| Job alert | Jobs 1 - 10 of 95 |
Sr. QA Specialist - Plant Ops
Roslin CT US Holdings,LLC
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Hopkinton, MA, 01748
... This includes developing QA specific procedures related to product disposition, line clearance and review and approval of GMP documentation including but not limited to Batch Records, Validation Protocols/Reports, and Calibration/Work Order Records ... - Apr 18
Senior Quality Systems Engineer
Discover International
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Massachusetts
... Strong knowledge of GMP, FDA regulations, ISO 13485. Skilled in deviation, nonconformance, CAPA, and complaint handling. Familiarity with electronic document management systems. Works independently with minimal supervision. Adaptable to fast-paced ... - May 02
Quality Control Technician
US Tech Solutions
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Worcester, MA, 01609
Duration: 12 Months contract, Full-Time Employment Type: W-2 Responsibilities: • Performs routine Environmental Monitoring testing within a GMP environment. • Performs Environmental Monitoring (EM) during a fill operation. • Supports other lab ... - May 03
QC Associate
Pyramid Consulting, Inc
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Massachusetts
... Key Requirements and Technology Experience: BS with minimum of 3-4 years of experience in a GMP QC lab is required (or equivalent experience in a related biopharmaceutical GLP or GMP lab environment). Strong technical lab skills using pipettes, ... - Apr 18
Director GxP Quality Assurance
Hobson Prior
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Massachusetts
... The successful candidate will be responsible for developing and maintaining the GMP/GDP specific aspects of the Quality Management System to meet country specific requirements. This role will also involve leading country level inspections, ... - Apr 21
Senior Manager, Quality Control
AbbVie
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Worcester, MA
... In this role, you will play a crucial part in ensuring the GMP method performance of analytical chemistry and molecular-based assays. You will also be responsible for establishing GMP procedures required for laboratory operations. Your expertise ... - Apr 21
QC Associate
Pyramid Consulting, Inc
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Massachusetts
... Key Requirements and Technology Experience: BS with minimum of 1 year of experience in a GMP QC lab is required (or equivalent experience in a related biopharmaceutical GLP or GMP lab environment). Strong technical lab skills using pipettes, ... - May 04
Documentation Specialist- Onsite
Select Source International
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Marlborough, MA, 01752
Job Description Job Description: The Documentation Coordinator I is responsible for the control of Quality Management System (QMS) and quality specific GMP critical documentation. Key responsibilities include: Develops, produces, and maintains a ... - May 02
Principal Microbiologist, QC
Replimune, Inc.
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Framingham, MA
... Qualifications Experience and skill requirements: · Minimum 10 years GLP/GMP laboratory-based experience in a Microbiology testing capacity in a GMP-Regulated environment. Good analytical skills and technical experience is a must, preferentially ... - Apr 20
Sr. QA Specialist- Plant Operations
RoslinCT
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Hopkinton, MA, 01748
... This includes developing QA specific procedures related to product disposition, line clearance and review and approval of GMP documentation including but not limited to Batch Records, Validation Protocols/Reports, and Calibration/Work Order Records ... - Apr 20