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Temporary Biotech Regulatory Affairs Jobs (NOW HIRING)

Oterra

Regulatory Affairs Manager

Mount Pleasant, WI

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for ... biotechnology regulations. As the regulatory leader for North America, this position serves as the ...

Oterra

Regulatory Affairs Manager

Mount Pleasant, WI · On-site

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for ... biotechnology regulations. As the regulatory leader for North America, this position serves as the ...

Oterra

Regulatory Affairs Manager

Mount Pleasant, WI · On-site

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for ... biotechnology regulations. As the regulatory leader for North America, this position serves as the ...

Legend Biotech US

Director, Regulatory Affairs

Somerset, NJ · On-site

$158K - $209K/yr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Role Overview The Director of Regulatory Affairs is responsible for independently developing ...

Oterra

Regulatory Affairs Manager

Sturtevant, WI · On-site

The Regulatory Affairs Manager is responsible for leading regulatory compliance activities for ... biotechnology regulations. As the regulatory leader for North America, this position serves as the ...

Legend Biotech USA, Inc.

$158K - $209K/yr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Role OverviewThe Director of Regulatory Affairs is responsible for independently developing ...

PrideStaff

Regulatory Affairs Associate

Tustin, CA · On-site

$32 - $36/hr

Regulatory Affairs Associate for a biotechnology company located in Tustin. Temporary to Hire opportunity. Paying $32-36/hr, depending on qualifications. Hours are 9:00 AM - 5:00 PM, Monday-Friday.

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Temporary Biotech Regulatory Affairs information

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How much do temporary biotech regulatory affairs jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for temporary biotech regulatory affairs in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

What is the difference between Temporary Biotech Regulatory Affairs vs Temporary Biotech Quality Assurance?

AspectTemporary Biotech Regulatory AffairsTemporary Biotech Quality Assurance
Primary FocusRegulatory compliance, submissions, and interactions with authoritiesProduct quality, standards, and process validation
Required CredentialsLife sciences degree, knowledge of regulations (FDA, EMA)Quality management systems, GMP knowledge, certifications
Work EnvironmentRegulatory agencies, biotech companies, documentation-heavyManufacturing sites, labs, quality control departments
Industry UsageCommonly used in biotech and pharmaceutical sectorsUsed across biotech, pharma, and manufacturing industries

While both roles support biotech companies, Temporary Biotech Regulatory Affairs focuses on ensuring compliance with regulations and managing submissions to authorities. Temporary Biotech Quality Assurance emphasizes maintaining product quality and adherence to standards. Understanding these differences helps candidates and employers align expectations and skills for each position.

What cities are hiring for Temporary Biotech Regulatory Affairs jobs?

Cities with the most Temporary Biotech Regulatory Affairs job openings:

What are the most commonly searched types of Biotech Regulatory Affairs jobs?

The most popular types of Biotech Regulatory Affairs jobs are:

What states have the most Temporary Biotech Regulatory Affairs jobs?

States with the most job openings for Temporary Biotech Regulatory Affairs jobs include:

Temporary Biotech Regulatory Affairs jobs near you

Senior Director, Regulatory Strategy

Scorpion Therapeutics

Washington, DC • On-site

$150 - $200/hr

Other

Posted 9 days ago

Job description

Key Duties & Responsibilities
  • Lead development of regulatory strategy for multiple/complex development projects (first-in-human to post-marketing), including regulatory submission documents and Health Authority communications.
  • Represent Global Regulatory Affairs (GRA) on core/project teams; collaborate with regional leaders to ensure unified regulatory input into clinical programs and commercial strategy.
  • Address complex regulatory issues; provide guidance to cross-functional teams; counsel senior management on global Regulatory Affairs strategies, tactics, procedures, and practices.
  • Develop and manage project plans/timelines; assign/manage resources to prioritize work and meet goals on time.
  • Influence regulatory environment via conferences, industry/agency regulatory meetings, committees, and trade associations; stay current on regulations, policy, intelligence, and competitive issues.
  • Lead continuous improvement of department processes/strategies.
  • Lead GRA functional team(s); coach, develop, and provide performance feedback.
  • People management may include financial and HR responsibilities for assigned staff.
Required Knowledge & Skills
  • Business-minded strategic leader; innovative solutions to regulatory problems.
  • Excellent communication skills; ability to influence decisions; present and document regulatory strategy.
  • Regulatory leadership in cross-functional, matrix environments.
  • Deep expertise in regulatory affairs science and global/regional/local frameworks for human pharmaceutical development (research & development, preclinical/clinical, registration, maintenance).
  • Advanced data/protocol/safety reporting/labeling interpretation across drug development phases.
  • Expertise in proposing regulatory paths and clinical plans; lead productive Health Authority interactions.
  • Ability to assess regulatory pathway adequacy and guide refinements based on regulatory outcomes.
  • Ability to align with strategic vision/core values; improve internal regulatory policies/programs.
  • Cultural sensitivity; embraces diversity; mentors and develops staff.
Required Education & Experience
  • Bachelor's degree in Biology, Chemistry, or related discipline.
  • Typically 12 years' relevant pharmaceutical/biotech regulatory affairs experience and 5 years' supervisory/management experience (or equivalent).
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