Radiopharmaceutical QC Scientist (Method Development & Technology Transfer) (m/f/d)

At our site in Warsaw, a team of around 30 dedicated experts develops and produces state-of-the-art PET tracers that significantly improve patients’ lives. We combine scientific precision with a pioneering spirit—within an open, international environment where you can take responsibility, drive innovation, and truly make a difference. Join our growing team and help shape the next chapter of our success story!

Shape the future of radiopharmaceuticals with vision, structure, and determination.

• Plan, develop and optimize analytical quality control methods for radiopharmaceuticals (e.g., HPLC, GC, TLC) including method validation and analytical method transfer according to GMP requirements.
• Perform and document quality control testing of radiopharmaceuticals in accordance with Good Manufacturing Practice (GMP) requirements (e.g., testing instructions) for development, validation and technology transfer batches.
• Participation in scale-up activities of radiopharmaceutical synthesis processes by providing analytical and quality control support.
• Participate in the planning and execution of analytical method transfer for radiopharmaceutical products, including support for implementation at other Alliance Medical sites.
• Prepare and maintain development reports, analytical validation protocols and reports, and technology transfer documentation.
• Support the preparation of analytical and quality documentation for product registration submissions.
• Contribute to the development and revision of SOPs, manufacturing instructions, and process documentation.
• Collaborate with Production, QA, QC, and Regulatory Affairs teams to ensure compliance with GMP requirements.
• Participate in regular internal project meetings to discuss and plan activities.
• Participate in regular meetings with contract organizations to provide project updates via teleconference or on-site visits, as appropriate.

• This position requires on-site presence with daytime working hours, which may be adjusted depending on laboratory availability.
• University degree in pharmaceutical sciences, chemistry, or a related scientific discipline.
• Knowledge of GMP requirements.
• At least 2 years of experience in R&D, TT or QC department in pharmaceutical industry.
• Experience in radiopharmaceutical industry will be an advantage.
• Strong problem-solving skills with the ability to identify and address critical issues effectively.
• Creative mindset with the ability to think outside the box and challenge current projects development strategies.
• Excellent teamwork and interpersonal skills, with the ability to collaborate effectively in multidisciplinary environments.
• Strong communication skills, with the ability to communicate clearly and professionally at all organizational levels and proactively drive topics forward.
• Willingness to travel and work within an international and partly remote team environment.
• Fluency in Polish and English (written and spoken).

• Employment contract
• Opportunities for professional development 
• International pharmaceutical work environment
• Support from an experienced team
• Medical package
• Sports card
• Bonus system
• Training

Wir sind ein Team von hands-on arbeitenden und kreativen Köpfen, die die Herausforderungen in unserer kleinen, innovativen Umgebung mit familiärer Atmosphäre schätzen. Geführt von unserem internationalen Umfeld liefern wir von 9 Standorten in 3 Ländern zuverlässig unsere hochmodernen Arzneimittel an Patienten, die von unserem nachhaltigen und expandierenden Service profitieren.

Werde Teil unseres wachsenden Teams und entwickle dich mit uns stetig weiter!