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 to patients worldwide. Don't miss out on this exciting opportunity!