qa specialist (medical sterilization), stargard

stargard, zachodniopomorskie
job type
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job details

stargard, zachodniopomorskie
experience level
powyżej 24 miesięcy

job type
job category
Manufacturing & Production
contract type
umowa o pracę
working time
pełen etat
work system


elżbieta kamińska+48 697 742 288
reference number
/503/03/2021/MB - 68957

job description

For an international company in the medical industry we are looking for a QA Specialist of medical sterilization. If you have experience in a similar position, speak English fluently and are not afraid of business trips, this offer is for you.

what we offer

  • regular contract after 3-monthly trial period
  • competitive salary with the possibility of earn a bonus
  • comprehensive on-the-job trainings
  • opportunity for professional development in an international environment and gaining valuable experience
  • development in a dynamic company with a strong lean culture
  • private medical care
  • life insurance - possibility to join group life insurance
  • benefit cards (e.g. co-funding of the sports card)
  • fresh fruits and drinks
  • interesting integration meetings

your tasks

  • support review and approval of validation and requalification of EO sterilization processes
  • provide guidance for QMS and regulatory compliance in an FDA regulated and ISO compliant environment for Sterilization
  • take part in the Quality assurance activities as an active member of relevant project teams
  • keep updated knowledge of standards, regulatory requirements and directives applicable for Medical Devices/IVD and ensure updating relevant parts of the QA system

what we expect

  • knowledge of Global Labeling requirements, ISO-11135 and ISO-8 within Sterilization and Clean rooms
  • at least 5 years of experience
  • experience of working with multicultural and in a matrix organization
  • demonstrated Product Release Skills: effective document review, understanding of analytical methods and their results
  • great verbal and written communication skills
  • good planning and organizational skills
  • QA Design Control experience from the medical device or IVD industry or other similar regulated industries
  • English on fluent level
  • knowledge of using MS Office

Agencja zatrudnienia – nr wpisu 47