Scientist / Senior Scientist, Radiopharmaceutical Development and Technology Transfer

Job Description

Scientist / Senior Scientist, Radiopharmaceutical Development & Technology Transfer

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Location: Salt Lake City, Utah

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Travel: Approximately 10% (US travel)

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Level: Scientist or Senior Scientist, depending on the experience and background of the successful candidate

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About the Opportunity

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Hartmann Young is partnered with a growing radiopharmaceutical biotechnology company seeking a Scientist or Senior Scientist, Radiopharmaceutical Development & Technology Transfer to join its team in Salt Lake City, Utah.

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This role will focus on the development, optimisation, and transfer of radiopharmaceutical manufacturing processes to internal and external GMP manufacturing sites. The position offers significant cross-functional exposure across CMC, Manufacturing, Quality, Regulatory, and external CDMO partners. Regular collaboration with colleagues based at the company's Boston headquarters is expected through virtual meetings and periodic onsite visits.

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Position Summary

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The successful candidate will lead process development and technology transfer activities supporting the advancement of radiopharmaceutical programs from development through clinical manufacturing. This is an excellent opportunity for a hands-on scientist with experience in radiopharmaceutical manufacturing, GMP environments, and external partner management who is looking to make a significant impact within a growing organisation.

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About the Opportunity

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Key Responsibilities

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• Develop and optimise radiopharmaceutical production processes to support pipeline advancement.
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• Transition early-stage manufacturing processes into GMP-ready manufacturing processes.
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• Design and execute process development strategies, including qualification, verification, and validation activities.
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• Lead technology transfer activities at internal manufacturing sites and external CDMO partners.
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• Act as the primary technical contact during process transfers and manufacturing implementation.
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• Deliver technical training and support to manufacturing personnel.
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• Author and review Master Batch Records, development reports, technology transfer documents, qualification protocols, validation reports, and regulatory submission content.
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• Support deviation, OOS, and OOT investigations, including root cause analysis and CAPA implementation.
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• Ensure compliance with cGMP, GLP, data integrity, and regulatory requirements.
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• Collaborate with Manufacturing, Quality, Regulatory Affairs, CMC, and external partners to meet development timelines.
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Qualifications

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• PhD in a relevant scientific discipline with 4+ years of experience, MSc with 8+ years, or BSc with 10+ years.
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• Hands-on experience working with radioactive materials.
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• Demonstrated experience in radiopharmaceutical process development and manufacturing.
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• Strong understanding of cGMP principles and GMP manufacturing operations.
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• Technology transfer experience within a pharmaceutical or radiopharmaceutical environment.
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• Excellent technical writing skills.
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• Experience working cross-functionally and managing external partners.
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• Strong communication, organisational, and project management skills.
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• High attention to detail and commitment to quality and compliance.
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Preferred Experience

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• Radioligand therapy or radiopharmaceutical drug development experience.
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• CDMO management experience.
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• Experience supporting IND and IMPD submissions.
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• Knowledge of process validation and lifecycle management.
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• Experience with chromatography systems, LIMS, and related manufacturing technologies.
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What's on Offer

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• Opportunity to join a growing leader in radiopharmaceutical development.
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• High level of scientific ownership and visibility.
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• Collaborative and innovative culture.
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• Competitive compensation package aligned to experience and level.
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