team members and liaise with group of professionals from an external firm. Perform analytical review including variance analysis for purposes of team and management assessment of accuracy of regulatory filings. Liaise with the governance teams to ensure compliance for the US Legal Entities. Develop more robust reporting and analytics supporting regulatory and tax requirements. Analyze foreign exchange exposure and document hedging strategies Controllership for intergroup loans and liase with international affiliates Ensure Sarbanes-Oxley compliance by documenting and updating operational procedures including testing in line with GE approved criteria. Working with a wider team on accomplishing team/organizational goals. Provide support on various strategic projects.
Qualifications/Requirements:	Bachelor's Degree Minimum 2 years Controllership or Financial Planning and Analysis Experience with the closing and reporting process Proficient use of financial systems and analysis tools to include Microsoft Excel, Business Objects, and Access Eligibility Qualifications: Must submit your application for employment through gecareers.com to be considered (Internals via COS) Must be 18 years or older Must be willing to comply with pre-employment screening, including but not limited to drug testing, reference verification, and background check. Must be willing to work out of an office in Stamford, CT Must be willing to travel up to 10%, if applicable - MUST BE ABLE TO SATISFY THE REQUIREMENTS OF SECTION 19 OF THE FEDERAL DEPOSIT INSURANCE ACT. For U.S. employment opportunities, GE hires U.S. citizens, permanent residents, asylees, refugees, and temporary residents. Temporary residence does not include those with non-immigrant work authorization (F, J, H or L visas), such as students in practical training status. Exceptions to these requirements will be determined based on shortage of qualified candidates with a particular skill. GE will require proof of work authorization.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	Bachelor's Degree in Accounting, Finance or Business Administration. CPA, Master’s degree, or equivalent certification. Strong GE Accounting knowledge and practical experience in areas of derivative/swap, inter/intra company and GE investment/equity accounting. Experience with Regulatory Reporting. Financial Management Program / Corporate Audit Staff graduate. Demonstrated oral and written communication skills and ability to work cross functionally at all levels. Strong analytical skills to clearly link financial results to operational performance drivers, generate alternatives and drive positive change Ability to prioritize/multitask and work effectively under time constraints and fast paced environment Experience working in complex corporate environments (i.e., multiple systems, multiple products / businesses, multiple reporting environments, multiple GAAPs, multiple regulatory, legal or country jurisdictions. Uncompromised levels of integrity, ethical and personal values in decisions, communications and actions

Risk Analyst – Regulatory Reporting Job (Norwalk, CT, United States)

