Validation Specialist

Republic of Ireland  ‐ Onsite
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Description

As part of the Validation team, the Validation Specialist will be responsible for the performance and execution of Process, Equipment and Cleaning Validation.

The primary focus of the role will be on validation transfers of existing products to new equipment within the site.

Other key duties and responsibilities may include:
  • Responsibility for the co-ordination of Process Validation, Cleaning Validation activity and Equipment Validation in the Production Department.
  • Performance of qualification activities
  • Validation report writing
  • Process FMEA
  • Preparation and execution of validation and re-validation protocols and reports, (IQ / OQ / PQ), for the validation of equipment, systems, products and projects.
  • Responsible for Investigating and resolving deviations associated with validation studies.


Essential Requirments:
  • Must have 5+ years recent experience in validation of product/processes/equipment.
  • Must have good interpersonal and organisational skills
  • Must have proficient computer skills ( MS office etc)
  • Applicants should have a third level degree or equivalent in a Pharmacy/Science/Engineering
  • Demonstrated Validation experience in Granulation, Tabletting and Coating areas would be beneficial.
  • Strong leadership, communication and interpersonal skills and an ability to achieve objectives without close supervision in a team based environment are essential for this position.


If you would like to apply please contact Sarah Irvine on or reply with a copy of your up to date CV. We also offer shopping vouchers for any successful referrals.
Start date
09/2015
From
Real Staffing
Published at
08.09.2015
Project ID:
980690
Contract type
Freelance
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