Manufacturing Technician, Albumin Purification

Grifols

. Set up, operate, and clean manufacturing equipment, including buffer preparation skids, centrifuges, fractionation skids and filter presses, TFF skids and columns, chromatography skids, filtration skids, filling lines within an isolator, and automated packaging lines .

Posted 11/5/2026full-timeMontreal • CanadaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in operating and troubleshooting manufacturing equipment within a cGMP environment, ensuring compliance with safety procedures and quality standards. Proficient in executing manufacturing batch records and participating in validation processes while maintaining accurate documentation.

Highest-signal resume keywords

Manufacturing Equipment OperationCGMP ComplianceVisual InspectionCleanroom ExperienceBilingual in French and English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Buffer Preparation SkidsCentrifugesChromatography SkidsFiltration SkidsCIP/SIP SkidsAutoclavesPackaging Equipment TroubleshootingManufacturing Batch RecordsEnvironmental MonitoringEquipment Calibration

Soft Skills

Ability to Work IndependentlyTeam CollaborationTime Management

Tools & Technologies

Label Verification Vision SystemsVial LabelersShrink-Banding MachinesParts Washers

Industry Keywords

Pharmaceutical TechnologyBiopharmaceutical IndustryHealthcare IndustryCGMPGDP

About the role

Key responsibilities & impact

Set up, operate, and clean manufacturing equipment, including buffer preparation skids, centrifuges, fractionation skids and filter presses, TFF skids and columns, chromatography skids, filtration skids, filling lines within an isolator, and automated packaging lines
Set up and operate CIP/SIP skids, autoclaves, and parts washers
Set up, operate, and troubleshoot packaging equipment, label verification vision systems, vial labelers, vial cartoners, shrink-banding machines, and related equipment
Conduct periodic challenges for packaging systems
Inspect packaged and pre-packaged products for defects through manual and semi-automated visual inspection
Accurately count products before and after packaging
Execute manufacturing batch records in designated areas
Immediately escalate issues that may affect cGMP compliance or manufacturing processes
Participate in sampling, process and cleaning validation, environmental monitoring, clean utilities, in-process testing, weighing, equipment calibration, and maintenance
Participate in the drafting and implementation of GMP documents and maintain records in accordance with GDPs
Perform daily, weekly, and monthly cleaning in the manufacturing area
Maintain and replenish manufacturing supplies
Work safely in accordance with cGMPs, SOPs, safety procedures, and company policies

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 involve working in a refrigerated environment
Experience working in a cleanroom preferred
Bilingual in spoken and written French and English
English is required for documentation, reports, and interactions with Health Canada, the FDA, and multidisciplinary departments located outside Quebec and Canada
Vision examination, including color-vision testing, required for manufacturing technicians performing visual inspection as a qualified function