Project Scientist, PET Radiopharmaceuticals

Project Scientist, PET Radiopharmaceuticals (24-Month Contract)
Jubilant Radiopharmacies
Help Advance the Future of Nuclear Medicine
At Jubilant Radiopharmacies, we are committed to expanding access to innovative PET radiopharmaceuticals that support critical diagnostic imaging and patient care. As we continue to grow, we are seeking a skilled Project Scientist to support technology transfer and product implementation initiatives across our PET manufacturing network.
This is an excellent opportunity for a radiochemist, scientist, or technical professional who enjoys working at the intersection of science, manufacturing, and innovation while helping bring new radiopharmaceutical products into commercial production.
Role Overview
As a Project Scientist, PET, you will serve as a technical subject matter expert supporting technology transfer activities, validation programs, and new product onboarding across multiple PET manufacturing sites. Working closely with Operations, Quality, Project Management, and external partners, you will help ensure new products and processes are successfully implemented while maintaining compliance with regulatory and quality requirements.
Location
This is a home-based position located in the United States. Travel to Jubilant Radiopharmacies manufacturing and radiopharmacy sites, as well as customer locations, will be required to support project execution and successful technology transfers.
Key Responsibilities
Serve as the technical lead for PET technology transfer projects across the manufacturing network.
Support new product onboarding, process implementation, and commercial product launches.
Prepare, review, and approve technology transfer, validation, and GMP documentation.
Partner with site teams to support engineering runs, process validation, troubleshooting, and manufacturing readiness activities.
Support equipment qualification, cleaning validation, method qualification, continued process verification, and change control activities.
Collaborate with cross-functional teams and external partners to ensure successful project execution.
Ensure compliance with FDA regulations, cGMP requirements, quality systems, and customer commitments.
Qualifications
Bachelor's degree in Chemistry, Pharmaceutical Sciences, Engineering, or a related scientific discipline; advanced degree preferred.
Minimum 5 years of experience in technology transfer, product development, manufacturing support, or related activities within the pharmaceutical or radiopharmaceutical industry.
Experience supporting commercial manufacturing within a cGMP environment.
Strong knowledge of PET radiopharmaceutical manufacturing and applicable regulations, including FDA 21 CFR Part 212, FDA 21 CFR Part 211, FDA Part 11, ICH Q9, USP <825>, GAMP 5, and ISPE guidance.
Experience with validation, qualification, risk assessments, change controls, investigations, and GMP documentation.
Strong technical writing, communication, problem-solving, and project management skills.
Experience working collaboratively across multiple sites and functions.
Lean Six Sigma Green Belt and/or PMP certification is an asset.
Why Join Jubilant Radiopharmacies?
Play a key role in expanding access to PET radiopharmaceuticals across the United States.
Work on innovative products and technology transfer programs that directly support patient care.
Collaborate with experienced radiochemists, scientists, manufacturing leaders, and quality professionals.
Enjoy the flexibility of a remote-based role with meaningful site engagement.
Be part of a growing organization at the forefront of nuclear medicine.
Benefits
We offer competitive compensation, comprehensive health and dental coverage, generous vacation, and 401(k) matching.
Our Commitment to Inclusion
Jubilant Radiopharmacies is committed to creating an inclusive workplace where all employees are treated with dignity and respect. We welcome applicants from diverse backgrounds, experiences, and perspectives. All qualified applicants will receive consideration for employment based on job-related qualifications, and reasonable accommodations are available throughout the recruitment and employment process.

Work arrangement
No