Technicien de production, 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 automatic packaging lines.

Posted 10/6/2026full-timeMontreal • CanadaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in operating and maintaining manufacturing equipment in compliance with cGMP standards, including experience in clean room operations and visual inspection processes. Proficient in executing manufacturing batch records and maintaining GDP-compliant documentation.

Highest-signal resume keywords

Manufacturing Equipment OperationCGMP ComplianceVisual InspectionClean Room OperationBilingualism (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 TroubleshootingGMP DocumentationEnvironmental MonitoringEquipment Calibration

Soft Skills

Ability to Work IndependentlyTeam CollaborationTime Management

Tools & Technologies

Label Verification Vision SystemsVial LabelersShrink-Banding MachinesParts Washers

Certifications & Qualifications

High School DiplomaCEGEP/College Diploma in Pharmaceutical Technology

Industry Keywords

BiopharmaceuticalPharmaceuticalHealthcareCGMPGDP

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 automatic 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 labeling equipment.
Conduct periodic challenges for packaging systems.
Inspect packaged and pre-packaged products for defects through manual and semi-automatic visual inspection.
Accurately count pre- and post-packaged products.
Execute manufacturing batch records in designated areas.
Immediately escalate issues potentially impacting cGMP or manufacturing processes.
Participate in sampling, validation, 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 according to SOPs.
Maintain and replenish manufacturing supplies.

Requirements

What you’ll need

High school diploma or CEGEP/College diploma in Pharmaceutical Technology.
Preferred 1-year experience within the biopharmaceutical, pharmaceutical, healthcare industry.
Ability to work in a fast-paced environment and manage multiple priorities.
Ability to work independently as well as in a team environment.
Must be able to lift, push, pull at least 15kg and wear PPE as required.
Some tasks will involve working in a refrigerated environment.
Experience in clean room operation preferred.
Bilingualism (French and English) both spoken and written.
For manufacturing technicians performing visual inspection as a qualified person: eye sight exam including color blindness testing.

Benefits

Comp & perks

Regular Full-Time employment
Night shift