Project Manager - Technology Transfers

Jubilant Pharma Limited

Kansas

On-site

USD 90,000 - 130,000

Part time

12 days ago

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Benefits offered by this job

Competitive compensation
Generous vacation
Health/dental benefits
401(k) matching

Job summary

Jubilant Radiopharmacies is seeking an experienced Project Manager to lead technology transfer initiatives for PET and SPECT products across the U.S. This home-based role requires coordinating cross-functional teams to ensure readiness of documentation, batch records, and validation activities while meeting regulatory and timeline requirements.

You will partner with Operations, Manufacturing, Quality, and Business Development to expand patient access to radiopharmaceutical therapies and

Qualifications

  • Bachelor's degree in Life Sciences, Pharmacy, Engineering, or a related field.
  • Minimum 5 years of project management experience in pharmaceutical/biotech/radiopharmaceutical industry.
  • Experience with technology transfer, process validation, manufacturing scale-up, or related activities.
  • Experience in cGMP-regulated manufacturing environments.
  • Strong understanding of FDA regulations, FDA 211/212 requirements, and quality systems.

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.

Skills

Project management
Cross-functional teamwork
FDA regulations
cGMP
Process validation
PMP certification
PET/SPECT knowledge
Communication

Education

Bachelor's degree in Life Sciences/Pharmacy/Engineering

Job description

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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