Pharma Data Integrity Specialist — Onsite in Waterford

EFOR; Munster; Presencial; EUR 70.000 - 90.000; Jornada completa

Descripción de la vacante

EFOR Group is seeking a Manufacturing Data Remediation Specialist to join a Waterford-based site on onsite basis. You will ensure CPV data is traceable from batch records, MES/eBR and process historians, enabling accurate trending and decision making.

You will remediate data, backfill from source records, standardise naming and units, and document mappings to GMP data integrity standards while coordinating two junior CPV Production Support consultants.

Formación

• Degree in Process, Chemical, Automation or Computer Engineering, Data Science or similar.
• Experience with pharma manufacturing data, MES, automation or digital manufacturing (3–6 years).
• Knowledge of data integrity (ALCOA+) and GMP data standards.

Responsabilidades

• Map CPV data requirements to source systems: batch records, MES/eBR, process historian and ERP.
• Assess data completeness, accuracy and integrity; log and prioritise gaps.
• Define and carry out remediation: data cleansing, backfill from source records, and standard parameter naming and units.
• Prepare data for contextualisation (batch, phase and equipment hierarchy) and support loading into the digital trending platform.
• Document source-to-target mappings and rationale for fixes to GMP data integrity standards.
• Coordinate the daily data work of two junior CPV Production Support consultants.

Conocimientos

Data integrity

SQL

Python

Power BI

MES/eBR

GMP compliance

Batch data CPV

Leadership

Educación

Engineering degree

Herramientas

AVEVA PI

OSIsoft PI

Data lake concepts

Descripción del empleo

EFOR Group is seeking a Manufacturing Data Remediation Specialist to join a Waterford-based site on onsite basis. You will ensure CPV data is traceable from batch records, MES/eBR and process historians, enabling accurate trending and decision making.

You will remediate data, backfill from source records, standardise naming and units, and document mappings to GMP data integrity standards while coordinating two junior CPV Production Support consultants.