Downstream Biologics Purification Technologist

Centre de production de produits biologiques Inc; Montreal; On-site; CAD 65,000 - 90,000; Full time

Benefits offered by this job

On-site parking

Competitive compensation

RRSP with employer contributions

Comprehensive benefits

Job summary

Biologics Manufacturing Centre (BMC) Inc. seeks a Manufacturing Technologist, Downstream, to join a highly technical team handling purification activities for biologics and vaccines.

You will operate chromatography systems, perform calibration, and document data in GMP-compliant records, contributing to batch records and client reports. The role requires a life sciences diploma and at least 1 year of biopharma manufacturing experience, with regular daytime hours and potential overtime.

Qualifications

• Post-secondary diploma in life sciences or equivalent.
• Minimum of 1 year of manufacturing or laboratory experience in biopharmaceuticals.
• Hands-on experience with purification processes and chromatographic steps.
• Experience with process control software is an asset.

Responsibilities

• Perform large-scale purification activities in compliance with client requirements.
• Operate chromatography columns and AKTA Ready/Readyflux systems; use Unicorn interfaces.
• Calibrate, verify performance, and troubleshoot equipment for reliability.
• Participate in GMP training and follow SOPs and manufacturing procedures.
• Draft and record data in SOPs, logs, batch records, and client reports.
• Collect samples, perform environmental monitoring, and ensure safety standards.
• Assist in cleaning manufacturing areas per procedures.

Skills

Purification processes

Chromatography

TFF

Nanofiltration

Process control software

Education

Post-secondary diploma in life sciences

Tools

AKTA Ready

Unicorn software

Job description

Biologics Manufacturing Centre (BMC) Inc. seeks a Manufacturing Technologist, Downstream, to join a highly technical team handling purification activities for biologics and vaccines.

You will operate chromatography systems, perform calibration, and document data in GMP-compliant records, contributing to batch records and client reports. The role requires a life sciences diploma and at least 1 year of biopharma manufacturing experience, with regular daytime hours and potential overtime.