Important multinational Pharmaceutical company FDA approved.


The candidate will be responsible for all aspects of quality assurance in accordance  with the corporate guidelines.

The role reports to the Quality Director.

Main activities:

  • Develop, implement, and train facility workers on a quality plan in order to be in compliance with quality regulations

  • Interact with customers in addition to other departments to main product supply and help introduce new product

  • Implement quality procedures

  • Ensure execution of corrective action plans

  • Monitor performance

  • Supervising technical staff

  • Writing technical and management systems reports

  • Represent the company in FDA regulatory inspections and customer compliance audits



  • Bachelor Degree in Biology, Chemistry, CTF or equivalent;

  • Professional experience minimum 5 years  in quality assurance activities in multinational organizations in the pharmaceutical field.

  • Strong knowledge in all compliance /regulatory aspects (FDA,GMP, etc)

  • Knowledge in Continuous improvement tools

  • Excellent leadership skills including strong communication skills

  • Fluency in English and Italian


Location:  LATINA area


Please send a CV, mentioning the authorization to the processing of personal data in accordance with EU 2016/679 and included reference to the position:
Email: uff.firenze@standler.it

L'offerta di lavoro si intende estesa a entrambi i sessi (L. 903/77). Aut. Min. Lav. prot. nr. 1417 del 22/01/2007.

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