Lead Quality Investigator - Andover, MA

Job summary · The QA Investigation Reviewer is responsible for the independent review and approval of GMP investigations, ensuring compliance with cGMP regulations, site procedures, and global quality standards.This role supports product quality, patient safety, · and timely batc ...

Our client is seeking an experienced Investigations Lead to support Cell & Gene Therapy manufacturing operations across Boston and Cambridge sites. · ...

The Quality Investigations Specialist conducts timely and thorough investigations into grievances, complaints and alleged human rights violations. They manage internal and regulator-assigned grievances and complaints, conducting interviews with stakeholders, writing initial repor ...

The Quality Investigations Specialist is an important part of the Quality team responsible for conducting timely and thorough investigations into grievances, · complaints and alleged human rights violations. · ...

The Quality Investigations Specialist is an important part of the Quality team responsible for conducting timely and thorough investigations into grievances, · complaints and alleged human rights violations.Collaborates with Assistant Director of Quality and Quality Improvement S ...

This role focuses on real-time issue triage and investigation ownership across cell manufacturing Quality Control materials and facilities in a GMP-regulated environment. · ...

Join a leading biopharmaceutical organization supporting manufacturing and quality operations as a Quality Control Investigation Consultant. · ...

We are hiring a Quality Records Investigator for one of our clients. The ideal candidate will have experience in tracking and management of QC Quality Records. · Serves as the Quality Record (PR) Subject Matter Expert (SME) for the Quality Control team · Leads complex technical i ...

+We are looking for a Quality Assurance Investigations Manager to join our Cell Therapy team at Bristol Myers Squibb. As a member of our team you will have the opportunity to grow and thrive through opportunities uncommon in scale and scope. · + · Author review approve technical ...

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits · At Bristol Myers Squibb we are reimagining the future of cell therapy. · The Senior Manager Quality Assurance Investigations will ...

+Job summary · Transforming patients' lives through science · +ResponsibilitiesReview and approve investigations/ CAPAs / effectiveness checks associated with the manufacturing site including but not limited to materials, manufacturing, laboratory, facility, and computer systems. ...

Working at Bristol Myers Squibb is anything but usual. Here uniquely interesting work happens every day in every department. From optimizing a production line to the latest breakthroughs in cell therapy this is work that transforms the lives of patients and careers. · Bristol Mye ...

The Andover QC Microbiology non-testing group is looking for an individual to fill a QC Associate role responsible for writing investigations generated within the QC Microbiology testing group in Andover. · Perform thorough, detailed, and timely investigations. · Generate high-qu ...

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 ...

· Job Description · I am Zach from Pioneer Data System, Inc. We have an immediate requirement for a Manufacturing Process Investigator/ Pharma Industry in Andover, Massachusetts · If you are interested please call me at ( or respond to this email. · Position Details: · Job Titl ...

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

· Job Description · Position Details: · Job Title: Quality Assurance Analyst / Pharma Manufacturing · Duration: 12 months contract, extendable up to 18 months · Location: Andover, MA · Note: · Client has the right-to-hire you as a permanent employee at any time during or after ...

· Company Description · Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, ...

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 ...

· Company Description · Makro Scientific: · Growing Pharmaceutical, Biotechnology and Medical Device companies always need TOP Talent. Since 1996, MakroScientific's proven staffing solutions have helped many Life Sciences companies succeed and visualize their goals by increasing ...