A prominent medical device company is currently searching for skilled Validation Engineers with diverse backgrounds & experience, including Process, Equipment, Utilities, and Software Validation. 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 process, equipment, utilities, or software validation.
Experience within Medical Device or Pharmaceutical Industries preferred
For a confidential discussion and more information on the role, please contact Kevin Griffin
Kevin Griffin
kevin.griffin@collinsmcnicholas.ie
(021) 2427108