Manufacturing Deployment Lead Remote

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US USA
- Remote

Updated:
Tuesday, 13 October 2026

Telix Pharmaceuticals is a dynamic, fast-growing radiopharmaceutical company with offices in Australia (HQ), Belgium, Japan, Switzerland, and the United States. Our mission is to deliver on the promise of precision medicine through targeted radiation.
At our core, we exist to create products that seek to improve the quality of life for people living with cancer and rare diseases. You will be supporting the international roll-out of our approved prostate cancer imaging agent and helping us to advance our portfolio of late clinical-stage products that address significant unmet need in oncology and rare diseases.

The Manufacturing Deployment Lead oversees the deployment of new manufacturing facilities and the transfer of TELIX diagnostic and therapeutic product technologies. This role coordinates the transfer of manufacturing processes, equipment, analytical methods, documentation, and technical knowledge from development teams or established manufacturing sites to new TMS facilities, ensuring a smooth handoff to TMS Operations.

Supporting both greenfield developments and expansions at existing TMS sites, this position partners with Operations, Quality Assurance, Quality Control, Engineering, Regulatory Affairs, Supply Chain, EHS, and external vendors to ensure facilities and processes meet applicable regulatory requirements. This position reports to the Senior Director, Manufacturing Deployment and Tech Transfer.

• Execute technology transfers for TELIX diagnostic and therapeutic products at designated manufacturing
• Support manufacturing deployment from facility readiness through regulatory approval and handoff to TMS
• Conduct activities in accordance with applicable cGMP requirements, including 21 CFR Parts 210, 211, and

• Provide on-site technical support for facility commissioning, equipment installation, manufacturing and QC laboratory readiness, personnel implementation, and qualification and validation activities.
• Support QC laboratory startup, analytical method qualification and validation, and operational

Mandatory travel to TMS manufacturing sites is required to support facility startup, qualification campaigns, validation activities, and regulatory approval processes.

• Transition technology transfer documentation from CMC into the TMS quality management
• Develop and review cGMP procedures, specifications, protocols, and reports required for product technology
• Support validation and implementation of the electronic quality management system across the TMS
• Partner with Manufacturing, Quality Assurance, Regulatory Affairs, Supply Chain, and other stakeholders to align facility expansion and technology transfer plans with organizational objectives.

Perform other duties as assigned.

• BS/BA in a science field or related degree preferred
• Minimum of 5 years of operational experience, preferably in the pharmaceutical or biotechnology industry (radiopharmaceuticals preferred)
• Strong knowledge of regulatory requirements and industry standards related to pharmaceutical manufacturing facilities, including FDA regulations, BOP regulation, cGMP guidelines, NRC regulations and environmental health and safety standards
• Excellent interpersonal skills, with the ability to work in a team environment and collaborate with cross functional teams
• Strong analytical and problem-solving skills, with the ability to identify issues, develop solutions, and drive continuous improvement initiatives
• Location:
  
  US Frequent travel to TMS manufacturing facilities is mandatory and an essential requirement of this role.

• Strong interpersonal, organizational, and managerial skills
• Excellent verbal and written skills communication skills are required
• Excellent attention to detail in the execution of job responsibilities
• Positive attitude with excellent interpersonal skills with a proven ability to create and maintain strong working relationships with internal and external stakeholders
• Possess proven…