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Equipment Validation Specialist

Reference ID : NHAT01
Category :
  • Medical Devices
  • Science
  • Pharma / Biotech
  • General Manufacturing
Date Posted : Sep 3, 2018
Job Location
:
  • Munster
- Tipperary
Experience : 5+ Yrs
Salary : Neg
Employment Type
:
Contract
Consultant
:
Nicola O'Sullivan
Contact Number : 087 0622429
Equipment Validation Specialist required for Munster based pharmaceutical multinational

Principal Responsibilities

QA Validation Specialist

An excellent opportunity for a QA Validation Specialist has arisen within a global pharmaceutical leader based in the Munster region.

The successful candidate will Validate/qualify equipment, systems, and processes in accordance with regulatory requirements and support, follow and implement company manufacturing standards policies and procedures.

Key Duties:

  • Executes and reviews Qualification / Re-Qualification and Validation activity of Equipment / System / Facility and Plant utilities as QA Validation.
  • Generates and executes project validation plans and validation master plans.
  • Co-ordinates with manufacturing / engineering personnel for respective Qualification / Validation / Re-qualification activity for timely completion of activities.
  • Investigates any deficiencies related with qualification activities and determines corrective actions.
  • Preparation and review of SOPs and Drawings as related to validation.
  • Review and approval of calibration and PM activities (e.g. schedules) and Work orders.

Qualifications & Requirements

Qualifications and Experience:

  • Degree qualified in a Science or Engineering discipline
  • 5 – 8 years experience in a similar role within the pharmaceutical or med device industry
  • Have a good understanding of regulatory requirements
  • Strong communication and presentation skills
  • Excellent interpersonal, project management and motivational 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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