Senior Scientist, Radiochemistry
Location: Canada – Remote
Updated: Thursday, 16 October 2025
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, improving the quality of life for people living with cancer and rare diseases.
As part of our team, you will support the international roll-out of our approved prostate cancer imaging agent and contribute to advancing our portfolio of late clinical-stage products addressing unmet medical needs in oncology and rare diseases.
Position Overview
The Senior Scientist, Radiochemistry will support the development of clinical-stage radiopharmaceutical assets, overseeing manufacturing and quality control (QC) development to ensure compliance with corporate, GMP, and regulatory standards.
This position involves collaborating with internal and external stakeholders to manage process development, validation, and optimization required for clinical and commercial manufacturing readiness.
Key Accountabilities
1. Development and Process Management
Interface with key stakeholders, including external CMOs, to manage the development of manufacturing and QC procedures for clinical-stage radiopharmaceutical assets in compliance with GMP regulations.
Manage the development and validation of manual and automated manufacturing procedures.
Lead the development and validation of non-compendial QC methods as required.
Perform method transfer activities and support process optimization efforts.
2. Documentation and Regulatory Compliance
Prepare and maintain development, validation, and method transfer protocols and reports.
Author CMC sections for INDs, NDAs, BLAs, and international equivalents.
Develop and maintain SOPs for manufacturing and QC activities in alignment with Telix’s QMS and GMP standards.
Ensure all documentation complies with corporate and regulatory quality systems.
3. Technical and Operational Support
Provide technical support for manufacturing and QC procedures for all Telix products.
Participate in scale-up, streamlining, and commercial readiness activities for manufacturing processes.
Collaborate cross-functionally to ensure technical consistency and operational excellence.
Education and Experience
Required Qualifications
Bachelor’s degree with 8+ years of experience, or
Master’s degree with 6+ years of experience, or
Doctorate with 5+ years of experience.
Practical radiochemistry experience.
Experience developing HPLC, TLC, or GC QC methods for radiopharmaceuticals.
Experience in GMP-compliant manufacturing environments.
Strong written and verbal communication skills.
Preferred Qualifications
Experience in biologic conjugation and radiolabeling.
Experience in method development supporting regulatory filings (IND/NDA/BLA).
Key Competencies
Strong analytical, problem-solving, and organizational skills.
Ability to manage multiple CMOs and projects independently.
Excellent documentation precision and attention to detail.
Strong collaboration and interpersonal communication.
Knowledge of GMP, GLP, and regulatory expectations for radiopharmaceuticals.
Why Join Telix
At Telix, everyone counts. We strive for excellence, act with integrity, and pursue our mission with determination.
You’ll be part of a supportive global team committed to helping patients with cancer and rare diseases live longer and better-quality lives.
We offer:
Competitive salary and annual performance-based bonuses
Equity-based incentive program
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. We evaluate qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other legally protected characteristic.
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Apply Now
For more information on Telix’s global opportunities, visit our [LinkedIn page].
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