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Transamerica is organized by lines of business (Life Insurance, Annuities, Mutual Funds, Retirement Plans, and Employee Benefits), which are supported by Transamerica Corporate (Corporate Development; Finance; Internal Audit; Legislative, Regulatory & Policy; Office of the CEO; People and Places; Brand; Corporate Affairs; Risk; and Technology.
$110,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This role will also be responsible for establishing and maintaining regulatory and legislative environments that support Vantage's economic development, energy, community engagement, and sustainability strategies.
$135,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Responsible for the distribution of Transamerica's mutual funds to the Institutional and large market Registered Investment Advisor (RIA) marketplace in a defined territory. Be Well Company holistic wellness program, which includes Wellness Coaching and Reward Dollars.
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Bachelor's degree in Engineering, Graphic Design, Life Sciences, Regulatory Affairs, or related discipline. Collaborate with cross-functional teams, including R&D, Regulatory Affairs, Quality Assurance, and Marketing, to ensure accurate and timely product label updates.
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This position will report to the Vice President of Regulatory Affairs for the Western Region. The Director, Regulatory Affairs will represent Invenergy before and manage relationships with state economic and environmental regulators, transmission system operators, and regional trade associations in Texas on behalf of Invenergy's existing assets as well as its pipeline of development projects.
$208,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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You’ll be engaged in projects dealing with International tax, mergers and acquisitions, state and local tax accounting, regulatory processes, tax reporting and strategy. Real Estate: Advise clients on their federal, local and overseas tax affairs, while acting as a strategic consultant related to: deals and transactions (including mergers, acquisitions and investments, conversions, reorganizations, dispositions, joint ventures, fund formation and structuring, etc.
$44.75 an hourFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Collaborating compliantly with colleagues from Medical Affairs and other corporate functions, the MSL engages in scientific exchange and enters into strategic discussions as they relate to medical/clinical, health economics and outcomes research (HEOR) data with health care professionals.
$195,000 a yearFull-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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This position reports to the Executive Director of MSLs. The MSL will have contact with internal colleagues in compliance, regulatory, pharmacovigilance, marketing, sales, research and development, medical science, medical information, market access, training, strategy and portfolio management, and HOVA. This internal collaboration is considered a fundamental and essential part of the position.
$181,500 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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This position is part of Quality and Regulatory Affairs located in Fargo, ND and will be fully remote. The Director of Global Regulatory Affairs will be responsible for developing and executing regulatory strategies for drug development and commercialization ensuring compliance with global regulations and standards across multiple markets.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Works with and assists the executive director in executing programs to influence issues of concern to industry including; regulatory and local government matters. Under the supervision of the executive director, manage assigned regulatory and local government issues.
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Strong business acumen, analytical skills, and experience working with various internal business partners (especially Sales, Marketing, Clinical, Regulatory, Legal, and Government Affairs staff) to provide insight into key economic and reimbursement issues for transcatheter heart valve products.
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For further information, visit: Recognition of Foreign Qualifications | International Affairs Office (ed.gov). The position is located in the Office of Research and Development, Veterans Health Administration and will be responsible for serving as the regulatory expert and consultant on policies, procedures, guidance, and FAQs related to biospecimens in VA conducted research studies.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Collaborate with the global regulatory affairs team on cybersecurity product submissions. Experience with medical device product cybersecurity regulatory submission requirements (globally.
$135,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Since being founded the team has seen phenomenal and sustained organic growth, working across Medical Affairs, Publications, Promotional, Commercial and Regulatory spaces for their roster of blue-chip pharmaceutical companies and biotech's.
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Job DescriptionResponsibilitiesCollaborate with Regulatory Affairs team members in the West region and across regions, as well as other internal departments. Knowledge of FERC and NERC standards related to transmission and interconnections, including Open Access Transmission Tariff (OATT.
$86,000 a yearFull-timeExpandApply NowActive JobUpdated 5 months ago
regulatory affairs jobs in Denver, Turner, Oregon
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