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02.10.2022 02 października 2022

Quality Control Bioassay Specialist

Pracodawca: Polpharma Biologics Group Numer referencyjny: 90474 Data publikacji: 14 września 2022 Lokalizacja: Gdańsk - Pomorskie Rodzaj umowy: - Doświadczenie: 1-3 lata Branże:
Przemysł i inżynieria: Mikrobiologia, biotechnologia
Środowisko naturalne, bioróżnorodność: Badania naukowe

Opis stanowiska

  • Conducting biological analyzes using the following methods: ELISA, qPCR, in vitro with the use of cell cultures, etc. in accordance with applicable documentation
  • Preparation and review of protocols, reports, instructions, test methods, procedures, and other documents in the Department of Biological Quality Control
  • Planning and execution of validation and transfer of analytical methods along with the preparation of all related documentation
  • Checking and verification of the analytical results and validation and transfer documentation, in accordance with the applicable procedures
  • Development of Standard Operating Procedures, Instructions and Analytical Methods and conducting trainings on them
  • Close cooperation and communication with other teams at Polpharma Biologics
  • Performing maintenance, calibration, and qualification of laboratory equipment in accordance with applicable instructions and procedures
  • Supervising the work of lab technicians as part of the assigned tasks
  • Performing standard activities related to work in the laboratory, i.e. preparation of reagents, waste management (including hazardous waste), keeping records of consumables and reagents and their replenishment
  • Writing and checking of the certificates of analyses for the results obtained in Polpharma Biologics and in cooperation with external companies
  • Participation in trainings designated by the supervisor and training of co-workers
  • Performing tasks other than those listed above at the request of the supervisor

Wymagania

  • University degree in the field of microbiology, biotechnology, biology, chemistry or related
  • Minimum 3 years of experience in laboratory work in a regulated environment (preferably in a biotech lab and/or pharmaceutical industry)
  • Very good knowledge of GLP, GMP and GDP rules
  • Ability to independently solve problems and work in a team
  • Fluent English
  • Laboratory precision
  • Analytical thinking
  • Good organization of work
  • Very good ability to collaborate with others to solve problems
  • Ability to prioritize tasks, according to timelines
  • Very good knowledge of MS Office

Oferujemy

  • Fixed-term employment​ (1,5 year)
  • Private healthcare
  • Cutting-edge technology equipment
  • Attractive salary
  • International work environment
  • Relocation package
  • And much more…

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Polpharma Biologics Group

Operator techniczny bierze udział w procesie utrzymania w sprawności technicznej systemów i urządzeń technologicznych

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