Technicien de production, Albumin Purification

Grifols

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

Posted 11/4/2026full-timeMontreal • CanadaMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in operating and maintaining manufacturing equipment within the biopharmaceutical industry, with a strong focus on compliance with cGMP and GDP standards. Proficient in conducting inspections, executing batch records, and participating in validation processes while ensuring product quality and safety.

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 Manage Multiple PrioritiesTeam CollaborationIndependent Work

Tools & Technologies

Label Verification Vision SystemsVial LabelersCartonersShrink-Banding MachinesParts Washers

Certifications & Qualifications

High School DiplomaCEGEP/College Diploma in Pharmaceutical Technology

Industry Keywords

BiopharmaceuticalPharmaceuticalHealthcareManufacturing Batch RecordsCleaning Validation

About the role

Key responsibilities & impact

Set up, operate, and clean manufacturing equipment including buffer preparation skids, centrifuges, fractionation skids, filter presses, TFF skids and columns, chromatography skids, filtration skids, filling lines, 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, 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-automatic visual inspection.
Accurately count pre- and post-packaged products.
Execute manufacturing batch records in designated areas.
Escalate issues potentially impacting cGMP 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 required records and data according to GDPs.
Perform daily, weekly, and monthly cleaning in the manufacturing area.
Maintain and replenish manufacturing supplies.
Develop multidisciplinary skills by rotating among Albumin Purification, Fractionation, IGIV Purification, Filling, and Packaging areas.

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.