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Vice President, Regulatory Affairs Jobs

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Vice President, Regulatory Affairs (ex-US)

Aegerion Pharmaceuticals, Inc.

Working in a team environment, the Vice President will provide regulatory oversight, support and guidance for all company functions, provide key input to regulatory strategy for products in development and in commercial distribution, and be responsible for planning and

3/28/2015  Cambridge, MA  Save This Job

Regulatory Affairs Specialist

T2 Biosystems, Inc.

Stage 2: Product Development 

Tracking Code 29-093 Job Description The Regulatory Affairs Specialist must be a talented and highly motivated individual. The position will participate in quality audits and support on-going compliance in the product development process. The position will assist in the

4/5/2015  Lexington, MA  Save This Job

Director, Regulatory Affairs

Acceleron Pharma

About Acceleron: Acceleron is a publicly traded, clinical stage biopharmaceutical company focused on the discovery, development and commercialization of novel protein therapeutics for cancer and rare diseases. The company is a leader in understanding the biology of the TGF-?

4/11/2015  Cambridge, MA  Save This Job

Vice President, Research Biology

Relypsa

Company Overview Relypsa, Inc. is a late clinical-stage pharmaceutical company leading the discovery and development of novel non-absorbed polymeric drugs for important applications in cardiovascular and renal diseases. Relypsa's lead product candidate is patiromer, a

4/26/2015  Redwood City, CA  Save This Job

Senior/Executive Director, Medical Affairs

Aegerion Pharmaceuticals, Inc.

Reporting into the Vice President of Medical Affairs, the Senior/Executive Director will be part of the Medical Affairs organization at Aegerion headquarters in Cambridge and will contribute to the medical/clinical output from that team. A key part of this role will be to serve

3/28/2015  Cambridge, MA  Save This Job

Quality Engineer

Tactile Systems Technology

Reports to: Vice President, Quality and Regulatory Affairs Scope of Supervision: None EDUCATION, BUSINESS EXPERIENCE AND PHYSICAL REQUIREMENTS ? Minimum 5 years? experience as a Quality Engineer in the medical device industry ? BA/BS degree in science or other technical field ?

5/4/2015  Minneapolis, MN  Save This Job

Complaint Coordinator

Tactile Systems Technology

Reports to: Vice President, Quality and Regulatory Affairs Scope of Supervision: None EDUCATION, BUSINESS EXPERIENCE AND PHYSICAL REQUIREMENTS ? Minimum 3 years? experience in the medical device industry with demonstrated quality system knowledge including 21 CFR Part 820 (QSR) &

5/4/2015  Minneapolis, MN  Save This Job

Companies: Vice President, Regulatory Affairs Jobs