Regulatory Specialist Jobs

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Regulatory Affairs Consultant
MechelenNegotiable

We are looking for an experienced Regulatory Affairs Consultant to support MDR transition, risk management, and validation documentation activities within a highly regulated pharmaceutical/medical device environment. This 12‑month hybrid assignment is based in Antwerp, working 2-3 days on‑site. Key ResponsibilitiesUpdate and rewrite Risk Management...

Regulatory Affairs/ CMC Consultant
ColumbiaNegotiable

We are seeking an experienced Regulatory & CMC Lead to guide the chemistry, manufacturing, and controls strategy for a regulated cannabis inhalation product targeting medical and medically‑adjacent markets. This is a part‑time, long‑term contract role focused on building pharma‑grade documentation, specifications, and regulatory readiness appropria...

Principal Regulatory Affairs Specialist Advertising & Promotion
MinneapolisNegotiable

A leading global medical device company is seeking a Regulatory Affairs Principal to support the review and approval of advertising, promotional, sales, and training materials for its interventional cardiology portfolio. This role applies a risk‑based regulatory mindset to ensure content is accurate, balanced, well‑substantiated, and compliant with...

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Selby Jennings Start Your Career In Recruitment
Regulatory Specialist
MichiganNegotiable

Regulatory Specialist (Contract - W2 Only)Location: Remote (occasional travel within the U.S.) Contract Length: 2 Years Hours: 40 per week Start Date: ASAPAbout the RoleA leading global MedTech client is seeking an experienced Regulatory Specialist to support regulatory strategy and submissions for their orthopaedic device portfolio. This is an exc...

Regulatory Affairs Specialist II
DublinNegotiable

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 ...

Regulatory Affairs Specialist II
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 ...