Emplois “FDA” au Canada – Page 22

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• 1 mois

  Project Manager II / Gestionnaire de projet II (Canada)

  Montréal, QC

  Télétravail

  

  Indero

  5+ ans3+ gestionBaccalauréat 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

  1 mois

  Project Manager / Gestionnaire de projet (Canada)

  Montréal, QC

  Télétravail

  

  Indero

  3+ ansB.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

  1 mois

  Clinical Trial Delivery Trainer

  Montréal, QC

  Télétravail

  

  Indero

  5+ ansIndero 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

• 1 mois

  Staff Software Engineer - Experience

  Télétravail au Canada

  TélétravailTemps plein

  H

  Helix

  10+ ansCandidates need 10+ years of professional software engineering experience with a record of impact at scale. Helix requires strong backend skills in Go, Java, Python, Scala or Rust, full-stack web experience with React, Next.js, Vue.js or similar, and experience with cloud infrastructure such as AWS, GCP or Azure.

  AWS, GCP, Azure, React, Next.js, Vue.js

• 1 mois

  Senior Director, Technical Development Lead, Device

  Toronto, ON

  Sur placeTemps plein

  BT

  BlueRock Therapeutics Canada ULC

  12+ ansCandidates need an advanced degree in biomedical, mechanical or materials engineering, over 12 years of progressive medical device experience, and senior leadership in biotech or medtech. Strong knowledge of device regulations, design controls and combination products is required.

  Biomedical engineering, Mechanical engineering, Materials science

• 1 mois

  Spécialiste, Affaires réglementaires

  Saint-Bernard, QC

  Temps plein

  

  duBreton

  5+ ansBaccalauréat 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

• 1 mois

  Executive Director, Clinical Trials - Sunnybrook Health Sciences Centre - Regular Full-time 2026-17838

  Toronto, ON

  Temps plein

  SH

  Sunnybrook Health Sciences Centre

  10+ ansCandidates need an MBA or equivalent graduate degree and 10 to 15 years of senior academic clinical research leadership. They must have built or transformed a clinical trials enterprise, know GCP, ICH and Health Canada rules, and engage investigators and industry partners.

  Clinical trials, Leadership, Research, Data management, Team leadership, Translation

• 1 mois

  Reliability Engineer

  Télétravail au Canada

  TélétravailContrat

  

  Sapsol Technologies Inc: A Process-Centric AI & Quantum company

  10+ ansCandidates 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

• 1 mois

  Production Manager

  Ontario

  62 $/hTemps plein

  

  Kelly Services

  10+ ansCandidates 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

• 1 mois

  Quality Assurance Associate

  Brantford, ON

  30 $/hSur placeTemporaire

  ?

  Do you have a passion for quality, an eye for detail, and experience working in a regulated manufacturing environment?; This role is ideal for a quality professional with pharmaceutical, radiopharmaceutical, or…

  Quality assurance, Quality control systems, Quality control, Good manufacturing practices, Documentation, MasterControl

• 1 mois

  Product Cybersecurity Expert

  Ontario

  

  Sonova AG

  5+ ansSonova 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

  1 mois

  Regulatory Systems Analyst Co-op

  Ontario

  

  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

• 1 mois

  Director, Quality Assurance

  Hamilton, ON

  Temps plein

  

  AtomVie Global Radiopharma Inc.

  15+ ans5+ gestionCandidates 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

  1 mois

  VP Quality

  Hamilton, ON

  Temps plein

  

  AtomVie 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

  1 mois

  Microbiologist

  Hamilton, ON

  58k $/anTemps plein

  

  AtomVie 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

  1 mois

  Analytical Development Chemist

  Hamilton, ON

  74k $/anTemps plein

  

  AtomVie 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

  1 mois

  Microbiology - Technical Writer & Data Reviewer

  Hamilton, ON

  79k $/anTemps plein

  

  AtomVie 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

  1 mois

  Quality Assurance Associate- Batch Release

  Hamilton, ON

  65k $/anTemps plein

  

  AtomVie 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

  1 mois

  CQV Specialist I (Lab)

  Hamilton, ON

  64k $/anTemps plein

  

  AtomVie 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

• 1 mois

  Production Manager

  Etobicoke, ON

  57–67 $/hContrat

  

  Randstad Canada

  10+ ansCandidates need a bachelor's degree or equivalent industry experience and 10+ years of progressive production management in regulated industries such as medical devices or optics. They must know ISO 13485, GMP, FDA and Health Canada rules and have experience leading cross-functional teams.

  NetSuite, SAP, Oracle

  1 mois

  Adjoint à la logistique et aux achats

  Sainte-Julie, QC

  50k–60k $/anTemps plein

  

  Randstad Canada

  2+ ansPlus de 2 ans en administration, logistique de transport ou service fournisseurs; Maîtrise de Microsoft Office, surtout Excel et Outlook; Expérience pratique d'un ERP, Maximum est un atout

  Microsoft Excel, Microsoft Outlook, ERP, Maximum

• 1 mois

  Hygiéniste dentaire, technicien(ne) – Service périnatalité, petite enfance et jeunesse

  Quebec

  Temps partiel

  SQ

  Santé Québec Capitale-Nationale

  DEC en techniques d'hygiène dentaire; Membre de l'Ordre des hygiénistes dentaires du Québec; Permis de conduire valide et véhicule

  Dental hygienist, Collaboration, Leadership, Work in teams

  1 mois

  Hygiéniste dentaire, technicien(ne) – Postes et remplacement

  Quebec

  Temps partiel

  SQ

  Santé Québec Capitale-Nationale

  Diplôme et permis d'hygiéniste dentaire; Permis de conduire et véhicule requis; Déplacements fréquents entre plusieurs CHSLD et sites

  Appareil de radiographie dentaire portatif (ARDP), Matériel de détartrage, Fluorure diamine d'argent (FDA)

• 1 mois

  VP, Late-Stage & Commercial Biologics Development

  Vancouver, BC

  Temps plein

  

  AbCellera: AbCellera is a clinical-stage biotechnology company focused on discovering and developing antibody-based medicines in the areas of endocrinology,…

  18+ ans8+ gestionCandidates need a post-secondary degree in a biological or chemical field and 18 to 20+ years in biopharmaceutical process development or CMC, including at least 8 years in leadership. They need a record of taking biologics through PPQ and approval, plus experience with CDMO tech transfers and combination products.

  Troubleshooting, Coaching, Process improvement, Quality assurance, Regulatory affairs, Supply chain management

13 entreprises