Denn durch unsere intensiven Beziehungen und Netzwerke über alle Industriebranchen hinweg vermitteln wir Ihnen als Engineering-Fachleuten spannende Projekte und attraktive Positionen. Ganz nach Ihren Interessen und abhängig von Ihren Erfahrungen und Qualifikationen. Sie profitieren dabei von einer professionellen Betreuung von der ersten Ansprache bis zum Antritt Ihres neuen Projektes bzw.
Denn durch unsere intensiven Beziehungen und Netzwerke über alle Industriebranchen hinweg vermitteln wir Ihnen als Engineering-Fachleuten spannende Projekte und attraktive Positionen. Ganz nach Ihren Interessen und abhängig von Ihren Erfahrungen und Qualifikationen. Sie profitieren dabei von einer professionellen Betreuung von der ersten Ansprache bis zum Antritt Ihres neuen Projektes bzw.
Denn durch unsere intensiven Beziehungen und Netzwerke über alle Industriebranchen hinweg vermitteln wir Ihnen als Engineering-Fachleuten spannende Projekte und attraktive Positionen. Ganz nach Ihren Interessen und abhängig von Ihren Erfahrungen und Qualifikationen. Sie profitieren dabei von einer professionellen Betreuung von der ersten Ansprache bis zum Antritt Ihres neuen Projektes bzw.
Register now and look forward to many interesting and suitable positions and projects. Be the voice of patients and Roche users in every product related discussion Identify user profiles, tasks, hazard-related use scenarios, usability risks and requirements Responsible for translating UX research insights, user needs, business requirements and technical requirements into pleasant and efficient User Experiences Responsible for creating medical device usability deliverables according to IEC 62366 Create and facilitate workshops with the product teams to gather system-level information and to coordinate the design deliverables Plan formative and summative usability studies and coordinate external suppliers in the process Prepare, maintain and review Usability Engineering Files Advocate for accessibility, quality and usability for end-users at Roche Diagnostics Provide guidance and mentorship to more junior designers supporting them on professional development, output and productivity Masters degree in Science, Industrial Engineering, Human Factors Engineering or other related technical field Strong experience in applied Human Factor Engineering and in Design Control Management Experience in the Usability Engineering process for medical devices made of both hardware and software Experienced in planning, executing and documenting usability studies in the medical field Experience collecting and analyzing physiological and behavioral data Experience in creating, facilitating and analyzing workshops with customers and stakeholders Excellent presentation skills and ability to communicate know-how, experiences, ideas, solutions and deliverables effectively and persuasively Knowledge of the IEC 62366 standard and the latest FDA guidance on applying human factors engineering Fluency in English is required - additional language skills are considered an advantage Dynamic and innovative market environment A very renowned company Ihr Kontakt Referenznummer 887297/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Register now and look forward to many interesting and suitable positions and projects. Be the voice of patients and Roche users in every product related discussionIdentify user profiles, tasks, hazard-related use scenarios, usability risks and requirementsResponsible for translating UX research insights, user needs, business requirements and technical requirements into pleasant and efficient User ExperiencesResponsible for creating medical device usability deliverables according to IEC 62366Create and facilitate workshops with the product teams to gather system-level information and to coordinate the design deliverablesPlan formative and summative usability studies and coordinate external suppliers in the process Prepare, maintain and review Usability Engineering FilesAdvocate for accessibility, quality and usability for end-users at Roche DiagnosticsProvide guidance and mentorship to more junior designers supporting them on professional development, output and productivity Masters degree in Science, Industrial Engineering, Human Factors Engineering or other related technical fieldStrong experience in applied Human Factor Engineering and in Design Control ManagementExperience in the Usability Engineering process for medical devices made of both hardware and softwareExperienced in planning, executing and documenting usability studies in the medical fieldExperience collecting and analyzing physiological and behavioral dataExperience in creating, facilitating and analyzing workshops with customers and stakeholdersExcellent presentation skills and ability to communicate know-how, experiences, ideas, solutions and deliverables effectively and persuasivelyKnowledge of the IEC 62366 standard and the latest FDA guidance on applying human factors engineeringFluency in English is required - additional language skills are considered an advantage Dynamic and innovative market environmentA very renowned company Ihr Kontakt Referenznummer 887297/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Register now and look forward to many interesting and suitable positions and projects. Compliance and Quality Lifecycle: Manage non-conformities, changes, and documentation in SAP (covering processes, methods, materials, and equipment) Manage technical relationships with external suppliers and collaborate closely with internal departments—including Logistics, Development, and Quality - to ensure a seamless product supply Root Cause Analysis: Enact structured problem-solving processes to ensure fact-based, data- driven root cause analysis and identify effective countermeasures Deviation Management: Support the investigation and processing of deviations within the S&C sensors and reagents production Process Optimization: Adopt and optimize production processes to improve quality, increase yield, and lower costs for your respective products Control Loops: Establish, maintain, and continuously improve control loops Stakeholder Management: Independently communicate with and gather crucial information from various cross-functional stakeholders Regulatory Compliance: Ensure strict adherence to existing frameworks, regulatory guidelines, and department-specific requirements.
