Quality Control Bioassay Specialist

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Quality Control Bioassay Specialist

Ogłoszenie wygasło

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