Technical Writer

09 January 2026
100%
Permanent position
Zurich

Job summary

Join Thoratec Switzerland GmbH, part of Abbott Laboratories, a leader in medical devices. Be part of a dynamic team in Zurich focusing on lifesaving technology.

Tasks

Create and manage project documentation for manufacturing processes.
Collaborate with R&D and Quality teams to ensure compliance.
Ensure proper documentation traceability and modifications.

Skills

Bachelor’s or Master’s in Engineering or related field required.
Strong technical writing experience in a manufacturing environment.
Proficient in PLM and ERP software, preferably Windchill and SAP.

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About the job

Thoratec Switzerland GmbH is part of Abbott Laboratories, one of the world’s leading companies in medical devices and healthcare. We are the global market leader for implantable and extracorporeal blood pump systems based on magnetic bearings. Our lifesaving medical devices, which are developed and produced on-site in Zurich, are used for the short- and long-term treatment of patients suffering from severe heart disease.Our Zurich site employs approximately 150 people, covering areas including R&D and manufacturing. Currently, we are expanding our innovative and high-caliber team in Zurich and an exciting opportunity exists for a motivated and talented software engineer.Technical Writer – Medical DeviceAs part of the New Product Introduction (NPI) team you will create, edit and manage the project and product documentation regarding the manufacturing processes, part specifications, inspection procedures and the design. You will help the manufacturing team to ensure that the product and project documents are properly managed and traced and approved by the management and all changes to the product or process are correctly reflected in all modified documentation. This position requires an engineering background, strong technical writing experience, good communication skills and an independent problem-solving mindset.What You'll Do<ul><li>Create, edit, manage and modify all product and process documentation using PLM and ERP software packages.</li><li>Be a part of the Manufacturing team with extensive interactions with the R&D and Quality departments.</li><li>Ensure traceability and compliance of the documents with the Quality templates and instructions as well as global regulatory requirements.</li></ul>What We're Looking For<ul><li>Bachelor’s or Master’s or other technical degrees in Engineering or related fields.</li><li>3 to 6 years of experience in Engineering, Quality or Technical Writing at a manufacturing environment.</li><li>Experience with medical device manufacturing of electro-mechanical equipment.</li><li>Good written and oral English communication skills. German speaking an advantage.</li><li>Previous experience with some PLM and ERP software packages ideally with Windchill and SAP.</li><li>Familiarity with IT data services and regulated document authentications and safeguards.</li></ul>We Offer<ul><li>A challenging position in a fast-growing crisis independent industry</li><li>To become part of a young, dynamic, highly educated, highly skilled, and motivated team</li><li>Flat hierarchies, open appreciative mentality, and efficient, constructive lines of communication</li><li>Multi-national environment, where we foster the development of our talents within the enterprise</li><li>Competitive compensations and benefits</li><li>A workplace in the centre of Zurich with R&D and manufacturing under one roof</li></ul>Looking forward to receiving your application documents including CV, motivation letter, and job certificates in PDF format.Please follow our Career site and check for available openings: <a href="https://www.jobs.abbott/us/en" target="_blank">Abbott Jobs | Apply Now | Abbott Laboratories Careers</a>

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Technical Writer

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