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Senior Scientist, Radiochemistry

5-8 years
Not Disclosed
10 Oct. 31, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Scientist, Radiochemistry

Location: USA – 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.

You will play a vital role in supporting the global rollout of our approved prostate cancer imaging agent and advancing our portfolio of late clinical-stage radiopharmaceutical products that address significant unmet medical needs.


Position Overview

The Senior Scientist, Radiochemistry will support the development of clinical-stage radiopharmaceutical assets, ensuring that manufacturing and quality control (QC) procedures align with corporate, regulatory, and GMP requirements.

This role involves managing development activities across multiple CMOs, supporting regulatory submissions, and ensuring a smooth transition to commercial-stage manufacturing.


Key Accountabilities

1. Development and Compliance

  • Partner with internal teams and external CMOs to manage development of manufacturing and QC procedures in alignment with GMP regulations.

  • Ensure all documentation and procedures meet corporate quality standards and regulatory compliance requirements.

2. Manufacturing & QC Management

  • Oversee development and validation of manual and automated manufacturing procedures.

  • Develop and validate non-compendial QC methods, including analytical techniques like HPLC, TLC, and GC for radiopharmaceuticals.

  • Generate comprehensive protocols and reports for development, validation, and method transfer activities.

3. Regulatory Documentation

  • Author CMC sections for INDs, NDAs, BLAs, and international regulatory filings.

  • Prepare SOPs for manufacturing and QC processes in accordance with Telix’s QMS and GMP principles.

4. Technology Transfer and Scale-Up

  • Support method transfers to external manufacturing partners and ensure successful implementation.

  • Participate in process optimization, streamlining, and scale-up of manufacturing for commercial readiness.

  • Provide technical support for existing and new Telix product manufacturing and QC operations.


Education & 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.

  • Hands-on experience in radiochemistry.

  • Experience developing HPLC, TLC, and GC QC methods for radiopharmaceuticals.

  • Experience in GMP-compliant manufacturing environments.

  • Strong technical writing and communication skills.

Preferred Qualifications

  • Experience in biologic conjugation and radiolabeling.

  • Experience in method development to support regulatory submissions (IND/NDA/BLA).


Key Skills & Competencies

  • Strong analytical and problem-solving mindset.

  • Excellent attention to detail and documentation accuracy.

  • Ability to manage multiple projects and external vendors independently.

  • Collaborative approach with internal and cross-functional teams.

  • Proven ability to operate in a regulated, fast-paced biotech environment.


Why Join Telix

At Telix, everyone counts. We strive for excellence, act with integrity, and pursue our goals with determination.

You will be part of an engaged, supportive global team united by a shared mission — helping people with cancer and rare diseases live longer, better-quality lives.

We offer:

  • Competitive compensation and annual performance-based bonuses

  • Equity-based incentive program

  • Generous vacation and paid wellness days

  • Learning and development support

  • Flexible hybrid and remote work options


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 roles, visit our [LinkedIn page].