Lead Product Quality Vigilance Engineer

7555-Janssen Pharmaceutica NV Legal Entity

Geel

Sur place

EUR 73 000 - 115 000

Plein temps

Il y a 8 jours
Générateur de candidature

Une candidature sur mesure pour ce poste — un CV et une lettre de motivation personnalisés qui correspondent à l’offre.

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Avantages offerts par ce poste

Annual bonus
Vacation days
Parental leave
Well-being reimbursement

Résumé du poste

Johnson & Johnson is seeking a PQV Quality Engineer 4 in Belgium to lead investigations of Product Quality Complaints for Innovative Medicine products across manufacturing sites. You will ensure thorough analysis, documented failures, and global knowledge transfer.

You will coordinate with R&D, NPI, and site teams to ensure readiness, drive improvements, and act as Single Point of Contact for PQV investigations while supporting audits and risk management.

Qualifications

  • 5+ years in Quality Assurance and/or Quality Control in regulated industry.
  • Knowledge of medical safety environment and regulation.
  • Experience in Medical Device or Pharmaceutical industry required.

Responsabilités

  • Lead and support investigations of product quality complaints (PQC) across sites.
  • Coordinate with R&D, NPI and cross-functional teams for readiness and escalation.
  • Ensure documented, data-driven decision making and adherence to regulatory requirements.
  • Act as SPOC for PQV investigations and support audits/inspections.

Connaissances

Coaching
Consistency
Controls Compliance
Critical Thinking
Data Savvy
Engineering
Lean Thinking
Process Improvements

Formation

BA/BS in technical, scientific or engineering
MA/MS/MBA in technical, scientific or engineering (desirable)

Outils

Six Sigma Green Belt
Six Sigma Black Belt
CQE (ASQ)

Description du poste

Johnson & Johnson is seeking a PQV Quality Engineer 4 in Belgium to lead investigations of Product Quality Complaints for Innovative Medicine products across manufacturing sites. You will ensure thorough analysis, documented failures, and global knowledge transfer.

You will coordinate with R&D, NPI, and site teams to ensure readiness, drive improvements, and act as Single Point of Contact for PQV investigations while supporting audits and risk management.

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