Technical Supplier Manager (m/f/d)

Work Selection AG; Risch-Rotkreuz; Presencial; CHF 120.000 - 180.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Diversity & Inclusion

Moderne Campusumgebung

Betriebsrestaurant

Parkplätze vor Ort

Mobilitätsrabatte

Descripción de la vacante

Work Selection AG sucht eine engagierte Fachkraft als Technical Supplier Manager – Technical Project Lead und Process Design. Sie steuern Fertigungsprozesse, begleiten Technologietransfers zu externen Herstellern und sichern Qualität entlang des Lieferkettenzyklus.

Zu Ihren Aufgaben gehören DfX, Validierungskonzepte (IQ/OQ/PQ) sowie pFMEA und SPC-Analysen. Reisetätigkeit ca. 20–30% wird erwartet; Zusammenarbeit mit Roche Diagnostics in Rotkreuz ist Teil des Auftrags.

Formación

• Abgeschlossenes Hochschulstudium in Maschinenbau, Elektrotechnik, Mechatronik, Verfahrenstechnik oder vergleichbare Fachrichtung.
• Mindestens 5–6+ Jahre Erfahrung in Manufacturing Process Design, technischer Lieferantenführung oder Industrialisation, ideal in Medizinprodukte/IVD.
• Nachweis in Design for Manufacturing/Assembly, SPC, Cpk, MSA, pFMEA; Führung in komplexen technischen Projekten; Zertifizierungen PM von Vorteil.

Responsabilidades

• Gestaltung, Optimierung und Industrialisierung von Fertigungs- und Testprozessen für Bauteile und Baugruppen.
• Leitung technischer Transfers zwischen externen Herstellern und Lieferanten (External-to-External).
• Aufbau von QMPs, Meilensteinplanung und Berichterstattung an Führungskräfte; Zusammenarbeit mit RS/QA/RA.

Conocimientos

Process Design

pFMEA

SPC

MSA

Projektleitung

Educación

Bachelor/Master oder HTD

Herramientas

QMPs

pFMEA Tools

Change Control Systems

Descripción del empleo

As a first-tier supplier to our renowned business partner Roche Diagnostics in Rotkreuz, we are currently looking for a motivated and dedicated Technical Supplier Manager – Technical Project Lead und Process Design for a temporary assignment of 18 months, with high probability of extension.

Tasks und Responsibilities

Manufacturing 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 RundR)
• Design for Excellence (DfX): Partner closely with RundD 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 (pFMEA), establish poka-yoke (error-proofing) controls, and drive root-cause investigations to engineer out process vulnerabilities

Technical Project Leadership und External-to-External (E2E) Transfers

• Lead 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 Support

• Supplier 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 (8D, 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 Haves

• A 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 pFMEA
• 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

Benefits

• Become 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.