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Regulatory Jobs

608 Job Offers

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Senior Consultant - Regulatory Affairs
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Italy , Firenze; Milano; Rome
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Product Life Group
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Program Manager, AV Compliance - Regulatory Response and Compliance Monitoring
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United States , San Francisco
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137000.00 - 169000.00 USD / Year
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Waymo
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Senior Regulatory Consultant - Regulatory Project/Program Manager
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United States
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Parexel
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US regulatory report FR Y-14 Senior Analyst- Assistant Vice President
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Senior Analyst role in Citi’s Controllers Organization, supporting U.S. regulatory reporting (FR Y-14, FR Y-9C, Call Report) in Mumbai. Requires 5+ years in financial services with deep knowledge of Basel III, CCAR, and GAAP/SEC reporting. Drive process improvements, manage key metrics, and colla...
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India , Mumbai
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Citi
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US Regulatory Report FR Y-14 Lead Analyst- Vice President
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India , Mumbai
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Citi
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Regulatory Operations - Client Assets Team Manager
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United Kingdom , Belfast
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Citi
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Regulatory Policy and Intelligence Senior Manager
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United States
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141588.75 - 191561.25 USD / Year
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Amgen
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Regulatory Quality Assurance Manager
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United Kingdom , Guildford
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Alliance Medical Ltd
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Regulatory Reporting Analyst
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Join Barclays in Chennai as a Regulatory Reporting Analyst. Leverage your expertise in UK/US regulatory reporting and Basel 3/3.1 to mitigate prudential risks and prepare key reports. Ideal for MBA Finance/Economics graduates with strong analytical skills. Enjoy benefits like an onsite medical cl...
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India , Chennai
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Barclays
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QM Associate - Regulatory Affairs
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Join Brainlab in Munich as a QM Associate in Regulatory Affairs, driving global regulatory strategies for innovative medical devices. You’ll interpret requirements, support FDA 510(k) submissions, and collaborate with international teams. Ideal for candidates with a degree in engineering or life ...
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Germany , Munich
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Brainlab
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Japan Regulatory Strategy Manager
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Amgen seeks a Japan Regulatory Strategy Manager in Tokyo to lead drug development strategies and interface with Japanese authorities. This role requires 10+ years of experience, including 5+ in Regulatory Affairs, with deep knowledge of Japan’s pharmaceutical regulations. You will drive local and...
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Japan , Tokyo
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Amgen
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United States Regulatory Manager – Obesity and Related Conditions
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Amgen seeks a United States Regulatory Manager to lead U.S. regulatory strategy for Obesity and Related Conditions. You will manage FDA submissions, support labeling negotiations, and drive global regulatory tactics. Ideal candidates have a relevant degree and regulatory experience. Join a missio...
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United States
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112.00 - 152.00 USD / Year
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Amgen
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Associate Regulatory Affairs
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Egypt , Cairo
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Amgen
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Director, Global Regulatory Lead – Obesity & Related Conditions (Chronic Weight)
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United States , Thousand Oaks
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195640.25 - 264689.75 USD / Year
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Amgen
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Senior Associate Regulatory Affairs - Clinical Studies (CDMX)
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Senior Associate Regulatory Affairs sought for Amgen’s clinical studies in Mexico City. Drive local regulatory strategy and ensure compliant clinical trial authorizations under NOM-012 and COFEPRIS. Requires a Master’s in health sciences with clinical regulatory experience in Mexico. Enjoy compet...
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Mexico , Mexico City
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Amgen
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Global Regulatory Director Lead – Obesity & Related Conditions (Type II Diabetes)
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Global Regulatory Director Lead sought to drive strategy for obesity and Type II diabetes programs. This role requires deep expertise in metabolic biology, global submissions, and Health Authority interactions (FDA, EMA). Lead cross-functional GRTs, develop regulatory plans, and shape clinical de...
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United States
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189632.45 - 256561.55 USD / Year
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Amgen
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Mea Regulatory Affairs Senior Associate
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Seeking a **MEA Regulatory Affairs Senior Associate** in **Cairo, Egypt** to manage labeling and packaging for Amgen’s pipeline and biosimilars. Requires 2+ years of RA experience, a pharmacist/biology background, and fluency in English & Arabic (French a plus). Drive lifecycle management, e-labe...
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Egypt , Cairo
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Amgen
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Quality Regulatory Manager
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Quality Regulatory Manager sought for a Bengaluru-based role. Requires a Master’s/Ph.D in Life Sciences or Biomedical Engineering with 6-10 years in IVD/medical device regulatory affairs. Must have deep expertise in ISO 13485, EU IVDR, US FDA 21 CFR 820, and global submissions. Lead audits and dr...
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India , Bengaluru
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Randstad
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Senior Counsel - EU Product & Chemical Regulatory Compliance
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Senior Counsel sought to lead Avantor’s new EU Product & Chemical Regulatory function. This role provides strategic legal counsel on REACH, CLP, and GMP compliance across Europe, with a focus on Germany. Ideal for a 10+ year attorney with deep regulatory expertise in pharma or chemicals. Drive co...
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Germany; United Kingdom; Poland; Ireland
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Avantor
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Corporate Counsel, Innovation and Regulatory
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United States , New York
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140000.00 - 170000.00 USD / Year
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Antech Diagnostics
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About the Regulatory role

Explore a world of opportunity in regulatory jobs, a dynamic profession at the critical intersection of law, science, and business. Regulatory professionals are the essential guardians of compliance, ensuring that products, processes, and organizations operate within the complex frameworks of local and international laws. Their work is fundamental across diverse industries—from pharmaceuticals, medical devices, and biotechnology to chemicals, consumer goods, agriculture, and healthcare—making these roles both versatile and in high demand.

Individuals in regulatory affairs and compliance careers typically serve as strategic navigators and operational experts. Their core mission is to interpret evolving regulations, translate legal requirements into actionable business strategies, and secure necessary approvals from governmental and accreditation bodies. Common responsibilities include managing product registration and licensing submissions, maintaining comprehensive regulatory documentation, and ensuring accurate safety data sheets and labeling. They conduct rigorous internal audits, lead readiness initiatives for inspections, and serve as the primary liaison with external agencies. A significant part of the role involves proactive monitoring of the regulatory landscape, assessing the impact of new guidelines, and implementing compliance programs to mitigate risk. Furthermore, they provide critical guidance to cross-functional teams such as Research & Development, Quality Assurance, Manufacturing, and Marketing, ensuring compliance is integrated from product conception through to market launch and beyond.

To thrive in regulatory jobs, a specific blend of skills and qualifications is essential. A strong educational foundation in a scientific, legal, or health-related field is typically required, with advanced degrees often preferred for senior positions. Professionals must possess meticulous attention to detail, exceptional analytical abilities, and superb written and verbal communication skills to articulate complex requirements clearly. Strategic thinking is paramount, as is the ability to influence stakeholders and lead teams through intricate compliance challenges. Key requirements often include direct experience with relevant regulatory frameworks—such as FDA regulations, REACH, CLP, ISO standards, or Joint Commission accreditation—depending on the sector. Certifications like RAC (Regulatory Affairs Certification) or CPHQ (Certified Professional in Healthcare Quality) are highly valued. Ultimately, successful regulatory professionals are continuous learners, adept problem-solvers, and trusted advisors who protect their organizations while facilitating innovation and market access. Discover your path in this impactful field where expertise drives safety, quality, and global commerce.

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