ZipRecruiter

Log In

1

Regulatory Affair Associate Project Manager Jobs

Amgen

Sr Associate Project Manager - Remote

Bachelor's degree and 2 years of Project Management experience OR * Associate's degree and 6 years ... Bachelor's or advanced degree in a life science discipline, regulatory affairs, business, or a ...

ITW Car Care

Regulatory Affairs Associate

Houston, TX · Hybrid

Position Summary The Regulatory Affairs Associate supports the organization's product stewardship ... Customer Focus * Project Management * Continuous Learning * Effective Communication Working ...

BioSpace

Regulatory Affairs Associate II

Rockville, MD · On-site

... project and operational management of initiatives in support of the National Center for Advancing ... The regulatory affairs associate will work closely with Leidos Biomed/DDD leadership, NIH team ...

New

next page

Showing results 1-20

All JobsGovernment JobsGovernment Services JobsRegulatory Affairs Specialist JobsRegulatory Affair Associate Project Manager Jobs

Regulatory Affair Associate Project Manager information

See salary details

$17

$32

$48

How much do regulatory affair associate project manager jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for regulatory affair associate project manager in the United States is $32.21, according to ZipRecruiter salary data. Most workers in this role earn between $24.52 and $38.22 per hour, depending on experience, location, and employer.

What are popular job titles related to Regulatory Affair Associate Project Manager jobs?

For Regulatory Affair Associate Project Manager jobs, the most frequently searched job titles are:

Infographic showing various Regulatory Affair Associate Project Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $66,992 per year, or $32.2 per hour.

Regulatory Affairs Associate

Piscataway, NJ • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Re-posted 12 days ago

Job description

Hi,

My name is Karthik Mutyala, and I am a Recruitment Manager with Stark Pharma Solutions, specializing in opportunities across the Pharmaceutical, Biotechnology, Medical Device, and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Role: Regulatory Affairs Associate

Location: United States

Duration: Long Term contract

Position Summary

We are seeking a detail-oriented Regulatory Affairs Associate to support regulatory activities for medical devices, pharmaceuticals, biotechnology products, or combination products. The successful candidate will assist in preparing regulatory submissions, maintaining regulatory documentation, monitoring compliance requirements, and supporting product registrations to ensure adherence to FDA and global regulatory standards.

Key Responsibilities

  • Prepare, compile, review, and submit regulatory documentation to support product approvals and registrations.
  • Assist in the preparation of FDA submissions, including 510(k), PMA, IND, NDA, ANDA, or other regulatory filings as applicable.
  • Support regulatory strategy development for new products, product modifications, and market expansions.
  • Maintain regulatory files, product registrations, licenses, and submission records.
  • Review product labeling, promotional materials, and technical documentation for regulatory compliance.
  • Monitor changes in U.S. and international regulations and communicate regulatory impacts to internal stakeholders.
  • Collaborate with Quality Assurance, R&D, Clinical, Manufacturing, and Marketing teams to support regulatory initiatives.
  • Assist with regulatory agency correspondence, inspections, audits, and information requests.
  • Support change control assessments and evaluate regulatory impact of product or process changes.
  • Participate in cross-functional project teams to ensure timely regulatory deliverables.

Required Qualifications

  • Bachelor's degree in Regulatory Affairs, Life Sciences, Pharmacy, Biology, Chemistry, Biomedical Engineering, or a related scientific discipline.
  • 1–3 years of Regulatory Affairs experience within the pharmaceutical, biotechnology, medical device, or healthcare industry.
  • Working knowledge of FDA regulations, guidance documents, and regulatory submission processes.
  • Strong technical writing, documentation, and organizational skills.
  • Ability to manage multiple projects and deadlines in a fast-paced environment.
  • Excellent verbal and written communication skills.