QC Physicochemical Specialist
Duchnice (pow. warszawski zachodni)

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

  • Participating in the project related to the launch of a new laboratory and other projects implemented in the Quality Control;
  • Performing transfer and validation of physicochemical methods;
  • Performing qualitative and quantitative physicochemical tests in tested products and starting materials;
  • Verification of the correctness of test documentation in accordance with applicable procedures;
  • Collection and registration of clean media, raw materials, semi-finished products, products ready for analytical testing;
  • Participation in the development of the GMP system in the Quality Control Laboratory;
  • Conducting investigations, corrective and preventive actions regarding the results of OOS, OOT and complaints regarding product quality;
  • Participation in the preparation of the Quality Control area for GMP audits and certification;
  • Working out of standard procedures, instructions and analytical methods as well as training in them;
  • Performing maintenance, calibration and qualification of laboratory equipment in accordance with applicable instructions and procedures.

If you have

  • Higher education, with a specialization in the fields: chemistry, biotechnology, biochemistry or related,
  • Experience of working in an analytical laboratory or quality control laboratory in a pharmaceutical or biotech works (at least 5 years),
  • Experience in working with instrumental analytical techniques in the field of physicochemical tests of biotechnological drugs and raw materials: chromatography (HPLC, UPLC, GC), UV/VIS spectrophotometry, FT-IR, capillary electrophoresis,
  • Practical and theoretical knowledge in the field of validation and transfer of analytical methods;
  • Knowledge of regulations and guidelines for good laboratory practice (GLP) and Good manufacturing Practice (GMP) contained in the ICH, FDA, EMEA and national guidelines,
  • Experience in testing of biotechnological products;
  • Knowledge of MS Office;
  • Very good English spoken and written;
  • Organizational skills;
  • Strong communication skills.

We offer

  • Private healthcare;
  • Life insurance;
  • Pension plan above national standards;
  • Relocation package;
  • Additional free day;
Join our Team!

Why you should work with us