On‑Site Senior QA Leader, GMP & Compliance

0011 Evonik Canada Inc._11; Burnaby; Hybrid; CAD 102,000 - 135,000; Full time

Benefits offered by this job

Competitive base compensation

Health & dental benefits

RRSP & pension plans

Generous vacation & time off

Fitness membership support

Training & development

Job summary

EVONIK Vancouver Laboratories is seeking a seasoned QA professional to maintain QA procedures, ensure cGMP compliance, and review batch records for early‑phase products at the Vancouver facility.

You will lead QA activities, guide investigations, oversee deviations and CAPAs, manage change controls, audits, and supplier qualifications, and support process development with strong regulatory knowledge.

Qualifications

• Minimum B.S. degree in chemistry, biology, microbiology, biomedical or chemical engineering or equivalent education.
• Strong leadership and mentoring capabilities in QA environments.
• Experience with cGMP/QC for pharmaceutical/biotech products.
• Excellent communication and cross-functional collaboration skills.

Responsibilities

• Maintain and revise QA procedures as needed.
• Perform QA batch record review and disposition for early-phase products.
• Provide final QA approval of investigations and disposition of impacted batches.
• Manage deviations, CAPAs, and change controls for facilities, equipment, and processes.
• Coordinate internal audits/self-inspections and supplier qualifications.
• Support process development teams with QA expertise and validation planning.
• Communicate effectively with client QA personnel and support audit responses.

Skills

Leadership

Problem solving

Organizational skills

Communication

Education

B.S. in chemistry/biology/biomed/engineering

Tools

Word

Excel

Access

Job description

EVONIK Vancouver Laboratories is seeking a seasoned QA professional to maintain QA procedures, ensure cGMP compliance, and review batch records for early‑phase products at the Vancouver facility.

You will lead QA activities, guide investigations, oversee deviations and CAPAs, manage change controls, audits, and supplier qualifications, and support process development with strong regulatory knowledge.