Validation and Quality Specialist

Republic of Ireland  ‐ Onsite
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Description

Supports the management of GMP compliance systems through the following activities:

* Carries out tasks related to the administration of project and site nonconformance management systems:
* Reviews and/or approves nonconformance investigations and their associated documentation.
* Manages entry of nonconformance records into the appropriate electronic system.
* Tracks investigations from the initiation through closure processes and advises relevant personnel on the status of investigations and associated CAPA and commitments, as appropriate.
* Coordinates investigation activities to ensure root causes are identified and that corrective actions are appropriate.
* Approves closure of nonconformance investigations on completion of the investigation and associated corrective actions.
* Carries out tasks related to the management of project and site change control systems:
* Reviews and/or approves change control requests, implementation actions, and request closures.
* Manages entry of change control records into the appropriate electronic system.
* Equipment Validation, knowlegde of IQ, OQ & PQ

This is an urgent requirement with competitive hourly rates. If you are interested in applying please contact Sarah Irvine on or reply with a copy of your current CV. We also offer vouchers for any successful referrals so if you know of anyone who may be looking please feel free to get in touch.
Start date
05/2015
From
Real Staffing
Published at
22.04.2015
Project ID:
890270
Contract type
Freelance
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