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Technical Writer

Abbott

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Technical Writer

full-timePosted: Jan 12, 2026

Job Description

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 Device

As 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

  • Create, edit, manage and modify all product and process documentation using PLM and ERP software packages.

  • Be a part of the Manufacturing team with extensive interactions with the R&D and Quality departments.

  • Ensure traceability and compliance of the documents with the Quality templates and instructions as well as global regulatory requirements.

What We're Looking For

  • Bachelor’s or Master’s or other technical degrees in Engineering or related fields.

  • 3 to 6 years of experience in Engineering, Quality or Technical Writing at a manufacturing environment.

  • Experience with medical device manufacturing of electro-mechanical equipment.

  • Good written and oral English communication skills. German speaking an advantage.

  • Previous experience with some PLM and ERP software packages ideally with Windchill and SAP.

  • Familiarity with IT data services and regulated document authentications and safeguards.

We Offer

  • A challenging position in a fast-growing crisis independent industry

  • To become part of a young, dynamic, highly educated, highly skilled, and motivated team

  • Flat hierarchies, open appreciative mentality, and efficient, constructive lines of communication

  • Multi-national environment, where we foster the development of our talents within the enterprise

  • Competitive compensations and benefits

  • A workplace in the centre of Zurich with R&D and manufacturing under one roof

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:  

Abbott Jobs | | Abbott Laboratories Careers 

Locations

  • Zurich, Zurich, Switzerland

Salary

Estimated Salary Rangemedium confidence

55,000 - 95,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • technical writingintermediate
  • PLM and ERP software (Windchill, SAP)intermediate
  • document managementintermediate
  • communication skillsintermediate
  • problem-solvingintermediate

Required Qualifications

  • Bachelor’s or Master’s in Engineering or related fields (experience)
  • 3 to 6 years experience in Engineering, Quality or Technical Writing in manufacturing (experience)
  • Experience with medical device manufacturing (experience)
  • Good English communication skills (German advantage) (experience)
  • Familiarity with IT data services and regulated documents (experience)

Responsibilities

  • Create, edit, manage and modify product and process documentation
  • Interact with Manufacturing, R&D and Quality departments
  • Ensure traceability and compliance with Quality templates and regulatory requirements

Benefits

  • general: Challenging position in fast-growing industry
  • general: Dynamic, highly skilled team
  • general: Flat hierarchies and open communication
  • general: Multi-national environment with talent development
  • general: Competitive compensations and benefits

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Abbott logo

Technical Writer

Abbott

Other Jobs

Technical Writer

full-timePosted: Jan 12, 2026

Job Description

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 Device

As 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

  • Create, edit, manage and modify all product and process documentation using PLM and ERP software packages.

  • Be a part of the Manufacturing team with extensive interactions with the R&D and Quality departments.

  • Ensure traceability and compliance of the documents with the Quality templates and instructions as well as global regulatory requirements.

What We're Looking For

  • Bachelor’s or Master’s or other technical degrees in Engineering or related fields.

  • 3 to 6 years of experience in Engineering, Quality or Technical Writing at a manufacturing environment.

  • Experience with medical device manufacturing of electro-mechanical equipment.

  • Good written and oral English communication skills. German speaking an advantage.

  • Previous experience with some PLM and ERP software packages ideally with Windchill and SAP.

  • Familiarity with IT data services and regulated document authentications and safeguards.

We Offer

  • A challenging position in a fast-growing crisis independent industry

  • To become part of a young, dynamic, highly educated, highly skilled, and motivated team

  • Flat hierarchies, open appreciative mentality, and efficient, constructive lines of communication

  • Multi-national environment, where we foster the development of our talents within the enterprise

  • Competitive compensations and benefits

  • A workplace in the centre of Zurich with R&D and manufacturing under one roof

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:  

Abbott Jobs | | Abbott Laboratories Careers 

Locations

  • Zurich, Zurich, Switzerland

Salary

Estimated Salary Rangemedium confidence

55,000 - 95,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • technical writingintermediate
  • PLM and ERP software (Windchill, SAP)intermediate
  • document managementintermediate
  • communication skillsintermediate
  • problem-solvingintermediate

Required Qualifications

  • Bachelor’s or Master’s in Engineering or related fields (experience)
  • 3 to 6 years experience in Engineering, Quality or Technical Writing in manufacturing (experience)
  • Experience with medical device manufacturing (experience)
  • Good English communication skills (German advantage) (experience)
  • Familiarity with IT data services and regulated documents (experience)

Responsibilities

  • Create, edit, manage and modify product and process documentation
  • Interact with Manufacturing, R&D and Quality departments
  • Ensure traceability and compliance with Quality templates and regulatory requirements

Benefits

  • general: Challenging position in fast-growing industry
  • general: Dynamic, highly skilled team
  • general: Flat hierarchies and open communication
  • general: Multi-national environment with talent development
  • general: Competitive compensations and benefits

Target Your Resume for "Technical Writer" , Abbott

Get personalized recommendations to optimize your resume specifically for Technical Writer. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Technical Writer" , Abbott

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Technical Writer @ Abbott.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.