Quality Control Specialist jobs in Middlesex, MA

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SUPERVISORY QUALITY ASSURANCE SPECIALIST

Plans and directs Quality Assurance (QA) Group operations. Plans the accomplishment of QA Group functions within the resources provided by and the policies and regulations established at higher levels. Utilizes risk based techniqu...

CompanyUs Defense Contract Management Agency
AddressTewksbury, MA
CategoryManufacturing
Salary$139,147 - $183,709 a year
Job typeTemporary | Full-time
Date Posted 2 months ago See detail

Supervisory Quality Assurance Specialist

Us Defense Contract Management Agency

Tewksbury, MA

$139,147 - $183,709 a year

Plans and directs Quality Assurance (QA) Group operations. Plans the accomplishment of QA Group functions within the resources provided by and the policies and regulations established at higher levels. Utilizes risk based techniqu...

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...

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...

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...

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...