AtomVie Global Radiopharma Inc. ("AtomVie"), incorporated in late 2021, is a global leading CDMO for the GMP manufacturing and distribution of clinical and commercial radiopharmaceuticals and the most recent spinout from the Centre for Probe Development and Commercialization (CPDC). AtomVie offers the full range of scientific, technical, regulatory, quality, logistics and business expertise combined with a specialized infrastructure for the development of your…
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Empowering Next Generation Radiotherapeutics
AtomVie Global Radiopharma Inc. ("AtomVie"), incorporated in late 2021, is a global leading CDMO for the GMP manufacturing and distribution of clinical and commercial radiopharmaceuticals and the most recent spinout from the Centre for Probe Development and Commercialization (CPDC). AtomVie offers the full range of scientific, technical, regulatory, quality, logistics and business expertise combined with a specialized infrastructure for the development of your radiopharmaceuticals from Phase 1 to the commercial marketplace. With a state-of-the art purpose-built facility that will be operational in Q4 2025, AtomVie empowers the development of your radiotherapeutics. For more information about AtomVie, visit our website or contact: [email protected].
Currency and observation date were not supplied; this is not a current valuation or a funding round.
AtomVie Global Radiopharma Inc. has 12 open jobs in Canada as of November 6, 2026. Top locations: Hamilton.
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AtomVie Global Radiopharma Inc.
3+ YOECandidates need a diploma or degree in supply chain, logistics or business, and at least 3 years of logistics, transportation or export experience. Knowledge of IATA, TDG and radioactive material shipping is an asset.
Microsoft Office, ERP systems
AtomVie Global Radiopharma Inc.
15+ YOE5+ MgmtCandidates need a science degree (BSc, MSc or PhD), about 15 years of pharmaceutical or biotech QA experience with at least 5 years managing direct reports, and deep knowledge of Health Canada, FDA and EU GMP rules for sterile products.
electronic quality management system
AtomVie Global Radiopharma Inc.
15+ YOE10+ MgmtCandidates 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
AtomVie Global Radiopharma Inc.
1+ YOECandidates 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
AtomVie Global Radiopharma Inc.
1+ YOECandidates need a college diploma or B.Sc. in chemistry, biotechnology or a related field, plus 1 to 3 years of analytical lab experience with HPLC, GC, TLC or microbiology tests. Proficiency with Empower, Excel and Word, good English communication and the ability to lift up to 23 kg are required.
HPLC, GC, TLC, Empower, Excel, Word
AtomVie Global Radiopharma Inc.
AtomVie Global Radiopharma needs candidates with a college diploma in chemistry, biotechnology, biology or a related field, or two years of university. Previous lab experience, pharmaceutical cGMP or aseptic work, and Canadian Nuclear Safety Commission experience are assets. Candidates must lift up to 10 kg, wear PPE, and be proficient in spreadsheets and word processing.
pH meter, analytical balance, dose calibrator, water bath, sonicator, biological safety cabinet
AtomVie Global Radiopharma Inc.
3+ YOECandidates 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
AtomVie Global Radiopharma Inc.
2+ YOECandidates 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
AtomVie 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
AtomVie Global Radiopharma Inc.
3+ YOECandidates 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
AtomVie Global Radiopharma Inc.
5+ YOECandidates 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
AtomVie Global Radiopharma Inc.
2+ YOECandidates 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
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