#PolpharmaBiologics is a state-of-the-art biological R&D and manufacturing facility, one of the most modern in Europe. We have a fantastic, international team of experienced experts and dynamic young scientists with common goals and values. Biotechnology is our passion. Together we develop medicine, offering new hope to patients suffering from serious diseases.
We create a passionate and friendly workplace environment. Join us!
- International work environment
- Attractive salary
- Cutting-edge technology equipment
- Conferences and trainings around the world
- Being the single point of contact for all analytical topics within an project from development to product discontinuation. Coordinating analytical activities and compiling analytical documents to support the project
- Actively managing analytical knowledge of a certain project by communicating to all people involved in analytical activities and having an overview on these activities
- Overseeing and coordinating method development, stability indicating studies, method qualification and validation, method transfer, method monitoring and improvement
- Supporting all analytical activities to increase understanding of all properties of a molecule like quality attribute assessment, defining the stability profile of the molecule, structure function relationships
- Overseeing and coordinating specific analytical activities of a certain project like: comparability studies, establishment of analytical standards, cleaning validation of manufacturing units
- Participating in project team meetings and other project related meetings representing all analytical aspects of a certain project
- Compiling documents like product specifications, sampling plans, analytical method transfer protocols and reports, leachable and extractable studies
- Supporting preparation of reports of other departments (e.g. USP development, DSP development, manufacturing) by providing analytical data collected in analytical departments both development and QC and support interpretation of these data
- Supporting any troubleshooting activities with analytical knowledge and coordinating and performing any analytical activities
- Presenting analytical topics of a certain project during internal and external audits
- Supporting preparation of regulatory submissions; participate in meetings with regulatory authorities as needed
- Preparation, reviewing and approval of procedures, protocols and reports
- Communication with any external companies to align on analytical tasks
- Higher education with a specialization in the fields: biotechnology, analytical chemistry, biochemistry, pharmacy, or related
- Practical and theoretical knowledge about development, transfer and validation of analytical methods, stability studies, liquid chromatography concerning work with biologic drugs (such as: peptide mapping, SEC, IEC), capillary electrophoresis, ELISA, UV-VIS spectrophotometry, pharmacopoeial methods used for release raw materials, intermediates and final drug products
- 5 years’ experience in regulated laboratory environment (preferred biotechnological lab). Very good knowledge of GLP and GDP rules
- Project management experience
- Fluent English
- Sport Card
- Development programs
- Private healtcare
- Relocation package
- Fruit day
- Integrations events
- Benefit platform
- and more
Aleksandra Bufnal
aleksandra.bufnal@PolpharmaBiologics.com
Poznaj
Rezon Bio
Dołącz do zespołu ponad 1300 specjalistów produkujących zaawansowane leki biologiczne, które poprawiają jakość życia pacjentów na całym świecie.
Bazując na doświadczeniu Polpharma Biologics, Rezon Bio działa jako partner CDMO (Contract Development and Manufacturing Organization).
Dzięki nowoczesnym centrom biotechnologicznym w Gdańsku i Warszawie-Duchnicach oferujemy szeroki wachlarz możliwości karierowych w obszarach naukowych, technicznych i biznesowych.