Quality Engineer I

  • Cork
  • Temporary 12 months
  • JO-1907-64610_1562073723

Summary

Responsibilities:

  • Supervision of QA Technician personnel and scheduling of duties
  • Responsibility for tracking customer complaints / co-ordinating close-out and investigations
  • Lot review of lots and release of same into inventory
  • Review of validation protocols/lots and release of same. Approval of shipping requests
  • Responsibility for ensuring that all activities in the plant comply to ISO and GMP requirements. Drive quality improvements and initiatives within the plant
  • Hold department quality meetings for the plant
  • Responsible for the disposition of non-conforming in-process and finished product
  • Communicate with customers where necessary
  • Has responsibility for the implementation of those parts of the Merck quality system relating to the QA function
  • Updates, reviews and drafts quality documentation such as test methods and standard operating procedures, management procedures, test specifications and protocols
  • Adhere to company safety requirements

Requirements:

  • A degree in an appropriate science/engineering discipline and at least 3 years relevant experience. Preferably in a regulated Medical Device or GMP manufacturing site.
  • Excellent communication skills.
  • Good leadership and planning skills.
  • Technical ability and a good approach to problem solving.

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