<p>For our client, an international leader in the energy technology sector, we are looking for a skilled and driven R&D Test and Process Engineer with a specialized focus on high voltage (HV) testing and manufacturing process development. Based at their production and research site in Zurich, you will play a critical role in bridging R&D and manufacturing, ensuring the performance, safety, and compliance of next-generation energy systems.<br /><br /><br /><br /><br /> </p><h3>General Information</h3><br /><ul><li><p>Location: Zurich, Switzerland</p></li><li><p>Start Date: ASAP / By agreement</p></li><li><p>Duration: Permanent</p></li><li><p>Working Hours: Full-time (100%)</p></li><li><p>Remote Work: No (On-site laboratory and manufacturing environment)<br /><br /><br /><br /><br /> </p></li></ul><h3>Your Responsibilities</h3><br /><ul><li><p>High Voltage Testing: Lead and execute HV testing activities in strict compliance with IEC, IEEE, and internal quality standards.</p></li><li><p>Test Design & Implementation: Design sophisticated test setups, including the selection of appropriate HV equipment and specialized methodologies.</p></li><li><p>Data Analysis & Reporting: Analyze complex test data, document technical results, and lead root cause investigations to implement corrective actions.</p></li><li><p>Cross-Functional Collaboration: Partner with R&D and manufacturing teams to define comprehensive test strategies and manufacturing process requirements.</p></li><li><p>Process Optimization: Proactively drive continuous improvement within testing and prototyping workflows to enhance overall efficiency and product quality.</p></li><li><p>Equipment Governance: Ensure the rigorous maintenance, calibration, and safe operation of all high voltage test equipment.</p></li><li><p>Prototyping Support: Facilitate prototyping activities and assess process feasibility within a large-scale manufacturing environment.</p></li><li><p>Safety & Compliance: Promote a world-class safety culture, ensuring total adherence to ISO 9001, ISO 45001, and internal corporate policies.<br /><br /><br /><br /><br /> </p></li></ul><h3>Your Qualifications</h3><br /><ul><li><p>Education: Bachelor’s or Master’s degree in Electrical Engineering.</p></li><li><p>Experience: Minimum 2 years of hands-on experience in high voltage testing; additional experience in process engineering is highly advantageous.</p></li><li><p>Technical Skills: Deep knowledge of HV testing protocols, equipment, and safety practices. Familiarity with IEC, IEEE, ISO 9001, and ISO 45001 standards is required.</p></li><li><p>Analytical Mindset: Proficient in data analysis, failure mode identification, and technical problem-solving.</p></li><li><p>Communication: Excellent communication skills with the ability to translate complex test results into actionable manufacturing insights.</p></li><li><p>Languages: Fluency in German and a good command of English (both written and spoken) are essential.</p></li></ul>

<p>Für unseren Kunden, ein führendes internationales Unternehmen im Life-Science-Sektor mit Sitz in Rotkreuz, suchen wir eine proaktive Persönlichkeit als MSAT Automation Engineer (m/w/d). In dieser Rolle werden Sie Teil des Manufacturing Science and Technology (MSAT) Automation Chapters und unterstützen die Produktion im Bereich Sensors and Cartridges (S&C) Operations.<br /><br /><br /> </p><p>Sie agieren als technischer Experte an der Schnittstelle zwischen laufender Produktion, Kapazitätserweiterungsprojekten und Systemintegration. Dabei stellen Sie den Software-Lifecycle sowie die Hochverfügbarkeit der Produktionsanlagen und QC-Anwendungen sicher.<br /><br /><br /><br /> </p><h3>Allgemeine Informationen:</h3><br /><ul><li><p>Start: Ab sofort oder nach Absprache</p></li><li><p>Dauer: 1 Jahr (Verlängerung wahrscheinlich)</p></li><li><p>Arbeitsplatz: Rotkreuz </p></li><li><p>Workload: 100%</p></li><li><p>Remote/Home-Office: Bis zu 20% (1 Tag pro Woche) nach Absprache möglich</p></li><li><p>Reisetätigkeit: Keine<br /><br /><br /> </p></li></ul><h3>Aufgaben & Verantwortlichkeiten:</h3><br /><ul><li><p>Projekt- & Betriebsbetreuung: Selbstständige Durchführung von Automatisierungsprojekten sowie Wartungsarbeiten an verschiedenen SPS- und Leitsystemen.</p></li><li><p>Troubleshooting: Direkte Unterstützung bei der Fehlersuche und Problemlösung für OT-Systeme in enger Abstimmung mit Engineering und IT.</p></li><li><p>Lifecycle Management: Verantwortung für die Softwareverwaltung, das Backup-Management und den Audit Trail sowie Monitoring der Server für das User Management.</p></li><li><p>Inbetriebnahme & Modernisierung: Aktive Mitarbeit bei der Qualifizierung und Inbetriebnahme neuer Anlagen im Rahmen von Kapazitätserweiterungen und Modernisierungsprojekten.</p></li><li><p>Compliance & Dokumentation: Erstellung und Aktualisierung von Spezifikationen (SDS, HDS, FS) und Arbeitsanweisungen in einem streng regulierten GMP-Umfeld.</p></li><li><p>Prozessoptimierung: Durchführung von Korrektur- und Präventivmassnahmen (CAPA) zur kontinuierlichen Verbesserung der OT-Umgebung.<br /><br /><br /><br /> </p></li></ul><h3>Qualifikationen & Anforderungen:</h3><br /><ul><li><p>Ausbildung: Abgeschlossene technische Grundausbildung oder Studium im Bereich Automatisierungstechnik, Elektrotechnik oder eine vergleichbare Fachrichtung.</p></li><li><p>Berufserfahrung: Mindestens 3 Jahre fundierte Erfahrung in der Automatisierungstechnik und/oder im Bereich MES.