Cleaning Validation Consultant- 12 Months Contract

NB - The candidate must hold a current full UK Driving Licence.

Qualifications

* First degree or equivalent in a scientific/engineering discipline.

Knowledge & Experience

* Minimum 5 Years Current Experience in Bio-Pharma Industry

* Minimum 3 Years Experience in a Validation Role (1 Year of which should be in Cleaning Validation)

* Detailed knowledge and practical experience of CIP Systems (Manual and Automatic) and their functionality.

* Understanding and application of GMP risk assessments.

* Demonstrated understanding and application of industry standard validation practices and documentation, i.e. IQ, OQ, PQ, PV etc

* A thorough understanding of Good Manufacturing Practice (cGMP) is essential.

Key Elements of Role

* Completion of review and analysis of the current Clean In Place procedures and equipment.

* Recommendations for improvement of current cleaning procedures/processes where required.

* Execution of required cleaning validation activities where identified by risk assessment.

* Preparation of documentation for Cleaning Validation activities complying with company procedures and industry standard practices.

* Preparation of project plans identifying key milestones and resolving resource bottlenecks in order to achieve stated deadlines. Generation of regular status reports

* Preparation of detailed validation reports, summarising validation exercise, identifying potential problem items and recommendations for resolving such issues.
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Please contact Rachel Smith as soon as possible if you are interested in this position. 0207 758 7322To find out more about Real please visit www.realstaffing.com