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.
