The Validation Specialist join a leading global pharmaceutical company that is rapidly expanding its international presence, with plans to double in both size and production in the coming years. The Validation Specialist will be responsible for executing and reviewing revalidations, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to support validation protocols and investigations. This role is essential in maintaining the accuracy of validation processes, identifying root causes of failures, and implementing corrective actions to enhance efficiency and quality.

QUALIFICATIONS OF THE VALIDATION SPECIALIST:

• Bachelor’s Degree in Engineering, Computer Science, or a related technical field.
• Minimum 2 years of validation experience within the pharmaceutical or medical device industry.
• Knowledge of core validation areas such as sterilization, cleaning, process validation, or computer validation.
• Familiarity with cGMP documentation and regulatory standards.
• Strong proficiency in Microsoft Word, Excel, and validation tracking tools.
• Experience with validation test equipment, including temperature mapping (e.g., Kaye Validator).
• Strong analytical, problem-solving, and organizational skills.