</p></li><li><p>Fachwissen: Tiefgreifende Kenntnisse in der Programmierung und Betreuung von SPS-, PLS- und MES-Systemen sowie Know-how in der Netzwerktechnik (Industrie 4.0 / OT).</p></li><li><p>Regulatorisches Umfeld: Erfahrung in der Arbeit innerhalb eines streng regulierten Umfelds (GxP, IVD oder Pharma).</p></li><li><p>Sprachen: Sehr gute Englisch- und gute Deutschkenntnisse in Wort und Schrift.<br /><br /><br /><br /><br /> </p></li></ul><h3>Von Vorteil (Nice to Haves):</h3><br /><ul><li><p>Methodik: Schnelle Auffassungsgabe und eine analytische Herangehensweise an komplexe technische Fragestellungen.</p></li><li><p>Persönlichkeit: Hohe Eigeninitiative sowie die Fähigkeit, konventionelle Denkmuster kritisch zu hinterfragen („Out-of-the-box“-Denken).</p></li><li><p>Soft Skills: Ausgeprägte Teamfähigkeit und Kommunikationsstärke in einem hochqualifizierten, interdisziplinären Ingenieursumfeld.</p></li></ul>

<p>For one of our clients, a world leader in in-vitro diagnostics, we are currently looking for Process Management Support.</p><p>General Information:</p><ul><li>Start Date: 01.07.2026</li><li>Latest Possible Start Date: 01.09.2026</li><li>Planned Employment Duration: 12 months contract with the possibility of extension</li><li>Workplace: Rotkreuz</li><li>Workload: 100%</li><li>Home Office: possible</li><li>Team: 30 people</li><li>Department: Design Control Excellence CH (DSRSPC)</li><li>Working Hours: Standard</li></ul><p>About the job:</p><p>The main purpose of the team is the support of development projects and product care activities with development processes like Requirement Management, Product Risk Management, Configuration Management and Defect Management. For this goal the team members are embedded into project teams and product teams, executing such processes by taking the responsibility of authoring the respective documents and ensuring that the processes are followed by the development teams.</p><p>The Perfect Candidate:</p><p>The product consists of a combination of Hardware, Software, Plasticware and Biochemistry. The perfect candidate would have experience in developing/handling all these types of materials and understanding how they come together. Additionally the ideal candidate should be able to navigate in a dynamic project environment, where quite often exceptional situations occur. Efficient process management is not only working according to a checklist, but also understanding the product and project team with its challenges and issues and finding process solutions which keep the compliance and benefit the project.</p><p>Tasks & Responsibilities:</p><ul><li>Responsible for process guidance, process optimization and documentation of various development projects (systems and assays) regarding Requirements- and Risk-Management, Configuration Management, Verification and Validation Management, defects management and/or Usability Engineering</li><li>Support translation of multi-level requirements via Requirements Management process</li><li>Conduct detailed risk assessments by analyzing documents, statistics, reports and market trends and with a team of cross functional representatives</li><li>Ensure all risks and requirements are maintained within a database and streamline approach across projects</li><li>Ensure the delivery of timely and good quality risk and requirements documentation</li><li>Establish and perform Configuration Management in complex development projects</li><li>Support development projects as Verification Manager (Planning, Guiding, Training, Reporting)</li><li>Managing project related interactions with Development, Global Platform Support, Design Quality Assurance, Regulatory, Medical Affairs, external suppliers and other internal departments</li><li>Information gathering from respective stakeholders including consolidation of information</li><li>Independent execution of work packages within area of responsibility</li><li>Organize and manage their own time within scope of assigned work packages</li><li>Ensure the delivery of timely and good quality documentation</li></ul><p>Must Haves:</p><ul><li>University degree in Life Sciences, Natural Sciences or Engineering</li><li>Good technical understanding of development processes</li><li>Excellent verbal and written communication skills in English</li><li>Database experience</li><li>First experience in product development in a highly regulated environment is preferred (n2H)</li><li>Good analytical thinking, a structured, reliable working manner, ability to prioritize, plan and manage multiple tasks and to instill a sense of urgency in teams</li><li>Ability to lead by influence, demonstrated effectiveness, drive decisions and account for results; ability to resolve conflicts and adapt to change, effective to drive results and achieve project goals</li><li>Excellent communication and presentation skills</li><li>Open minded team-player with an eye for details</li></ul><p>Nice to Haves:</p><ul><li>Systematic mindset, able to understand complex concepts</li><li>Process experience</li><li>Flexible mindset, able to find solutions in situations which are not described in a process</li><li>Dealing with resistance</li><li>Experience in the Diagnostics industry and experience within the GMP regulated environment</li><li>Experience in Process Management (Risk- Requirements- Configuration- and/or Verification Management) or Product Development such as testing</li><li>German skills</li></ul><p>Sounds interesting? Apply now – we’re looking forward to receiving your applications!</p><p>Application Submission Deadline: 12.05.2026</p>