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Fractionation Manufacturing Supervisor
GrifolsFractionation Manufacturing Supervisor overseeing plasma-derived medicine production at Grifols Canada. Leading cGMP shifts, personnel, documentation, equipment, and cross-functional manufacturing activities.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in leading manufacturing operations within a cGMP biopharmaceutical environment, ensuring compliance with safety and quality standards while effectively training and developing personnel. Proficient in troubleshooting manufacturing systems and equipment, with a strong understanding of aseptic processing and regulatory requirements.
Highest-signal resume keywords
Manufacturing LeadershipCGMP ComplianceAseptic Processing KnowledgeQuality Management SystemsBilingual Communication
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Manufacturing LeadershipCGMP KnowledgeAseptic ProcessingTroubleshootingProcess ControlEquipment ValidationBatch Record ReviewPreventive MaintenanceAutomated Control SystemsStatistical Analysis
Soft Skills
Excellent CommunicationOrganizational SkillsDocumentation SkillsProblem-Solving SkillsTraining and Development
Tools & Technologies
Microsoft WordMicrosoft ExcelMicrosoft PowerPointMicrosoft Project
Industry Keywords
BiopharmaceuticalFDA RegulationsOSHA ComplianceEPA RegulationsCGMP StandardsCleanroom OperationsQuality ControlQuality AssuranceMaterials ManagementValidation
Tech Stack
Tools & technologiesReact
About the role
Key responsibilities & impact- Lead and direct daily manufacturing shift activities in the Fractionation production area, assigning tasks and following up on progress
- Ensure quality, safety, delivery, and productivity objectives are met
- Issue and investigate quality and preventive-maintenance notifications in a timely manner
- Ensure manufacturing schedules, products, and materials are delivered
- Train Fractionation manufacturing personnel on processes, safety, and cGMP activities
- Identify development gaps and implement applicable plans and targets
- Review safety cases and identify or implement corrective actions
- Develop, train, and monitor personnel to ensure compliant product manufacturing
- Ensure compliance with site procedures, health and safety protocols, and applicable federal health-authority regulations
- Coordinate and prepare reviews of batch-related documents, including batch records and SOPs
- Execute quality management system assignments, including CAPA and change control, and ensure timely closure
- Ensure equipment operates properly and request equipment or facility repairs and modifications as needed
- Resolve operational and equipment issues and coordinate emergency repairs, modifications, and preventive maintenance
- Coordinate manufacturing activities with Quality Control, Materials Management, Quality Assurance, Validation, and other departments
Requirements
What you’ll need- CEGEP diploma or technical degree required
- BS degree in Science, Engineering, or a related field preferred
- Previous experience in biologics protein fractionation manufacturing is an asset
- 1–3 years of manufacturing leadership/supervisory experience in a cGMP biopharmaceutical environment
- Good understanding of process equipment operating principles
- Strong knowledge of technical and scientific principles associated with aseptic processing
- Familiarity with automated control systems
- Knowledge of cGMP, OSHA, EPA, and FDA facility requirements and regulations
- Knowledge of aseptic operations, statistics, equipment design, process control, process scale-up, aseptic pharmaceutical processes, and equipment validation
- Ability to troubleshoot and maintain manufacturing systems, equipment, and processes
- Ability to gown aseptically for cleanroom operations
- Ability to respond quickly to assess and resolve problems
- Excellent communication, documentation, organizational, and troubleshooting skills
- Ability to accurately read, understand, and follow company SOPs and guidelines
- Strong writing and computer skills
- Proficiency in Microsoft Word, Excel, PowerPoint, and Project
- Bilingual in spoken and written French and English; English required for documentation and communication with other Grifols sites
Benefits
Comp & perks- 🌐 Worldwide ❌ Jobs You've Hidden ⭐️ Saved Jobs ✅ Applied Jobs ✉️ Email Alerts 👤 Account Grifols Website LinkedIn All Job Openings 10,000+ employees Founded 1909 🏥 Healthcare 🏭 Manufacturing 🧬 Biotechnology Healthcare
- Manufacturing
- Biotechnology Grifols is a global healthcare company dedicated to improving the health and well-being of people around the world. They focus on the development, production, and distribution of innovative plasma-derived medicines and have a strong commitment to research and development in the pharmaceutical sector. Grifols aims to provide solutions for patients with rare diseases and chronic conditions, contributing significantly to the field of biotechnology and healthcare. Fractionation Manufacturing Supervisor 🔥 26 minutes ago 🏢 Montreal – Onsite ⏰ Full Time 🟢 Junior ✨ Supervisor 🗣️🇫🇷 French Required Apply Now Customize resume + cover letter Report problem ☆ Save ☑️ Mark as applied ❌ Hide 📋 Description