Register now and look forward to many interesting and suitable positions and projects. Compliance and Quality Lifecycle: Manage non-conformities, changes, and documentation in SAP (covering processes, methods, materials, and equipment)Manage technical relationships with external suppliers and collaborate closely with internal departments—including Logistics, Development, and Quality - to ensure a seamless product supplyRoot Cause Analysis: Enact structured problem-solving processes to ensure fact-based, data- driven root cause analysis and identify effective countermeasuresDeviation Management: Support the investigation and processing of deviations within the S&C sensors and reagents productionProcess Optimization: Adopt and optimize production processes to improve quality, increase yield, and lower costs for your respective productsControl Loops: Establish, maintain, and continuously improve control loopsStakeholder Management: Independently communicate with and gather crucial information from various cross-functional stakeholdersRegulatory Compliance: Ensure strict adherence to existing frameworks, regulatory guidelines, and department-specific requirements.Audit Readiness: Prepare for quality audits and successfully represent the Chapter during audit procedures Education: A University degree in Natural Sciences or Engineering (e.g., Biotechnology, Biology, Chemistry, Material Science, Mechanical/Electrical Engineering) and/or a completed apprenticeship with equivalent professional experience in a related fieldFirst proven professional experience within a highly regulated environment, backed by a strong quality awareness (GxP mindset)Essential knowledge in process and product developmentEssential knowledge in process and product developmentCollaboration: High motivation for teamwork, excellent communication skills, and the ability to work independently within and across multi-disciplinary teamsProactivity: Enthusiasm for taking on responsibility and proactively collaborating with a highly engaged team of engineers, operators, QA, and logisticsHands-on Approach: A genuine interest in learning manufacturing technologies and continuously improving diverse BG&E processes to support our in-house production efficientlyLanguages: Fluent communication skills in English and a good working knowledge of German (B2+) Work in a modern, technically challenging workshop environmentAttractive working conditions within an industry leaderCollaborate with a motivated and experienced team Ihr Kontakt Referenznummer 878730/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Register now and look forward to many interesting and suitable positions and projects. Review and evaluate qualification and validation documents and process risk analyses provided by our suppliers Oversee the assessment of deviations related to qualification and validation activities, ensuring they meet our rigorous standards Meticulously document the outcomes of your evaluations in compliance with established quality standards Actively engage in the continuous improvement of processes, providing support in technical matters and performing statistical data analyses Offer expert advice to suppliers on quality and compliance, ensuring adherence to all relevant quality standards and specifications Thrive in cross-departmental collaboration, working effectively within squads to achieve common goals A Bachelor's Degree in engineering, scientific/technical field Related work experience (Q&V, Auditing, or Quality functions) in Pharma or the medical device industry Experience with external manufacturing business Profound understanding of applicable standards and norms, along with expertise in injection molding, blow molding, or other automated production technologies Demonstrate a continuous desire for learning and improvement both for yourself and your team members Excellent communication skills in English and German (written and verbal) Advantageous: Knowledge of computerized systems validation and controlled environment qualification (ISO 14644) Advantageous: Familiarity with product risk management according to ISO 14971 Advantageous: Certified Lean Six Sigma Green Belt / Black Belt Fascinating, innovative environment in an international atmosphere A very renowned company Ihr Kontakt Referenznummer 874041/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Register now and look forward to many interesting and suitable positions and projects. Review and evaluate qualification and validation documents and process risk analyses provided by our suppliersOversee the assessment of deviations related to qualification and validation activities, ensuring they meet our rigorous standards Meticulously document the outcomes of your evaluations in compliance with established quality standardsActively engage in the continuous improvement of processes, providing support in technical matters and performing