Biotech Validation Jobs in Littleton, Massachusetts

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5 Littleton, MA Biotech Validation jobs found on Monster.

Jobs 1 to 5 of 5
SENIOR QA SUPPORT – DRUG SUBSTANCE TECH TRANSFER REQUIREMENT #14-01223 RECRUITER: CINDI PISNOY JOB LOCATION: DEVENS, MA NOVEMBER 7, 2014 Project Description: Provide Quality Assurance oversight to support the commercial technical transfer of drug substance from client’s facility to another facility. This position will be responsible for the following, but not limited to: · QA review and appr...
Hi, We have an excellent opportunity for “Quality Engineer” with direct Client. If this sounds interesting please send the details or do call me on 609-357-1858 ,609-454-3209 Ext 103 Quality Engineer –Drug Substance Tech Transfer Duration: 1 year Location: Devens, MA Employment type: w2 Description of Services: Provide Quality Assurance oversight to support the commercial technical transfer...
QUALITY ENGINEER contract opportunity at a well-respected manufacturing firm near Concord, MA. Projected 12+ month assignment. Need BS Degree and biopharmaceutical. Includes per diem. Responsibilities for the Quality Engineer Provide oversight to support the commercial technical transfer of drug substance between facilities Review and approval process facility fit reports, risk assessments, val...
Thank you for your interest in the Azzur Group. Please ensure your salary requirements are included with your resume. Summary: Provide Quality Assurance oversight to support the commercial technical transfer of drug substance from one site to another This position will be responsible for the following, but not limited to: • QA review and approval of process facility fit reports, process risk a...
GMS - Biologics Devens Devens, MA
Description The primary role of the Executive Director, Analytical Science and Technology is to provide leadership and direction for the AST function in its mission of delivering the post-approval analytical technical agenda for all in-line products which includes delivery of method improvements and innovation, regulatory filings, support and partnership with QC and manufacturing and partnership ...

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