Skill
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
- Employers
- 10
- Median pay
- —
- Disclose 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 ↗
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 ↗
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 ↗
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 ↗
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 ↗
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 ↗
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 ↗
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 ↗
Roles that use Regulatory Affairs
Employers hiring for Regulatory Affairs
10 in total, most open roles first.
- Bristol Myers Squibb5 roles
- Gilead Sciences4 roles
- Biogen2 roles
- IQVIA2 roles
- AAstranis1 role
- CACognition AI1 role
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