SMO Medtronic Europe Sàrl
Senior Process Engineer(m/w/x)
Vollzeitnur vor OrtSenior
Lausanne
ab CHF 111.200 - 166.800 / Jahr
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
SMSMO Medtronic Europe Sàrl
Equipment Development Engineer(m/w/x)
Lausanne
ab CHF 92.000 - 138.000 / Jahr
VollzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
Designing and automating production equipment for medical devices. 3+ years of equipment development experience required. Up to 20% travel, flexible benefits package.
Anforderungen
- Flexibility to travel up to 20%
- Bachelor's or Master's degree in engineering
- 3+ years of equipment development experience
- Proven project management experience
- Strong knowledge of equipment qualification processes
- Expertise in automation systems
- Familiarity with risk management tools
- Strong problem-solving skills
- Strong analytical skills
- Strong communication skills
- Knowledge of GMP, ISO, FDA standards
- PMP certification or equivalent training (plus)
Aufgaben
- Lead design and automation integration of production equipment
- Acquire and qualify production equipment for medical devices
- Combine technical expertise with project management
- Deliver robust, compliant, and cost-effective equipment solutions
- Drive cross-functional collaboration and supplier management
- Initiate continuous improvement initiatives for equipment reliability
- Develop specialized manufacturing equipment for medical devices
- Define and validate User Requirement Specifications (URS)
- Align URS with business and manufacturing needs
- Establish equipment architecture standards
- Ensure hardware, safety, ergonomics, and automation standards
- Collaborate with third-party manufacturers and integrators
- Oversee design, customization, and build of equipment
- Integrate MEX principles during design phases
- Lead full lifecycle of equipment acquisition projects
- Develop and manage project scope, budget, timelines, and risks
- Ensure on-time and on-budget project delivery
- Coordinate with suppliers, contractors, and integrators
- Ensure compliance with Medtronic quality standards
- Collaborate with Manufacturing, Quality, Regulatory, and Validation teams
- Prepare and deliver project updates to stakeholders
- Plan and lead Factory Acceptance Testing (FAT)
- Approve Site Acceptance Testing (SAT)
- Execute qualification protocols (IQ, OQ, PQ) for new equipment
- Provide technical leadership during debugging and commissioning
- Ensure equipment meets regulatory, performance, and safety requirements
- Define and integrate automation strategies
- Implement PLC programming, robotics, motion control, vision systems, and HMIs
- Conduct risk analyses (e.g., eFMEA)
- Ensure robust equipment performance and safety
- Optimize processes to improve cycle times and reduce costs
- Enhance product quality through process optimization
- Stay current on emerging automation technologies
- Implement innovative solutions where applicable
- Embed MEX methodology into equipment development
- Lead EEM activities for reliability, maintainability, and performance
- Support development of preventive and predictive maintenance strategies
- Drive standardization of best practices
- Ensure complete and accurate equipment documentation
- Guarantee compliance with FDA, ISO 13485, and GMP
- Provide technical expertise during internal and external audits
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- PLCs
- HMIs
- Robotics
- Sensors
- Vision systems
- Industrial communication protocols
- FMEA
- eFMEA
Benefits
Sonstige Vorteile
- Flexible benefits package
- Resources for career and life stages
Attraktive Vergütung
- Competitive compensation plans
Mitarbeiterrabatte
- Wide range of benefits
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens SMO Medtronic Europe Sàrl erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Noch nicht perfekt?
- SMO Medtronic Europe Sàrl
Senior Process Engineer(m/w/x)
Vollzeitnur vor OrtSeniorLausanneab CHF 111.200 - 166.800 / Jahr - SMO Medtronic Europe Sàrl
Intern Engineering Automation & Equipment Development(m/w/x)
VollzeitPraktikumnur vor OrtLausanne, Tolochenazab CHF 2.000 / Monat - SMO Medtronic Europe Sàrl
Quality Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenTolochenazab CHF 92.000 - 138.000 / Jahr - SMO Medtronic Europe Sàrl
Software Engineer I(m/w/x)
Vollzeitnur vor OrtKeine AngabeLausanneab CHF 123.480 / Jahr
SMSMO Medtronic Europe Sàrl
Equipment Development Engineer(m/w/x)
Lausanne
ab CHF 92.000 - 138.000 / Jahr
VollzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
Designing and automating production equipment for medical devices. 3+ years of equipment development experience required. Up to 20% travel, flexible benefits package.
