Senior Process Engineer (m/w/d) – Biotech Manufacturing
Shape the Future of Biologics Manufacturing – Join an Innovative Team!
Duration: 02.03.2026 – 29.02.2028
Location: Greater Lucerne Area
Type: Temporary Position
Salary: CHF 10,000 monthly gross
About Our Client
For 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 Responsibilities
* Lead 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 product
* Drive innovation as a change champion, introducing new technologies, digitization initiatives, and modern working methodologies throughout the organization
* Coordinate cross-functional activities through tiered meeting structures with colleagues in the US and Ireland for seamless implementation of novel manufacturing processes
* Evaluate and harmonize innovative equipment solutions for batch and continuous manufacturing paradigms, ensuring flexible switching capabilities between production modes
* Develop capital funding requests and user requirement specifications for new technologies, software, and instruments that streamline GMP manufacturing and administrative workflows
* Create and review GMP documentation including risk assessments, batch records, sampling plans, qualification protocols, and standard operating procedures
* Provide subject matter expertise on quality assurance and GMP compliance within global, interdisciplinary project teams
* Centralize process knowledge to establish robust knowledge management systems and support continuous learning initiatives
Your Profile
* Minimum 5 years of professional experience in the pharmaceutical or biotechnology industry with hands-on manufacturing exposure
* Proven project management skills leading cross-functional teams in complex technical environments
* Strong knowledge of upstream and downstream unit operations for biologics manufacturing processes
* Analytical mindset with demonstrated ability to solve complex problems and develop practical, innovative solutions
* Business 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 automation
* Desirable: Deep understanding of Critical Process Parameters, Critical Quality Attributes, and equipment qualification principles
* Proactive team player who thrives under pressure and takes initiative in a collaborative environment
Your Benefits with Nemensis
* Nemensis AG is your specialized personnel recruiter in the Life Sciences sector with headquarters in Basel
* Comprehensive consultation and support throughout the application process by our experienced consultants
* Access to an extensive client network and exciting positions in Northwestern Switzerland
* Fast and uncomplicated entry through individual guidance and consulting during the application process
Ready 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!
Branche: Pharma-Industrie
Funktion: Produktion
Anstellungsart: Befristeter Vertrag