Senior Process Engineer MES (m/f/d) – Biopharmaceutical Manufacturing
Shape the Future of Biopharmaceutical Manufacturing – Your Expertise in MES Implementation Awaits!
Duration: 02.03.2026 to 26.02.2027
Type: Temporary position
About Our Client
For our client, a leading biopharmaceutical research and development company in the greater Lucerne area, we are seeking a highly skilled Senior Process Engineer MES (m/f/d). This innovative facility specializes in the development and manufacturing of biotechnological active ingredients for global clinical trials and operates one of only three forensic laboratories worldwide. With over 400 employees from more than 15 countries, the site plays a crucial role in advancing life‑saving medicines and represents a hub of cutting‑edge biotechnology and pharmaceutical excellence.
Your Responsibilities
Lead technical support for the deployment and ongoing maintenance of the Manufacturing Execution System (PAS‑X) within biotech production environments
Develop and maintain GMP‑compliant documentation including Standard Operating Procedures and Work Instructions for MES operations and electronic batch record management
Drive continuous improvement of electronic batch record execution through troubleshooting, optimization, and cross‑functional collaboration
Ensure seamless integration of MES capabilities with process workflows, quality management systems, and regulatory compliance standards
Participate actively in design reviews, system testing phases, and go‑live preparation for MES‑related projects
Provide operational support for clinical drug substance production, including resupply campaigns and process execution
Facilitate the introduction of new or modified equipment and processes through evaluation, implementation, and qualification activities
Train manufacturing and engineering teams on updated systems, processes, and procedural changes
Your Profile
Minimum 5 years of professional experience in pharmaceutical or biotechnology manufacturing environments
Proven expertise with Manufacturing Execution Systems; hands‑on experience with PAS‑X is highly valued
Strong background in GMP‑regulated operations and cross‑functional project collaboration
Practical knowledge of biologics manufacturing processes, including upstream and downstream operations
Demonstrated ability to author and maintain comprehensive GMP documentation
Solid understanding of equipment qualification principles and quality management systems
Excellent analytical and problem‑solving capabilities with the ability to remain proactive under pressure
Independent work style combined with strong team collaboration skills
Business fluent in English (C1 level) and German (B1 level) for effective written and oral communication
What We Offer
Nemensis AG is your specialized personnel recruitment partner in the Life Sciences sector, based in Basel
Comprehensive consultation and support throughout the entire application process through our dedicated consultants
Access to an extensive client network and exciting opportunities in Northwestern Switzerland
Fast and straightforward entry through individual guidance and consultation during the application process
Ready to Take the Next Step in Your Career?
At nemensis ag, we have already connected thousands of candidates with their dream jobs, providing them with opportunities to develop professionally or re‑enter the job market. What can we do for your career today? Get in touch with us!
Apply now for the position as Senior Process Engineer MES (m/f/d) in the Lucerne area and become part of an innovative team shaping the future of biopharmaceutical manufacturing!
You’re seeking a change of perspective, but this isn’t the right position for you? Then register with us – we’ll contact you for an introductory meeting to understand your wishes and needs and align ourselves accordingly.
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