About the Opportunity
About You
- Bachelor's Degree in a related science/technology field
- Minimum Five (5) years of experience in a GMP and/or UPS 797 environment (pharmaceutical, radiopharmaceutical or biopharmaceutical environment)
- Quality Management and Leadership experience in a GMP-compliant pharmaceutical production facility
- Strong working knowledge and formal training in Good Manufacturing Practices (GMP), USP 797
- Strong working knowledge of Health Canada guidelines (Guide 0001, Guide 0071, Positron Emitting Radiopharmaceuticals (PER)).
- Demonstrated knowledge of Health Canada and/or other regulatory agency inspections and internal and/or vendor audits (i.e. Canadian Nuclear Safety Commission (CNSC)).
- Proven track record in facilitating regulatory and/or client audits
- Extensive knowledge of radiopharmacy and radiochemistry is preferred.
- Competency with computer applications such as Microsoft Office and information/document management systems.
- Excellent organizational and time management skills
- Excellent oral and written communication skills
- Ability to work independently
- Knowledge of USP 797 standards is an asset.
- Competencies in other languages an asset, French preferred
Hours
- Permanent full-time position; 75 hours biweekly
Compensation and Benefits
Nova Scotia Health Authority
