Director of Quality Assurance - Lowell

The Quality Assurance Specialist is part of the QA/QC department at Plenus Group and is responsible for ensuring that all products and processes meet the company's high-quality standards and regulatory requirements. · Product Testing and Inspection: Perform regular routine quanti ...

Our well established, award winning client has an immediate need for a Quality Assurance Manager to join their growing team. This is a leadership role where the QA Manager will conduct internal AS9100 audits and customer audits as well as review customer RFQs. In addition, the QA ...

Our well-established, award-winning client has an immediate need for a Quality Assurance Leader to join their growing team. In this role, the QA Lead will conduct internal AS9100 audits and customer audits as well as review customer RFQs. In addition, the QA Lead will be responsi ...

Acute Care TechnologyAt ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and tr ...

Acute Care TechnologyAt ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and tr ...

Join our dynamic team as a Quality Assurance Manager and lead the charge in maintaining the highest standards of product quality and compliance. · ...

Acute Care TechnologyAt ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and tr ...

Acute Care TechnologyAt ZOLL, we're passionate about improving patient outcomes and helping save lives. We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and tr ...

We are hiring a Quality Assurance Specialist for one of our clients. · Perform Quality Assurance role in the Quality Assurance Site Support team with oversight of investigations (Manufacturing investigations), document approvals such as SOP approval, change control approval and l ...

This Quality position is an Andover based position which reports into PharmSci QA responsible for supporting the Pharmaceutical Sciences Organization. · Support day to day clinical manufacturing operations from a Quality support perspective (batch record review) · ...

This global role is responsible for Quality Assurance Validation (QAV) support to clinical pharmaceutical sciences biotherapeutic manufacturing and laboratory facilities.This includes QAV support to all areas including utility manufacturing laboratory and related computer systems ...

+ Job Summary · This Quality position is an Andover based position which reports into PharmSci QA responsible for supporting the Pharmaceutical Sciences Organization. The candidate works primarily in support of clinical manufacturing operations.Support day to day clinical manufac ...

This role will provide non-testing support for raw material testing in a cGMP Quality Control Analytical (QCA) department. · ...

· Company Description · Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on ...

· Company Description · Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation.  Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies ...

This role will provide non-testing support for raw material testing for new and existing product in a cGMP Quality Control Analytical (QCA) department. · Write change controls, protocols, investigations · ...

This position provides Quality Systems support for change controls product complaints investigation and CAPA program as it relates to supporting manufacturing of biotherapeutic drug substance at the Pharmaceutical Andover MA facility. This position will monitor progress of produc ...

This QA Specialist role will be responsible for supporting start-up of a new manufacturing suite at the Andover facility including support of applicable quality systems. · The role will transition to routine support when the suite is in GMP production, · including batch record , ...

· Company Description · At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies. · As speci ...

The Senior Quality Assurance Manager leads the development and execution of strategies to ensure compliance with quality and regulatory standards. · ...