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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Albumin Purification and related biopharmaceutical processes while adhering to cGMP regulations and maintaining high standards of cleanliness and safety. Proficient in operating and troubleshooting manufacturing and packaging equipment, with strong record-keeping and documentation skills.
Highest-signal resume keywords
Albumin PurificationCGMP ComplianceManufacturing Equipment OperationBilingual in French and EnglishCleanroom Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Albumin PurificationCGMP ComplianceManufacturing Equipment OperationPackaging Equipment TroubleshootingEnvironmental MonitoringIn-Process TestingGMP DocumentationEquipment CalibrationVisual InspectionChange Control System
Soft Skills
Ability to Work IndependentlyTeam CollaborationTime ManagementAdaptability
Tools & Technologies
CIP/SIP SkidsAutoclavesParts WashersLabel Verification Vision Systems
Certifications & Qualifications
High School DiplomaCEGEP/College Diploma in Pharmaceutical Technology
Industry Keywords
Biopharmaceutical IndustryPharmaceutical IndustryHealthcare IndustryPPE RequirementsRefrigerated Environment
About the role
Key responsibilities & impact- Primarily work in Albumin Purification while developing multidisciplinary skills through rotation in Fractionation, IGIV Purification, Filling, and Packaging
- Work in a manufacturing environment regulated by cGMPs, SOPs, safety procedures, and company policies
- Clean and maintain the workplace to control bioburden levels
- Clean operating equipment to prevent product contamination
- Maintain accurate records and logs
- Assist with operating process equipment safely
- Set up, operate, and clean manufacturing and packaging equipment
- Set up and operate CIP/SIP skids, autoclaves, and parts washers
- Set up, operate, and troubleshoot packaging equipment and label verification vision systems
- Conduct periodic packaging-system challenges
- Inspect packaged and pre-packaged products for defects
- Count products before and after packaging
- Execute manufacturing batch records
- Immediately escalate issues potentially impacting cGMP or manufacturing processes
- Participate in sampling, environmental monitoring, in-process testing, weighing, equipment calibration, and maintenance
- Write and implement GMP documents using the change control system and maintain GDP-compliant records
- Perform daily, weekly, and monthly cleaning
- Maintain and replenish manufacturing supplies
- Report to a Supervisor or Manager
Requirements
What you’ll need- High school diploma or CEGEP/college diploma in Pharmaceutical Technology
- One year of experience in the biopharmaceutical, pharmaceutical, or healthcare industry preferred
- Ability to work in a fast-paced environment and manage multiple priorities
- Ability to work independently and as part of a team
- Must be able to lift, push, and pull at least 15 kg and wear PPE as required
- Some tasks will involve working in a refrigerated environment
- Experience operating in a cleanroom preferred
- Bilingual in French and English, both spoken and written
- English is required for documentation, reports, and interactions with Health Canada, the FDA, and multidisciplinary departments based outside Quebec and Canada
- Vision examination, including color-vision testing, required for manufacturing technicians performing visual inspection as qualified personnel
Benefits
Comp & perks- Regular full-time employment
- Weekend shift: Friday, Saturday, and Sunday, from 12:00 p.m. to 12:00 a.m.