CPV Quality Quality Support

EFOR; Waterford; On-site; EUR 60,000 - 80,000; Full time

Job summary

EFOR Group is hiring a CPV Quality Support – QC Data Remediation Specialist in Waterford, Ireland. This onsite role supports a global pharmaceutical manufacturer within the CPV programme, focusing on making QC data complete, correct, and traceable.

The candidate will work with QC leads, QA and MSAT to close data gaps, ensure ALCOA+ data integrity, and apply fixes across LIMS and related systems while documenting the rationale for every change.

Qualifications

• Experience in GMP QC, QA or lab systems on a pharmaceutical site.
• Hands-on LIMS experience with data flows and data integrity.
• Strong Excel skills and ability to document data changes clearly.
• Awareness of ALCOA+ and EU GMP Annex 11 requirements.

Responsibilities

• List QC data per CPV plan: release, in-process, stability results.
• Compare source records with LIMS and other lab systems; fix gaps.
• Support master data alignment: specs, test methods, units, limits.
• Apply data integrity controls and document rationale for each fix.
• Produce data-quality status reports for the CPV programme.
• Collaborate with QC leads, QA and MSAT to close data gaps.

Skills

LIMS data remediation

Data integrity (ALCOA+)

Excel

Quality documentation

Education

Degree in Chemistry, Biochemistry, Microbiology, Pharmacy or similar

3–6 years in GMP QC, QA or pharmaceutical lab systems

Tools

LabWare

LabVantage

STARLIMS

SQL

Power BI

Job description

Now Hiring: CPV Quality Support – QC Data Remediation (Waterford, Ireland | Onsite)

Did you start out as a QC analyst and end up as the person everyone asks about LIMS? EFOR Group, a trusted Life Sciences consulting partner, is looking for a QC Data Remediation Specialist to join a global pharmaceutical manufacturer in Waterford. The role is part of a network-wide Continued Process Verification (CPV) programme. Your mission: make the site’s QC results complete, correct, traceable and ready to trend.

What you’ll do:

• 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

Your background:

• 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
• Strong knowledge of data integrity (ALCOA+), EU GMP Annex 11 and 21 CFR Part 11
• Good understanding of QC analytical methods and specifications, plus strong Excel skills
• LIMS data migration, data remediation or LIMS implementation experience is strongly preferred; SQL or Power BI is a plus
• Rigorous, an excellent documenter, and comfortable working through large datasets on your own

Why EFOR Group?

EFOR brings together more than 3,200 experts in 18 countries, delivering technical, quality and engineering excellence across the full Life Sciences product lifecycle. Join a team helping to build trusted lab data that underpins the quality of medicines.

Location: Waterford, Ireland (onsite)

Contract: approx. 5.5 months, starting Q4 2026

Ready to make every QC result count?

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