QC Data Analyst

Summary:
Our client, a bio pharmaceutical company located in Waterford, is currently looking for a QC Data Analyst. The ideal candidate will be defining, managing and maintaining a documentation control system for QC cGMP documents.

Responsibilities:

• Review QC testing data ensuring compliance to procedure, specifications, data integrity and cGMP standards.
• Identify OOT (out of trend) and OOS (out of specification) results and escalate as appropriate.
• Point of contact for results internally and to external sites.
• Support documentation issuance for lab activities.
• Maintain Good Documentation Practices (GDP) including laboratory documentation and analytical reports.

Qualifications & Experience:

• Degree in Science or Quality Engineering.
• 2-3 years’ experience in a similar GMP regulated environment.
• Excellent documentation skills.