Supporting the quality management system on review and approval of validation and engineering documents, test protocols, CAPAs, deviations, change controls and any technical documentation where QA needs to approve before implementation and upon completion
Keep up to date on cGMPs and regulatory requirement s as well as global procedures, guidelines and policies
Proactively identify and propose resolution to both technical and compliance issues/gaps, as well as development and implementation of Quality Systems
Temporary opportunity to start immediately Internationally operating business in the pharmaceutical sector
Bachelors or Masters in physical or biological sciences
Previous experience of the validation of laboratory, production equipment and knowledge of production methodology involved in biopharmaceutical drug substance production
Self-driven and take ownership and responsibility for own assignments
Be confident in making technical decisions
Fluent English, German is a plus
Flexibility - working weekends may occasionally be required
Our client, an internationally renowned Pharmaceutical company is recruiting. On its behalf we are now looking for a Quality Engineering Associate to work in the Solothurn area on a full-time temporary basis, for at least the next 3 months. Are you currently looking for a position within an international operating, dynamic business environment and enjoy communication and working together with different nationalities and teams? We look forward to receiving your application!