Fri, 14 Jun 2013 07:59:00 GMT

Job Number:	1741267
Business:	GE Capital
Business Segment:	Capital - Staff
About Us:	Headquartered in Norwalk, Connecticut, GE Capital offers consumers and businesses around the globe an array of financial products and services. For over 1 million businesses, we provide real estate, equipment and inventory financing; fleet services; working capital; and funds for corporate acquisitions, refinancing and restructurings. For our 130 million consumer customers, we offer credit cards, retail sales finance programs, home, car and personal loans and credit insurance.
Posted Position Title:	Risk Analyst – Regulatory Reporting
Career Level:	Experienced
Function:	Risk Management
Function Segment:	Risk Analytics
Location:	United States
U.S. State, China or Canada Provinces:	Connecticut
City:	Norwalk
Postal Code:	06851-1168
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. Support timely delivery of accurate & complete risk data from GECC’s centralized data warehouse to meet regulatory reporting requirements. Assist in risk reporting process improvement and simplification projects.
Essential Responsibilities:	Own processes that create quarterly/annual risk data reporting from GECC’s centralized data warehouse for regulatory reporting and monitor data accuracy and completeness to ensure the quality of the reports. Responsible for Risk Data collection for regulatory reporting purposes across GECC’s global portfolios with a focus on consistency and accuracy. Partner with regulatory reporting data owners to create / update data definitions & quality rules for data elements mandated by regulatory reporting requirements. Work effectively cross functions and establish strong relationships with key functional stakeholders (Risk, Finance, IT and Business Units). Perform data analysis to identify strategies for risk data sourcing and leverage other GECC systems for centralized risk reporting. Become subject matter expert on risk reporting tools & systems and become familiar with key risk metrics across multiple GECC business products. Identify risk system development requirements, outline desired state, perform gap analysis and develop project plans to remediate gaps and achieve the desired results. Support system build-out, testing and use technology to identify, track & improve data quality; Drive system automation and simplification for regulatory risk reporting processes.
Qualifications/Requirements:	Basic Qualifications: Bachelor’s Degree, preferred in Accounting, Finance or Business fields 5+ years of work experience in an accounting, finance, risk or business reporting role. Experience with software applications including Excel, Word, Power Point. Eligibility Qualifications: Must submit your application for employment through gecareers.com to be considered (Internals via COS). Must be able to satisfy the requirements of Section 19 of the Federal Deposit Insurance Act. Must be willing to comply with pre-employment screening, including but not limited to drug testing, reference verification, and background check. Must be willing to work out of an office in Norwalk, CT. Must be willing to travel up to 5% of the time. Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	Highly motivated and must be able to work under tight deadlines with multiple priorities. Demonstrated experience analyzing risk/business data with the ability to evaluate large amounts of information to address critical areas of focus. Experience in regulatory reporting and knowledge of FRY9C, FR14Q/A reporting. Knowledge of GECC businesses and products. Strong facilitation and communications skills. Strong project management skills. Strong Power Point and Excel skills. Experience in risk or financial reporting.

Chief Compliance Office Job (Seoul, Korea, Republic of)

Mon, 10 Jun 2013 07:59:00 GMT

Job Number:	1759581
Business:	GE Capital
Business Segment:	Capital - Asia Pacific
About Us:
Posted Position Title:	Chief Compliance Office
Career Level:	Experienced
Function:	Legal
Function Segment:	Compliance and Regulatory
Location:	Korea, Republic of
U.S. State, China or Canada Provinces:
City:	Seoul
Postal Code:	150-706
Relocation Assistance:	No
Role Summary/Purpose:	- Responsible for developing and implementing GE Capital’s overall regulatory/compliance strategy and program in Korea including working with business and compliance leaders at GE Capital Asia Pacific & GE GGO Korea to protect and promote the Company’s good name
Essential Responsibilities:	- Responsible for developing and implementing GE Capital’s overall regulatory/compliance strategy and program in Korea including working with business and compliance leaders at GE Capital Asia Pacific & GE GGO Korea to protect and promote the Company’s good name - Review of regulatory/ compliance matters for key operation of GE Capital’s Korea JVs, Hyundai Capital Services (HCS), Hyundai Card Co (HCC), Hi Network (HIN), and HCS’s invested companies located in Korea & foreign locations (collectively, “JVs”) in consultation with JVs compliance teams and other functions - Support day to day operation of GE Capital business & investments in Korea such as ABS vehicle SPCs - Provide regulatory/compliance expertise to the business leaders on transactions, regulatory matters, compliance issues, new product introductions, BD activities and other commercial matters - Assist the business leader and assist JVs general counsel and compliance leaders to manage and operate the compliance function - Ensure that a sound regular reporting rhythm is in place both locally with each business segment and externally to GE Capital Asia Pacific Region Regulatory/Compliance team and GE GGO Korea Compliance team (where appropriate): Prepare Session D and other GE regulatory/compliance reporting and updates - Partner with Asia Pacific Region legal counsels on key regulatory matters and support to structure key legal program and execution - Ensure rigorous program to identify, manage and abate key risks, including: - Improper payments – especially drive rigorous process on the JVs’ provision of gifts & entertainment. - Collect and report on information about regulatory risk areas: e.g. early warning system. metrics & testing - Assist the business to manage and build relationships/networks with key external parties, including customers, suppliers, government and regulators - Assist the JVs in preparing and holding Board of Directors meeting and Compliance Review Board - Proactively work with the JVs in preparing annual compliance plan and tracking progress of the plan - Periodically assess the effectiveness of the regulatory/compliance program: e.g. conduct his/her own risk assessment in regulatory/compliance perspectives
Qualifications/Requirements:	- Strong knowledge of Korean regulatory environment of consumer finance area - Strong understanding of consumer finance products, procedures and all applicable Korean regulatory/compliance issues - Knowledge of global compliance strategies and tools - At least 7 – 10 years of consumer finance related regulatory/compliance experience preferably in a reputable financial institutions or law firms - Experience in a senior regulatory/compliance role - Korea legal training/knowledge preferred, U.S. lawyer’s license or equivalent license is helpful - Strong commercial acumen - Fluency in both Korean and English
Additional Eligibility Qualifications:
Desired Characteristics:	- Outstanding influencing & communication skills, with the ability to influence & communicate effectively at different levels - Proven ability to develop relationships at various levels within the organization - Excellent leadership skills, ability to lead and motivate both direct team as well as the broader organization on key legal/compliance issues

