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Continued Process Verification Consultant - CR/604532_1785919669

Continued Process Verification Consultant

Anagni
Contract
Negotiable
Manufacturing
CR/604532_1785919669
Continued Process Verification Consultant

Location: Anagni, Scoppito

Contract length: 9-10 months

Number of positions: 6

Overview

We are supporting the implementation of a global Continued Process Verification (CPV) programme across pharmaceutical manufacturing sites in Italy. Consultants will play a key role in establishing site-level CPV strategies aligned with standardised global guidance whilst ensuring manufacturing and QC data are suitable for ongoing process monitoring and verification activities.
This is a hands-on role requiring close collaboration with site teams to remediate, organise, and contextualise critical manufacturing and quality data.

Responsibilities

  • Support deployment of site CPV strategies in line with global programme requirements.
  • Review and remediate Quality Control data to ensure suitability for CPV activities.
  • Review and remediate manufacturing process data from multiple systems and sources.
  • Support data contextualisation activities, linking process data to relevant operational and quality events.
  • Collaborate with Manufacturing, Quality, QC and technical teams to improve data quality and usability.
  • Identify data gaps, inconsistencies and integrity issues impacting CPV implementation.
  • Ensure data is structured and available for ongoing process monitoring and trending.
  • Contribute to standardisation and harmonisation initiatives across manufacturing sites.
  • Provide practical support during implementation and execution of CPV programmes.

Requirements

  • Previous experience within pharmaceutical, biotechnology or life sciences manufacturing.
  • Demonstrated experience with Continued Process Verification (CPV), Process Validation or related process monitoring activities.
  • Strong understanding of GMP and regulated manufacturing environments.
  • Experience with manufacturing data analysis and remediation.
  • Experience supporting QC data review, remediation or data integrity initiatives.
  • Ability to work effectively with stakeholders across technical and operational functions.
  • Strong analytical and problem-solving skills.
  • Fluent English; Italian language skills advantageous.

Ideal Candidate Profile

An ideal candidate will have a pharmaceutical manufacturing background with direct exposure to CPV, Process Validation, MS&T, Quality, or Manufacturing Excellence activities. They will be comfortable working with large manufacturing and QC datasets, identifying data quality issues, and supporting remediation and contextualisation efforts. Candidates who have previously supported global quality transformation programmes, process monitoring initiatives, or site readiness projects will be particularly relevant.

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