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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 and3/28/2015 Cambridge, MA Save This Job
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 the4/5/2015 Lexington, MA Save This Job
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
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, a3/21/2015 Redwood City, CA Save This Job
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 serve3/28/2015 Cambridge, MA Save This Job
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
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