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Quality Control Bioassay Specialist

Quality Control Bioassay Specialist
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 responsibilities include, but are not limited to:
  • Conducting biological analyzes using the following methods: ELISA, qPCR, in vitro using cell cultures etc. in accordance with the applicable analytical methods.
  • Acting as SME for analytical methods.
  • Development and reporting of the results of biological analyzes.
  • Verifying the results of biological analyzes performed by other analysts, obtained in Polpharma Biologics and the results provided by external companies.
  • Conducting the process of validation and qualification of analytical biological methods.
  • Carrying out the process of transferring biological methods to and from external companies and within the organization.
  • Creation and updating of analytical methods in the field of QC Bioassay.
  • Supporting the process of creating Certificates of Analysis.
  • Direct participation in audits and business visits.
  • Acting as owner responsible for Quality systems including Change Control and CAPA activities.
  • Managing the quality documentation of the Biological Quality Control team.
  • Performing and Supervising Data Integrity compliance activities.
  • Supervising the training status and supporting the team in the implementation of training and courses.
  • Conducting trainings for other team members.
  • Performing oversight of processes related to instruments, technical software qualifications and data integrity.
  • Cooperation with other departments of Polpharma Biologics.
  • Fulfilling the obligations in accordance with the current GMP regulation and other pharmaceutical guidelines.
  • Taking care of the laboratory and its contents and keeping it ready for routine activities and audit visits.
  • Performing other activities ordered by the supervisor.
If you have:
  • Higher education in the field of biology, chemistry, pharmacy, biotechnology.
  • Minimum 3 years of experience in laboratory work in regulated laboratory environment.
  • Very good knowledge of GLP, GMP and GDP rules.
  • Ability to independently solve problems and work in a team.
  • Very good knowledge of English language.
  • Laboratory precision.
  • Analytical thinking.
  • Good organization of work and time.
  • Very good ability to collaborate with others to solve problems.
  • Timeliness, the ability to prioritize tasks.
  • Very good knowledge of MS Office.
What we offer:
  • Competitive salary.
  • Private healthcare.
  • Life insurance.
  • Pension plan above national standards.
  • Relocation package.
  • Additional free day.
  • and more..
Why you should work with us
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