Validation
Overview
An experienced Validation Engineer is required to support manufacturing operations within a regulated pharmaceutical environment. This role will focus on validation activities, technical assessments, and continuous improvement initiatives across core production and support areas. The position is hands-on in nature and will involve close collaboration with cross-functional teams to ensure activities are delivered in line with established quality and compliance standards.
Key Responsibilities
- Support validation activities associated with manufacturing processes and supporting systems, ensuring alignment with internal procedures and industry expectations
- Contribute to the execution, review, and maintenance of validation documentation, including protocols and reports
- Perform structured assessments of equipment, process steps, and operational practices to support consistent performance
- Assist in the ongoing development and enhancement of validation approaches and methodologies
- Support the evaluation and improvement of cleaning and operational practices where required
- Collaborate with quality and operational teams to support routine activities, assessments, and continuous improvement efforts
- Contribute to the preparation of documentation to support internal and external review activities
- Ensure activities are delivered in a clear, organised, and compliant manner
Requirements
- Degree in Engineering, Life Sciences, or a related discipline
- Previous experience in validation within a regulated manufacturing environment
- Understanding of validation principles across process, equipment, or cleaning activities
- Ability to work in a structured and detail-oriented manner
- Familiarity with applicable regulatory and quality expectations
FAQs
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