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 within Medical Device, Pharmaceutical & Electrical Industries preferred
For a confidential discussion and more information on the role, please contact Kevin Griffin
Kevin Griffin
kevin.griffin@collinsmcnicholas.ie
(021) 2427108