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A prominent medical device company is currently searching for skilled Validation Engineers with diverse backgrounds & experience including Process Validation, Test Method Validation as well as Equipment Qualification. You will be part of a dynamic team working in a highly regulated industry, ensuring the safe and effective delivery of products to its customers.
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 withinMedical Device, Pharmaceutical & Electrical Industries preferred
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