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Role Overview
A leading pharmaceutical company based in the Waterford area is currently seeking a dedicated Validation Engineer to support a new project. As the Validation Engineer, you will play a crucial role in ensuring the ongoing validation and compliance of new equipment, systems, and processes.
Key Duties and Responsibilities
* Executing FAT/SAT/IOQ protocols, including the generation of protocols and reports.
* Designing, executing, and reporting on validation studies for equipment, systems, and processes.
* Ensuring validation studies are managed in conjunction with all required standards and legal requirements (Health & Safety, cGMP, construction, environmental etc.).
* Providing technical interpretation and guidance of current US FDA and EU validation requirements for aseptic processing, lyophilisation, sterilisation, and depyrogenation.
Role Requirements
* Relevant degree in a scientific or engineering discipline.
* Proven industry experience in a healthcare manufacturing environment, ideally within the pharmaceutical sector.
* A working knowledge and practical experience with validation protocols, quality management systems, and regulatory compliance.
Key Words
Validation Engineer / Pharmaceutical / Waterford / FAT / SAT / IOQ / cGMP / Aseptic Processing / Lyophilisation / Sterilisation / Depyrogenation / Quality Management / Regulatory Compliance / Equipment Validation / Process Validation
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Location: Waterford, County Waterford, Ireland
Employment type: Contract
Job function: Management and Manufacturing
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