Job Title

Validation Specialist – Kent – Pharmaceuticals About the Company:We are looking for an experienced Validation Specialist to join a pharmaceutical manufacturing site in Kent (commutable from SE London). You will have the opportunity to work in a newly built GMP manufacturing facility. This is a 1-year parental cover contract on a FTC. Responsibilities: • Completion of validation activities and projects for equipment and processes.• Maintenance of relevant documentation.• Preparation and execution of validation procedures and protocols for re-qualification, cleaning validation, and temperature mapping.• Maintenance of the re-qualification schedule for validated equipment.• Gathering and analysing validation data and prepare reports.• Assisting with the compilation of and maintain the validation master plan (VMP).• Providing advice and suggestions concerning changes and improvements.• Providing technical expertise in terms of investigation, trouble shooting and finding solutions.• Maintaining documentation and files.Requirements:• An understanding of and experience in IQ, OQ, PQ and PV.• Experience of temperature mapping and cleaning validations.• Experience working in a process and equipment validation position in the pharmaceutical, biopharmaceutical or biotechnology manufacturing industry.• Ability to write and carry out validation procedures.• An understanding of the principes of calibration.• Excellent communication skills.• An understanding of the requirements of GMP.