Executive Counsel - Regulatory Affairs Job (Norwalk, CT, United States)

Sat, 01 Jun 2013 05:00:00 GMT

Job Number:	1774924
Business:	GE Capital
Business Segment:	Capital - Staff
About Us:	Headquartered in Norwalk, Connecticut, GE Capital offers consumers and businesses around the globe an array of financial products and services. For over 1 million businesses, we provide real estate, equipment and inventory financing; fleet services; working capital; and funds for corporate acquisitions, refinancings and restructurings. For our 130 million consumer customers, we offer credit cards, retail sales finance programs, home, car and personal loans and credit insurance.
Posted Position Title:	Executive Counsel - Regulatory Affairs
Career Level:	Experienced
Function:	Legal
Function Segment:	Regulatory
Location:	United States
U.S. State, China or Canada Provinces:	Connecticut
City:	Norwalk
Postal Code:	06851-1168
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. This position provides Bank Regulatory advice and counsel company-wide as part of small team of regulatory lawyers reporting to Global Lead Regulatory Counsel. Position advises all functions and business units on all aspects of US bank regulatory law. Position includes staying current on evolving financial regulatory reform, laws and regulation, implications for GE Capital and advising Legal and business leadership on impact or risks.
Essential Responsibilities:	Provide US bank regulatory law interpretation, counsel and strategy. Responsibilities to include: Researching and monitoring developments in relevant pending legislation and proposed regulations, and using expertise to determine impact on company and business units. Working with Government Relations team and relevant trade associations to formulate action plans for responding. Provide legal counsel and training to assigned business unit(s) on US bank law and regulation and implications to transactions, new product development, merger, acquisition and disposition proposals and other general business activity. Develop operating procedures and processes with respect thereto. Coordinate with non-US counsel regarding non-US Banking regulations that may impact the parent company. Partner with non-US counsel and business management to resolve issues. Develop working knowledge of global regulatory and supervisory requirements that may impact the consolidated organization. Partner with supervision teams to formulate response action plan and provide support in drafting responses to various types of inquiries from examiners/supervisors or regulatory organizations (e.g., Federal Reserve, FDIC, OCC). Support compliance teams through legal advice and promoting awareness and consistency of compliance programs across organization. Execute regulatory filings as required (e.g., dividends, acquisitions, movement of assets, etc.). Provide advice on legal governance including responsibilities of officers and directors. Represent the company before regulatory agencies.
Qualifications/Requirements:	Basic Qualifications: Bachelor’s Degree. J.D. with 10+ years of relevant law firm, in-house and /or banking agency regulatory experience. Must be a member in good standing of one or more state bars or the D.C. bar and where required, in house counsel registration or admission to the local state bar. Experience working with and knowledge of banking laws and regulations. Experience working with financial services products, for example leasing, corporate lending, consumer products, etc. Experience analyzing complex banking regulations and advising stakeholders on implications. Experience in advising banks and/or their holding companies or other large financial institutions regarding federal banking laws and related regulations, including the National Bank Act, the Federal Reserve Act, the Federal Deposit Insurance Act and the Bank Holding Company Act. Experience leading large scale legal implementation/change projects. Eligibility Qualifications: Must submit application for employment through COS (internal candidates) or www.gecareers.com (external candidates) to be considered for this position. Legal authorization to work in the U.S. is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening. Must be willing to comply with pre-employment screening, including but not limited to, drug testing, reference verification and background check.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	Proven ability to convey complex matters clearly and concisely. Ability to respond creatively and practically to complex transactions and issues, particularly in applying bank regulatory concepts in a nontraditional environment. Must have proven ability to grasp complex structure and assess the implications of regulatory and supervisory requirements on that structure. Excellent advocacy and influencing skills. Excellent networking and relationship management skills. Experience working in a large financial institution preferred. Outstanding verbal and written communication skills. Ability to quickly identify and prioritize issues and devise solutions. Ability to multi-task and demonstrate a sense of urgency. Successful experience working in a highly matrixed environment. Abilitiy to work with minmal supervision.

