Validation Engineer- 4Months

Validation Engineer A client of mine are seeking Process Validation Engineer to support validation and revalidation efforts for CGMP equipment, systems, and processes in a pharmaceutical manufacturing environment. This role ensures compliance with global standards and regulatory requirements (FDA, HPRA, etc.), delivering customer satisfaction through validation and project work.
Location- Mayo
Duration- 4 Months
Key Responsibilities: Lead and implement the site validation master plan for process, equipment, and system validation.Oversee validation projects, ensuring timely completion of documentation and compliance with regulatory standards.Coordinate validation activities with relevant engineers and departments.Review, approve, and maintain validation documentation.Support audit preparations, regulatory reviews, and audit responses.Ensure compliance with internal EHS requirements and participate in continuous improvement efforts.Requirements: Bachelor's degree in a science or engineering discipline.Minimum of 2 years' experience in pharmaceutical or similarly regulated environments.Strong project management skills in Process Validation.Experience in Equipment/Cleaning Validation is beneficial.Proficiency in Microsoft Office.Excellent problem-solving and critical thinking skills.
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