Onsite QC Data Remediation Specialist for CPV & LIMS

EFOR; Munster; On-site; EUR 42,000 - 64,000; Full time

Job summary

EFOR Group is hiring a QC Data Remediation Specialist to join a global pharmaceutical manufacturer in Waterford. The role focuses on Continued Process Verification (CPV) to ensure QC results are complete, correct, traceable and ready to trend.

Key tasks include mapping CPV data needs, reconciling LIMS data, aligning master data, applying data integrity controls, and generating CPV status reports while collaborating with QC, QA and MSAT teams.

Qualifications

• Degree in Chemistry, Biochemistry, Microbiology, Pharmacy or similar.
• 3-6 years in GMP QC, QA or laboratory systems at a pharmaceutical site.
• Hands-on LIMS experience (e.g. LabWare, LabVantage, STARLIMS) and a good understanding of laboratory data flows.

Responsibilities

• List the QC data each product's CPV plan needs: release, in-process and stability results.
• Compare source records with LIMS and other lab data systems, then fix missing or inconsistent results.
• Support master data alignment: specifications, test methods, units and limits.
• Apply data integrity controls and document the rationale and traceability for every fix.
• Produce data-quality status reports for the CPV programme.
• Work with QC lab leads, QA and MSAT to agree what each product needs, and close the gaps.

Skills

LIMS

Data integrity

Excel

SQL

Power BI

QA

Education

Bachelor's degree in Life Sciences

Tools

LabWare

LabVantage

STARLIMS

Power BI

SQL

Job description

EFOR Group is hiring a QC Data Remediation Specialist to join a global pharmaceutical manufacturer in Waterford. The role focuses on Continued Process Verification (CPV) to ensure QC results are complete, correct, traceable and ready to trend.

Key tasks include mapping CPV data needs, reconciling LIMS data, aligning master data, applying data integrity controls, and generating CPV status reports while collaborating with QC, QA and MSAT teams.