Tecan Trading AG
Technical Writer(m/w/x)
Full-timeOn-siteExperienced
Männedorf
New Job?Nejo!
The AI Job Search Engine
ABAbbott Laboratories GmbH
Technical Writer – Medical Device(m/w/x)
Zürich
Full-timeOn-siteExperienced
Nejo AI Summary
Documenting manufacturing processes, part specifications, and inspection procedures for medical devices. Engineering degree and strong technical writing experience required. Work in a global healthcare enterprise.
Requirements
- Engineering background
- Strong technical writing experience
- Good communication skills
- Independent problem-solving mindset
- Bachelor’s or Master’s degree in Engineering or related fields
- 3 to 6 years of experience in Engineering, Quality or Technical Writing
- Experience with medical device manufacturing of electro-mechanical equipment
- Good written and oral English communication skills
- German speaking an advantage
- Previous experience with PLM and ERP software packages ideally with Windchill and SAP
- Familiarity with IT data services and regulated document authentications and safeguards
Tasks
- Create and edit project documentation
- Manage product documentation
- Document manufacturing processes and part specifications
- Outline inspection procedures and design details
- Ensure proper management and traceability of documents
- Reflect changes in product or process in documentation
- Modify documentation using PLM and ERP software
- Collaborate with the Manufacturing team and interact with R&D and Quality departments
- Ensure document compliance with Quality templates and global regulatory requirements
Work Experience
- 3 - 6 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- Windchill
- SAP
Benefits
Competitive Pay
- Competitive compensations
Diverse Work
- Challenging position
Informal Culture
- Flat hierarchies
- Open appreciative mentality
- Multi-national environment
Other Benefits
- Efficient communication
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Abbott Laboratories GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Not a perfect match?
- ThoratecSwitzerland GmbH
Change Control Specialist(m/w/x)
Full-timeOn-siteExperiencedZürich - HITACHI ENERGY LTD
Technische Redakteur:in(m/w/x)
Full-timeOn-siteExperiencedZürich - Abbott Laboratories GmbH
Test Engineer - Medical Device(m/w/x)
Full-timeOn-siteExperiencedZürich - Thoratec Switzerland GmbH
Senior Manufacturing Engineer(m/w/x)
Full-timeOn-siteSeniorZürich
ABAbbott Laboratories GmbH
Technical Writer – Medical Device(m/w/x)
Zürich
Full-timeOn-siteExperienced
Nejo AI Summary
Documenting manufacturing processes, part specifications, and inspection procedures for medical devices. Engineering degree and strong technical writing experience required. Work in a global healthcare enterprise.
Requirements
- Engineering background
- Strong technical writing experience
- Good communication skills
- Independent problem-solving mindset
- Bachelor’s or Master’s degree in Engineering or related fields
- 3 to 6 years of experience in Engineering, Quality or Technical Writing
- Experience with medical device manufacturing of electro-mechanical equipment
- Good written and oral English communication skills
- German speaking an advantage
- Previous experience with PLM and ERP software packages ideally with Windchill and SAP
- Familiarity with IT data services and regulated document authentications and safeguards
Tasks
- Create and edit project documentation
- Manage product documentation
- Document manufacturing processes and part specifications
- Outline inspection procedures and design details
- Ensure proper management and traceability of documents
- Reflect changes in product or process in documentation
- Modify documentation using PLM and ERP software
- Collaborate with the Manufacturing team and interact with R&D and Quality departments
- Ensure document compliance with Quality templates and global regulatory requirements
Work Experience
- 3 - 6 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- Windchill
- SAP
Benefits
Competitive Pay
- Competitive compensations
Diverse Work
- Challenging position
Informal Culture
- Flat hierarchies
- Open appreciative mentality
- Multi-national environment
Other Benefits
- Efficient communication
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Abbott Laboratories GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Abbott Laboratories GmbH
Industry
Healthcare
Description
Abbott ist ein weltweit führendes Unternehmen im Gesundheitswesen, das bahnbrechende wissenschaftliche Erkenntnisse nutzt und Lösungen zur Verbesserung der Gesundheit der Menschen entwickelt.
Not a perfect match?
- Tecan Trading AG
Technical Writer(m/w/x)
Full-timeOn-siteExperiencedMännedorf - ThoratecSwitzerland GmbH
Change Control Specialist(m/w/x)
Full-timeOn-siteExperiencedZürich - HITACHI ENERGY LTD
Technische Redakteur:in(m/w/x)
Full-timeOn-siteExperiencedZürich - Abbott Laboratories GmbH
Test Engineer - Medical Device(m/w/x)
Full-timeOn-siteExperiencedZürich - Thoratec Switzerland GmbH
Senior Manufacturing Engineer(m/w/x)
Full-timeOn-siteSeniorZürich