Validation Specialist

Reporting directly to the Validation Manager, you will be responsible to facilitate the implementation of new Global Quality Procedures

Responsibilities Include:

- To organise the site re-qualification activities in accordance with the VMP. To prepare the relevant protocols, collate and review the resulting data.
- To prepare the necessary Validation documents from templates, and develop new Validation Study protocols.
- To execute and/or oversee execution of Validation/Qualification protocols for specific items of new equipment, such as continuous flow centrifuges, fermenter vessels, filtration equipment and temperature controlled units.
- To review vendor FAT/SAT protocols and attend Factory Acceptance Testing at vendor sites as required.
- To provide technical validation support to project and production teams.
- To perform/assist in the preparation, execution and review of Process/Cleaning Validation protocols as required.
- To supervise validation contractor site visits, and schedule visits with production departments.
- To organise Production/QC teams involved in Validation Activities, particularly HVAC and Autoclave Validation Activities.

To be considered for this position, you will need to have:

- Minimum of three years experience within a Production, Validation, or Quality Assurance role in a pharmaceutical manufacturing environment.
- Hands on experience of equipment validation such as autoclaves, HVAC and large scale process equipment
- Experience of directing/coaching small teams of staff.
- Experience/involved in inspections by regulatory bodies.

This is a great opportunity to be a part of a multi national organisation with huge scope to progress in your career.

If you are interested in the position please send an updated CV to Jade Tetlow or call 0207 758 7311 for further details I would be happy to discuss.

Keywords: Validation, Production, Testing, Equipment qualification, Process Validation, Cleaning Validation, Operations, Utilities Validation, HVAC , Pharmaceuticals, GMP.To find out more about Real please visit www.realstaffing.com