Senior Process Engineer (m/w/d) – Biotech ManufacturingShape the Future of Biologics Manufacturing – Join an Innovative Team!Duration: 02.03.2026 – 29.02.2028Type: Temporary PositionSalary: CHF 10,000 monthly grossAbout Our ClientFor our client, a leading biopharmaceutical company in the greater Lucerne region, we are seeking a Senior Process Engineer (m/w/d). This innovative organization operates at the forefront of biologics development and clinical manufacturing, driving next-generation technologies and continuous improvement in GMP batch and continuous manufacturing processes. With a strong presence in Switzerland's thriving life sciences cluster and global connections across the US and Ireland, this company offers an exceptional environment for professional growth and technological innovation.Your ResponsibilitiesLead and mentor the Process Engineering team while coordinating efforts across local and international sites to implement cutting-edge technologies for GMP manufacturing of drug substance and drug productDrive innovation as a change champion, introducing new technologies, digitization initiatives, and modern working methodologies throughout the organizationCoordinate cross-functional activities through tiered meeting structures with colleagues in the US and Ireland for seamless implementation of novel manufacturing processesEvaluate and harmonize innovative equipment solutions for batch and continuous manufacturing paradigms, ensuring flexible switching capabilities between production modesDevelop capital funding requests and user requirement specifications for new technologies, software, and instruments that streamline GMP manufacturing and administrative workflowsCreate and review GMP documentation including risk assessments, batch records, sampling plans, qualification protocols, and standard operating proceduresProvide subject matter expertise on quality assurance and GMP compliance within global, interdisciplinary project teamsCentralize process knowledge to establish robust knowledge management systems and support continuous learning initiativesYour ProfileMinimum 5 years of professional experience in the pharmaceutical or biotechnology industry with hands-on manufacturing exposureProven project management skills leading cross-functional teams in complex technical environmentsStrong knowledge of upstream and downstream unit operations for biologics manufacturing processesAnalytical mindset with demonstrated ability to solve complex problems and develop practical, innovative solutionsBusiness fluent in English and German: Effective written and oral communication skills in English (C1 level) and German (B1 level)Desirable: Experience with quality management systems, quality auditing, Emerson DeltaV, SIPAT, and manufacturing automationDesirable: Deep understanding of Critical Process Parameters, Critical Quality Attributes, and equipment qualification principlesProactive team player who thrives under pressure and takes initiative in a collaborative environmentYour Benefits with NemensisNemensis AG is your specialized personnel recruiter in the Life Sciences sector with headquarters in BaselComprehensive consultation and support throughout the application process by our experienced consultantsAccess to an extensive client network and exciting positions in Northwestern SwitzerlandFast and uncomplicated entry through individual guidance and consulting during the application processReady for Your Next Career Move?At nemensis ag, we have already connected thousands of candidates with their dream jobs, giving them the opportunity to develop further or re-enter the job market. What can we do today for you and your career? Get in touch with us!Note: This message contains italic text in the original; formatting tag removed for consistency.Please use only the file formats pdf, doc, docx, png, gif, jpeg, odt with max. 8MB filesize.
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