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GE HealthCare

Technical Documentation Specialist

FIN03-01-Helsinki-Kuortaneenkatu 2

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hirly's read of this role

Seniority
Mid level
Country
FI
Work mode
On-site / unstated
First seen by hirly
13 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Job Description Summary

We are seeking a technically skilled Technical Documentation Specialist to support our production lines by creating and maintaining documentation for machine qualification activities. This role is critical to ensuring that production equipment meets functional and safety requirements through clear, accurate, and compliant documentation

Job Description

Roles and Responsibilities

  • Create and maintain machine qualification documentation , including Installation Qualification ( IQ ), Operational Qualification ( OQ ), and Performance Qualification ( PQ ) protocols and reports.
  • Collaborate closely with Engineering, Quality Assurance, and Production teams to gather technical information and ensure documentation accuracy and completeness.
  • Translate complex technical information into clear, structured, and easy-to-understand documentation for internal and external audits.
  • Ensure that all documentation complies with industry standards , internal procedures, and regulatory requirements.
  • Manage document version control and traceability within document management systems.
  • Support continuous improvement initiatives by updating documentation based on equipment upgrades, process changes, or audit findings.
  • Assist in the development of Standard Operating Procedures (SOPs) and work instructions related to machine operation and qualification.

Required Qualifications

  • Bachelor’s degree or equivalent qualification in a relevant field, preferably Engineering or a related technical discipline.
  • Proven experience in technical writing , preferably within a manufacturing, industrial, or regulated environment.
  • Familiarity with equipment qualification processes and documentation standards, including Installation Qualification ( IQ ), Operational Qualification ( OQ ), and Performance Qualification ( PQ ).
  • Solid understanding of manufacturing equipment , automation systems, and validation principles.
  • Excellent written and verbal communication skills in Finnish .
  • Written and verbal communication skills in English
  • Proficiency in using documentation tools such as Microsoft Word, Excel, Adobe Acrobat, and document management systems.
  • Ability to work independently and manage multiple documentation projects simultaneously

Desired Characteristics

  • Experience working in regulated environments , such as the medical device , pharmaceutical , or food manufacturing industries.
  • Ability to interpret CAD drawings , technical schematics, and equipment manuals.

What We Offer:

  • The opportunity to work in a dynamic and innovative manufacturing environment.
  • Competitive compensation and benefits.
  • Opportunities for professional development and training.
  • A collaborative team culture focused on quality and continuous improvement.
  • The chance to participate in exciting projects as part of a team responsible for ramping up production lines and ensuring that manufacturing equipment meets all defined functional and safety requirements

#LI-PW1

Additional Information

Relocation Assistance Provided: No

Original posting on GE HealthCare's site ↗

Listed on hirly, a job board. hirly is not the employer: GE HealthCare is hiring for this role.

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