Anforderungen
- Flexibility to travel up to 20%
- Bachelor's or Master's degree in engineering
- 3+ years of equipment development experience
- Proven project management experience
- Strong knowledge of equipment qualification processes
- Expertise in automation systems
- Familiarity with risk management tools
- Strong problem-solving skills
- Strong analytical skills
- Strong communication skills
- Knowledge of GMP, ISO, FDA standards
- PMP certification or equivalent training (plus)
Aufgaben
- Lead design and automation integration of production equipment
- Acquire and qualify production equipment for medical devices
- Combine technical expertise with project management
- Deliver robust, compliant, and cost-effective equipment solutions
- Drive cross-functional collaboration and supplier management
- Initiate continuous improvement initiatives for equipment reliability
- Develop specialized manufacturing equipment for medical devices
- Define and validate User Requirement Specifications (URS)
- Align URS with business and manufacturing needs
- Establish equipment architecture standards
- Ensure hardware, safety, ergonomics, and automation standards
- Collaborate with third-party manufacturers and integrators
- Oversee design, customization, and build of equipment
- Integrate MEX principles during design phases
- Lead full lifecycle of equipment acquisition projects
- Develop and manage project scope, budget, timelines, and risks
- Ensure on-time and on-budget project delivery
- Coordinate with suppliers, contractors, and integrators
- Ensure compliance with Medtronic quality standards
- Collaborate with Manufacturing, Quality, Regulatory, and Validation teams
- Prepare and deliver project updates to stakeholders
- Plan and lead Factory Acceptance Testing (FAT)
- Approve Site Acceptance Testing (SAT)
- Execute qualification protocols (IQ, OQ, PQ) for new equipment
- Provide technical leadership during debugging and commissioning
- Ensure equipment meets regulatory, performance, and safety requirements
- Define and integrate automation strategies
- Implement PLC programming, robotics, motion control, vision systems, and HMIs
- Conduct risk analyses (e.g., eFMEA)
- Ensure robust equipment performance and safety
- Optimize processes to improve cycle times and reduce costs
- Enhance product quality through process optimization
- Stay current on emerging automation technologies
- Implement innovative solutions where applicable
- Embed MEX methodology into equipment development
- Lead EEM activities for reliability, maintainability, and performance
- Support development of preventive and predictive maintenance strategies
- Drive standardization of best practices
- Ensure complete and accurate equipment documentation
- Guarantee compliance with FDA, ISO 13485, and GMP
- Provide technical expertise during internal and external audits
Berufserfahrung
- 3 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- PLCs
- HMIs
- Robotics
- Sensors
- Vision systems
- Industrial communication protocols
- FMEA
- eFMEA
Benefits
Sonstige Vorteile
- Flexible benefits package
- Resources for career and life stages
Attraktive Vergütung
- Competitive compensation plans
Mitarbeiterrabatte
- Wide range of benefits
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens SMO Medtronic Europe Sàrl erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
SMO Medtronic Europe Sàrl
Branche
Healthcare
Beschreibung
The company leads global healthcare technology and addresses challenging health problems by finding solutions.
Noch nicht perfekt?
- SMO Medtronic Europe Sàrl
Senior Process Engineer(m/w/x)
Vollzeitnur vor OrtSeniorLausanneab CHF 111.200 - 166.800 / Jahr - SMO Medtronic Europe Sàrl
Senior Process Engineer(m/w/x)
Vollzeitnur vor OrtSeniorLausanneab CHF 111.200 - 166.800 / Jahr - SMO Medtronic Europe Sàrl
Intern Engineering Automation & Equipment Development(m/w/x)
VollzeitPraktikumnur vor OrtLausanne, Tolochenazab CHF 2.000 / Monat - SMO Medtronic Europe Sàrl
Quality Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenTolochenazab CHF 92.000 - 138.000 / Jahr - SMO Medtronic Europe Sàrl
Software Engineer I(m/w/x)
Vollzeitnur vor OrtKeine AngabeLausanneab CHF 123.480 / Jahr