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