Quality Coordinator-HC Job (Waukesha, WI, United States)

Thu, 13 Jun 2013 05:00:00 GMT

Job Number:	1784075
Business:	GE Healthcare
Business Segment:	Healthcare Quality
About Us:
Posted Position Title:	Quality Coordinator-HC
Career Level:	Experienced
Function:	Quality
Function Segment:	Administration and Support
Location:	United States
U.S. State, China or Canada Provinces:	Wisconsin
City:	Waukesha
Postal Code:	53188-1696
Relocation Assistance:	No
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. To assist the GE Healthcare regulatory team in gaining approvals and maintaining the regulatory compliance of the business, the role will primarily be involved in (but not limited to) the collection, organization, submission and distribution of information related to obtaining Certificate to Foreign Governments (CFG). The role will also encompass general administrative support to the HCS regulatory and quality team to facilitate maintaining and monitoring a compliant business
Essential Responsibilities:	- Ensuring the accuracy and optimal presentation of information to regulatory authorities and internal presentations, and that they meet current best practice standards. - Liaising with relevant personnel within GEHC to ensure appropriate, timely input is provided to regulatory authorities and that all legally mandated deadlines for submission are met. - Providing administrative support to the quality and regulatory processes, (i.e. arranging payments to regulatory bodies, collecting and reporting metrics, supporting presentations). - Acting as regulatory functional expert in computer based support system in order to input, track and follow-up on information in the system.
Qualifications/Requirements:	1. Associate degree or high school diploma/GED plus 4 years working experience in Quality Engineering or Quality Assurance Management. 2. IT proficiency and experience in working with electronic databases. 3. Experience working with Microsoft Office applications (Word, Excel, Powerpoint). 4. Highly organized and attentive to detail. 5. Ability to handle multiple priorities and multi-task in an environment of changing priorities and deadlines. 6. Flexible attitude to the work environment with the ability to flex hours based on business need. 7. Demonstrates good interpersonal skills required to build relationships with internal departments, other GE Healthcare offices around the world and externally with relevant staff at regulatory authorities. 8. A self-starter able to work on own initiative and well in a team environment. 9. Should have a developing knowledge of the regulatory requirements relevant to the projects with which they are involved. 10. Will be expected to work on assigned projects to an agreed plan, under the guidance of a regulatory professional. 11. Good focus on customer needs with follow up on commitments and requests.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	1. Bachelors degree 2. One or more years relevant experience in the healthcare industry

Regulatory Reporting Manager Job (Stamford, CT, United States)

