Metrology Specialist: GMP Equipment Qualification

AtomVie Global Radiopharma Inc.; Hamilton; On-site; CAD 58,000 - 70,000; Full time

Benefits offered by this job

Health & dental benefits

RRSP matching

Wellness programs

Job summary

AtomVie Global Radiopharma Inc. is seeking a Metrologist (CQV Specialist) to support qualification, calibration, recertification, and documentation for GMP laboratory equipment.

The role involves coordinating with third-party contractors and driving continuous engineering improvements across sites. The position requires a technical diploma and 2–5 years GMP lab experience, with hands-on qualification tasks and strong regulatory knowledge.

Qualifications

• Minimum 2–5 years hands-on GMP pharmaceutical lab experience, metrology preferred.
• College Diploma in a technical field or equivalent experience.
• Ability to lift 50 lbs and work in small spaces.
• Experience with validation and CQV activities is a plus.

Responsibilities

• Manage and execute calibration and preventive maintenance programs with records.
• Perform equipment qualification and validation activities (e.g., HPLC, GC) and balance verification.
• Create/Develop lab SOPs and CMMS maintenance programs.
• Lead development and execution of qualification documentation for lab equipment and software validation.
• Coordinate with teams to ensure calibration programs align with cGMPs and Validation Plan.
• Investigate and troubleshoot CQV tasks and deviations; support deviations closure.
• Lead nonconformances and CAPAs; assist repairs of production and QC equipment.

Skills

Regulatory knowledge Health Canada FDA

Analytical troubleshooting

Technical report writing

Cross-team collaboration

Education

College Diploma in Metrology/Pharma or technical field

Tools

Empower CDS

Waters HPLC

Job description

AtomVie Global Radiopharma Inc. is seeking a Metrologist (CQV Specialist) to support qualification, calibration, recertification, and documentation for GMP laboratory equipment.

The role involves coordinating with third-party contractors and driving continuous engineering improvements across sites. The position requires a technical diploma and 2–5 years GMP lab experience, with hands-on qualification tasks and strong regulatory knowledge.