Specialist Quality Complaints jobs in Cambridge, MA

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SENIOR QUALITY SPECIALIST/ QUALITY MANAGER

Bachelors degree in sciences/engineering, minimum 8 years of biotech/pharmaceutical industry experience or 12 years of biotech/pharmaceutical industry experience in lieu of degree.By becoming a team member here at Vor, youll hav...

CompanyVor Bio
AddressCambridge, MA
CategoryManufacturing
Date Posted a week ago See detail

Senior Quality Specialist/ Quality Manager

Vor Bio

Cambridge, MA

Bachelors degree in sciences/engineering, minimum 8 years of biotech/pharmaceutical industry experience or 12 years of biotech/pharmaceutical industry experience in lieu of degree.By becoming a team member here at Vor, youll hav...

Senior Quality Specialist/ Quality Manager

Vor Bio

Cambridge, MA

$105K - $133K a year

Provide quality oversight of facility/utility and equipment for qualification activities. Provide quality oversight of validation program which includes but is not limited to Commissioning, Qualification, Validation, Analytical In...

Senior Specialist, GMP Quality Assurance

Nuvalent, Inc.

Cambridge, MA

$90.7K - $115K a year

Provide quality oversight throughout the CMC lifecycle management of Nuvalent's products with a primary focus on Drug Substance and Starting Materials. Conduct product release activities for all phases of development including rev...

Quality Specialist

Novo Nordisk

Watertown, MA

Education Level: Minimum BA/BS in a scientific discipline with 3+ years of relevant experience required. Advanced degree may be substituted for 2 years experience. An Advanced degree may be substituted for 2 years experience. Expe...

Specialist, Gas Quality Control

Eversource

Somerville, MA

$90,120 - $100,130 a year

Ensures safe work practices are being employed in accordance with the Companys Health and Safety Handbook and Contractor Safety Manual. Ensures all work activities are being performed in accordance with Gas Distribution construct...

Senior Specialist, Quality Commercial Batch Disposition (Hybrid)

Vertex Pharmaceuticals

Boston, MA

$99.9K - $126K a year

Master and Executed Batch Record review and resolution of comments/issues Archiving of batch documents in electronic document system Track data for the purpose of metrics generation Evaluations of Investigations/ OOS/ Change Contr...

Associate Director, Quality Product Complaints / Recalls

Vertex Pharmaceuticals Incorporated

Boston, MA

Responsible for all activities associated with the product complaint process, including reconciliation, training, complaint sample management, triage, trending, and SOP management, etc. Supports all activities associated with the...

Senior Quality Assurance Specialist, Global Product Quality

Cerevel Therapeutics

Boston, MA

Ensure GMP compliance for outsourced manufacturing, packaging, labeling, testing & distribution activities. Review GMP documentation such as Master Batch Records, Specifications, Analytical Test Methods, Stability Protocols/Report...

Senior Specialist, GMP Operational Quality (On-Site, 2nd Shift)

Vertex Pharmaceuticals

Boston, MA

$109K - $138K a year

Review batch data, including batch records, deviations, in-process data, EM data, QC release testing and other quality systems. Responsible for approval of COAs, generating BSE/TSE statement and product labelling. Responsible for...

Specialist II, Quality Control Investigations

Arranta Bio Llc

Watertown, MA

Actively participates in fostering a positive, collaborative work culture. Authoring and revision of standard operating procedures, test methods, protocols, and reports. Participate in execution of raw material testing, stabilit...

Quality Product Specialist

Mastech Digital

Woburn, MA

We are currently seeking a Quality Product Specialist for our client in the Engineering domain. We value our professionals, providing comprehensive benefits and the opportunity for growth. This is a Contract position, and the clie...

Sr. Specialist, Quality Assurance - Internal Audit

Lemaitre

Burlington, MA

$69.2K - $87.6K a year

Executes day to day activities based on quality objectives (goals) complementary to corporate policies and goals of building high quality medical devices. Audits the QMS and coordinates with external agencies to complete internal...