Site Quality Director
AstraZeneca · Hamilton, Ontario, Canada · Global
Posted 60+ days ago
Quality Improvement
–
Not yet analysed
Demand80
Career growth70
Healthcare fit65
Remote potential10
5-year outlook
Competitive director-level compensation in the pharmaceutical industry, with potential for growth in the expanding radiopharmaceutical sector.
Clinical license
Not required
Applicant reach
narrow
Seniority
senior
Employment type
full-time
Date found
2026-09-08
Intelligence details
Why this is worth applying to
Consider if you have significant QA/QC and regulatory compliance experience in pharmaceutical manufacturing; otherwise, it's a long shot. The role offers high impact in a cutting-edge field but requires deep industry expertise.
Who should apply
Pharmacists with pharma industry experience, doctors with quality management background, allied health professionals with lab and compliance experience.
CV angle
Highlight clinical knowledge of patient safety, attention to detail, understanding of regulatory requirements, and any experience with quality systems, audits, or compliance.
Skills to highlight
- cGMP
- QA/QC
- regulatory compliance
- CAPA
- leadership
- strategic planning
- budget management
- continuous improvement
Role summary
A senior leadership role overseeing quality assurance and compliance at a radiopharmaceutical manufacturing site, ensuring cGMP compliance and readiness for regulatory inspections.
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