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Regulatory Affairs Senior Manager Jobs

13 Job Offers

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Senior Regulatory Affairs & Entity Corporate Governance Manager (10 months FTC)
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Senior Manager, Government Affairs and Regulatory Policy
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Senior Manager, Regulatory Affairs
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Lead regulatory strategy and a team of professionals for AbbVie in Montreal. Requires 10+ years in pharma, 4+ years leading teams, and proven Health Canada submission success.
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Canada, Montreal
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Senior Manager, Regulatory Affairs (Energy Markets & Transmission)
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Lead PJM regulatory strategy for a fast-growing data center developer in Washington, DC. Requires 7+ years in wholesale energy markets, FERC/PJM filings, and stakeholder engagement. Shape large-load policy and transmission planning.
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United States, Washington D.C., DC
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Senior Manager Regulatory Affairs, Global Reg Strategy US & Canada
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Lead US & Canada regulatory strategy for AbbVie's pharmaceutical portfolio in North Chicago. Requires 6+ years in regulatory affairs, FDA liaison expertise, and strong negotiation skills. Drive RSTP development and execution.
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Senior Manager Regulatory Affairs, Global Reg Strategy US & Canada
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Lead US and Canada regulatory strategy for AbbVie's pharmaceutical portfolio in Florham Park. Requires 6+ years in regulatory affairs, FDA liaison expertise, and strong negotiation skills. Drive submissions and cross-functional alignment.
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United States, Florham Park
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Senior Manager Regulatory Affairs, Global Reg Strategy US & Canada
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Lead regulatory strategy for US and Canada at AbbVie in Irvine. Requires 6+ years in regulatory affairs, FDA liaison expertise, and strong negotiation skills. Drive RSTP for on-market and pipeline products.
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Senior Manager - Regulatory Affairs
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Senior Manager, Regulatory Affairs – Global Supply Chain Transformation
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Senior Regulatory Affairs Manager
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Senior Regulatory Affairs Manager sought to lead animal health drug development and regulatory strategy in Shawnee, US. Leverage 8+ years of veterinary regulatory expertise (CVM, GLP, GCP, GMP) to provide expert client advice, navigate complex submissions, and drive consulting growth. Ideal candi...
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Senior Manager Regulatory Affairs CZ&SK
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Senior Manager Regulatory Affairs CZ&SK sought by Amgen in Prague to lead affiliate regulatory strategy and lifecycle management. This role oversees a local team, serves as the primary contact with Czech and Slovak agencies, and ensures compliance with EU and local legislation. Requires fluency i...
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Senior Manager, Regulatory Affairs (Ad Promo)
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Senior Manager, Regulatory Strategy role in Raleigh, US. Leverage 7+ years of regulatory expertise to design clinical trials, develop submission plans, and advise ICON clients. Requires a Bachelor's in science/healthcare, supervisory experience, and strong strategic drug development skills. Benef...
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Senior Manager - CMC Regulatory Affairs Biopharm Development Projects
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Senior Manager, CMC Regulatory Affairs sought to lead global regulatory strategy for GSK’s biopharm development projects. Drive CMC submissions (IND/NDA/MAA) and risk mitigation across multiple complex programs. Requires a Life Sciences degree and 4+ years in CMC regulatory, with expertise in glo...
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United States, Collegeville, Wavre, Durham, Siena, London, Waltham
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144375.00 - 240625.00 USD / Year
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About the Regulatory Affairs Senior Manager role

Explore rewarding Regulatory Affairs Senior Manager jobs, a pivotal leadership role at the intersection of science, business, and law within the highly regulated life sciences industry. Professionals in these positions serve as strategic navigators, guiding pharmaceutical, biotechnology, and medical device companies through the complex global regulatory landscape to bring vital products to market and ensure ongoing compliance. This senior role is less about tactical dossier preparation and more about high-level strategy, team leadership, and influencing business decisions to mitigate risk and accelerate patient access to innovative therapies and technologies.

A Regulatory Affairs Senior Manager typically oversees a team of specialists and is responsible for developing and executing comprehensive regulatory strategies for product portfolios. This involves a deep analysis of regulatory pathways across multiple regions, anticipating Health Authority requirements, and identifying potential hurdles long before submission. Common responsibilities include leading the preparation, submission, and lifecycle management of critical regulatory applications such as INDs, NDAs, BLAs, MAAs, or device PMAs and CE Mark technical files. They act as the primary company liaison with regulatory agencies like the FDA, EMA, and others worldwide, managing communications, leading agency meetings, and negotiating approval terms. Furthermore, they ensure ongoing compliance with post-marketing obligations, manage regulatory aspects of product changes, and provide crucial regulatory intelligence to inform R&D and commercial planning.

The skill set required for these senior jobs is both broad and deep. A strong scientific background, usually with an advanced degree in life sciences, pharmacy, or medicine, is fundamental. Candidates must possess extensive, hands-on experience in regulatory submissions and a proven track record of successful agency interactions. Beyond technical expertise, exceptional leadership and people management skills are essential for mentoring teams and fostering talent. Strategic thinking, superior communication abilities for influencing cross-functional stakeholders, and sharp project management skills to drive complex timelines are critical. A keen understanding of global regulatory guidelines, risk assessment capabilities, and a proactive, problem-solving mindset define top performers in this field. For those seeking to shape the future of medicine while ensuring the highest standards of safety and efficacy, Regulatory Affairs Senior Manager jobs offer a challenging and profoundly impactful career path at the heart of the healthcare industry.