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QA Document Specialist (m/f) 100%

nemensis ag

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QA Document Specialist (m/f) 100%

As result of high work overload, we support our client, an international pharmaceutical firm in the Luzern area, in the search for two specialists for a project until end of 2017.

Your tasks:

  • To review and correct Quality GMP relevant documents
  • To compile and approve documentation related to releases of API or clinical supply (bulk and packaged) as well as issue deficiencies reports
  • To conduct routine QA audits in procedures, systems, computer systems and equipment
  • To ensure compliance with GMP and SOPs
  • To collaborate with team to solve audit issues and perform inspections

Your profile:

  • Completed laboratory technician training or Bachelor in Science
  • At least 2 years experience in a pharmaceutical company or drug regulatory institution with profound cGMP knowledge
  • Written and spoken English and German

What the company offers you in return:

  • Same consideration as internal employees
  • 40h./week, minimum 25 holidays/year , 15 bank holidays in 2017
  • 59 CHF/h. gross salary (holidays, bank holidays, 13th salary inclusive)
  • Easy reachable with public transport and car, modern facilities

Welcome to nemensis!

We are looking forward to getting to know you.