Technical Documentation Specialist

GE HealthCare; Finland; On-site; EUR 50,000 - 75,000; Full time

Job summary

GE HealthCare is seeking a Technical Documentation Specialist to create and maintain machine qualification documentation (IQ, OQ, PQ) supporting production lines in Finland. You will translate technical details into clear, audit-ready documents and collaborate with Engineering, QA, and Production to ensure accuracy and compliance.

Key requirements include a Bachelor's in Engineering or related field, proven technical writing experience in regulated environments, and proficiency with Word, Excel,

Qualifications

• Bachelor's degree in a relevant technical field.
• Proven experience in technical writing within regulated environments.
• Familiarity with IQ/OQ/PQ documentation processes.
• Strong understanding of manufacturing equipment and validation principles.
• Excellent Finnish and English written and verbal communication.
• Proficiency with Word, Excel, Acrobat, and document management systems.

Responsibilities

• Create and maintain machine qualification documentation (IQ, OQ, PQ) protocols and reports.
• Collaborate with Engineering, QA, and Production to gather information and ensure accuracy.
• Translate complex data into clear, auditable documentation for internal/external audits.
• Ensure compliance with industry standards and regulatory requirements.
• Manage document version control and traceability in the DMS.
• Support continuous improvement by updating docs after upgrades or audits.
• Assist in developing SOPs and work instructions related to machine operation.

Skills

Technical writing

Documentation tools

Education

Bachelor's degree in Engineering

Tools

Microsoft Word

Excel

Adobe Acrobat

Document management systems

Job description

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

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Additional Information

Relocation Assistance Provided: No