Pharma Data Integrity Specialist, CPV & MES Remediation

EFOR

Waterford

Sur place

EUR 70 000 - 100 000

Plein temps

Il y a 2 jours

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Résumé du poste

EFOR Group in Waterford, Ireland, onsite, seeks a Manufacturing Data Remediation Specialist to join a global pharma manufacturer on a ~6.5-month contract. You will map CPV data requirements to source systems, assess data integrity, perform remediation, and prepare data for digital trending.

You will oversee two junior CPV consultants and work across OT/IT, Production and Quality. The ideal candidate has 3–6 years in pharma data, experience with MES/eBR and PI historians, and solid knowledge of

Qualifications

Degree in Process, Chemical, Automation or Computer Engineering, Data Science or similar.
3–6 years in pharma manufacturing data, MES, automation or digital manufacturing.
Hands-on experience with MES/eBR, process historians (e.g. AVEVA/OSIsoft PI) and data lakes.
Strong knowledge of data integrity (ALCOA+), EU GMP Annex 11 / 21 CFR Part 11, and an awareness of computerised system validation.

Responsabilités

Map CPV data requirements to source systems: batch records, MES/eBR, process historian and ERP.
Assess the completeness, accuracy and integrity of manufacturing data, then 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 site’s digital trending platform.
Document source-to-target mapping and the rationale for each fix to GMP data integrity standards.
Coordinate the daily data work of two junior CPV Production Support consultants.