A prominent medical device company is seeking skilled Validation Engineers with diverse backgrounds and experience in Process Validation, Test Method Validation, and Equipment Qualification.
Key Responsibilities:
* Develop and implement validation strategies for various systems and processes.
* Create and maintain validation documentation, ensuring compliance with industry standards and regulations.
* Collaborate with cross-functional teams to ensure the safe and effective production of products that meet customer needs.
* Manage and update quality system procedures to align with evolving regulatory requirements.
* Monitor and maintain the quality and compliance status of associated records, procedures, work instructions, and training materials.
* Effectively communicate validation status, report metrics, identify trends, and suggest improvement initiatives.
* Review and approve validation documentation in accordance with company policies.
Qualifications and Experience:
* A relevant third-level qualification, preferably in Engineering, Manufacturing, or Science.
* 3-5 years of experience in equipment, facilities validation.
* Experience within Medical Device, Pharmaceutical & Electrical Industries preferred.