Quality Investigator - Cell Therapy Manufacturing
BioPharma Consulting JAD Group
Summary
Grow your quality career in cell therapy at a leading biotechnology company in Boston, Massachusetts. You will investigate manufacturing and QC deviations, find root cause and drive CAPAs to closure.
Job description
What you'll do
- Investigate standard-complexity deviations with interviews, GEMBA and root cause analysis tools.
- Propose CAPAs with SMEs; manage records in eQMS and meet due dates.
- Support change controls and effectiveness checks.
- Track deliverables and escalate risks to the team lead.
Qualifications
- Bachelor's degree in Engineering or related + 2–5 years.
- Pharma/biotech quality, manufacturing or engineering experience.
- Deviation/CAPA experience and eQMS.
- Clear technical writing.
Details
- Contract: 12 months, with possible extension
- Shift: On-site; shift set by the hiring manager (may be non-standard)
- Start: Immediate
Requirements
- Bachelor's degree in Engineering or related field
- 2–5 years of experience
- Pharma/biotech quality, manufacturing or engineering experience
- Deviation/CAPA experience
- eQMS experience
- Clear technical writing
Company overview
BioPharma Consulting JAD Group is a specialized consulting firm operating in the biotechnology and pharmaceutical sectors. The company provides expert advisory services to biopharmaceutical companies, research institutions, and healthcare organizations. Their consulting services likely encompass strategic planning, regulatory compliance, market access strategies, clinical development optimization, and commercialization support for biotech and pharmaceutical products. As part of the JAD Group network, the firm leverages collective expertise to address complex challenges in drug development, manufacturing, and market entry. Their focus on biotechnology research suggests they work closely with emerging biotech companies to navigate the intricate landscape of drug discovery, clinical trials, and regulatory pathways. The consulting group serves as a bridge between scientific innovation and commercial success, helping clients accelerate their research and development timelines while ensuring compliance with global regulatory standards.