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Regulatory Affairs Specialist Jobs

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Regulatory Affairs Specialist

Scientific Protein Laboratories

Up To Lead Regulatory Affairs Specialist Scientific Protein Laboratories LLC (SPL) is a biopharmaceutical world leader in the development and cGMP compliant manufacturing of pancreatic enzymes and heparin. We have an immediate opening in Waunakee, WI (Madison Area) for an

7/4/2016  Waunakee, WI  Save This Job

Regulatory Affairs Specialist (U.S.)

Globus Medical

Location:Audubon, PA Job Code:RAPMKB0515 Description The Regulatory Affairs Specialist assists in writing, submitting and gaining clearance for 510(k) submissions and approval for IDE/PMA submissions to the Food and Drug Administration (FDA) for class II and class III products.

6/26/2016  Audubon, PA  Save This Job

International Regulatory Affairs Specialist

Globus Medical

Location:Audubon, PA Job Code:IRPMLB0216 Description The International Regulatory Affairs Specialist writes, submits and gains approval of product registrations and other submissions to international Regulatory agencies. This position entails development of submissions in

6/26/2016  Audubon, PA  Save This Job

Regulatory Affairs Specialist II

Second Sight Medical Products

POSITION SUMMARY: The position is responsible for diverse regulatory functions, including but not exclusive to the development of Medical Device submissions and the implementation of Regulatory Compliance. ESSENTIAL DUTIES AND RESPONSIBILITIES: ? Prepare submissions for US and

7/10/2016  Sylmar, CA  Save This Job

Regulatory Specialist

Sciformix Corporation

Regulatory Specialist (United States; Russia; Egypt; Turkey; UAE; Israel; Saudi Arabia) Responsibilities Ensure compliance with regulatory agency regulations and interpretations Prepare responses to regulatory agencies? questions and other correspondence Organize and maintains

7/23/2016  Westborough, MA  Save This Job

Senior Regulatory Specialist

Penumbra, Inc.

ALAMEDA, CAREGULATORY AFFAIRSFULL-TIME APPLY FOR THIS JOB As a member of our Regulatory Affairs team, you will play a key role in expediting the availability of our lifesaving products worldwide by ensuring that they meet all requirements set forth by regulatory bodies in the

7/3/2016  Alameda, CA  Save This Job

Manufacturing Specialist

Tactile Systems Technology

Department: Manufacturing Operations Reports to: Director of Operations and Project Management Scope of Supervision: No Direct Reports EDUCATION, BUSINESS EXPERIENCE, AND PHYSICAL REQUIREMENTS ? Basic computer skills necessary ? Experience in Medical Device assembly and working

7/2/2016  Minneapolis, MN  Save This Job

Quality Assurance Compliance Specialist

Aprecia Pharmaceuticals

inShare Location: East Windsor, NJ Aprecia is a specialty pharmaceutical company committed to transforming customers' experience with highly prescribed high-dose medications. Built upon our proprietary three-dimensional printing (3DP) technology platform, we develop and

8/11/2016  Blue Ash, OH  Save This Job