Job Title

AtomVie Global Radiopharma Inc. About the Role The QA Associate for Batch Release is responsible for final disposition of incoming materials and final radiopharmaceutical drug product batches. This role ensures that all batches meet specifications, are manufactured/packaged in accordance with validated processes and are compliant with cGMP requirements and regulatory requirements. What You Will Do Determine final disposition of batches by reviewing all required documentation, including but not limited to batch records and change controls, and determining the status of deviations Complete media fill reviews, reporting any issues Participate in the creation and revision of standard operating procedures, and specifications Review Certificates of Analysis, material management or other similar documentation for internal and external customers Release incoming materials (e.g. activity, raw materials, components etc.) using the ERP system Act as liaison with clients for batch related issues. Assist in drafting and finalizing Annual Product Quality Reviews Provide support for the launch of new products Provide support for to Management by gathering and analyzing data Recommend, support and drive cross-functional and interdepartmental continuous improvement efforts Provide support to internal and external audits by AtomVie and participate in regulatory inspections of AtomVie facilities, as needed Plan, implement, and successfully complete assigned tasks in a timely fashion ensuring consistent high quality. Support and implement corrective actions (CAPA) where required Adhere to GMP regulations by maintaining complete records and ensuring compliance with Health Canada, FDA, and EMA requirements for sterile pharmaceuticals. Ensure compliance with Health and Safety for all policies, procedures and regulations applicable to their work. Complete other duties as assigned What You Bring To The Role Proficiency in the English language both written and oral and excellent communication skills; detail-oriented Ability to work independently and possess excellent organizational skills. A collaborative mindset, with the ability to work cross-functionally with various teams. High attention to detail and the ability to maintain accuracy in reviewing batch records, documentation, and regulatory compliance. Requirements A B.Sc or M.Sc in the life sciences with 2-5 years of experience in a GMP or equivalent regulated environment is preferred. In-depth knowledge of key regulations and guidance documents, pertinent to Product Development and Quality including Health Canada, FDA, EU GMP, ICH and ISO, with specific knowledge of the regulations as they pertain to sterile products Flexibility to support the operational needs of a 24/7 production environment. The work schedule for this position will include shifts scheduled from Sunday through to Saturday Compensation Annual salary starts at $60,000 Group Health & Dental Benefits (from day 1) RRSP Matching Program Employee Assistance and Wellness Programs AtomVie does not use artificial intelligence or automated decision-making tools in any part of the recruitment, screening, or selection process. We are committed to fostering a workplace that values diversity, equity, and inclusion. We believe that a diverse and inclusive workforce enhances our ability to innovate, collaborate, and better serve our clients and patients. We thank you for considering a career with AtomVie. Only those candidates selected for an interview will be contacted. Accommodations are available upon request for candidates taking part in all aspects of the recruitment and selection process. We are dedicated to ensuring that every qualified applicant has an equal opportunity to thrive within our organization. #J-18808-Ljbffr