Associate Director Quality Assurance Mdcp

Merck Sharp & Dohme Corp

Haarlem, Netherlands
Hybrid
Device assembly and packaging operations
Quality oversight of the device network
Medical device and combination product manufacturing
Merck Sharp & Dohme Corp is seeking an Associate Director of Quality Assurance for their Device Quality & Regulatory organization in Haarlem, Netherlands. The role involves providing quality oversight for medical device operations, specifically focusing on combination products, while collaborating with various stakeholders to ensure compliance and drive innovation

Job Summary

  • Provide quality oversight of the Device Network, with a specific focus on device assembly and packaging operations at the Haarlem, Netherlands site.
  • Collaborate closely with diverse stakeholders including Manufacturing, R&D, Quality Assurance, and suppliers to drive innovation and commercialization of medical devices and combination products.
  • Benefits include a competitive salary, 35.5 vacation days, 8% vacation allowance, 3% year-end bonus, incentive plan, excellent pension scheme, and various wellbeing support programs.

Matching Summary

Match Score: 85

Merck Sharp & Dohme Corp is seeking an Associate Director of Quality Assurance for their Device Quality & Regulatory organization in Haarlem, Netherlands. The role involves providing quality oversight for medical device operations, specifically focusing on combination products, while collaborating with various stakeholders to ensure compliance and drive innovation.

Skills & Requirements

Must-have

  • Device assembly and packaging operations
  • Quality oversight of the Device Network
  • Medical device and combination product manufacturing
  • Root cause investigations of deviations
  • CAPA activities for device assembly
  • Cross-functional partnerships

Nice-to-have

  • Independent contributor role
  • Fast-paced operating environment
  • Patient safety and product quality focus
  • Culture of early issue identification

Key Requirements

  • Minimum 5 years relevant experience
  • Bachelor's degree in relevant discipline
  • Experience with medical devices and combination products
  • Familiarity with device design verification and control

Work Rights

Not specified

Tailored Resume

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