Project Manager - Technology Transfers
jubilant pharmaTopeka, KS
Project Manager - Technology Transfers
jubilant pharmaTopeka, KSSenior L5
Research and Development in BiotechnologyPharmaceutical Preparation ManufacturingResearch and Development in the Physical, Engineering, and Life Sciences
APPLY NOW (opens in a new tab)24-months contract
Project Manager, Technology Transfers Help Expand Access to Life-Changing Radiopharmaceuticals
At Jubilant Radiopharmacies, we support healthcare providers across the United States by delivering radiopharmaceutical products used in diagnostic imaging and patient care. We're looking for an experienced Project Manager to lead technology transfer projects that bring new PET and SPECT products and capabilities to sites across our network.
Role Overview:
As Project Manager, Technology Transfers, you will lead cross-functional technology transfer projects from planning through implementation. Working closely with customers and internal teams, you will help ensure products, processes, documentation, and operational readiness are successfully transferred to receiving sites while meeting quality, regulatory, budget, and timeline 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:
Lead technology transfer projects for PET and SPECT radiopharmaceutical products across the U.S. 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 other 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.
Qualifications:
Bachelor's degree in Life Sciences, Pharmacy, Engineering, or a related field.
Minimum 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.
Proven ability to manage complex, multi-site projects and collaborate across diverse stakeholder groups.
Strong communication, organization, and problem-solving skills.
PMP certification preferred.
Experience in PET/SPECT radiopharmaceuticals, nuclear medicine, or specialty pharmaceutical manufacturing preferred.
Why Join Jubilant Radiopharmacies?
Lead high-impact projects that expand patient access to radiopharmaceutical therapies and diagnostics.
Partner with customers and industry experts across a growing national network.
Enjoy the flexibility of a home-based role while remaining connected to meaningful site and customer interactions.
Be part of a collaborative team advancing nuclear medicine and radiopharmaceutical manufacturing.
Benefits:
We offer competitive compensation, generous vacation, health/dental benefits and 401(k) matching. Our Commitment to Inclusion
Jubilant Radiopharmacies is committed to creating an inclusive workplace where everyone is treated with dignity and respect. We welcome applicants from diverse backgrounds and experiences and are committed to providing reasonable accommodations throughout the recruitment and employment process.
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Level
Senior L5
Location
Topeka, KS
Occupation
Project Management Specialists
Industry
Research and Development in Biotechnology
Posted
today