VP Quality
Hamilton, ONAtomVie Global Radiopharma Inc.
15+ ans10+ gestionCandidates need a relevant science degree (BSc, MSc or PhD), at least 15 years of pharmaceutical QA experience in an FDA, Health Canada or EMA regulated industry, and 10 years managing cross-functional QA and QC teams. Sterile manufacturing, facility design and validation, and leading regulatory inspections are must-haves.
Good manufacturing practices, Radiopharmaceuticals, Regulatory compliance, Strategic planning, Quality assurance, Quality control
Microbiologist
Hamilton, ONAtomVie Global Radiopharma Inc.
1+ ansCandidates need a B.Sc. in Microbiology or a related field and 1 to 3 years of microbiological testing experience. Strong spreadsheet skills, clear English writing and the ability to lift up to 23 kg are required.
Excel, Google Sheets
Analytical Development Chemist
Hamilton, ONAtomVie Global Radiopharma Inc.
3+ ansCandidates need a university degree in biology, biological chemistry, biotechnology or a related discipline, with an M.Sc. or Ph.D. preferred. They need 3-4 years of pharmaceutical cGMP experience with HPLC, GC, TLC and microbiology tests, plus written and spoken English and flexibility for shift work.
Empower, Waters HPLC, HPLC, GC
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
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
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