Regulatory Specialist Jobs

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Principal Reg Specialist
san francisco$125,000 - $150,000 USD a year

Influence Regulatory Strategy for Products That Reach Global MarketsThe OpportunityA global medical device manufacturer is looking for a Regulatory Affairs Specialist to join a well-established regulatory team supporting a diverse product portfolio.This is a role for someone who wants to move beyond transactional regulatory work and become a valued...

Senior Regulatory Affairs Specialist
Irvine$130,000 - $150,000 USD a year

A growing medical device company is seeking a Senior Regulatory Affairs Specialist to support global regulatory strategy and submissions across a diverse product portfolio. This role will partner cross-functionally with quality, clinical, and product development teams to ensure compliance with applicable regulations throughout the product lifecycle...

Regulatory Affairs Lead
Los Angeles$120,000 - $150,000 USD a year

Regulatory Affairs LeadPosition Summary The Regulatory Affairs Lead will provide strategic and operational regulatory support across the product lifecycle for Class III medical devices. This role will partner cross‑functionally to help ensure regulatory alignment, support global submissions, and maintain compliance with applicable regulations.Key ...

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Selby Jennings Start Your Career In Recruitment
Sr. Regulatory Affairs Consultant
ChicagoNegotiable

Contract: 12-month, full time contractStart date: ASAP Client: US based large MedTech Working hours: Supporting US Team, some requirements for availability in CST time zoneJob Description:Assesses regulatory intelligence to assist in the development of local, regional, and global regulatory strategiesParticipates in advocacy activities of a more ad...

Regulatory Affairs Project Manager (Delivery System)
Irvine, CANegotiable

Job Title: Senior Regulatory Affairs Specialist Supervisor/Manager Title: Senior Manager, Regulatory AffairsJob Description Summary: Responsible for timely preparation and submission of organized, scientifically valid global regulatory affairs submissions (clinical, pre- and post-market applications), query responses, and correspondence tracking. M...

Senior Regulatory Affairs Specialist
ColumbusNegotiable

A rapidly growing medical device organization is seeking a driven and detail‑oriented Regulatory Affairs Specialist II to join their Minneapolis team. This is an opportunity to step into a hands‑on role supporting innovative, life‑saving technologies while working closely with cross‑functional partners across product development, quality, and risk ...