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Bioconjugation Process Development & Manufacturing Lead at Telix Pharmaceuticals (AMER) · Katori

Asks for

The ad says“Extensive hands-on experience operating and configuring ÄKTA chromatography systems.”
The ad says“Minimum 2 years of hands-on experience in purification process development, purification process scale-up, or biologics manufacturing.”
The ad says“Design, execute, analyze, and document downstream process development studies, including chromatography, ultrafiltration/diafiltration, buffer exchange, impurity clearance purification activities.”
The ad says“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.”
The ad says“Design, execute, analyze, and document downstream process development studies, including chromatography, ultrafiltration/diafiltration, buffer exchange, impurity clearance purification activities.”
The ad says“Develop scalable purification processes from early-stage development through commercial manufacturing, leveraging Quality by Design (QbD) principles and process characterization approaches.”
The ad says“Minimum 2 years of hands-on experience in purification process development, purification process scale-up, or biologics manufacturing.”
The ad says“Minimum 2 years of hands-on experience in purification process development, purification process scale-up, or biologics manufacturing.”
The ad says“Develop scalable purification processes from early-stage development through commercial manufacturing, leveraging Quality by Design (QbD) principles and process characterization approaches.”
The ad says“Experience authoring development reports, technology transfer packages, protocols, manufacturing instructions.”
The ad says“Design, execute, analyze, and document downstream process development studies, including chromatography, ultrafiltration/diafiltration, buffer exchange, impurity clearance purification activities.”

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.
Strong understanding of purification process scale-up principles, control strategies, and manufacturing readiness.
Experience authoring development reports, technology transfer packages, protocols, manufacturing instructions.
Preferred: Knowledge of GMP requirements, quality systems, deviation management, change control, CAPA, and tech transfer best practices.
Preferred: Hands-on experience in bioconjugation process development, conjugation scale-up, conjugate purification, and manufacturing support.

Key Capabilities:

Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges

At Telix, we believe everyone counts, we strive to be extraordinary, and we pursue our goals with determination and integrity. You will be part of an engaged and supportive group of colleagues who all have a shared purpose: to help people with cancer and rare diseases live longer, better quality lives. Being a Telix employee means being a part of a unique, global, interdisciplinary team working to deliver what's next in precision medicine. We have hybrid and remote employees located all around the world. We offer competitive salaries, annual performance-based bonuses, an equity-based incentive program, generous vacation, paid wellness days and support for learning and development.

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, and other legally protected characteristics.

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