Well established, global client carrying out a major site upgrade and expansion - now looking for Validation Specialists on both contract and permanent basis. The roles will be responsible for and carry out the following functions - Leadership role within the Quality Department responsible for the management and co-ordination of … the site cGMP validation activities. Support validation activity during... more »
Well established, global client carrying out a major site upgrade and expansion - now looking for Validation Specialists on both contract and permanent basis. The roles will be responsible for and carry out the following functions - Leadership role within the Quality Department responsible for the management and co-ordination of … the site cGMP validation activities. Support validation activity during design, installation & commissioning of new equipment, processes, packaging lines & facilities and utilities. Ensure the validated status of site facilities, i.e., equipment, processes, CSV and utilities is complete and compliant with internal local and corporate procedures, relevant regulatory requirements and … industry guidance. Authoring, reviewing, executing and maintaining validation documentation including site Validation Master Plan and Site Validation Strategy. Support Production departments in validation activities for processes and equipment Preparation and management of validation plans, protocols and reports. Support and coordinate with corporate validation team. more »
Brightwork are currently recruiting for a ValidationSpecialist to join our client, a renowned manufacturer in their site in Ayrshire during an exciting period of expansion and growth. The ValidationSpecialist responsibilities include: Leadership role within the Quality Department responsible for the management and co-ordination … of the site cGMP validation activities. Support validation activity during design, installation & commissioning of new equipment, processes, packaging lines & facilities and utilities. Ensure the validated status of site facilities, i.e., equipment, processes, CSV and utilities is complete and compliant with internal local and corporate procedures, relevant regulatory requirements … and industry guidance. Authoring, reviewing, executing and maintaining validation documentation including site Validation Master Plan and Site Validation Strategy. Support Production departments in validation activities for processes and equipment. Preparation and management of validation plans, protocols and reports. Supporting external audits including customer and regulatory more »