Manufacturing Technician – Albumin Purification

Grifols

. Set up, operate, and clean 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 maintaining biopharmaceutical manufacturing equipment, ensuring compliance with cGMP and GDP standards. Proficient in conducting inspections, validations, and maintaining accurate manufacturing records while working effectively in a team-oriented and fast-paced environment.

Highest-signal resume keywords

Biopharmaceutical ManufacturingCGMP ComplianceVisual InspectionCleanroom ExperienceBilingual in French and English

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Buffer PreparationCentrifuge OperationChromatographyFiltrationPackaging Equipment TroubleshootingCIP/SIP OperationEnvironmental MonitoringEquipment CalibrationGMP DocumentationManufacturing Batch Records

Soft Skills

Ability to Manage Multiple PrioritiesTeam CollaborationIndependent Work

Tools & Technologies

Automated Packaging LinesLabel-Verification Vision SystemsVial LabelersShrink-Banding MachinesParts WashersAutoclaves

Industry Keywords

Pharmaceutical TechnologyHealthcare IndustryClean UtilitiesProcess ValidationSOP Compliance

About the role

Key responsibilities & impact

Set up, operate, and clean 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 pre- and post-packaged products.
Execute manufacturing batch records in designated areas.
Immediately escalate issues that may affect cGMP compliance or manufacturing processes to the responsible manager.
Participate in sampling, process and cleaning validation, environmental monitoring, clean utilities, in-process testing, weighing, equipment calibration, and maintenance.
Write and implement GMP documents and maintain records and data in accordance with GDPs.
Perform daily, weekly, and monthly cleaning in accordance with SOPs.
Maintain and replenish manufacturing supplies.
Develop multidisciplinary skills by rotating among Albumin Purification, Fractionation, IGIV Purification, Filling, and Packaging.

Requirements

What you’ll need

High school diploma or a 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 cleanrooms preferred.
Bilingual in French and English, both spoken and written.
For manufacturing technicians performing visual inspection as qualified personnel: vision examination, including color-blindness testing.