Sustainability Engineer

Telix Pharmaceuticals Limited

Sustainability Engineer providing technical support and training in radiopharmaceutical manufacturing at Telix Pharmaceuticals. Leading initiatives to improve compliance and efficiency across teams.

Posted 5/16/2026full-timeRemote • 🇺🇸 United StatesSeniorLeadWebsite

About the role

Key responsibilities & impact

Technical lead of tech transfer and manufacturing activities related to drug substance and drug product formulation, radiolabeling, and fill/finish of small molecule and biologic based radiopharmaceuticals
Analyze production processes and report results. Identify and communicate gaps, risks, and inefficiencies. Drive implementation of process improvements and risk mitigations. Lead manufacturing investigations and root cause analyses
Support implementation of cold and hot analytical methods under the guidance of internal QC SMEs, ensuring alignment with approved methods, validation requirements, and quality standards.
Provide support to Regulatory Affairs for product IND and new NDA submissions, support inspection readiness, participate in regulatory agency inspections, and provide audit support, as required
Manage technical collaborations with multiple CDMOs to provide technical support and achieve key project milestones
Author and review documents such as SOPs, batch records, protocols, and reports to produce clinical and/or commercial products
Ensure appropriate compliance through document creation/review/approval, quality investigations, corrective actions, and change control within a Quality system
Follows procedures to support intellectual property protection
Provide first line technical support for ongoing batch manufacturing as the first point of contact for technical questions, concerns, and/or escalations
Work closely and collaboratively with Quality Assurance to provide ongoing support to manufacturing partners

Requirements

What you’ll need

Bachelor’s or Master’s degree in science or engineering with > 7 years of experience in the radiopharmaceutical industry, including GMP; or PhD in science or engineering with >5 years of experience in radio-pharmaceutical or biopharmaceutical industry, including GMP
Hands‑on experience with multiple isotopes like F-18, Lu-177 and I-131 etc.
Demonstrated leadership and managerial skills
Experience working cross-functionally with a team of internal scientists and engineers, managing external CDMOs to ensure compliance with project timelines/cGMPs, and on-going manufacturing operations
Experience working in radiopharmaceutical manufacturing environments, including knowledge of radiation safety principles, ALARA, and applicable regulatory requirement
Experience in MS Office suite applications (e.g., Excel, Word, Project)
Experience in authoring challenging technical documents, including but not limited to, protocols, reports, SOPs, and quality investigations
Experience in radiopharmaceutical and process development

Benefits

Comp & perks

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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

GMPradiolabelingprocess improvementsroot cause analysisanalytical methodstechnical documentationquality investigationschange controlradiopharmaceutical manufacturingprocess development

Soft Skills

leadershipmanagerial skillscross-functional collaborationcommunicationproblem-solvingtechnical supportrisk managementaudit supportteam managementinterpersonal skills