GMP CQV Specialist

Position: GMP CQV Specialist Role
Elevate your career as a CQV Specialist at Atom Vie Global Radiopharma in Hamilton, Ontario. Focus on ensuring laboratory equipment qualifications and compliance through effective documentation practices onsite.

Reporting to the Engineering Manager, you will assist the Engineering department by managing calibration programs and executing equipment qualifications. This role requires collaboration across teams to address and resolve CQV-related challenges while maintaining adherence to cGMP guidelines. Continuous improvement of engineering processes will also be a priority.

Key Responsibilities:

• Manage internal calibration and maintenance initiatives

• Execute HPLC annual qualification and validation activities

• Develop operational SOPs for laboratory instruments

• Lead documentation for equipment and software validation

• Provide technical support during CQV investigations

Requirements:

• Technical College Diploma or relevant experience

• 2-5 years in a GMP Pharmaceutical lab

• Capacity to lift 50lbs and work in confined spaces

• Familiarity with Health Canada and FDA regulations

• Strong verbal and written communication skills

Utilize your technical expertise in quality assurance and validation to make a difference at Atom Vie.
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