Overview
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
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.
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
Qualifications
* 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
Benefits
* 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?
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