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Speciality

Regulatory affairs jobs for people who move products through approval.

Roles in submissions, regulatory writing, publishing and lifecycle management with pharmaceutical, biotech and medical device teams.

Every product that reaches patients passes through regulatory professionals. They plan the strategy, assemble the evidence, write the documents agencies read, and keep approvals current as products change. Companies call us when a submission deadline is close, when a team is stretched by agency questions, or when a new market brings unfamiliar rules. If that is your work, we want to talk to you.

What hiring teams look for

Hiring managers want to hear about submissions you prepared or managed, the agencies you worked with, and the document types you know well: clinical and nonclinical summaries, CMC sections, labeling, or device technical documentation. Experience with electronic submissions and publishing tools is valued, as is a clear record of meeting deadlines without sacrificing accuracy. For device roles, familiarity with 510(k) and De Novo pathways, EU MDR and IVDR technical files, and post-market obligations often decides between candidates.

We recruit at every level, from regulatory associates building their first submissions to managers who have led programs through approval. Roles may be onsite, hybrid or remote depending on the company.

Engagement types

Submission peaks and remediation projects create many contract roles with clear end dates, often with the chance to extend or convert. Growing companies also hire permanent regulatory staff as products approach the market. Your recruiter will explain which kind of role you are considering before you apply.

Roles we recruit for

  • Regulatory Affairs Associate
  • Regulatory Affairs Specialist
  • Regulatory Affairs Manager
  • Regulatory Writer
  • Medical Writer (regulatory)
  • Regulatory Operations / Publishing Specialist
  • CMC Regulatory Specialist
  • Labeling Specialist
  • Regulatory Project Manager
  • Device Regulatory Specialist (510(k), EU MDR / IVDR)
  • Regulatory Intelligence Analyst
  • Lifecycle / Post-Approval Specialist

How we help you

A recruiter who understands regulatory work reviews your submissions history, presents it in the language hiring managers use, and matches you with teams where it counts. We submit you only with your consent and tell you how each application is going.

Have this experience? Let us find your next role.

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