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.

See Yourself at Telix

This role provides technical and analytical expertise for early phase biologics process development and manufacturing activities for multiple technology areas (e.g. analytical, purification, formulation, and bioconjugation) ensuring manufacturing processes are sufficiently developed to meet program objectives, safety standards, regulatory expectations, and quality compliance. This role is responsible for managing projects in multiple technology areas (e.g. analytical, purification, formulation, or bioconjugation) at internal sites and external CMC partners, as well as contributing to internal cross-functional collaborations to develop and execute clinical manufacturing.

The Principal Scientist, Biologics acts as the Biologics lead for a specific therapeutic program and should be comfortable communicating with cross-functional teams in formal settings and third-party meetings, be knowledgeable in several technical areas as well as their focus technology area (e.g. analytical, purification, formulation, or bioconjugation), and manage their own workload to complete assignments autonomously with some feedback from senior-level colleagues, matrix team members,

and/or their manager for more complicated topics.

Key Accountabilities

Leads development projects for multiple technology areas (e.g. analytical, purification, formulation, or bioconjugation) ensuring the appropriate process knowledge, technology transfer, analytical method transfer, design space and/or control strategy definition, optimization, and/or qualification to produces clinical drug substance intermediates.
Supports review and approval of manufacturing operation documents such as SOPs, batch records, protocols, analytical procedures, etc., and development reports for multiple technology areas (e.g. analytical, purification, formulation, or bioconjugation) to produce clinical drug substance intermediates.
Ensures appropriate compliance of multiple technology areas (e.g. analytical, purification, formulation, or bioconjugation) through document creation/review/approval, quality investigations, corrective actions, and change control within a Quality system.
Authors and/or reviews source documents and CMC content related to several technology areas (e.g. analytical, purification, formulation, or bioconjugation) to support IND, NDA, BLA and similar regulatory agency applications, especially in areas requiring more sophisticated acumen such as comparability and risk-based approach
Leads collaborations with internal sites and external CMC partners to develop selection criteria, assess capabilities, coordinate activities, plan process technology /analytical method activities, troubleshoot and analyze operational performance, conduct risk assessments, and manage timely deliverables.

Mentors Senior Scientists and other level Scientists on both technical topics as well as Telix values.

Education and Experience

Science or engineering degree with minimum relevant experience as applicable: BS with 11 years of experience, MS with 9 years of experience, PhD with 8 years of experience.
Minimum 5 years of experience in GMP, quality management system, and CMC compliance and
Demonstrated understanding and application of project management principles and
Ability to work in cross-functional, virtual
Travel expectation: 10 – 25% for key in-person meetings, partner site visits, and SME/technical person-in-plant