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Mammalian Cells Bioprocess Specialist - USP

  • Gdańsk, pomorskie pokaż mapę
  • Specjalista
  • 15.06.2018

    Pracodawca ma prawo zakończyć rekrutację we wcześniejszym terminie.

    if you want to work

    in one of the
    most modern biotechnology
    centres in Europe
    in place where
    from all over
    the world work
    on the highest-quality equipoment
    in the production
    of biotechnological
    drugs, which dive
    access to effective
    therapy to more
    in a company that will
    dive you stable
    employment competetive
    remuneration attracive
    benefits and the
    opportunity to participate
    in training at home
    and abroad
    Currently we’re looking for
    Mammalian Cells Bioprocess Specialist - USP

    Join “start-up” Biologics division with strong international and local team at site!


    We are waiting just for you!


    What will you do?

    • Carry-out and monitoring of biotechnological production processes according to technological documentation, GMP rules and internal quality requirements
    • Analysis of achieved process data according to compliance with technological documentation and internal requirements
    • Participation in technology transfer and process validation in cooperation with Research and Development Department
    • Preparation of documentation according to GMP rules and Company internal requirements
    • Preparation of qualification documentation for production equipment, participation and carry out of equipment qualification
    • Preparation of Standard Operational Procedures and instructions and trainings for its introduction
    • Guarantee of effective production activities preparation and carry out, responsibility for production process continuity, reporting of performed actions statuses
    • Supervision of proper raw materials expenditure during technology transfer and production processes.
    • Shift work

    What do we expect?

    • Higher education (at least Msc) in Biotechnology, Pharmacy or similar
    • At least two year experience in biotechnological or pharmaceutical industry
    • Good knowledge of cGMP and FDA requirements
    • Experience in keeping records in production documentation according to GMP requirements
    • Excellent knowledge of aseptic techniques especially used in in vitro cell cultures is required
    • Knowledge and experience in mammalian cell cultures (especially coherent cell lines) is required
    • Experience in work with bioreactors will be an additional advantage
    • Experience in work with recombinant proteins will be an additional advantage
    • Experience in single use materials usage for biopharmaceutical production will be an additional advantage
    • Very good speaking and writing English skills
    • Knowledge of MS Office
    • Good work organization and individual problem solving skills are required
    • Good communication, team cooperation skills and being open for new tasks is required