Technical Supplier Manager (m/f/d) in Zug

As a first-tier supplier to our renowned business partnerRoche Diagnostics in Rotkreuz , we are currently looking for a motivated and dedicatedTechnical Supplier Manager – Technical Project Lead und Process Designfor a temporary assignment of 18 months, with high probability of extension. Tasks und ResponsibilitiesManufacturing Process Design und Industrialization (Core Activity)Process Architecture und Development: Actively design, optimize, and industrialize robust manufacturing and testing processes for instrument components, electronics, and precision assemblies across the external supply base Process Capability und Validation: Define process validation strategies (IQ/OQ/PQ), design verification protocols, and establish process capability baselines (Cp/Cpk analysis, tolerance studies, and Gage Rund R) Design for Excellence (Df X): Partner closely with Rund D during early product development to embed Design for Manufacturing, Assembly, and Testability principles into component designs, preventing manufacturing bottlenecks and driving yield optimization Process Risk und Mitigation: Lead process failure mode and effects analysis (p FMEA), establish poka-yoke (error-proofing) controls, and drive root-cause investigations to engineer out process vulnerabilities Technical Project Leadership und External-to-External (E2 E) TransfersLead Technology Transfers: Steer end-to-end technical transfers between external contract manufacturers and suppliers (External-to-External), including production line relocations, tool duplications, and second-source qualifications Project Governance und Milestones: Establish qualification master plans (QMPs), define project schedules, align critical milestones, and report progress transparently to cross-functional leadership within MSAT and GIN Cross-Partner Synchronization: Lead technical alignment and change control across originating sites, receiving supplier facilities, Roche Global Sourcing, Quality Assurance, and Regulatory Affairs Technical Supplier Stewardship und Operations SupportSupplier Performance und Monitoring: Monitor supplier process stability, technical KPIs, and component quality trends across the complete instrument lifecycle Deviation Handling und SCARs: Lead technical problem-solving teams (8 D, Ishikawa, 5-Why) for component deviations; resolve Supplier Corrective Action Requests sustainably Supplier Technical Assessments: Conduct technical evaluations and audits of potential and existing suppliers as part of the formal supplier qualification process Operations Projects: Steer supplier-side engineering changes (without spec change), capacity expansions, and continuous line stabilization initiatives Must HavesA University degree (Bachelorund#39;s, Masterund#39;s, or Higher Technical Diploma) in Mechanical Engineering, Electrical Engineering, Mechatronics, Process Engineering, Industrial Engineering, or a related technical field At least 5–6+ years of relevant industry experience in manufacturing process design, technical supplier management, industrialization, or manufacturing engineering, ideally within medical devices, in-vitro diagnostics (IVD), pharmaceuticals, or precision high-tech equipment Process Design Expertise: Proven hands-on track record in designing, qualifying, and optimizing manufacturing and test processes; strong command of statistical process control (SPC), capability studies (Cpk), measurement systems analysis (MSA), and p FMEA Technical Project Leadership: Demonstrated leadership in complex technical projects, specifically external-to-external technology transfers, second-sourcing initiatives, or major line ramp-ups; formal PM certification (PMP, IPMA, Agile) is an asset Manufacturing Technologies: Deep technical understanding of precision manufacturing technologies (e.g., injection molding, precision mechanics/machining, electronics assembly, automated testing) along with an understanding of production cost drivers and cycle time optimization Regulatory und Quality Standards: Practical knowledge of ISO 13485, GMP/FDA regulations, process validation frameworks (IQ/OQ/PQ), and formal change management procedures Mindset und Communication: Pragmatic, innovative problem solver with a "think-out-of-the-box" attitude and strong intercultural stakeholder management and communication skills Languages und Mobility: Professional fluency in English and German (written and spoken); willingness to travel globally (approx. 20–30%) for supplier on-site process reviews, audits, and transfer milestones BenefitsBecome part of one of the most prestigious pharmaceutical companies and actively shape the future of healthcare Experience a work culture that promotes diversity and inclusion and where all employees feel valued Work on a state-of-the–art campus featuring green spaces, meeting areas, and an inspiring atmosphere Work with modern and up-to-date tools in an innovative work environment Start with a professional onboarding process and a thorough introduction to your new role during the Welcome Days Benefit from financial support for your professional development plans Enjoy a selection of high-quality meals in modern staff restaurants As part of a sustainable mobility concept, on-site parking spaces are available to you Take advantage of unbeatable, year-round discounts at renowned retailers and over 200 top brands Benefit from fleet discounts when purchasing new cars or receive constant fuel discounts Wir wertschätzen Vielfalt und begrüßen daher alle Bewerbungen – unabhängig von Geschlecht, sozialer Herkunft, Religion, Alter und Identität. Zur leichteren Lesbarkeit und besseren Verständlichkeit verwenden wir nur eine Gender-Form. Selbstverständlich sind im jeweiligen Kontext alle Genderformen gleichermassen gemeint.