Microbiology - Technical Writer & Data Reviewer
Hamilton, ONAtomVie Global Radiopharma Inc.
2+ ansCandidates need a science degree, 2 to 3 years of GMP-regulated experience, and experience reviewing lab documents and writing technical reports. Strong writing, attention to detail, and comfort with CAPAs and quality systems are essential.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Electronic quality management system
Production Technician
Hamilton, ONAtomVie Global Radiopharma Inc.
Candidates need a biotechnology certificate or a relevant diploma, prior experience in a GMP or aseptic environment, and the ability to lift 23 kilograms. Flexibility to work rotating shifts and weekends is required.
Packaging materials
Quality Assurance Associate- Batch Release
Hamilton, ONAtomVie Global Radiopharma Inc.
3+ ansCandidates need a B.Sc or M.Sc in the life sciences and 3-5 years of experience in a GMP or similarly regulated environment, preferred. They must know Health Canada, FDA, EU GMP, ICH and ISO rules for sterile products, communicate well in English, and work flexible shifts.
ERP system
QA - Data Reviewer, Associate
Hamilton, ONAtomVie Global Radiopharma Inc.
5+ ansCandidates need post-secondary education in engineering, chemistry, microbiology or a related field, plus at least 5 years of analytical testing or data review in pharmaceutical or radiopharmaceutical work. GMP experience, strong knowledge of data integrity and 21 CFR Part 11, and excellent English communication are required.
HPLC, GC, TLC, pH meter
CQV Specialist I (Lab)
Hamilton, ONAtomVie Global Radiopharma Inc.
2+ ansCandidates need a college diploma in a technical field or relevant experience, typically 2 to 5 years in a GMP pharmaceutical lab, ideally in metrology. They need knowledge of Health Canada and FDA regulations, experience with Empower CDS and Waters HPLC systems, and strong technical writing skills. The role also requires being able to lift 50 lbs and work in confined spaces.
Empower CDS, Waters HPLC, Gas chromatography, CMMS