We are seeking a motivated and detail-oriented Validation Engineer to join our Quality team at {company}, a leading pharmaceutical company in Cork.
As a key member of our team, 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 to ensure compliance with cGMP and regulatory guidelines.
* Conduct risk assessments and manage CAPA processes to address deviations, maintaining thorough documentation throughout.
* Collaborate with cross-functional teams to support new product introductions and process optimizations, streamlining validation processes using paperless qualification systems.
Qualifications
* A degree in Engineering or a related field is required.
* 2-5 years of experience in validation or automated manufacturing environments is essential.
* A strong understanding of cGMP and regulatory requirements is necessary.
* Excellent communication, project management, and problem-solving skills are required.
If you're passionate about ensuring quality in pharmaceutical manufacturing and eager to contribute to a dynamic team, we encourage you to apply.