Biologics QA Associate: GMP, mAbs & ADCs

Eurofins-Canada-Biopharma; Mississauga; On-site; CAD 63,000 - 77,000; Full time

Benefits offered by this job

Health & dental coverage

Life and disability insurance

RRSP with 3% company match

Paid holidays

Paid time off

Job summary

Eurofins CDMO Alphora, Inc. is seeking a QA Associate – Biologics to support cGMP compliance for biotechnology products, including mAbs and ADCs.

The role involves quality oversight of GMP activities, batch records, and release documentation within a Biologics facility in a fast‑paced environment. The ideal candidate has a BSc in Biochemistry or Microbiology with 2–5 years of pharmaceutical quality experience and strong cGMP knowledge.

Qualifications

• 2-5 years of pharmaceutical quality experience preferred.
• Strong understanding of cGMP and related regulations.
• Excellent written and verbal communication skills.

Responsibilities

• Provide quality oversight for GMP activities within the Biologics unit.
• Review batch records, release documentation and change controls.
• Assist with deviations, investigations and CAPA.
• Support environmental monitoring and contamination control programs.
• Participate in audits and continuous quality improvement.

Skills

Quality oversight

cGMP knowledge

Documentation

Multi-tasking

Communication

Education

BSc in Biochemistry/Microbiology or related

Job description

Eurofins CDMO Alphora, Inc. is seeking a QA Associate – Biologics to support cGMP compliance for biotechnology products, including mAbs and ADCs.

The role involves quality oversight of GMP activities, batch records, and release documentation within a Biologics facility in a fast‑paced environment. The ideal candidate has a BSc in Biochemistry or Microbiology with 2–5 years of pharmaceutical quality experience and strong cGMP knowledge.