Ge Healthcare

QC Specialist with expertise within chromatography, chromatographic data system (CDS) and method validation. The role is part of the CDS administrator group and will also be involved in lifecycle management of analytical methods.

QC systems is supporting the GMP-regulated analytical areas at Oslo Site (QC, Tech. Ops. and R&D). Currently Our main deliveries are administration of Global QC-IT Systems, installation and validation of analytical computerised systems and other analytical instrumentation, but we are also strengthening our capacity and competence within method validation and regulatory communication.
Essential Responsibilities

• Analyst supprot and troubleshooting
• Preparation of method validation documentation
• CDS maintenance
• CDS validation
• CDS template build and testing

Qualifications/Requirements

• Experienced analyst within a GMP-regulated environment
• Good knowlegde of ICH-guideline for validation (Q2 and Q14)
• Good knowledge in CDS applications
• Good communication skills