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Regulatory Affairs Generalist

  • Regulatory Affairs Generalist job type Posted on: Nov 08, 2026
  • Regulatory Affairs Generalist experience level Kelly Science, Engineering, Technology & Telecom
  • Regulatory Affairs Generalist employment type Bridgewater, Iowa
  • Regulatory Affairs Generalist employment type Onsite
  • Regulatory Affairs Generalist salary Full-time

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Job Title :

Regulatory Affairs Generalist

Job Type :

Full-Time

Job Location :

Bridgewater Iowa United States

Remote :

No

Jobcon Logo Job Description :

Location: Bridgewater, NJKelly® Science & Clinical is seeking a Regulatory Affairs Generalist for a contract opportunity supporting our client in the life sciences industry. If you’re experienced in preparing FDA submission materials, committed to accuracy and regulatory compliance, and thrive in a fast-paced, professional environment, trust The Experts at Hiring Experts to guide your next career move.Position OverviewIn this role, you will provide hands-on regulatory writing, document review, proofreading, and quality-control support for FDA submissions across investigational and marketed products. You will collaborate with Regulatory Affairs leadership and cross-functional subject matter experts to help ensure submission documents are accurate, complete, and prepared in accordance with applicable regulatory requirements.9Interested candidates should apply directly to this job posting. Please do not send an email or InMail.

Jobcon Logo Position Details

Posted:

Nov 08, 2026

Reference Number:

10440_4484516603

Employment:

Full-time

City:

Bridgewater

Job Origin:

APPCAST_CPC

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Location: Bridgewater, NJKelly® Science & Clinical is seeking a Regulatory Affairs Generalist for a contract opportunity supporting our client in the life sciences industry. If you’re experienced in preparing FDA submission materials, committed to accuracy and regulatory compliance, and thrive in a fast-paced, professional environment, trust The Experts at Hiring Experts to guide your next career move.Position OverviewIn this role, you will provide hands-on regulatory writing, document review, proofreading, and quality-control support for FDA submissions across investigational and marketed products. You will collaborate with Regulatory Affairs leadership and cross-functional subject matter experts to help ensure submission documents are accurate, complete, and prepared in accordance with applicable regulatory requirements.9Interested candidates should apply directly to this job posting. Please do not send an email or InMail.

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