Job Title

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 RoleThe Radiopharmaceutical Scientist serves as a technical subject matter expert in radiochemistry, automated synthesis, purification, and process development. This is an advanced-level individual contributor role responsible for driving product development activities from early-stage research through readiness for routine GMP manufacturing. The Scientist applies deep expertise in process design, optimization, and characterization to ensure development programs are executed efficiently, delivered on time and within scope, and aligned with regulatory and GMP requirements.Working collaboratively with Process Development, Manufacturing, Quality, and Regulatory teams, the Scientist supports process scale-up, technology transfer, and commercialization while maintaining accountability for Product Development deliverables and scientific integrity. The role contributes to resolving development and manufacturing challenges through data-driven recommendations and technical guidance, particularly during tech transfer and early-stage GMP execution, without direct oversight of Manufacturing activities.This posting is for an existing vacancy to support the expansion of the company.Location: AtomVie Global Radiopharma Inc, Hamilton ON (Onsite)What You Will DoDesign and execute radiopharmaceutical process development, including radiolabeling, conjugation, purification, and formulation for therapeutic and diagnostic programs.Design and implement phase-appropriate process development strategies, including DOE, process optimization, and process characterization.Develop robust and scalable processes suitable for clinical and commercial GMP manufacturing.Identify and define Critical Process Parameters (CPPs), Critical Quality Attributes (CQAs), and control strategies.Interpret and critically evaluate experimental data to ensure scientific integrity, troubleshoot development challenges, and define next-stage development strategies.Provide hands-on technical support and guidance to ensure successful execution of development activities.Serve as a subject matter expert in radiochemistry and process chemistry.Evaluate and introduce new technologies and process improvements to enhance development efficiency and robustness.Support planning and execution of development programs to meet project timelines, scope, and budget expectations.Contribute to process scale-up, technology transfer, validation, and launch activities.Ensure development activities are executed in accordance with defined process specifications and expected outcomes.Maintain working knowledge of regulatory guidance, pharmacopeial standards, internal procedures, and SOPs.Author, review, and maintain technical documentation, including process development reports, validation protocols, and SOPs, in accordance with Good Documentation Practices.Support preparation of CMC sections for regulatory submissions (IND, CTA, NDA, etc.).Support non-conformances (NCR's), investigations, CAPAs, and change controls related to development activities.Promote quality-by-design (QbD) principles and a right-first-time culture.Act as a technical interface for internal teams and clients during development stages.What You Bring to the Role5+ years of relevant industry experience.Hands-on experience in radiochemistry, radiopharmaceutical development, or process chemistry.Experience working in or supporting GMP environments.Experience with radiolabeling and isotope handling (therapeutic and/or diagnostic isotopes).Familiarity with CMC development and regulatory documentation is strongly preferred.Experience with analytical characterization techniques relevant to radiopharmaceuticals.Requirements PhD in Chemistry (preferred), Biochemistry, Chemical Engineering or related field.Compensation: Annual salary starts at $95k. AtomVie OffersGroup Health & Dental Benefits (from day 1)RRSP Matching ProgramPerkopolisEmployee Assistance and Wellness ProgramsParking AllowanceAtomVie 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.