Validation Specialist (facility and process equipment)

Validation Specialist Are you a Validation Specialist with experience in the pharmaceutical industry? Do you thrive in a fast-paced environment and enjoy working on cutting-edge projects? Our client, a leading pharmaceutical company, is seeking a talented individual like you to join their team as a Validation Specialist for a 6 month contract. If you are passionate about ensuring the quality and compliance of facility and process equipment validations, this opportunity is for you! As a Validation Specialist, you will have the opportunity to contribute to the success of our client's organisation by: Performing facility and process equipment validations in a GMP environment. Ensuring computer systems are validated and compliant with regulations. Upholding data integrity principles throughout the validation process. Collaborating with cross-functional teams to ensure QA requirements are met. Being a quick learner and adapting to new validation processes and techniques.Requirements: A minimum of 3 years of experience in facility and process equipment validation in a GMP environment. Familiarity with computer system validation and data integrity principles. Prior QA experience is a plus. Availability to be on-site a minimum of 3 days a week. Join our client's dynamic team and make a difference in the pharmaceutical industry! Apply now to showcase your expertise as a Validation Specialist and contribute to their mission of delivering quality products…