Senior Scientist, Radiochemistry

Telix Pharmaceuticals Limited

Senior Scientist managing development of clinical-stage radiopharmaceutical assets at Telix Pharmaceuticals. Ensuring QC procedures meet corporate requirements and supporting clinical trials.

Posted 7/28/2026full-timeRemote • 🇺🇸 United StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing the development and validation of manufacturing procedures for clinical-stage radiopharmaceuticals, ensuring compliance with GMP principles and regulatory requirements. Proficient in authoring CMC sections for INDs and NDAs while effectively interfacing with external CMOs.

Highest-signal resume keywords

Practical Radiochemistry ExperienceHPLC QC Method DevelopmentGMP-Compliant Manufacturing ExperienceCMC Section Authoring for INDs and NDAsStrong Written and Verbal Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

RadiochemistryHPLC Method DevelopmentTLC Method DevelopmentGC Method DevelopmentManufacturing Procedure ValidationRegulatory Filing SupportConjugation of BiologicsRadiolabeling of Biologics

Soft Skills

Strong Communication SkillsStakeholder Management

Industry Keywords

Clinical-Stage RadiopharmaceuticalsCMCINDNDAQMSGMP

About the role

Key responsibilities & impact

Support the development of clinical-stage radiopharmaceutical assets.
Manage the development required to ensure manufacturing and QC procedures meet corporate requirements.
Interface with key stakeholders, including external CMOs.
Demonstrate ability to manage multiple CMOs with little oversight.
Manage the development and validation of manufacturing procedures.
Author CMC sections for INDs, NDAs, and other submissions.
Ensure all documentation aligns with Telix QMS and GMP principles.

Requirements

What you’ll need

Bachelor’s degree plus 8 years experience, or Masters degree plus 6 years experience, or doctorate plus 5 years experience.
Practical radiochemistry experience is required.
Experience developing HPLC, TLC, or GC QC methods for radiopharmaceuticals is required.
Experience working in GMP-compliant manufacturing is required.
Strong written and verbal communication skills.
Experience with conjugation and radiolabeling of biologics is preferred.
Experience of method development to support regulatory filings is preferred.

Benefits

Comp & perks

Competitive salaries
Annual performance-based bonuses
Equity-based incentive program
Generous vacation
Paid wellness days
Support for learning and development