Wed, 22 May 2013 05:00:00 GMT

Job Number:	1766660
Business:	GE Capital
Business Segment:	Capital - Treasury
About Us:	GE Treasury team is responsible for global funding, cash & foreign exchange management, and other treasury services for all of GE's worldwide operations. Almost all of GE's debt is issued through GE Capital to support its financial services businesses. We fund ourselves through the issuance of long term debt, commercial paper, CDs & bank deposits, and other debt products as well. imagination at work? GE is an Equal Opportunity Employer. GE offers a competitive salary, outstanding benefits & the professional advantages of an environment that supports your development & recognizes your achievements. GE offers an inclusive environment where employees have the opportunity to succeed and diversity is embraced as a competitive advantage in the marketplace. The passion that our people bring to their work extends to their private worlds, and GE encourages a healthy balance between the two. GE values education and is dedicate to providing the tools and training for your professional development.
Posted Position Title:	Regulatory Reporting Manager
Career Level:	Experienced
Function:	Finance
Function Segment:	Controllership
Location:	United States
U.S. State, China or Canada Provinces:	Connecticut
City:	Stamford
Postal Code:	06905-3417
Relocation Assistance:	Yes
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. Manager Regulatory Reporting role is a critical part of a global controllership organization headquartered in Stamford with operations throughout North America, Europe and Asia. The role execute on the Regulatory Reporting strategy within the Functional Currency Simplification team, by providing FAS 52 analysis and support the efforts enhance controllership, compliance and reporting for various legal entities within FX Controllership area of GE Treasury.
Essential Responsibilities:	1. Collect and consolidate Regulatory Reporting within area of focus 2. Apply solid knowledge of Finance concepts and principles to Regulatory Reporting. 3. Perform detailed validation work on the data collected by the team and address unexpected results or inconsistencies in data. 4. Should be able to critically analyze data at legal entity level and able to explain the results in the context of the overall funding and hedging strategy. reporting capabilities to streamline data gathering. 5. Communicate results to management and provide visibility into details of underlying work. 6. Ensure the financial results at Legal entity level are consistent with GE Capital's hedging and funding strategies. 7. Ensure Sarbanes-Oxley compliance by documenting and updating operational procedures including testing in line with GE approved criteria. 8. Provide direction to other team members and liaise with group of professionals from an external firm. Working with a wider team on accomplishing team/organizational goals. 9. Develop more robust reporting and analytics supporting regulatory and tax requirements. 10. Provide support on various strategic projects. 11. Occasionally interface with headquarters Regulatory Reporting leadership Use interpretive and analytical skills to drive operational excellence in above areas and offer solutions to further enhance
Qualifications/Requirements:	Bachelor's Degree. Minimum 4 years controllership or financial planning and analysis experience. Experience with the closing and reporting process. Demonstrated leadership experience. Experience managing projects. Demonstrated oral and written communication skills and ability to work cross functionally. Proficient use of financial systems and Microsoft Office (eg. Excel, Word, PowerPoint). Eligibility Qualifications: Must submit your application for employment through gecareers.com to be considered (Internals via COS) Must be 18 years or older Must be willing to comply with pre-employment screening, including but not limited to drug testing, reference verification, and background check. Must be willing to work out of an office in Stamford, CT Must be willing to travel up to 10%, if applicable - MUST BE ABLE TO SATISFY THE REQUIREMENTS OF SECTION 19 OF THE FEDERAL DEPOSIT INSURANCE ACT. For U.S. employment opportunities, GE hires U.S. citizens, permanent residents, asylees, refugees, and temporary residents. Temporary residence does not include those with non-immigrant work authorization (F, J, H or L visas), such as students in practical training status. Exceptions to these requirements will be determined based on shortage of qualified candidates with a particular skill. GE will require proof of work authorization.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	- Minimum 4 years of experience related to FX derivative instruments, including understanding of use in risk management, related hedge accounting strategies and methods, leading practices and associated system based solutions - Experience in FX accounting and derivative knowledge preferred - Bachelor’s Degree in finance, accounting or related field - Certified Public Accountant (CPA) or equivalent certification - Financial services industry experience - Public Accounting experience - Financial Management Program (FMP) grad or Corporate Audit Staff (CAS) grad - Minimum 4 years of experience in accounting preferably within a corporate treasury organization or financial services business - Experience with Regulatory Reporting - Strong interpersonal & communication skills, can-do-attitude / self-starter - Experience in a matrix and global environment preferred - Prior experience with treasury management and hedge accounting - Demonstrated ability to manage multiple priorities.

