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Hays
8+ YOECandidates need at least 8-10 years in the food industry, ideally in high-speed automated pick-pack fulfillment, plus proven budget, P&L and operating cost management. Lean Six Sigma or similar continuous improvement experience and HACCP/GMP food safety knowledge are must-haves.
Warehouse operations, Process improvement, Material handling, Inventory management, HACCP, Good manufacturing practices
Agilus Work Solutions: Experts in Specialized Talent for Nearly 50 years. Canada's largest, full service, privately-owned recruiting firm.
6+ YOECandidates need a bachelor's degree in health, clinical or biological sciences and about 6 years of clinical data management experience. Experience with EDC, CTMS and FDA 21 CFR Part 11 compliant systems is required.
EDC system, CTMS, Project management tools
Mars
5+ YOE3+ MgmtCandidates need a bachelor's degree in a relevant science or engineering field, 5 to 8 years of sanitation experience in food, pharma or CPG manufacturing, and at least 3 years leading teams. Strong knowledge of FDA, USDA, FSMA, HACCP and GMPs is required, along with willingness to work nights and weekends.
Microsoft Office, Sanitation management software
Indero
7+ YOECandidates need a related B.Sc., at least 7 years of industry experience with 5 years in Phase I-III clinical trial project management and financial accountability, and experience leading multinational trials over $25M USD. Strong knowledge of GCP, ICH, FDA and Health Canada rules and fluent English are required; PMP and dermatology experience are assets.
Microsoft Office, Trial Master File (TMF) system
Indero
2+ YOEBaccalauréat scientifique ou équivalent; Au moins 2 à 3 ans d'expérience en recherche clinique (CRO ou pharma); Expérience en démarrage d'études essentielle
Regulatory affairs, Leadership, Clinical trials, Translation, Clinical research, Google Cloud
Indero
5+ YOE3+ MgmtIndero needs a candidate with a bachelor's degree in clinical research or a related field and at least 5 years in clinical research, including 3 years managing Phase I and II trials. Strong knowledge of GCP, ICH, FDA and Health Canada rules is required, with dermatology trial experience strongly preferred.
Microsoft Office Suite, Trial Master File (TMF)
Indero
5+ YOE3+ MgmtBaccalauréat dans un domaine lié à la recherche clinique; Au moins 5 ans d'expérience dans l'industrie; Au moins 3 ans en gestion d'essais cliniques de phases I à III
Microsoft Office, eCRF, TMF
Indero
3+ YOEB.Sc. dans un domaine lié à la recherche clinique; Minimum 3 ans d'expérience dans l'industrie pharmaceutique, biotechnologique ou CRO; Au moins 2 ans de coordination d'essais cliniques
Microsoft Office, Excel
Indero
5+ YOEIndero requires a bachelor's degree in a relevant field and at least 5 years of clinical research experience in biotech, pharma or CRO work. Candidates need prior clinical trial delivery experience, training or coaching experience, and good knowledge of ICH-GCP and Health Canada, FDA and EMA rules.
Microsoft Copilot, ChatGPT, Gemini
duBreton
5+ YOEBaccalauréat en agroalimentaire, sciences alimentaires, biologie, chimie ou domaine connexe; 5 à 7 ans d'expérience en affaires réglementaires, idéalement dans la viande; Connaissance approfondie des réglementations ACIA
Microsoft 365
Sapsol Technologies Inc: A Process-Centric AI & Quantum company
10+ YOECandidates need 10+ years of reliability engineering experience, ideally in medical devices, plus a Bachelor's degree in an engineering discipline. Strong skills in test planning, fixtures, statistical analysis and regulatory standards such as ISO 13485 and 21 CFR 820 are required.
Minitab, JMP, Reliasoft, PTC Windchill, Python, Matlab
Kelly Services
10+ YOECandidates need a bachelor's degree in engineering or operations (or equivalent experience) and 10+ years of progressive production management in medical devices or similar regulated industries. Required skills include ISO 13485, GMP, FDA and Health Canada knowledge, ERP/MRP systems such as NetSuite, SAP or Oracle, and proven cross-functional leadership.
NetSuite, SAP, Oracle ERP, MRP
Sonova AG
5+ YOESonova AG needs candidates with 5+ years in software, architecture, product development or DevSecOps, including 3+ years in cybersecurity. They should know secure development, threat modeling and vulnerability management, and communicate well in English.
CI/CD pipelines
Sonova AG
Candidates need a current or recent bachelor's degree in engineering, life sciences or a related field, plus interest in regulatory affairs and quality assurance. They also need strong analytical skills, fluent English, and proficiency with Microsoft Office.
Microsoft Office
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.
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
14 companies