QA Specialist (6603)

QA Specialist – 6603 ADA

Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a:QA Specialist for a contract role of 9 months (with potential extension), based in the Visp, Switzerland.

Main Responsibilities:

·      Generating and maintaining accurate reports of compliance activities and documents, including trending of key quality indicators, e.g. for non-conformities, CAPAs, changes, training status, among others

·      Supporting implementation of corporates documents at local level

·      Collaborating with other departments to ensure harmonization throughout the site on QMS related topics

·      Identifying and managing projects that focus on QMS needs, as required

·      Active participation in audits and inspections as well as following up

·      Performing other duties as assigned

Qualifications and Experience:

·      Relevant working/residency permit or Swiss/EU-Citizenship required

·      Bachelor (B.Sc.) or Master (M.Sc.) in natural sciences or related field

·      3 to 5 years of work experience in a GMP regulated environment; preferably within a Quality unit

·      Ability to interact with several stakeholders and handle multiple tasks simultaneously

·      Very good knowledge of written and spoken English; German as an advantage

·      Proficiency with Microsoft tools – especially Excel and Power Point.