Validation Engineer

A leading pharmaceutical company in Cork is seeking a motivated and detail-oriented Validation Engineer to join our Quality team. In this role, you will play a pivotal part in ensuring our manufacturing processes meet the highest regulatory standards, driving continuous improvement across our operations.

Key Responsibilities:

• Develop, execute, and review IQ, OQ, and PQ protocols for production equipment.
• Conduct risk assessments and manage CAPA processes to address deviations.
• Collaborate with cross-functional teams to support new product introductions and process optimizations.
• Maintain thorough documentation in compliance with cGMP and regulatory guidelines.
• Utilize paperless qualification systems to streamline validation processes.

Qualifications:

• Degree in Engineering or a related field.
• 2-5 years of experience in validation or automated manufacturing environments.
• Strong understanding of cGMP and regulatory requirements.
• Excellent communication, project management, and problem-solving skills.

If you're passionate about ensuring quality in pharmaceutical manufacturing and eager to contribute to a dynamic team, I want to hear from you!

Apply today to join us in delivering high-quality, life-saving products to patients worldwide.