USP Bioprocess Engineer

vor 2 Wochen

Visp, Schweiz Hays Vollzeit

USP Bioprocess Engineer (m/f/d) Freelance/temporary employment for a project Visp Start date: asap Reference number: /1 Diesen Job teilen oder drucken Responsibilities Develop, enhance, and implement documentation systems to optimize production and service processes in a GMP-regulated environment Independently review manufacturing and cleaning batch records in accordance with internal SOPs and ensure timely completion Participate in cross-functional review meetings with QA and production teams to ensure compliance and continuous improvement Maintain and update documentation lists ( KPIs, issuance logs) and support production teams with document preparation and archiving Create production certificates upon batch completion and manage controlled copies of work instructions Evaluate existing documentation processes and propose improvements to increase efficiency, quality, and compliance Provide general documentation support to project teams, including label checks, document collection, and prototype testing Support administrative tasks such as presentation creation, office supply orders, and document archiving Profile Solid experience in a pharmaceutical or GMP-regulated environment Completed vocational training or equivalent professional qualification Strong understanding of current cGMP regulations and documentation standards Excellent written and verbal communication skills in English; German is advantageous Proficient in MS Office and digital documentation systems Detail-oriented with a structured and reliable working style Ability to organize daily tasks independently and ensure timely completion Communicative and a strong team player Benefits Work in a high-impact role within a regulated and innovative pharmaceutical setting Close collaboration with QA and production teams Opportunities for professional development in process optimization and documentation systems 

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