statistical data analysesOffer expert advice to suppliers on quality and compliance, ensuring adherence to all relevant quality standards and specificationsThrive in cross-departmental collaboration, working effectively within squads to achieve common goals A Bachelor's Degree in engineering, scientific/technical fieldRelated work experience (Q&V, Auditing, or Quality functions) in Pharma or the medical device industryExperience with external manufacturing businessProfound understanding of applicable standards and norms, along with expertise in injection molding, blow molding, or other automated production technologiesDemonstrate a continuous desire for learning and improvement both for yourself and your team membersExcellent communication skills in English and German (written and verbal)Advantageous: Knowledge of computerized systems validation and controlled environment qualification (ISO 14644)Advantageous: Familiarity with product risk management according to ISO 14971Advantageous: Certified Lean Six Sigma Green Belt / Black Belt Fascinating, innovative environment in an international atmosphereA very renowned company Ihr Kontakt Referenznummer 874041/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Ideally, you bring a proven track record of developing functional consumables with a focus on cost-optimized, large-scale series production Proven Lifecycle Expertise: Extensive professional experience driving all phases of mechanical development, with deep-rooted expertise in Design for Manufacturability (DFM) Stakeholder & Vendor Management: Demonstrated success working in multidisciplinary teams, with strong capabilities in managing external development partners and suppliers CAD & Standards Proficiency: Proficiency and willingness to perform hands-on CAD design (SolidWorks preferred, integrated with SAP) in strict compliance with ISO 8015 / Geometrical Product Specifications (GPS) for 2D drawings and 3D models Analytical Mindset: A strong affinity for methodical, systematic approaches in the early phases of product development, backed by solid fundamentals in physics and engineering Medical Device Background: Desired experience developing complex medical systems and integrating components such as pumps, valves, sensors, and temperature control elements within a regulated environment Agile Adaptability: Ready and motivated to thrive in a fully agile, transparent, and collaborative team environment Language Skills: Professional in English is essential (project language); listening and reading comprehension in German is a distinct advantage Fascinating, innovative environment in an international atmosphere Ihr Kontakt Referenznummer 885388/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Ideally, you bring a proven track record of developing functional consumables with a focus on cost-optimized, large-scale series productionProven Lifecycle Expertise: Extensive professional experience driving all phases of mechanical development, with deep-rooted expertise in Design for Manufacturability (DFM)Stakeholder & Vendor Management: Demonstrated success working in multidisciplinary teams, with strong capabilities in managing external development partners and suppliersCAD & Standards Proficiency: Proficiency and willingness to perform hands-on CAD design (SolidWorks preferred, integrated with SAP) in strict compliance with ISO 8015 / Geometrical Product Specifications (GPS) for 2D drawings and 3D modelsAnalytical Mindset: A strong affinity for methodical, systematic approaches in the early phases of product development, backed by solid fundamentals in physics and engineeringMedical Device Background: Desired experience developing complex medical systems and integrating components such as pumps, valves, sensors, and temperature control elements within a regulated environmentAgile Adaptability: Ready and motivated to thrive in a fully agile, transparent, and collaborative team environmentLanguage Skills: Professional in English is essential (project language); listening and reading comprehension in German is a distinct advantage Fascinating, innovative environment in an international atmosphere Ihr Kontakt Referenznummer 885388/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt
Solution-oriented, autonomous, and proactive working style Experience in PCBA design, microcontrollers, firmware support as well as EMC and functional safety requirements Fluent in German (both spoken and written), English as a strong asset Nice to have: Experience in laboratory diagnostics and/or service & support, as well as supporting HW and SW, are additional assets Nice to have: Experience in ECAD Mentor expeditions Fascinating, innovative environment in an international atmosphere A very renowned company Ihr Kontakt Referenznummer 869713/1 Kontakt aufnehmen Telefon:+41 44 225 50 00 E-Mail: positionen@hays.ch Anstellungsart Freiberuflich für ein Projekt