Quality Specialist, Chemistry

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 role is located in Seneffe, Belgium, with the role reporting to the local Quality Control Manager. The primary responsibility of this role will be to carry out and to coordinate Quality control operations in the scope of product development as well as for clinical and commercial productions in accordance with cGMP.

Key Accountabilities

• Conduct and organize, as per the delegation of the Quality Control Manager, QC inspections and tests on raw materials, packaging, intermediate or finished products. Some QC tests are performed in a laboratory and require the handling of radioactive substances (short-lived isotopes)
• Document testing according to procedures and within our electronic Quality Management System or paper based (GLP)
• Participate in management of the QC sample outsourced to external laboratories
• Coordinate management of QC laboratory materials, including consumables and chemicals
• Support the lifecycle management of laboratory equipment, including installation, qualification, calibration, maintenance and requalification
• Contribute to the day-to-day operation of the QC laboratory, including organisation, housekeeping and backup activities such as environmental monitoring
• Participate in management of deviations, out-of-specification results and the implementation of corrective and preventive actions
• Support the writing and updating of Quality Control procedures
• Review Analytical development as per ICH Q14
• Prepare validation protocols in compliance with ICH Q2R2, execute validation studies and author validation reports in line with internal procedures and regulatory requirements
• Understand and adhere to GMP policies and procedures

Education And Experience

• Education in chemistry, radiochemistry, pharmacy or biochemistry; or Laboratory technician education
• 3+ years of Experience with Good Manufacturing Practices (GMP)
• 3+ years of Experience in analytical chemistry techniques (Chromatography and others)
• Experience in radiopharmaceuticals or radiochemistry is an asset
• Professional proficiency in French and English required

Key Capabilities

• 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
• Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to 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
• Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
• Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
• Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
• Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills

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-b