Regulatory Reporting Lead Analyst Job (Alpharetta, GA, United States)

Fri, 24 May 2013 05:00:00 GMT

Job Number:	1769050
Business:	GE Capital
Business Segment:	Capital - Retail Finance
About Us:	GE Capital’s Retail Finance business is among the country’s most successful retail lenders, with more than 75 years of experience in consumer financing. The business, which originates loans as a unit of GE Capital Retail Bank, provides credit card programs to retailers and consumers in the United States and Canada. We build better businesses through customized private label and bankcard credit programs to national and regional retailers in the U.S., as well as private label credit card programs, promotional and installment lending, bankcards and financial services for consumers through dealers; national, regional and independent retailers; contractors; manufacturers; healthcare practices; and service providers across nearly 20 industries. At GE Capital Retail Finance, we are committed to being an employer of choice, offering competitive rewards, compensation and benefits. When you join our team, you become part of a stimulating work environment with vast opportunities to sharpen your skills and embrace new leadership challenges. GE provides tools to enable you to build your development and chart your own career path. As a member of the GE Capital Retail Finance team, you'll join over 8,000 colleagues who are passionate about their work! The United States has regulations that govern the hiring of current or former U.S. Government employees. If you currently work for (or have in the past) the U.S. Government (in any capacity), you may have certain responsibilities under these regulations and certain restrictions may apply to your potential employment with GE. Therefore, if GE regarding a position of employment contacts you, and you have worked for the U.S. Government at any time, please immediately inform the GE representative of this fact.
Posted Position Title:	Regulatory Reporting Lead Analyst
Career Level:	Experienced
Function:	Finance
Function Segment:	Controllership
Location:	United States
U.S. State, China or Canada Provinces:	Georgia
City:	Alpharetta
Postal Code:	30005-8378
Relocation Assistance:	Yes
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. Own the regulatory reporting readiness and subsequent preparation of the business submissions for FR Y-11 & FR 2314 for Capital HQ consolidation. Analyze reporting requirements, data availability, coordinate with Risk and Finance functions to train and obtain data to prepare submissions. Support the implementation of Capital HQ initiatives related to regulatory reporting and legal entity purity. Identify process improvements and work independently on tasks.
Essential Responsibilities:	Prepare quarterly and annual FR Y-11/ FR 2314 reports as required Cross functional coordination & maintenance of supporting documentation. Maintaining/enhancing control environment. Coordination of review process of call report prior to submission. Responding to regulator requests. Driving automated initiatives at business to ensure efficient and timely reporting. Coordinating closely with SEC/ USGAAP/ FR Y-9C reporting team to ensure consistency. Drive/Support Regulatory reporting projects and initiatives rolled out by Capital HQ Controllership and Regulatory team. Timely collection of Regulatory Reporting within area of focus. Preparation of work papers to support regulatory reporting. Perform detailed validation work on the data collected and address or escalate further any unexpected results or inconsistencies in data. Drive the remediation of current data / process gaps. Identify and implement simplification and automation opportunities. Apply solid knowledge of Finance concepts and principles to Regulatory Reporting. Verify and perform the consolidation of Regulatory Reporting data utilizing provided tools. Communicate results to manager and provide visibility into details of underlying work. Drive operational excellence in above areas and offer solutions to further enhance processes. May be responsible for providing direction to other team members.
Qualifications/Requirements:	Bachelor's Degree. Minimum 2 years controllership/accounting experience including month end close and quarterly reporting. 2 years of SEC reporting experience. Controllership / Finance experience including the closing and reporting process. Proficient use of financial systems and Microsoft Office (e.g.. Excel, Word, PowerPoint). YOU MUST BE ABLE TO SATISFY THE REQUIREMENTS OF SECTION 19 OF THE FEDERAL DEPOSIT INSURANCE ACT Eligibility Requirements : All applications for employment must be submitted through either http://www.gecareers.com or the Career Opportunity System (COS) to be considered You must be 18 years or older You must have a high school diploma or equivalent You must be willing to take a drug test, submit to a background investigation and submit fingerprints as part of the selection process If currently a GE employee, you must have been in your current position for at least 6 months (AP) or 24 months (PB or greater), have at least a "consistently meets expectations" performance rating and have the approval of your manager to post (or the approval of your manager and HR to apply if you don't meet the time-in-job or performance requirement) For U.S. employment opportunities, GE hires U.S. citizens, permanent residents, asylees, refugees, and temporary residents. Temporary residence does not include those with non-immigrant work authorization (F, J, H or L visas), such as students in practical training status. Exceptions to these requirements will be determined based on shortage of qualified candidates with a particular skill. GE will require proof of work authorization. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	Experience in GAAP and regulatory / SEC reporting in a corporate environment or financial institution industry. GAAP and SEC reporting within the financial services or credit card industry. US GAAP experience. Experience with banking products. Experience with regulatory reporting such as - FR Y-9, FR Y-11 and/or 2314 reporting for example. Proficient use of financial systems and analytical tools including Hyperion databases and Oracle Discoverer. Bachelor’s Degree in Finance or Accounting or Business Administration. Master's degree, Certified Public Accountant (CPA) or equivalent certification. Demonstrated ability to solve complex issues related to data from multiple systems/environments. Financial Management Program (FMP) grad or Corporate Audit Staff (CAS) grad. Ability to lead multiple projects/priorities and drive each to completion. Excellent analytical and problem solving skills. Excellent organizational and follow-up skills. Ability to influence and motivate people. Excellent communication skills – both oral and written.

