Cell Therapy Quality Investigator: CAPA & Deviation Expert

BioPharma Consulting JAD Group; Boston (MA); On-site; USD 90,000 - 120,000; Full time

Job summary

BioPharma Consulting JAD Group in Boston, MA seeks a quality-focused professional to investigate deviations in cell therapy manufacturing and QC, drive CAPAs with SMEs, and manage records in the eQMS. The role supports change controls, effectiveness checks, and risk escalation.

The ideal candidate has 2–5 years in pharma/biotech quality or engineering, with strong technical writing skills and experience in CAPA processes. Start immediately on a 12-month, on-site contract.

Qualifications

• Bachelor's degree in Engineering or related field with 2–5 years of experience.
• Pharma/biotech quality, manufacturing or engineering experience.
• Deviation/CAPA experience and familiarity with eQMS.
• Clear technical writing skills.

Responsibilities

• Investigate standard-complexity deviations using 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 elevate risks to the team lead.

Skills

Pharma/biotech quality, manufacturing,

Deviation/CAPA experience

Clear technical writing

Education

Bachelor's degree in Engineering or related

Tools

eQMS

Job description

BioPharma Consulting JAD Group in Boston, MA seeks a quality-focused professional to investigate deviations in cell therapy manufacturing and QC, drive CAPAs with SMEs, and manage records in the eQMS. The role supports change controls, effectiveness checks, and risk escalation.

The ideal candidate has 2–5 years in pharma/biotech quality or engineering, with strong technical writing skills and experience in CAPA processes. Start immediately on a 12-month, on-site contract.