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.
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