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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

5/15/2016  Schaumburg, IL  Save This Job

Manager/Associate Director GMP QA

Paratek Pharmaceuticals

Department: Regulatory Affairs and Quality Assurance Hiring Manager: Director of Regulatory Affairs Summary of Position: Under the direction of the Director of Quality Assurance, the Manager/Associate Director GMP QA is responsible for providing QA and Technical support to

6/6/2016  Boston, MA  Save This Job

Sr. Clinical Supply Manager

Merrimack Pharmaceuticals

Clinical Operations Cambridge, MA, United States Merrimack is a fully integrated biopharmaceutical company that views cancer as a complex engineering challenge. Through systems biology, which brings together the fields of biology, computing and engineering, Merrimack aims to

6/21/2016  Cambridge, MA  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

5/22/2016  Cambridge, MA  Save This Job

Senior Manager, GCP Compliance

Alder Biopharmaceuticals

This newly created position reports to the Director, Quality Assurance Compliance and is responsible for assuring GCP compliance with Alder SOPs, ICH and FDA/EMA regulations. Specific responsibilities will include: Provide GCP compliance support: participate in Clinical Project

6/24/2016  Bothell, WA  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

5/9/2016  Mountain View, CA  Save This Job