Validation Engineer
A Validation Engineer will play a key role in ensuring the safe and effective delivery of medical devices to customers. The successful candidate will be responsible for developing and implementing validation strategies for various systems and processes.
The ideal candidate will have experience in equipment and facilities validation, with a strong understanding of industry standards and regulations. They will collaborate with cross-functional teams to ensure the production of high-quality products that meet customer needs.
Main Responsibilities:
* Develop and Implement Validation Strategies: Create and implement validation strategies for various systems and processes, ensuring compliance with industry standards and regulations.
* Create and Maintain Validation Documentation: Develop and maintain validation documentation, including procedures, work instructions, and training materials.
* Collaborate with Cross-Functional Teams: Work collaboratively with cross-functional teams to ensure the safe and effective production of products meeting customer needs.
* Manage Quality System Procedures: Manage and update quality system procedures aligning with evolving regulatory requirements.
* Maintain Quality and Compliance Status: Monitor and maintain quality and compliance status of associated records, procedures, work instructions, and training materials.
* Communicate Validation Status: Effectively communicate validation status, report metrics, identify trends, and suggest improvement initiatives.
Qualifications and Experience:
* A relevant third-level qualification preferably in Engineering, Manufacturing, or Science.
* 3-5 years of experience in equipment and facilities validation.
* Experience within Medical Device, Pharmaceutical, and Electrical Industries preferred.