Manufacturing Engineer Line Support 100% Thoratec Switzerland GmbH is part of Abbott Laboratories, one of the world's leading manufacturers of medical devices. We are the global market leader for implantable and extracorporeal blood pumps based on magnetic levitation technology. Our life‑saving systems, developed and manufactured in Zurich, are used for acute and long‑term therapy in patients with severe heart disease.
Our location in Zurich has around 150 employees in development and production of the Centri MagTM system and the HeartMate 3TM motor.
Responsibilities
Provide first‑level support for the manufacturing floor in cases of technical problems, ensuring production can continue with minimal disruption.
Investigate and evaluate production deviations (Event Descriptions), determine material disposition in collaboration with Quality Engineering, and elevate to an NCMR when required.
Investigate and solve issues arising in production as part of a team responsible for complaint investigations.
Suggest corrective and preventive actions based on detailed engineering analysis and review using root‑cause analysis tools and techniques.
Monitor and analyze yield and manufacturing performance metrics, identify trends and improvement opportunities, and translate data into concise management insights.
Drive continuous and measurable process improvements using Operational Excellence (OPEX) methodologies and tools.
Perform change management in our Product Lifecycle System (PLS) Windchill and provide training to the affected audience accordingly.
Support audit activities as subject‑matter expert.
Qualifications
B.Sc./M.Sc. in Electrical, Mechanical or Industrial Engineering (University, Fachhochschule, or comparable education).
0–3 years of professional experience, preferably in a MedTech environment.
Highly curious and proactive learner.
Conscientious, well‑structured and independent way of working.
Strong service orientation with a proactive mindset and passion for supporting manufacturing operations.
Advanced German and English language skills.
Experience with continuous improvement and teamwork.
Knowledge of ISO 13485 / FDA 21CFR Part 820 / GxP regulations is a benefit.
We are offering opportunities for development for a highly motivated specialist who thinks along and enjoys being part of a small, young team with broad responsibilities.
Apply today by submitting motivation, curriculum vitae, letter of recommendation and diplomas in PDF format.
#J-18808-Ljbffr
Our location in Zurich has around 150 employees in development and production of the Centri MagTM system and the HeartMate 3TM motor.
Responsibilities
Provide first‑level support for the manufacturing floor in cases of technical problems, ensuring production can continue with minimal disruption.
Investigate and evaluate production deviations (Event Descriptions), determine material disposition in collaboration with Quality Engineering, and elevate to an NCMR when required.
Investigate and solve issues arising in production as part of a team responsible for complaint investigations.
Suggest corrective and preventive actions based on detailed engineering analysis and review using root‑cause analysis tools and techniques.
Monitor and analyze yield and manufacturing performance metrics, identify trends and improvement opportunities, and translate data into concise management insights.
Drive continuous and measurable process improvements using Operational Excellence (OPEX) methodologies and tools.
Perform change management in our Product Lifecycle System (PLS) Windchill and provide training to the affected audience accordingly.
Support audit activities as subject‑matter expert.
Qualifications
B.Sc./M.Sc. in Electrical, Mechanical or Industrial Engineering (University, Fachhochschule, or comparable education).
0–3 years of professional experience, preferably in a MedTech environment.
Highly curious and proactive learner.
Conscientious, well‑structured and independent way of working.
Strong service orientation with a proactive mindset and passion for supporting manufacturing operations.
Advanced German and English language skills.
Experience with continuous improvement and teamwork.
Knowledge of ISO 13485 / FDA 21CFR Part 820 / GxP regulations is a benefit.
We are offering opportunities for development for a highly motivated specialist who thinks along and enjoys being part of a small, young team with broad responsibilities.
Apply today by submitting motivation, curriculum vitae, letter of recommendation and diplomas in PDF format.
#J-18808-Ljbffr
Manufacturing Engineer Line Support 100% Arbeitgeber: Thoratec Switzerland GmbH
Abbott in Zürich bietet eine dynamische Arbeitsumgebung, die Innovation und Zusammenarbeit fördert. Als Senior NPI Engineer profitieren Sie von umfangreichen Entwicklungsmöglichkeiten in einem internationalen Team, das sich auf die Herstellung komplexer medizinischer Geräte spezialisiert hat. Die Unternehmenskultur legt Wert auf Eigenverantwortung und kontinuierliches Lernen, während die Lage in Zürich Ihnen Zugang zu einer lebendigen Stadt mit hoher Lebensqualität bietet.
Kontaktdaten:
Thoratec Switzerland GmbH Recruiting-Team
