CQV Specialist AtomVie

Position: CQV Specialist Job with AtomVie
Join Atom Vie Global Radiopharma Inc. as a CQV Specialist I, where you will ensure laboratory compliance and lead crucial equipment qualification tasks. This role emphasizes collaborative efforts in a GMP environment.

Reporting to the Engineering Manager, the CQV Specialist will assist in calibration programs and laboratory document management. You will collaborate with teams to address equipment issues and enhance operational compliance. This position is vital for enforcing high-quality standards in pharmaceutical production.

Key Responsibilities:

• Execute internal calibration and maintenance programs

• Perform HPLC and equipment qualification activities

• Develop SOPs for laboratory instruments and maintenance

• Support investigations into qualification and validation challenges

• Author non-conformance reports and manage CAPAs

Requirements:

• College Diploma in technical fields (Metrology, Pharmaceutical Sciences)

• 2-5 years relevant GMP lab experience

• Physical capability to lift and maneuver in tight spaces

Bring your technical expertise in calibration and validation to Atom Vie and play a key role in patient care.
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