- Lead and direct daily manufacturing shift activities in the Fractionation production area, assigning tasks and following up on progress
- Ensure quality, safety, delivery, and productivity objectives are met
- Issue and investigate quality and preventive-maintenance notifications in a timely manner
- Ensure manufacturing schedules, products, and materials are delivered
- Train Fractionation manufacturing personnel on processes, safety, and cGMP activities
- Identify development gaps and implement applicable plans and targets
- Review safety cases and identify or implement corrective actions
- Develop, train, and monitor personnel to ensure compliant product manufacturing
- Ensure compliance with site procedures, health and safety protocols, and applicable federal health-authority regulations
- Coordinate and prepare reviews of batch-related documents, including batch records and SOPs
- Execute quality management system assignments, including CAPA and change control, and ensure timely closure
- Ensure equipment operates properly and request equipment or facility repairs and modifications as needed
- Resolve operational and equipment issues and coordinate emergency repairs, modifications, and preventive maintenance
- Coordinate manufacturing activities with Quality Control, Materials Management, Quality Assurance, Validation, and other departments 🎯 Requirements
- CEGEP diploma or technical degree required
- BS degree in Science, Engineering, or a related field preferred
- Previous experience in biologics protein fractionation manufacturing is an asset
- 1–3 years of manufacturing leadership/supervisory experience in a cGMP biopharmaceutical environment
- Good understanding of process equipment operating principles
- Strong knowledge of technical and scientific principles associated with aseptic processing
- Familiarity with automated control systems
- Knowledge of cGMP, OSHA, EPA, and FDA facility requirements and regulations
- Knowledge of aseptic operations, statistics, equipment design, process control, process scale-up, aseptic pharmaceutical processes, and equipment validation
- Ability to troubleshoot and maintain manufacturing systems, equipment, and processes
- Ability to gown aseptically for cleanroom operations
- Ability to respond quickly to assess and resolve problems
- Excellent communication, documentation, organizational, and troubleshooting skills
- Ability to accurately read, understand, and follow company SOPs and guidelines
- Strong writing and computer skills
- Proficiency in Microsoft Word, Excel, PowerPoint, and Project
- Bilingual in spoken and written French and English; English required for documentation and communication with other Grifols sites Apply Now 📊 Check your resume score for this job Improve your chances of getting an interview by checking your resume score before you apply. Check Resume Score 🌐 Worldwide Built by Lior Neu-ner. I'd love to hear your feedback — Get in touch via DM or support@remoterocketship.com Search Search Jobs by country Search jobs by city Search jobs by job title Search entry-level jobs Search junior-level jobs Search senior-level jobs Search jobs by tech stack Search jobs by contract type Search remote internships Search remote part-time jobs Remote jobs Anywhere in the World Companies Hiring Anywhere in the World Companies Hiring Sales People Anywhere in the World Companies Hiring Software Engineers Anywhere in the World Resources Advice Tips for finding remote jobs Interview questions and answers Resume examples Cover letter examples Post a job Affiliates About us Is Remote Rocketship legit? Privacy policy Terms of service Job board SEO course Remote Job Search MasterClass AI Apply Copilot OpenClaw job finder Find jobs using your resume Jobs by Country Remote jobs anywhere in the world (Worldwide remote jobs) Remote jobs United States Remote jobs Australia Remote jobs Brazil Remote jobs Canada Remote jobs France Remote jobs Ireland Remote jobs Germany Remote jobs Netherlands Remote jobs Spain Remote jobs UK Popular Jobs Remote data analyst jobs Remote customer support jobs Remote executive assistant jobs Remote marketing jobs Remote product designer jobs Remote product manager jobs Remote project manager jobs Remote recruiter jobs Remote sales jobs Remote software engineer jobs Jobs by Type Remote full-time jobs Remote part-time jobs Remote contract jobs Remote internship jobs Remote entry-level jobs Remote jobs with no experience required Remote junior jobs (1-3 years of experience) Digital nomad jobs Remote jobs with no degree required Freelance remote jobs Temporary remote jobs Remote jobs hiring now Stay at home mom jobs