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QA Validation Document Review Specialist

Reference ID : NHR02
Category :
  • Pharma / Biotech
  • Science
  • Medical Devices
  • General Manufacturing
Date Posted : May 8, 2018
Job Location
:
  • Munster
- Limerick
Experience : 3-4 Yrs
Salary : Neg
Employment Type
:
Contract
Consultant
:
Nicola O'Sullivan
Contact Number : 087 0622429
Document Reviewer required to join the QA validation team of a leading biopharma multinational

Principal Responsibilities

QA Validation Specialist

 

A QA Validation Specialist is required to become an integral member of the quality team within a dynamic Munster based Biotech facility.  The successful candidate will be experienced in continuing validation and complete document preparation and execution activities for cleaning validation on site.

 

Key Duties:

  • Continuing validation, maintaining a qualified state in relation to equipment
  • Gap analysis assessments
  • Technical writing, deviation/change control writing
  • Continuing assessment of equipment
  • Generate, review, approval of protocols
  • Maintain and update continuing validation plan and continuing schedule
  • Generate reports
  • Actively look for continuous improvements

Qualifications & Requirements

Qualifications and Experience:

  • Third level degree in a Science or Engineering discipline
  • 5+ years previous experience
  • Experience in continuing validation
  • Experience in deviation/change control writing
  • Excellent understanding of how cleaning validation/HVAC/cleaning equipment works
  • Extensive experience on writing and approving deviations
  • Good project management skills
  • Strong communication skills.

For more information contact Nicola on 087 0622429 or email your CV in the strictest confidence to jobs@headcount.ie



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