Validation Technologist

Summary:
Alex Dobson is currently recruiting for a Validation Technologist for one of the UK’s leading Contract Development Manufacturing Organizations. This is an exciting opportunity for someone looking to develop their skills within the pharmaceutical industry.  

Role:
The Facilities Validation department supports the manufacture and development of the companies products. It is responsible for ensuring compliance to the cGMP guidelines on Validation for all systems involved in the manufacture, storage and testing of PBL products.

The purpose of this role is to take the lead to execute validation activities relating to Temperature controlled units, Utilities and Sterilisation systems. This will involve coordination with Engineering, Production, QC and QA departments to ensure a timely delivery of the qualification report. The post holder may be expected to supervise contractor resource where appropriate with responsibility to ensure adequate training and supervision is provided. 

The post holder will be required to write, review and where appropriate approve validation reports prior to execution, followed by report generation. The scope of the work will involve (but not limited to) the qualification of Fridges, Freezers, Incubators, Autoclaves, Hot air ovens, HVAC systems, Clean rooms, Compressed gasses, Wfi, Purified Water and Clean steam systems.

Company:
The company have a long standing history within the UK and have been responsible for developing some of our modern day medication. They have worked in close collaboration with some of the world’s leading pharmaceutical companies and provide a very efficient service under strict GMP guidelines.

Keywords:
GMP, GDP, ISO, Pharmaceutical, Deviation, CAPA, Compliance, Salisbury, Wiltshire.