Process Chemist

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 RoleReporting to the Lead, Radiopharmaceutical Technology, the Process Chemist will apply their technical expertise and experience in radiochemistry and process chemistry to support current products and future drug development within AtomVie’s portfolio of CDMO functions. The Process Chemist plays a vital role in the development of products through successful experiment design, execution, and data analysis of AtomVie’s clinical pipeline. The Process Chemist will work as part of a highly skilled group of individuals employing industry leading development activities within the radiopharmaceutical industry while ensuring regulatory compliance, site safety and radiation protection guidelines are continuously upheld.This hands-on role will work on site with some flexibility for remote work. Some weeknight and weekend work may be expected according to production schedules.What You Will DoAct as a technical expert in GMP process development for AtomVie’s clinical and commercial portfolioDesign and conduct radiochemistry experiments for clinical and commercial drug developmentsCritically evaluate data, determine appropriate conclusions and a plan of action in collaboration with internal stakeholders to develop phase-appropriate GMP production processesProvide project data and progress status updates to management and clientsWork with cross-functional teams on the development of synthesis, purification, formulation and aseptic filling processes, including process transfer, scale-up, validation and launch activitiesSupport the preparation and review of written procedures, batch records, experimental protocols and reports, specifications and qualification/validation protocolsPrepare technical reports and documents, including SOPs and investigational reportsEmphasize safety in new and existing design and safe practices in all experimental activities for all staff membersConduct work according to best practices and, where appropriate, regulatory guidance, GMPs, established business processes and protocols, and applicable standard operating proceduresTake ownership over the projects you lead and feel a sense of accomplishment and pride in the work you produceWhat You Bring to the Role Passion about radiochemistry and the field of radiopharmaceutical sciencePlanning, designing and executing development activitiesAbility to successfully lead multiple projects at a given time while maintaining quality Exhibit strong ability to multitask by prioritizing workloadExcellent communication skills and ability to collaborate well with multiple stakeholders across the entire organizationStrong oral and written communication skillsAbility to work under minimal supervision and provide key updates to team members and management where requiredAttention to detail and well organized Excellent troubleshooting and analytical skillsThrive in a team setting and exhibit a high degree of trust and integrityMaintain the highest standards with respect to safety and radiation protection in all work activitiesFlexibility in work schedule to support a 7-day work week in support of nightshift-type production environmentRequirementsAt minimum BSc in chemistry, radiochemistry, biochemistry or equivalent discipline with at least 2 years of relevant laboratory experience and expertise in process development and formulation. MSc or PhD in the abovementioned disciplines is preferred. Strong knowledge in chemistry, process chemistry, or aseptic manufacturing experience in a pharmaceutical setting is considered an asset.Knowledge of validation principles, technology transfer of manufacturing processes and GMP concepts is highly desirable. 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.