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.
Responsibilities of the Validation Specialist:
Revalidation & Compliance Oversight:
Validation Process Management:
Continuous Improvement & Quality Assurance:
Qualifications of the Validation Specialist:
Compensation & Benefits:
Key Words: Validation Specialist, Pharmaceutical Validation, Revalidation, IQ/OQ/PQ, Root Cause Analysis, cGMP Compliance, Change Control, Process Validation, Sterilization, Cleaning Validation, Technical Documentation, Audits & Inspections, Quality Assurance
If you are passionate about ensuring high standards in validation, compliance, and process improvement, we encourage you to apply today!
This job opens for applications on 5/1. Applications for this job will be accepted for at least days from the posting date.
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Validation Specialist • Clayton, NC
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