Description
A global pharmaceutical company is seeking a senior validation specialist to join their Engineering Validation Department. You will be expected to be capable of co-ordinating and executing the validation activities for new and refurbished facilities and equipment for potentially any part of the production facility.Responsibilities:
*Assessing the validation requirements for new projects and preparing time and cost estimates. *Writing and reviewing validation protocols and reports.
* Co-ordinating and performing validation activities, including tracking and reporting the progress of projects.
* Training staff in validation procedures and principles.
*Managing external Validation contractors.
*Ensuring that resource, raw materials and documentation are available at the appropriate time.
The successful individual will have at least 5 years validation experience within the Pharmaceutical industry. You will have great communication skills, be able to interact with all levels of staff, suppliers, customers and regulatory bodies and have the mentality to ensure all work is successfully completed.