Senior QA Specialist - Project Manager

m/f/d, Wallis

As a member of the quality assurance team (Bioconjugates), you will be responsible to ensure production of API`s is in accordance with Good Manufacturing Practice (GMP).

Start date: Immediately:

End date: 31.12.2024

Location: Valais, on site

Support the contract manufacturing and advise members of development, production and analytical departments on all aspects of GMP
Responsible for checking manufacturing documentation for conformity, processing of change controls and reviewing and approving of deviations and OOS-results
In addition, you will be the quality contact for our clients, and will present during their GMP audits

Requirements

A degree in Life Science (microbiology, biotechnology, chemistry)
Relevant experience in the biopharmaceutical industry, ideally in GMP area
Strong communication skills, experience in working with stakeholders from different departments
Experience with TrackWise, SAP, LIMS and DMS is a plus
Fluency in English

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