Your role at KLOCKE Pharma-Service

Quality management assistant (m/f/d)

Job description:

  • You will edit Product Quality Reviews,
  • assess and evaluate our suppliers,
  • create, process and manage qualification and validation plans and reports in cooperation with our specialist departments
  • perform various samplings (wipe, swab and rinse tests, etc.) in order to monitor microbiological contamination and for cleaning validations.
  • Your tasks involve the management and maintenance of QM databases as well as the follow-up procedures (in particular processes such as Change Control and CAPA management) and other administrative activities.

Your profile:

  • Scientific and / or technical studies or vocational training plus professional experience, e.g. as a pharmaceutical or chemical technical assistant (PTA or CTA)
  • Some professional experience in an pharmaceutical environment (GMP) is desirable, especially for qualification and validation tasks
  • You are confident in using common MS Office applications,
  • a responsible and reliable person,
  • autonomous, structured and team-oriented at work.
  • You have the ability to openly communicate.
  • You are very proficient in both: written and spoken German and English.

We offer:

  • Flexitime
  • Professional education and training
  • Air-conditioned workspaces
  • The possibility to work from home as agreed with the team, extensive onboarding training, ergonomic workspaces in an international environment, welcoming work atmosphere, a fair and adequate salary with common German social benefits.

Position available on a fixed-term contract basis for a 2-year parental leave.

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