Senior Device Lifecycle Engineer – MedTech & Packaging

Johnson & Johnson Co.

Beerse

Sur place

EUR 73 000 - 115 000

Plein temps

Il y a 9 jours

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Avantages offerts par ce poste

Annual bonus
Vacation days
Parental leave
Bereavement leave
Caregiver leave
Well-being reimbursement

Résumé du poste

Johnson & Johnson is seeking a Senior Device Lifecycle Engineer to support device & packaging lifecycle activities in Beerse/Schaffhausen locations. You will bridge development and manufacturing, managing design changes, CAPA, tech transfers, and regulatory compliance.

The role emphasizes cross-functional collaboration, data-driven improvement, and adherence to cGMP standards for pharmaceutical and medical devices within the MSAT framework.

Qualifications

  • Bachelor's degree in Engineering or Science required.
  • Experience with device design/control and regulatory compliance.
  • Fluent in English with strong communication skills; Flemish/German a plus.

Responsabilités

  • Own lifecycle engineering for device & packaging products within the MSAT network.
  • Lead design changes, tech transfers, CAPA and complaint handling.
  • Coordinate with site operations and quality leadership for area of responsibility.
  • Ensure validation and production activities comply with cGMP and regulatory standards.
  • Drive continuous improvement using Six-Sigma and data-driven methods.
  • Guide cross-functional teams in capacity scaling and supplier development.

Connaissances

Agile Decision Making
CAPA
Problem Solving
Process Engineering
Statistical Analysis
Six-Sigma
Cross-functional Collaboration

Formation

BS in Engineering or Science

Description du poste

Johnson & Johnson is seeking a Senior Device Lifecycle Engineer to support device & packaging lifecycle activities in Beerse/Schaffhausen locations. You will bridge development and manufacturing, managing design changes, CAPA, tech transfers, and regulatory compliance.

The role emphasizes cross-functional collaboration, data-driven improvement, and adherence to cGMP standards for pharmaceutical and medical devices within the MSAT framework.

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