GxP Quality Assurance - Third-Party Systems (Pharma)

Pauwels Consulting

Geel

In loco

EUR 60.000 - 85.000

Tempo pieno

2 giorni fa
Candidati tra i primi
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Descrizione del lavoro

Pauwels Consulting is seeking a Quality Management professional to oversee the quality of third-party computerized systems providers for a global pharmaceutical client in Belgium. You will perform qualifications, risk-based evaluations, maintain quality agreements, manage the qualified third-party database, monitor performance, and ensure documentation of all activities.

Candidates hold a life sciences/engineering/computer sciences degree with 2+ years in a GxP-regulated environment and

Competenze

  • Bachelor or Master in Life Sciences, Engineering, Computer Sciences, or a related field.
  • 2+ years of experience in a GxP-regulated environment with a focus on third-party quality management.
  • Knowledge of FDA 21 CFR Part 11, EU Annex 11, and GAMP 5.
  • Strong analytical and risk assessment skills.
  • Fluent in Dutch and English.

Mansioni

  • Perform qualification assessments of third-party computerized systems providers to verify suitability and competence.
  • Conduct risk-based evaluations of external partners to determine appropriate quality control and oversight levels.
  • Develop and maintain quality agreements and contractual quality clauses with third-party suppliers.
  • Manage and update the qualified third-party database to ensure accurate referential data.
  • Monitor routine quality performance of qualified partners and lead continuous improvement initiatives.
  • Ensure comprehensive documentation and record-keeping of all third-party quality activities.

Conoscenze

Analytical skills
Risk assessment
Dutch (fluent)
English (fluent)

Formazione

Bachelor or Master in Life Sciences, Engineering, Computer Sciences, or related field

Strumenti

CSV

Descrizione del lavoro

Pauwels Consulting is seeking a Quality Management professional to oversee the quality of third-party computerized systems providers for a global pharmaceutical client in Belgium. You will perform qualifications, risk-based evaluations, maintain quality agreements, manage the qualified third-party database, monitor performance, and ensure documentation of all activities.

Candidates hold a life sciences/engineering/computer sciences degree with 2+ years in a GxP-regulated environment and

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