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Manager, Regulatory Affairs International Jobs

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Group Manager, Regulatory Affairs

Globus Medical

Location:Audubon, PA Job Code:GMRALB0816 Description The Group Manager, US Regulatory, is responsible for preparing, filing and gaining approval of 510(k), IDE, and PMA submissions to the U.S. Food and Drug Administration (FDA) for class II and class III products. This position

8/7/2017  Audubon, PA  Save This Job

Sr Associate Regulatory Affairs, Post Approval

Sagent Pharmaceuticals

Application Deadline: September 16, 2017 Location: Schaumburg, IL, USA Job Summary / Overview: Responsible for support of post-approval regulatory affairs activities under direction of the department Manager. Post-approval regulatory affairs activities may include but are not

8/30/2017  Schaumburg, IL  Save This Job

Regulatory Affairs Manager, Global-CMC (4641)

Aegerion Pharmaceuticals, Inc.

Req Id 4641 - Posted 03/03/2017 - United States - Massachusetts - Cambridge - Regulatory Affairs ? Job Description Print Preview Apply Apply Using LinkedIn? Save Job Email Job to Friend Return to List The Regulatory Affairs Manager Global-CMC is responsible for

8/9/2017  Cambridge, MA  Save This Job

Manager, Quality Systems

High Throughput Genomics

Job Location Tucson, Arizona Essential Duties Responsible for the maintenance and improvement of key Quality systems and processes. The incumbent will work in a multidisciplinary environment requiring a broad range of experience, analytical, communications and interpersonal

7/11/2017  Tucson, AZ  Save This Job

Manager, Technical Operations and Manufacturing

MaxCyte

About MaxCyte: MaxCyte is the leader in cell transfection with a world-wide marketed flow electroporation platform spanning the discovery, development, clinical, and manufacturing applications of virtually all classes of innovative therapeutics. MaxCyte's customers and

7/23/2017  Gaithersburg, MD  Save This Job