Specialist, Technology Transfer

Location: Atlanta

Join Us at Jubilant Radiopharmacies
At Jubilant Radiopharmacies, we help make advanced diagnostic imaging possible for patients across the country. Our teams work with care, precision, and purpose every day. If you want to use your technical expertise to support meaningful healthcare innovation-and be part of a company that values collaboration, curiosity, and continuous learning-we'd love to meet you.

We are looking for a Specialist, Technology Transfer to support the transfer of PET radiopharmaceutical manufacturing processes, analytical methods, equipment, and related technologies across Jubilant Radiopharmacy (JDR) sites. In this role, you'll help ensure that new or updated processes are successfully integrated into routine GMP operations, in full alignment with 21 CFR Part 211, 21 CFR Part 212, USP <823>, USP <825>, and internal quality standards. You will work closely with cross-functional teams to ensure technical readiness, strong documentation, and smooth transitions throughout the transfer lifecycle.

• Coordinate and execute technology transfer activities for PET drug manufacturing processes, analytical methods, and supporting systems.
• Develop, review, and maintain transfer plans, protocols, reports, and summaries that align with GMP expectations and internal procedures.
• Ensure processes and methods comply with 21 CFR Parts 211 and 212, approved regulatory filings, and validated states.
• Partner with Quality, QC, Validation, Operations, Engineering, and Regulatory teams to ensure seamless and compliant process transfers.
• Support process familiarization, equipment suitability assessments, and method verification or qualification activities.
• Identify potential risks during technology transfer and support mitigation using structured risk-management tools.
• Contribute to change control, deviation management, CAPA development, and investigations tied to transfer activities.
• Ensure receiving sites receive clear documentation, training, and technical knowledge.
• Support site start-ups, expansions, and new product introductions from a technology transfer perspective.
• Participate in regulatory inspections and audits by providing subject matter expertise and transfer-related documentation.

• Bachelor's degree in Engineering or Life Sciences.
• 3+ years of experience in pharmaceutical or radiopharmaceutical manufacturing, technology transfer, or technical operations.
• Experience with PET drugs and 21 CFR Part 212 requirements (preferred).
• Experience with analytical method transfer, equipment qualification, and process scale-up (preferred).
• Experience supporting or preparing for FDA inspections and audits (preferred).
• Strong understanding of pharmaceutical manufacturing and technology transfer principles.
• Knowledge of FDA 21 CFR Part 211, FDA 21 CFR Part 212, USP <823>, USP <825>, and GMP requirements.
• Understanding of validation, qualification, and change control processes.
• Strong written and verbal communication skills.
• Excellent organizational, analytical, and problem-solving abilities.
• Ability to manage multiple projects and work effectively across teams.
• Detail-oriented, with strong technical writing skills.
• Proficiency in English.

We offer competitive compensation, an annual performance bonus, generous vacation, and 401K matching.

We welcome applicants from all backgrounds and are committed to creating a workplace where everyone feels respected and valued. We encourage individuals of all abilities, identities, and experiences to apply. Jubilant Radiopharmacies is proud to be an equal opportunity employer.