Regulatory Reporting Analyst Job (Norwalk, CT, United States)

Fri, 24 May 2013 05:00:00 GMT

Job Number:	1748100
Business:	GE Capital
Business Segment:	Capital - Real Estate
About Us:	At GE Capital Real Estate, we apply our global insight, knowledge and expertise to meet the special needs of those in the commercial real estate market. We offer financing and asset management services to help our borrowers, investors and tenants build their businesses and to do it all with greater efficiency. Join us, and you’ll find yourself in an open, diverse and collaborative environment – one which will challenge your intellect and advance your career development. If you’re a flexible, ambitious leader who is open to learning and developing new skills, then join GE’s rich heritage of building and supporting growth around the world. Visit www.gecapitalrealestate.com to learn more. imagination at work? GE is an equal opportunity employer. GE offers a competitive salary, outstanding benefits and the professional advantages of an environment that supports your development and recognizes your achievements. GE is inclusive: employees have the opportunity to succeed, and diversity is embraced as a competitive advantage. The passion our people bring to their work extends to their private worlds. GE encourages a balance between the two. GE also values education and provides the tools and training for your professional development.
Posted Position Title:	Regulatory Reporting Analyst
Career Level:	Experienced
Function:	Finance
Function Segment:	Controllership
Location:	United States
U.S. State, China or Canada Provinces:	Connecticut
City:	Norwalk
Postal Code:	06851-1168
Relocation Assistance:	Yes
Role Summary/Purpose:	GE is an equal opportunity employer, offering a great work environment, challenging career opportunities, professional training and competitive compensation. Provide regulatory analysis and reporting support to GE Capital Real Estate management including collecting, reconciling and validating data. This role will assist with the design, implementation and maintenance of regulatory reporting processes. Provide analysis and support to regulatory team leadership. Evaluate complex situations using multiple sources of data and analytical skills.
Essential Responsibilities:	Role Summary/Purpose continued: Responsible for meeting and oversight over multiple financial reporting requirements, including those pertaining to external regulatory bodies, and reviewing work product of various team members, creating and/or reviewing original analyses and reconciliations, coordinating automation and process improvement projects. This role offers high visibility in a new regulatory environment. Preparation of specific regulatory filings for certain CRE entities. Direct and coordinate the activities of other CRE members in the completion of these regulatory filings. Liaise with other CRE platforms in the ultimate completion of the filings. Assist with the monthly, quarterly and annual closing and reporting processes of certain CRE reporting entities pertaining to internal and external reporting requirements, including local management and various external regulatory bodies. Preparation of financial statements and disclosures. Provide training and guidance to outside contractors and CRE platforms on regulatory accounting principles and practices, product information, and reporting processes. Ensure and where applicable, participate in month-end close reviews of various legal entities including the review of trial balance grouping, original reconciliation work produced by platforms and additional analyses to ensure all balances have been accurately reconciled and appropriately classified under US GAAP. Prepare and/or review periodic analytic review of certain CRE entity balance sheets and income statements. Prepare certain top-side journal entries relating to certain legal and/or reporting entities where appropriate. Prepare intercompany reporting and reconciliation and review processes for on and/or off balance sheet items of certain