GMP Data Integrity & CSV Remediation Lead

Life Science Recruitment

Lyon

Sur place

EUR 90 000 - 150 000

Plein temps

Il y a 13 jours

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Résumé du poste

Life Science Recruitment is recruiting an experienced cGMP Data Integrity and CSV Remediation Specialist to support a regulatory compliance project at a regulated manufacturing site in Lyon. This senior onsite contract role requires assessing data integrity controls, identifying compliance risks and delivering a structured remediation strategy.

The role covers gap assessments across manufacturing, labs, quality and computerised systems, prioritising risks, developing remediation plans and CAPAs,

Qualifications

  • Strong experience within pharmaceutical or biotechnology manufacturing.
  • Demonstrable data integrity assessment and remediation experience.
  • Strong working knowledge of Computer System Validation.
  • Experience applying GAMP 5 and EU Annex 11 requirements.
  • Experience supporting regulatory inspections or remediation programs.
  • Fluent in French and English, including technical writing.
  • Availability for onsite contract deployment in France.

Responsabilités

  • Perform comprehensive cGMP data integrity gap assessments across manufacturing, laboratory, quality and computerised system environments
  • Identify and prioritise data integrity and GMP compliance risks using a structured, risk-based methodology
  • Develop remediation strategies, quality remediation plans and implementation roadmaps
  • Support the development and execution of corrective and preventive actions
  • Assess electronic and paper-based records against applicable data integrity expectations
  • Review computerised systems and validation controls against GAMP 5 and EU Annex 11 requirements
  • Support improvements to validation processes, quality systems, procedures and governance
  • Conduct mock inspections and inspection readiness assessments
  • Review documentation for completeness, traceability, accuracy and regulatory compliance
  • Communicate findings and recommendations to quality, manufacturing, laboratory, IT and site leadership teams
  • Support the site during regulatory remediation and inspection preparation activities

Connaissances

cGMP
Data Integrity
CSV remediation
GAMP 5
EU Annex 11
Regulatory inspections
French & English writing

Description du poste

Life Science Recruitment is recruiting an experienced cGMP Data Integrity and CSV Remediation Specialist to support a regulatory compliance project at a regulated manufacturing site in Lyon. This senior onsite contract role requires assessing data integrity controls, identifying compliance risks and delivering a structured remediation strategy.

The role covers gap assessments across manufacturing, labs, quality and computerised systems, prioritising risks, developing remediation plans and CAPAs,

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