Process Validation Specialist

vor 1 Monat


Genf, Genf, Schweiz Michael Page Vollzeit
Job Description

We are seeking a highly skilled Process Validation Engineer to join our team at Michael Page.

Key Responsibilities
  • Collaborate with cross-functional teams to ensure seamless transfer of new products from design to production.
  • Develop and implement process validation plans to guarantee the maintenance of validated statuses.
  • Contribute to the validation protocols and participate in the continuous assessment and optimization of manufacturing processes.
  • Represent the validation department during inspections and/or audits by regulatory agencies.
Requirements
  • Degree in medical technology, engineering, or a related field.
  • Fluency in English.
  • First experience in industrialization and validation within the Medical device industry.
  • Strong knowledge of ISO quality management systems and risk management for Medical Devices.
Personal Qualities
  • Strong ethics, creativity, and problem-solving abilities.
  • Proactive and able to initiate and self-start projects.
  • Excellent planning, communication, and presentation skills.



About Michael Page

Michael Page is a leading recruitment agency providing expert recruitment solutions to businesses across various industries.



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