Supports the Site Managers in Compliance Relevant topics
Support deviations, investigations, CAPA's, and changes for the production site
Responsible for Risk Assessments within site
Responsible to implement, check or revise new Quality regulations and support updates of local GMP documents, such as SOP's
Serves as a point of contact for WAG GCS Compliance topics
Supports Walkthrough Audits and Internal Audits
Tracks and monitors local operational and quality performance. Escalates issues to the local Managers as appropriate
Assists in development and delivery of metrics
Unlimited temporary contract to start as soon as possible Opportunity in International Company
Minimum 3 years' experience in Quality function, related Business Operations or GMP regulated environment
Demonstrated Quality experience in the areas of pharmaceutical and / or biologics manufacturing or packaging
Ability to work within a matrix organization and leverage expertise from other functions and departments
Knowledge of cGMPs, data management, collection, and analysis
Fluency in German and English
We are currently searching for a professional and precise Quality Control Specialist to support the Site Manager of our client, an international Pharmaceutical company in the Lucerne area, on an unlimited temporary basis, with the aim of taking the position permanently. Do you want to play an important part in a global business? Do you value being responsible for the efficiency and quality of products? Do you enjoy surrounding yourself with lively people? Then do not hesitate and apply online now!
