Manufacturing Engineering – Maintenance & Facility Control

Take ownership of maintenance and facility control processes, supporting high equipment availability and reliability. Plan and implement improvement activities to strengthen compliant facility and utility operations. Act as technical owner for assigned equipment, utilities, or facility systems throughout their lifecycle. Manage change control activities in our PLM system (Windchill), including impact assessments and stakeholder training. Ensure clear, accurate, and GMP-compliant documentation in our asset management system (Infor). Plan and execute qualification and validation activities for equipment, facilities, and utilities. Investigate deviations, non-conformances, or incidents in close collaboration with Quality Engineering. Lead improvement initiatives in area of responsibility or represent the department in large scale projects, e.g. in cooperation with Abbott sites in the US. Support internal and external audits and inspections as a subject-matter expert. Ensure compliance with GMP, EHS, Abbott standards, and regulatory requirements.

At Thoratec Switzerland GmbH, part of the Abbott medical device division, we design and manufacture life-saving blood pump systems that support patients with advanced heart failure around the world. Our technologies — including the CentriMag and HeartMate 3 — are developed and produced at our Zurich site and are used every day in critical care settings. With around 140 colleagues in Development, Quality, and Production, our Zurich team combines deep technical expertise with a shared sense of purpose. As we continue to grow, we are looking for a Manufacturing Engineer – Maintenance and Facility Control who enjoys learning, collaborating, and contributing to something meaningful.

• Bachelor’s or Master’s degree in Electrical or Mechanical Engineering (ETH/FH or equivalent)

• 1–4 years of relevant professional experience (early-career profiles welcome)

• A structured, reliable, and independent working style

• Fluent English (C2) and communicative German

• Experience in medical devices or other regulated industries (ISO 13485, FDA 21 CFR 820, GxP)

• Exposure to production support functions

• Experience or interest in qualification and validation activities