AtomVie Global Radiopharma Inc. is a global leading GMP manufacturer and distributer of clinical and commercial radiopharmaceuticals. We work with our partners to transform patients lives by advancing high quality drugs for the treatment and diagnosis of diseases. We are a community that challenges ourselves professionally, takes pride in what we can accomplish together and values the impact we can make with our partners and patients across the globe.Start your career with AtomVie today and help us achieve our vision: to transform lives by revolutionizing healthcare. About the Role The QC Analyst I will be responsible for working in accordance with company policies and within GMPs while contributing technical expertise to support current products and develop future drugs within the AtomVie portfolio. They will also be responsible for quality control testing of materials and finished drug products, specifically radiopharmaceuticals. The ideal candidate will be proficient in executing chemical tests using advanced analytical techniques, including HPLC, GC, TLC, bacterial endotoxin testing, and pH measurements, while adhering to standard operating procedures (SOPs) and Good Manufacturing Practices (GMP). This position involves set evening, night, or early morning shifts, with weekend availability required (e.g., Thursday to Monday ). What You Will Do Quality control testing of materials and finished drug products (radiopharmaceuticals) including chemical tests using various analytical techniques such as HPLC, GC, TLC, bacterial endotoxin testing, pH, etc. according to standard operating procedures. Perform routine calibration/maintenance of equipment. Responsible for the facility maintenance and housekeeping, maintain inventory of reagents and supplies, waste disposal, etc. Peer review of laboratory records Conducting investigations for testing failure and non-conformances Author, revise, and review technical documents, including SOPs, validation documents, standard test methods according to good documentation practices and reports. Support analytical method transfer and validation activities as required. Adhere to Canadian Nuclear Safety Commission and GMP regulations. What You Bring to the Role Experience routinely executing chemistry techniques such as HPLC, GC and TLC is preferred for this role. Good math skills are critical in this role. Experience with other lab equipment such as ICP, Gamma Spectroscopy, or Liquid Scintillation Counter is an asset. Experience working with sterile products is considered an asset Requirements B. Sc. in Chemistry, Biotechnology or a related field 1-3 years of relevant experience working in a GMP or ISO environment is required Ability to lift 23 kilograms required Shift flexibility to support 24-hour/7-day manufacturing schedule AtomVie Offers Group Health & Dental Benefits (from day 1) RRSP Matching Program Perkopolis Employee Assistance and Wellness Programs Parking Allowance AtomVie is 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.
Job Title
QC Analyst I