Join AtomVie Global Radiopharma Inc. as a Lab CQV Specialist, where you will manage laboratory equipment qualifications and uphold GMP compliance standards.
Reporting to the Engineering Manager, this role focuses on executing calibrations, managing third-party contractors, and enhancing the engineering department’s performance. You'll actively contribute to troubleshooting CQV issues, ensuring that qualifications and compliance meet required standards.
Key Responsibilities:
• Perform annual qualifications and calibrations of lab equipment.
• Develop and implement SOPs for lab instruments.
• Lead documentation for equipment qualification and validation.
• Coordinate compliance updates with management and QA.
• Troubleshoot equipment and validation-related issues.
Requirements:
• Technical diploma or relevant experience required.
• 2-5 years in a GMP lab setting essential.
• Knowledge of Empower CDS and Waters HPLC systems.
• Must be able to lift up to 50lbs.
• Excellent written and verbal communication skills.
Leverage your specialized skills to help redefine innovation in healthcare at AtomVie.
#J-18808-Ljbffr

📌 Lab CQV Specialist at AtomVie (Hamilton)
🏢 AtomVie Global Radiopharma
📍 Hamilton