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Regulatory Affairs

Legal and Compliance

Regulatory affairs is a profession, primarily in industries like pharmaceuticals, medical devices, and biotechnology, focused on ensuring products meet the requirements of regulatory agencies such as the FDA or EMA. Regulatory affairs specialists prepare submissions, manage approval processes, and liaise between companies and regulators to bring products to market legally and safely. They also monitor ongoing compliance as regulations evolve after product launch.

Regulatory Affairs in the job market

Last checked October 28, 2026

Open roles
19

on Career App

Employers
10

hiring for it

Median pay
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Open roles requiring Regulatory Affairs (19)

Compliance Pharmacist, Non-Sterile Compounding

Hims and Hers

Full-time · New Albany, OH

This role oversees regulatory compliance and quality assurance for a high-volume non-sterile compounding pharmacy, serving as the Designated Person to ensure operations meet federal and state standards. It suits an experienced pharmacist with compounding expertise who thrives in regulated environments and can translate complex requirements into practical workflows.

Listed on Hims and Hers’s careers site · Apply there ↗

Bristol Myers Squibb

Senior Director, Worldwide Cell Therapy Autoimmune Medical Affairs, Neurology/LCM

Bristol Myers Squibb

Full-time · $229,380 – $277,956

This role leads global medical strategy for Bristol Myers Squibb's cell therapy programs across neurology and autoimmune indications, partnering with clinical, commercial, and regulatory teams to translate emerging science into clinical practice. It suits an experienced medical affairs leader with deep expertise in cell therapy, advanced therapeutics, or immunology who can drive cross-functional strategy and external engagement at the enterprise level.

Listed on Bristol Myers Squibb’s careers site · Apply there ↗

Colonial Pipeline

Manager, Environmental Programs

Colonial Pipeline

Alpharetta, GA

This role leads Colonial Pipeline's environmental compliance programs across air, water, waste, and remediation while supervising a small team. It suits experienced environmental professionals with oil and gas industry background who can manage regulatory relationships and drive program improvements across a large organization.

Listed on Colonial Pipeline’s careers site · Apply there ↗

IQVIA

Director, Medical Safety- Sponsor-Dedicated (Home-based)

IQVIA

This role oversees medical safety and pharmacovigilance for a CRO's client programs, reviewing trial data and regulatory documents while leading a team of physicians and safety professionals. It suits experienced medical safety physicians who want to manage complex, multi-stakeholder projects with both clinical and people leadership responsibilities.

Listed on IQVIA’s careers site · Apply there ↗

Biogen

Director, Risk Intelligence and Analytics

Biogen

Full-time · Cambridge, MA · $188,000 – $259,000

This director-level role leads a team building data systems and intelligence to monitor risks across Biogen's manufacturing and supply network, translating complex operational data into executive guidance for strategic decisions. The position suits experienced analytics leaders with deep pharmaceutical manufacturing knowledge who can combine technical rigor with clear stakeholder communication.

Listed on Biogen’s careers site · Apply there ↗

Merck

Senior Clinical Director, Clinical Research, Hematology

Merck

Full-time · $282,200 – $444,200

This role leads clinical research strategy and execution for blood cancer medicines across all development phases, from early-stage work through post-market studies. It suits experienced physician-scientists who want to shape drug development strategy and collaborate across functional teams in a large pharmaceutical environment.

Listed on Merck’s careers site · Apply there ↗

Moderna

Global Medical Affairs Lead, Oncology

Moderna

$210,900 – $379,200

Lead global medical strategy and scientific direction for Moderna's oncology mRNA programs from early development through commercialization, managing cross-functional teams and external stakeholder relationships. Ideal for an experienced medical affairs leader with deep oncology expertise who thrives in fast-paced, matrix environments and wants to shape the future of cancer treatment.

Listed on Moderna’s careers site · Apply there ↗

Gilead Sciences

Senior Director - U.S. Ethics & Compliance Advisor (HIV)

Gilead Sciences

Full-time · United States - California - Foster City · $226,185 – $292,710

This role leads ethics and compliance efforts for Gilead's HIV prevention and treatment business, serving as a trusted advisor to commercial, medical, and legal teams on regulatory and compliance matters. The position requires extensive experience in pharmaceutical or biotech compliance, with proven ability to manage a team and navigate complex healthcare regulations.

Listed on Gilead Sciences’s careers site · Apply there ↗

VP, U.S. Policy

Cognition AI

Washington, DC

Lead policy strategy and government affairs for an AI software company, shaping how federal policymakers approach AI adoption and regulation. This role suits experienced policy professionals with strong government relationships and the ability to translate technical AI concepts into actionable policy positions.

Listed on Cognition AI’s careers site · Apply there ↗

Senior Solutions Engineer

Astranis

Full-time · San Francisco, CA · $140,000 – $200,000

Astranis seeks a hands-on engineer to design and optimize satellite networks for commercial and government clients, balancing technical analysis with customer-facing sales support. The role spans from pre-sales through operations, requiring deep knowledge of satellite communications systems and the ability to navigate competing technical and business constraints.

Listed on Astranis’s careers site · Apply there ↗

View all 19 on Jobs

Employers hiring for Regulatory Affairs

10 in total, most open roles first.

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