Description
The Cleaning Validation Specialist will be responsible for the management of the qualification of Cleaning Processes within a highly regulated pharmaceutical manufacturing environment during a significant period of projects.Key Responsibilities:
*Take responsibility for creating site wide cleaning validation strategies.
*Co-ordinate with other groups with responsibilities for process/cleaning validation activities directly related to validation, e.g. Project Engineering.
*Provide up to date information to Line Management on activities and time lines relating to validation work, utilising appropriate techniques.
*Review/produce supporting validation documentation, as required, as part of a validation exercise.
*Write and review Cleaning validation protocols and reports for new and existing equipment.
Ideal Skills and Experience:
*Degree qualified in Engineering based subject or related experience in a Cleaning Validation role.
*Experience within pharmaceutical Manufacturing environments with an understanding of tablet packaging.
*Solid experience of project lifecycle cleaning validation activities to include the qualification of equipment in conjunction with Project engineering/CAPEX teams.
*Demonstrable experience in drafting, executing and reporting of validation documentation ie IQ, OQ, PQ protocols.
*Work autonomously
This initial 12 month contract opportunity requires an experienced Cleaning Validation professional with strong full lifecycle validation experience