Drive high-quality pharmaceutical practices as a CQV Specialist I at AtomVie Global Radiopharma Inc., focusing on laboratory equipment validation and compliance initiatives. This role is crucial for adhering to GMP standards.

The CQV Specialist will work under the Engineering Manager's guidance to execute calibration and maintenance tasks and lead equipment qualification efforts. Collaboration with diverse teams is essential to troubleshoot issues and support continuous improvements, all aimed at enhancing patient outcomes.

Key Responsibilities:
• Manage vendor calibration and technical maintenance efforts
• Conduct qualifications for lab equipment and software
• Create operational SOPs for laboratory instruments
• Investigate and resolve equipment issues promptly
• Lead CAPA initiatives related to equipment non-conformance

Requirements:
• Technical College Diploma or equivalent experience
• 2-5 years hands-on GMP experience in a lab
• Ability to perform physical tasks in confined spaces

Utilize your problem-solving and communication skills at AtomVie, advancing healthcare through innovation.
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📌 Laboratory CQV Specialist at AtomVie Global (Ontario)
🏢 AtomVie Global Radiopharma
📍 Ontario