Analytical Process Development Leader
Gdańsk
Boost your career with us
Polpharma Biologics 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 medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
Your role:
Leads a team of analysts at Process Development Analytics Team, coordinates the work related to the development, qualification, transfer of analytical methods, coordinates the work for team.
Your responsibilities
- Supervising the work of a team of analysts in Polpharma Biologics
- Monitoring of compliance of the works with internal standards
- Supporting staff and consultation in the development and implementation of analytical methods
- Consulting the research in projects through substantive, technical and expert support
- Participating in tasks related to research and development projects
- Overseeing the proper maintenance and validation of laboratory equipment entrusted
- Monitoring of compliance with safety rules in the analytical laboratory
- High interpersonal skills and ability to motivate co-workers
- Ability to plan and optimize the analytical studies to support the development process of biotechnological molecules
- Supervising the process of creating and implementing protocols, reports, methods, procedures and other documents required by internal rules and procedures
- Training analytical laboratory team
If you have
- higher education, with a specialization in the fields: chemistry, biotechnology, molecular biology, biochemistry, pharmacy, medicine or related
- minimum 5 years of experience
- knowledge of analytical techniques such as: liquid chromatography, electrophoresis, UV/VIS, ELISA, blotting, PCR
- 5 years of experience in laboratory work (analytical or quality control laboratory) in biotechnological or pharmaceutical company
- experience in team management and conducting research and development projects
- knowledge of regulations and guidelines for good laboratory practice (GLP) and Good Manufacturing Practice (GMP) contained in the ICH, FDA, EMEA and national guidelines.
- fluent English spoken and written
- fluent MS Office skills
- good organization of work and time
- ability to cooperate with others in order to solve problems
- high interpersonal skills and ability to motivate coworkers
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.