Senior Process Engineer (mf/d) 100%

Description du poste Senior Process Engineer (mf/d) 100% à Suisse

Senior Process Engineer (m/w/d) – Biotech Manufacturing
Shape the Future of Biologics Manufacturing – Join an Innovative Team!
Duration:02.03.2026 – 29.02.2028Location:
Greater Lucerne Area
Type:
Temporary Position
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 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 product
Drive innovationas a change champion, introducing new technologies, digitization initiatives, and modern working methodologies throughout the organization
Coordinate cross-functional activitiesthrough tiered meeting structures with colleagues in the US and Ireland for seamless implementation of novel manufacturing processes
Evaluate and harmonizeinnovative equipment solutions for batch and continuous manufacturing paradigms, ensuring flexible switching capabilities between production modes
Develop capital funding requestsand user requirement specifications for new technologies, software, and instruments that streamline GMP manufacturing and administrative workflows
Create and review GMP documentationincluding risk assessments, batch records, sampling plans, qualification protocols, and standard operating procedures
Provide subject matter expertiseon quality assurance and GMP compliance within global, interdisciplinary project teams
Centralize process knowledgeto establish robust knowledge management systems and support continuous learning initiatives
Your Profile
Minimum 5 years of professional experiencein the pharmaceutical or biotechnology industry with hands-on manufacturing exposure
Proven project management skillsleading cross-functional teams in complex technical environments
Strong knowledge of upstream and downstream unit operationsfor biologics manufacturing processes
Analytical mindsetwith 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 playerwho 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!?
Phill Rogers, Consultant,Write an email
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