Senior Process Engineer (mf/d) 100%

Senior Process Engineer (m/w/d) – Biotech ManufacturingShape the Future of Biologics Manufacturing – Join an Innovative Team!Duration:02.03.2026 – 29.02.2028Location:Greater Lucerne AreaType:Temporary PositionAbout 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 mentorthe 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 innovationas a change champion, introducing new technologies, digitization initiatives, and modern working methodologies throughout the organizationCoordinate cross-functional activitiesthrough tiered meeting structures with colleagues in the US and Ireland for seamless implementation of novel manufacturing processesEvaluate and harmonizeinnovative equipment solutions for batch and continuous manufacturing paradigms, ensuring flexible switching capabilities between production modesDevelop capital funding requestsand user requirement specifications for new technologies, software, and instruments that streamline GMP manufacturing and administrative workflowsCreate and review GMP documentationincluding risk assessments, batch records, sampling plans, qualification protocols, and standard operating proceduresProvide subject matter expertiseon quality assurance and GMP compliance within global, interdisciplinary project teamsCentralize process knowledgeto establish robust knowledge management systems and support continuous learning initiativesYour ProfileMinimum 5 years of professional experiencein the pharmaceutical or biotechnology industry with hands-on manufacturing exposureProven project management skillsleading cross-functional teams in complex technical environmentsStrong knowledge of upstream and downstream unit operationsfor biologics manufacturing processesAnalytical mindsetwith 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 playerwho 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!? Phill Rogers, Consultant,Write an emailYou're looking for a change of perspective, but this isn't the right position for you? Then register with us – we'll contact you for an initial meeting to understand your wishes and needs and align ourselves accordingly.