Job Title: Radiochemist – Talent Community
Location: USA (Remote)
Updated: October 9, 2025
Company: Telix Pharmaceuticals
About Telix Pharmaceuticals
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.
We focus on improving the quality of life for people living with cancer and rare diseases by developing innovative radiopharmaceutical solutions.
You will support the global roll-out of our approved prostate cancer imaging agent and help advance a portfolio of late-stage clinical products addressing significant unmet needs in oncology and rare diseases.
Position Overview
Telix is seeking Radiochemists (multiple levels) to support the development of clinical-stage radiopharmaceutical assets.
This role involves managing the development and validation of manufacturing and quality control (QC) procedures in compliance with GMP regulations.
Ideal for candidates experienced in radiochemistry manufacturing under GMP who thrive in a fast-paced, collaborative environment and want to contribute to the next generation of radiopharmaceutical drugs.
Key Responsibilities
Interface with key stakeholders, including external CMOs, to manage the development of manufacturing and QC procedures for radiopharmaceutical assets in compliance with GMP.
Develop and validate manual or automated manufacturing procedures.
Develop and validate non-compendial QC procedures.
Prepare development, validation, method transfer, and related protocols and reports.
Support regulatory filings by contributing to CMC sections for INDs, NDAs, BLAs, and foreign equivalents.
Generate Standard Operating Procedures (SOPs) for manufacturing and QC activities.
Support method transfers to external manufacturers.
Participate in process optimization, streamlining, and scale-up for commercial supply.
Provide technical support for manufacturing and QC activities across all Telix products.
Ensure all documentation aligns with Telix QMS and GMP principles.
Education & Experience Requirements
Bachelor’s degree + 5 years of experience, OR
Master’s degree + 3 years of experience, OR
Doctorate (Ph.D.) + 2 years of experience
Required Skills:
Practical radiochemistry experience
Experience developing HPLC, TLC, or GC QC methods for radiopharmaceuticals
Experience in GMP-compliant manufacturing
Strong written and verbal communication skills
Preferred Skills:
Experience working with radiometals
Experience in conjugation and radiolabeling of biologics
Experience in method development supporting regulatory filings
Why Join Telix?
At Telix, we believe:
Everyone counts
We strive to be extraordinary
We pursue our goals with determination and integrity
You’ll join a global, interdisciplinary, and supportive team dedicated to delivering breakthroughs in precision medicine.
Employee Benefits:
Competitive salaries
Annual performance-based bonuses
Equity-based incentive programs
Generous vacation and paid wellness days
Learning and development support
Hybrid and remote work flexibility
Equal Opportunity Statement
Telix Pharmaceuticals is an equal opportunity employer.
All qualified applicants are evaluated without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristic.
How to Apply
Submit your application of interest — our team will contact you when suitable openings arise.
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