Polpharma Biologics is part of the Polpharma Group, one of the largest pharmaceutical companies in Central and Eastern Europe. We focus on the development and production of biological medicines. Our international team consist of experiences experts and young scientists. We share common goal - to improve the quality of patients' ;ife with more availabe biological medicines of the hishest quality.
Head QC
Location: Gdańsk
If you want to work:
- in one of the most modern biotechnology centres in Europe
- in a place where professionals from all over the world work on the highest-quality equipment
- in the production of biotechnological drugs, which give access to effective therapy to more patiens
- in a company that will give you stable employment, competitive renumerations, attractive benefits and the opportunity to participate in trainings at home and abroad
Currently we’re looking for
1
Head QC
Join “start-up” Biologics division with strong international and local team at site!
We are waiting just for you!
What will you do?
- Set up of QC labs and organization of QC teams, motivates employees towards achieving the objectives set
- Perform all duties according to current GMP regulations and other pharmaceutical regulations
- Preparation, reviewing and approval of procedures, instructions and other QC's documents
- Ensure the performance of all necessary tests and evaluation of related records
- Timely release or rejection of tested raw materials, packaging materials and intermediates, product in bulk and final product. Timely and reliable performance of analysis
- Ensure compliance with the HSE (health, safety and environment) requirements
- Participate and represent the company, both in internal and external audits.
- Ensuring the performance of all appropriate method transfers and validation
- Ensuring the maintenance and qualification of premises and equipment in department
- Participation and representation of the company in internal and external audits
- Management and supervision of stability studies
- Approval and monitoring of contract analysts and laboratories
What do we expect?
- Education background in Biochemistry, Biotechnology or related field, ideally Master or PhD level
- Practical and theoretical knowledge in transfer and validation of analytical methods, stability studies, analysis of biologic drugs, analysis of release raw materials, intermediates and final drug product
- At least 5 years’ experience in regulated laboratory environment (preferred biotechnological lab)
- Strong knowledge of GMP and GDP rules and ability to conduct them in laboratory and supervise compliance with these rules
- Very good abilities to organizing team's and own work and ability to work under time pressure
- Fluent in English, willing to learn Polish language
- Ability of analytical thinking
Poznaj
POLPHARMA S.A.
Zdrowe jutro zaczyna się od ludzi, którzy tworzą Polpharmę – od ich wiedzy, zaangażowania i pasji. Wspólnie dbamy o zdrowie innych i tworzymy środowisko, w którym każdy może być sobą. Rozwijamy się w zgodzie z własnymi ambicjami, niezależnie od obszaru, w jakim działamy. Razem z nami możesz realnie wpływać na zdrowie i dobrostan innych.