Facharzt Allgemeine Innere Medizin (m/w) für Hausärzte am Bahnhofplatz, Winterthur ‐ Allgemeine Innere Medizin 50 ‐ 100 %
Praxisplus Kehrsatz
Date de publication :
13 août 2024Taux d'activité :
100%Type de contrat :
Durée indéterminée- Lieu de travail :Zürich
Join a Leading Biopharma Company as a MS Process Engineer!<br /> <br /> On behalf of our client, a multinational pharmaceutical company, Swisslinx is seeking a MS Process Engineer for the Fill and Finishing department.<br /> <br /> Contract Type: Contract<br /> Start Date: ASAP<br /> Location: Neuchatel<br /> Workload: 100%<br /> Duration: 12 months with possible extension<br /> <br /> Your mission: <br /> â ¢ Lead process improvement projects or activities<br /> â ¢ Develop and optimize process parameters<br /> â ¢ Ensure process performances through Quality by Design (QbD) and Continuous Process Verification (CPV) approaches<br /> â ¢ Identify business opportunities<br /> â ¢ Ensure communication and act proactively in case of performance trending <br /> â ¢ Lead and/or support investigations related to deviation/CAPA process <br /> â ¢ Perform product impact assessment for deviation<br /> â ¢ Lead projects or activities related to FF process or equipment (from User Requirements Specifications to Process Performance Qualification)<br /> â ¢ Support validation activities<br /> â ¢ Support or present topic during regulatory inspections<br /> â ¢ Support technology transfer<br /> <br /> Your background:<br /> â ¢ Minimum 3-5 years of experience FF area for recombinant protein.<br /> â ¢ Degree Engineering or in Biotechnology <br /> â ¢ Language skills: Fluent in English and French<br /> â ¢ Knowledge of cGMP and quality requirements<br /> â ¢ Able to deal with statistics <br /> â ¢ Strong energetic team player with good communication skills,<br /> â ¢ Ability to lead effectively and efficiently process validation topics<br /> â ¢ Ability to manage multiple priorities in a manufacturing plant setting<br /> â ¢ Ability to analyze, review and interpret validation data<br /> â ¢ Must have uncompromising dedication to quality and an excellent understanding of cGMPs and other regulatory guidelines<br /> â ¢ Interpersonal skills that enable you to work with people at all levels<br /> â ¢ Ability to plan, multitask, and manage time effectively<br /> â ¢ Must display eagerness to learn, to innovate, drive for solutions and continuously improvement<br /> <br /> Whatâ s on Offer?<br /> â ¢ A chance to showcase your expertise in a leading global biopharma company.<br /> â ¢ Join a dynamic team and be a part of a positive, collaborative company culture.<br /> If this sounds like the right opportunity for you, donâ t hesitate to apply here or reach out directly to Veronika von Mentzer, Recruiter: E-Mail schreiben