QA Specialist II – Lot Review (GMP Biotech)

Lonza; Alberta; On-site; CAD 70,000 - 90,000; Full time

Job summary

A global leader in life sciences is seeking a Quality Assurance Specialist 2 to support day-to-day quality assurance activities in compliance with SOPs in a GMP environment. The ideal candidate will have a degree and 3-5 years of experience, or a diploma with 5-7 years of experience. Key responsibilities include reviewing documentation, ensuring compliance, and leading projects. Located in Alberta, Canada, this role offers competitive compensation and a dynamic working culture.

Benefits

Competitive compensation

Professional growth opportunities

Comprehensive medical insurance

Company transport from designated locations

Qualifications

• 3 to 5 years’ experience in a similar industry or role.
• 5 to 7 years’ experience with a diploma.
• Fair knowledge of regulatory requirements like FDA, EMEA.

Responsibilities

• Support day-to-day QA activities in compliance with SOPs.
• Review and approve SOPs, protocols, and reports.
• Lead deviation investigations and provide corrective guidance.

Skills

Quality management system

Regulatory requirements

GxP compliance

Problem-solving

Team collaboration

Education

Degree from a recognized institution

Diploma

Job description

A global leader in life sciences is seeking a Quality Assurance Specialist 2 to support day-to-day quality assurance activities in compliance with SOPs in a GMP environment. The ideal candidate will have a degree and 3-5 years of experience, or a diploma with 5-7 years of experience. Key responsibilities include reviewing documentation, ensuring compliance, and leading projects. Located in Alberta, Canada, this role offers competitive compensation and a dynamic working culture.