Senior QA Compliance Lead — cGMP & Audit Expert

Lonza; Alberta; On-site; CAD 80,000 - 100,000; Full time

Job summary

A leading life sciences company in Alberta is seeking a Senior QA Specialist to support Quality Assurance activities in a cGxP contract manufacturing facility. The ideal candidate will have a degree in Engineering or Science, 5 to 10 years of quality experience in the biopharmaceutical industry, and strong interpersonal skills. Key responsibilities include leading deviation investigations and participating in audits. This role offers an opportunity to contribute to impactful solutions in the life sciences sector.

Qualifications

• 5 to 10 years’ experience in Quality in the Biopharmaceutical industry.
• Familiar with Regulator requirements and local Codes & Standards.
• Good knowledge of quality management systems in GMP facilities.

Responsibilities

• Support day-to-day Quality Assurance activities according to SOPs.
• Lead complex deviation investigations and CAPA proposals.
• Participate in Customer / Agency Audits and Inspections.

Skills

Quality Management

Analytical Skills

Interpersonal Skills

Effective Communication

Education

Degree in Engineering/Science or higher

Job description

A leading life sciences company in Alberta is seeking a Senior QA Specialist to support Quality Assurance activities in a cGxP contract manufacturing facility. The ideal candidate will have a degree in Engineering or Science, 5 to 10 years of quality experience in the biopharmaceutical industry, and strong interpersonal skills. Key responsibilities include leading deviation investigations and participating in audits. This role offers an opportunity to contribute to impactful solutions in the life sciences sector.