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Analytical Process Development Leader

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!
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
Join our Team!
Why you should work with us
Contact us
career@polpharmabiologics.com


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