About Jubilant Radiopharma
At Jubilant Radiopharma, we help healthcare professionals deliver essential patient care through high-quality nuclear medicine products. We value collaboration, innovation, and respect for people. We are committed to creating an inclusive workplace where everyone can contribute, learn, and grow.
Role Overview
As Project Manager, Technology Transfers, you will lead technology transfer projects from planning through implementation. Working closely with customers and cross-functional teams, you will help ensure products, processes, documentation, and operational readiness activities are successfully transferred to receiving sites while meeting quality, regulatory, budget, and timeline requirements.
12-months contract
Key Responsibilities
- Lead technology transfer projects for PET and SPECT radiopharmaceutical products across the network.
- Serve as the primary customer contact and manage project scope, timelines, risks, and deliverables.
- Coordinate cross-functional teams including Operations, Manufacturing, Quality, Supply Chain, Commercial, and Business Development.
- Ensure readiness of batch records, SOPs, validation protocols, analytical methods, and all required documentation.
- Facilitate project meetings, customer updates, and leadership reviews.
- Support business development activities through feasibility assessments and site capability evaluations.
- Ensure projects are executed in compliance with FDA regulations, cGMP requirements, and company quality standards.
- Build strong partnerships with stakeholders to support smooth transitions and successful technology transfer execution.
Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, Engineering, or a related field.
- Minimum of five (5) years of project management experience in the pharmaceutical, biotech, or radiopharmaceutical industry.
- Experience with technology transfer, process validation, manufacturing scale-up, or related activities.
- Experience working in cGMP-regulated manufacturing environments.
- Strong understanding of FDA regulations, FDA 211/212 requirements, and quality systems.
- Demonstrated ability to manage complex, multi-site projects and collaborate across diverse stakeholder groups.
- Strong communication, organization, and problem-solving skills.
- Excellent communication skills in both French and English as the incumbent must regularly communicate and collaborate with regulatory agencies and business stakeholders outside Quebec.
- PMP certification preferred.
- Experience in PET/SPECT radiopharmaceuticals, nuclear medicine, or specialty pharmaceutical manufacturing preferred.
- Willingness to travel in support of project execution and technology transfer activities.
