Quality Assurance Specialist - fixed-term
GE HealthCare · Oslo, Norway
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Role summary
GE HealthCare seeks a quality-focused specialist for a one-year temporary role at its Oslo sterile and aseptic pharmaceutical manufacturing facility. The position emphasizes GMP compliance, SAP process quality assurance, packaging material approvals, and continuous improvement within a regulated environment.
What they're looking for
- Bachelor's or Master's degree in pharmacy, chemistry, biotechnology, engineering, or equivalent scientific discipline
- Pharmaceutical industry experience, preferably in sterile or aseptic manufacturing
- Strong knowledge of GMP regulations including EU GMP and Annex 1
- Experience with SAP systems and quality-related processes for master data and material management
- Experience approving artwork, labels, or packaging materials
- Fluent Norwegian and English, spoken and written
- Analytical skills and structured problem-solving approach
What you'll be doing
- Ensure GMP compliance and quality standards in sterile and aseptic pharmaceutical manufacturing
- Perform quality assessments and approvals in SAP for material data, specifications, and product structures
- Approve artwork, labels, packaging materials, and associated changes per regulatory requirements
- Support production, laboratory, and ancillary functions with quality assurance expertise
- Drive continuous improvement using LEAN principles and participate in audits and regulatory inspections
Privacy & handoff
This role links to GE HealthCare's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.