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Regulatory Affairs /Quality Assurance Manager Jobs

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Regulatory Affairs Manager

Genocea Biosciences, Inc.

Position Summary The Manager of Regulatory Affairs is accountable for the preparation and management of simple and complex regulatory submissions. They will act as liaison between Regulatory Affairs and other functional areas on various projects including external CROs, partners,

5/26/2016  Cambridge, MA  Save This Job

Quality Assurance Complaint Specialist

Sagent Pharmaceuticals

Application Deadline: May 31, 2016 Location: Schaumburg, Illinois, USA Job Summary / Overview: To provide Quality Assurance support and guidance for customer complaints received by managing the Sagent customer complaint program. Proactively support the existing quality systems

5/10/2016  Schaumburg, IL  Save This Job

Director of Quality Assurance and Regulatory Affair

TeraRecon

Location:USA - CA Company Order Number:397 # of openings:1 Description About the Company TeraRecon is the largest independent, vendor neutral medical image viewing solution provider with a focus on advanced image processing innovation. TeraRecon iNtuition and iNteract+ solutions

4/20/2016  San Mateo, CA  Save This Job

International Regulatory Associate

Globus Medical

Location:Audubon, PA Job Code:IRALB0516 Description The International Regulatory Associate maintains CE Technical Files and registrations for international Regulatory agencies. This position entails working knowledge of products under review and of relevant regulations and

5/17/2016  Audubon, PA  Save This Job

Clinical Supply Manager

Merrimack Pharmaceuticals

Product Supply Cambridge, MA, United States We are looking for a talented Clinical Supply Manager to join our team in Cambridge! Job Responsibilities: Work closely with Clinical Operations to monitor and track clinical trial enrollment plans and actual enrollment Collaborate

5/17/2016  Cambridge, MA  Save This Job

International Regulatory Project Manager

Globus Medical

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

4/17/2016  Audubon, PA  Save This Job

TECHNICAL WRITER

ViewRay

REPORTS TO THE SENIOR MANAGER, REGULATORY AFFAIRS Responsibilities Create and maintain the manuals for a medical device, detailing Installation, Operation, Quality Assurance, Servicing, and other topics Understand validation and design change control; assist the Product

5/5/2016  Mountain View, CA  Save This Job