4 days ago

QA Document Specialist (m/f) 100%

nemensis ag

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 Please refer to alpha.ch in your application

QA Document Specialist (m/f) 100%

We support our client, an international pharmaceutical company in the northwest region of Switzerland, for a project until November 2018.

Your responsibilities:

  • To review GMP relevant documentation for compliance with SOPs and support in the resolution of deviations
  • To write QA documents: CoAs, CoCs, BRR sheets, SOPs, etc.
  • To collaborate with colleagues by supporting the requirements of electronic systems and act as contact person as required
  • To archive quality documents: Audit reports, CoCs, BRR, CoAs, etc.
  • To collaborate with the training of new employees

Your profile:

  • Professional education as Laboratory Technician, BSc or MSc in Life Sciences
  • Minimum 2 years previous experience in pharmaceutical environment and practical experience within Quality Assurance
  • Good written and spoken English and German

What the company offers you in return:

  • Company easily reachable by public transport and/or private car
  • Workload: 40 h/week
  • Gross hourly salary: Up to 41 CHF/h depending on age and experience (holidays, bank holidays and 13th salary already included)
  • Temporary position until end of November 2018

Welcome to nemensis!

We are looking forward to meeting you!