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

The Bioconjugation Process Development and Manufacturing Lead will provide technical leadership and hands-on execution for purification process development, technology transfer, process optimization, scale-up, and manufacturing support of bioconjugate programs. This role is responsible for developing and transferring purification and conjugation processes for proteins from development laboratories to GMP manufacturing environments.

The successful candidate will be an experienced process development and manufacturing scientist with expertise in chromatography-based purification platforms, process scale-up, and GMP manufacturing operations. The individual will independently design and execute laboratory studies, author development and technology transfer documentation, establish scalable manufacturing processes, and support manufacturing campaigns at internal facilities. This position requires significant hands-on experience operating, troubleshooting, and commissioning chromatography systems similar to ÄKTA Avant, ÄKTA Pure, and ÄKTA Pilot systems in both non-GMP and GMP environments.

Key Accountabilities

Design, execute, analyze, and document downstream process development studies, including chromatography, ultrafiltration/diafiltration, buffer exchange, impurity clearance purification activities.
Lead technology transfer, optimization, scale-up of purification processes for pre-conjugated and post-conjugated proteins from development laboratories to GMP manufacturing facilities.
Develop scalable purification processes from early-stage development through commercial manufacturing, leveraging Quality by Design (QbD) principles and process characterization approaches.
Provide hands-on operation, setup, troubleshooting, and execution of purification runs using ÄKTA Avant, ÄKTA Pure, and ÄKTA Pilot systems in both development and GMP manufacturing environments.
Support GMP manufacturing operations by performing or overseeing purification activities, troubleshooting process performance, investigating deviations, and implementing corrective actions.
Manage GMP bioconjugation activities while working with associated manufacturing and quality control teams.
Provide technical leadership for process scale-up activities including equipment fit assessments, process performance evaluation, facility readiness reviews, and manufacturing campaign support.

Education and Experience

Science or engineering degree with minimum relevant experience as applicable: BS with 5 years of experience, MS with 3 years of experience, PhD with 2 years of experience.
Minimum 2 years of hands-on experience in purification process development, purification process scale-up, or biologics manufacturing.
Demonstrated hands-on experience developing, optimizing, and scaling chromatography-based purification processes for recombinant proteins, monoclonal antibodies, antibody fragments, fusion proteins, and/or bioconjugates.
Demonstrated experience transferring manufacturing processes from development laboratories into GMP manufacturing facilities.
Hands-on experience working in both non-GMP and GMP environments.
Experience supporting clinical and/or commercial biologics manufacturing campaigns.
Experience managing complex projects is a plus
Ability to work in radiation areas after appropriate safety training.

Technical Requirements

Extensive hands-on experience operating and configuring ÄKTA chromatography systems.