Radiochemist - Talent Community

Telix Pharmaceuticals (AMER)

6d

About The Position

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. We are seeking Radiochemists at multiple levels to join our team! Please submit your application of interest and our team will be in contact with you when we have an opening. See Yourself at Telix Telix is seeking a Radiochemist to support the development of its clinical-stage radiopharmaceutical assets. The successful candidate will be responsible for managing the development required to ensure manufacturing and QC procedures meet the corporate requirements to support clinical trials, regulatory submissions, and transition to commercial-stage manufacturing. This is an ideal role for radiochemists with experience manufacturing under GMP regulations who are comfortable in a fast-paced environment and who are motivated to make vital contributions to the next generation of radiopharmaceutical drugs.

Requirements

• Bachelor’s degree plus five years experience, or Masters degree plus three years experience, or doctorate plus two years experience required
• Practical radiochemistry experience is required
• Experience developing HPLC, TLC, or GC QC methods for radiopharmaceuticals is required
• Experience working on GMP-compliant manufacturing is required
• Strong written and verbal communication skills are required

Nice To Haves

• Experience working with radiometals is preferred
• Experience with conjugation and radiolabeling of biologics is preferred
• Experience of method development to support regulatory filings is preferred

Responsibilities

• Interface with key stakeholders, including external CMOs, to manage the development of manufacturing and QC procedures for clinical-stage radiopharmaceutical assets in compliance with all applicable GMP regulations.
• Manage the development and validation of manual or automated manufacturing procedures as required.
• Manage the development and validation of non-compendial QC procedures as required.
• Generate development, validation, method transfer, and various other types of protocols and reports.
• Support regulatory filings via completion of CMC sections for INDs, NDAs, BLAs, and foreign equivalents.
• Generate SOPs for manufacturing and QC procedures.
• Support method transfers to external manufacturers.
• Participate in the streamlining, optimization, and scale-up of manufacturing procedures in preparation for commercial supply.
• Provide technical support for manufacturing and QC procedures for all Telix products as required.
• Ensure all documentation generated is consistent with Telix QMS and general principles of GMP manufacturing.

Benefits

• We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 251-500 employees