#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
- Performing quality control testing at every production stage as well as Drug Substance and Drug Product release and stability testing and results processing and interpretation. Verification of other analysts’ results
- Collection and registration of samples, raw materials, semi-finished products, finished products for analytical and microbiological tests (if required). Sample management
- Planning and performing analytical methods validation including preparing all related documentation
- Analytical methods results and transfer and validation documentation verification and review according to approved procedures
- Creating (with supervisor consultation) Standard Operating Procedures, Instructions and Analytical Methods and conducting trainings on them
- Close cooperation and communication with other Polpharma Biologics teams
- Performing maintenance, calibration and qualification of laboratory equipment according to instructions and procedures
- Supervising work of technicians in the assigned tasks
- Performing common laboratory tasks i.e.: reagents preparation, waste management (including hazardous waste), reagents and materials management and re-ordering
- Collection of quotations from vendors and placing orders including preparing all related documentation (under supervision)
- Participation in trainings (scheduled by supervisor) and training other analysts
- Higher education with specialization in the fields of biology, biotechnology, biochemistry, chemistry or related
- Minimum 3 years of laboratory experience (in regulated environment)
- Knowledge of bioanalytical methods, i.e. blotting, ELISA, SPR, RT-PCR used for testing biological drugs
- Practical and theoretical knowledge of transfer and validation of methods; bioanalytical methods: bioassay's like ELISA, SPR, RT-PCR
- Knowledge of pharmacopeial methods of raw materials testing would be considered an advantage
- Good knowledge of spoken and written English
- Knowledge of MS Office
- Ability to solve problems independently and good teamwork
- Good work and time organization
- 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.