Senior Quality Assurance III - Boston

We invite motivated candidates who are passionate about quality and patient safety to apply and join a team dedicated to supporting reliable, compliant, and impactful medical device solutions. · Partner with cross‑functional teams to provide quality guidance during development, m ...

A client I'm working with is seeking a motivated and detail‑oriented Quality Assurance Engineer III to join their team in supporting the development, manufacture, and ongoing reliability of our medical device products. · Partner with cross‑functional teams to provide quality guid ...

This position will support Blueprint Medicines' Quality Systems & Compliance functions in product complaint handling, document control, and regulatory inspection preparation. · ...

At Boston Scientific we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees tackling some of the most important health industry challenges. · ...

+ Design Assurance Engineer III · At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. · About the role: We have an excit ...

· DescriptionThe Quality Assurance Professional will work in the US External QA team responsible for Contract Manufacturing (CMO) and Contract Test Laboratories (CTL) oversight within the Biologics Operation Unit Quality Assurance Department This unit oversees contract manufactu ...

The QA Investigation Reviewer is responsible for the independent review and approval of GMP investigations within the Andover biopharma manufacturing facility.This role ensures non-conformances/deviations, OOS/OOTs, and other quality events are thoroughly investigated, · and comp ...

+ Job Summary: · Support all testing requirements for a SAFe agile team through the entire software development life cycle (SDLC) to deliver features and enhancements to the applications that support our transactional websites. · Develop test strategies and scripts. · Coordinate ...

We are seeking an experienced and detail-oriented Laboratory Technician to join our Hardware Failure Analysis team in Robotics. · ...

Support all testing requirements for a SAFe agile team through the entire software development life cycle to deliver features and enhancements to the applications that support our transactional websites. · Analyze requirements, develop test strategies and scripts, coordinate exec ...

Support all testing requirements for a SAFe agile team through the entire software development life cycle (SDLC) to deliver features and enhancements to the applications that support our transactional websites. Enable optimal team performance by ensuring that the testing for feat ...

We are seeking an experienced and detail‑oriented Laboratory Technician to join a Hardware Failure Analysis team. This role supports failure analysis investigations by preparing and analyzing samples, troubleshooting issues with attention to detail, and assisting engineers by wor ...

The QA Investigation Reviewer is responsible for the independent review and approval of GMP investigations within the Andover biopharma manufacturing facility. · This role ensures non-conformances/deviations, OOS/OOTs, and other quality events are thoroughly investigated, and com ...

The Genetics and Genomics Group in the R&D Center seeks a highly motivated genomics scientist / computational biologist to work in a dynamic and cross-functional team supporting genomics and translational research and therapeutic product development. · ...

+We have an exciting opportunity for an Information Systems Security Officer (ISSO) to join our Security Classification team.+ · +Assists leadership in interpreting regulations as they apply to information systems, platforms, and IT operating processes, practices and procedures. ...

The QA Investigation Reviewer is responsible for the independent review and approval of GMP investigations within the Andover biopharma manufacturing facility. · ...

About This Opportunity · In this role, you will be responsible for interfacing with and provide quality input to client's manufacturing programs that are in early stages of development or manufacture customized medicines. · This includes interfacing with clients that are nearing ...

We are partnering with a well-established global biopharmaceutical organization seeking Clinical Quality Assurance Managers for Phase I–III programs. · Lead GCP audits investigator sites CROs vendors internal processes · Provide quality oversight Phase I–III clinical trials · ...

We are partnering with a well-established global biopharmaceutical organization seeking Clinical Quality Assurance Manager to play critical role in clinical compliance audit execution inspection readiness across Phase I–III programs. · ResponsibilitiesLead and execute GCP audits ...

The Quality Assurance Analyst III is responsible for leading testing for CRM & Admissions applications. · 5-7 years of IT work experience with Salesforce knowledge. · Demonstrated knowledge of QA Testing methodologies. · ...