Job Description Summary

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Job Description

Key Responsibilities

• Validation Lifecycle Management
  • Lead the lifecycle validation activities for computerized systems including automated production equipment DBR DCS BMS and FMS.
  • Compile review and execute validation blueprints including User Requirement Specifications (URS) Functional Specifications (FS) Risk Assessments and Validation Plans.
• Protocol Execution & Testing
  • Author and execute Installation Qualification (IQ) Operational Qualification (OQ) and Performance Qualification (PQ) protocols.
  • Document test deviations perform thorough root-cause analysis and manage Corrective and Preventive Actions (CAPAs) through to closure.
• Regulatory Compliance & Data Integrity
  • Ensure all computerized systems strictly comply with GxP GAMP5 Annex 11 and FDA 21 CFR Part 11 regulations.
  • Conduct ALCOA data integrity assessments on PLCs HMIs and environmental monitoring databases to ensure secure data tracking.
• Audit Readiness & Maintenance
  • Maintain computerized systems in a continuous state of control and audit readiness.
  • Support internal and external regulatory inspections (such as NoMA/Statens legemiddelverk or FDA) as the subject matter expert for CSV.
• Cross-Functional Collaboration
  • Partner closely with automation engineers IT and Quality Assurance to execute system changes via formal Change Control procedures.
  • Bridge technical communication gaps by explaining complex validation strategies fluently in both Norwegian and English.

Technical Requirements

• CSV Expertise: Strong proficiency in GAMP5 methodologies and validating automated manufacturing and facility systems.
• System Familiarity: Hands-on validation experience with Siemens/Rockwell PLC/HMI platforms Honeywell EBI BMS and validated environmental monitoring software (FMS).
• Industry Experience: Minimum of 5-7 years of dedicated CSV experience within a validated pharmaceutical biotech or medical device manufacturing plant.
• Quality Systems: Direct experience using formal Change Control Deviation Management and Risk Management frameworks.

Language & Soft Skills

• Norwegian: Native or professional fluency (B2/C1 minimum) required for local regulatory compliance documentation and team collaboration.
• English: Professional working proficiency required for corporate reporting global policy alignment and international audits.
• Attention to Detail: Exceptional documentation skills with a commitment to maintaining precise compliant records under tight timelines.

GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition turn ideas into world-changing realities and join an organization where every voice makes a difference and every difference builds a healthier world.

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race color religion national or ethnic origin sex sexual orientation gender identity or expression age disability protected veteran status or other characteristics protected by law.

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus and drive ownership always with unyielding integrity.

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything youd expect from an organization with global strength and scale and youll be surrounded by career opportunities in a culture that fosters care collaboration and support.

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