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Your search generated 160 results
Quest Diagnostics Incorporated

Senior Specialist, Regulatory Affairs

San Juan Capistrano, California

Quest Diagnostics Incorporated

Job Description Provide regulatory guidance in product design, clinical studies, market authorization strategies, labeling, advertising, and product withdrawals and recalls. Provide pre-market and post-market regulatory strategy and impleme...

Job Type Full Time
Quest Diagnostics Incorporated

Bioinformatics Quality Documentation Lead

Denton, Texas

Quest Diagnostics Incorporated

Job Description The Bioinformatics Quality Management Lead is responsible for overseeing quality, compliance, and regulatory needs for bioinformatics operations in a clinical diagnostics lab under CAP/CLIA requirements. This role requires a...

Job Type Full Time
Boston Scientific

Senior Regulatory Affairs Specialist

Maple Grove, Minnesota

Boston Scientific

Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit- High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and h...

Job Type Full Time
Boston Scientific

Senior Regulatory Affairs Specialist - Endoscopy

Marlborough, Massachusetts

Boston Scientific

Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and ...

Job Type Full Time
Revance

Senior Regulatory Operations Specialist

Nashville, Tennessee

Revance

Job Summary: The Sr. Regulatory Operations Specialist is responsible for planning, preparing, publishing, and managing regulatory submissions to global health authorities, with a focus on U.S. FDA electronic submissions (INDs, BLAs, supplem...

Job Type Full Time
Remote
Revance

Senior Regulatory Operations Specialist

Tennessee

Revance

Job Summary: The Sr. Regulatory Operations Specialist is responsible for planning, preparing, publishing, and managing regulatory submissions to global health authorities, with a focus on U.S. FDA electronic submissions (INDs, BLAs, supplem...

Job Type Full Time
Nintendo of America Inc.

3D Approval Specialist

Redmond, Washington

Nintendo of America Inc.

Nintendo of America Inc. About Nintendo of America: From the launch of the Nintendo Entertainment System more than 30 years ago, Nintendo's mission has been to create smiles through unique entertainment experiences. Here at Nintendo of Amer...

Job Type Full Time
bioMerieux Inc.

Regulatory Affairs Specialist

Salt Lake City, Utah

bioMerieux Inc.

Description Position Summary: An RA Specialist on the Regulatory Affairs Lifecycle Management (RA LCM) team is responsible for developing regulatory strategies and assessing regulatory risks related to product changes throughout their life ...

Job Type Full Time
Smith & Nephew

Sr. Regulatory Affairs Specialist (Austin, TX)

Memphis, Tennessee

Smith & Nephew

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. The Senior Regulatory Affairs Specialist role is responsible for preparing and supporting US and International regulatory submissions and...

Job Type Full Time
Smith & Nephew

Regulatory Affairs Specialist (Memphis, TN)

Memphis, Tennessee

Smith & Nephew

Life Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living. Are you passionate about navigating regulatory landscapes? Do you thrive in fast-paced environments? We're looking for a Regulatory Affai...

Job Type Full Time

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