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 role
Participate in Quality Management System (QMS) building in Technical and Development Department (TR&D) in Gdańsk site. Revision and archiving of scientific projects data and equipment maintenance documentation.
Maintaining of Quality registers and training system for TR&D. Support in area preparation for inspections.
Your responsibilities
Support in implementation and monitoring of the Quality System in the TR&D Department
Support in preparation of the TR&D area for inspections and audits
Verification of documentation in TR&D areas in terms of compliance with the applicable internal procedures and current regulations
Contact with the TR&D Department of Polpharma Biologics to adapt the procedures and quality requirements to the standards of Polpharma Biologics
Revision and approval of the documentation related to technical and computerized systems in TR&D
Archiving of documentation
Maintaining registers of documentation, equipment calibration and maintenance activities
Working with electronical documentation systems
Preparation of presentations associated with Quality System in TR&D
If you have
Master’s or Bachelor degree in a relevant field (pharmacy, biology, biotechnology, biochemistry, chemistry)
Good knowledge of spoken and written English
Knowledge of MS Office
Good organization of work and time
Ability to cooperate with others to solve problems
Motivation to work and development 