legal and/or reporting entities. Ensure timely feedback is sought and provided in connection with the research and resolution of intercompany breaks. Assist in the management of the Genpact team through maintaining open item lists, assisting staff in prioritizing tasks and providing status reports. Liaise with multiple departments (including FP&A, tax, and legal) to resolve various financial and accounting issues. Oversee the maintenance and development of organizational accounting procedural policies for applicable roles and responsibilities assigned. Assist with automation and process improvement efforts by identifying, developing and implementing automation enhancements. Lead and develop the testing of new or enhanced applications and reports.
Qualifications/Requirements:	Basic Qualifications: Bachelor's degree and a minimum 2 years of Controllership or Financial Planning and Analysis experience (OR in lieu of degree, high school diploma/GED with 6 years of Controllership or Financial Planning and Analysis experience OR equivalent military experience/training) Experience with the closing and reporting process Proficient use of financial systems and analysis tools to include Microsoft Office Suite Eligibility Requirements: MUST be able to satisfy the requirements of Section 19 of the Federal Deposit Insurance Act. MUST submit application for employment through COS (internal candidates) or www.gecareers.com (external candidates) to be considered for this position. MUST be at least 18 years of age. MUST be willing to comply with pre-employment screening, including but not limited to, drug testing and background check. MUST be willing to travel up to 5% of the time. MUST be willing to work out of the Norwalk, CT office. Legal authorization to work in the United States is required. We will not sponsor individuals for employment visas, now or in the future, for this job opening.
Additional Eligibility Qualifications:	GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen.
Desired Characteristics:	Bachelor's Degree in Accounting, Finance or Business Administration 3+ years of Controllership or Financial Planning and Analysis experience Graduate of GE Leadership Program, such as Financial Management Program (FMP), Experienced Commercial Leadership Program (ECLP) or Corporate Audit Staff (CAS), or current GE Leadership Program employee graduating with the upcoming class Experience with Regulatory Reporting Knowledge of GAAP Ability to work across functions at all levels Strong communication, project management, and presentation skills Prior experience working for a large multinational corporation This posting will remain active at least through May 6, 2013.

GECI Projects & Reporting Consultant Insurance Job (Sydney, Australia)

Mon, 17 Jun 2013 05:00:00 GMT

Job Number:	1776557
Business:	GE Capital
Business Segment:	Capital - Asia Pacific
About Us:
Posted Position Title:	GECI Projects & Reporting Consultant Insurance
Career Level:	Experienced
Function:	Regulatory and Compliance
Function Segment:	Compliance Risk Area Management
Location:	Australia
U.S. State, China or Canada Provinces:
City:	Sydney
Postal Code:	2000
Relocation Assistance:	No
Role Summary/Purpose:	The purpose of this postion is to support all members of the Risk and Compliance team to: 1.enhance & deliver all risk, compliance and regulatory reporting 2.support the delivery of risk and compliance project and quality improvement initiatives and 3.prepare reports and returns to regulatory bodies such as FOS,FSC, ASIC,APRA and RBNZ
Essential Responsibilities:	R & C Reporting and analytics Regulatory reporting R & C Projects and Process Initiatives Policy and Procedure updates
Qualifications/Requirements:	Tertiary Qualifications in a relevant degree Experience in a Compliance Risk or Legal role (2 years) Excellent oral and written communbication skills Presentation preparation Broad Governance, policy and Procedural knowledge
Additional Eligibility Qualifications:
Desired Characteristics:	Experience in project management or process improvement