Validation Engineer

We are working with a Leading Medical Device company to recruit for a Validation Engineer based in Waterford.

Key Responsibilities:

• Write the necessary validation plans, protocols, reports & amendments of the Quality Management System ensuring compliance with the latest Regulatory Agencies (HPRA, FDA) directives / requirements within the Medical Device and Pharma Sector.
• Generate applicable quality documentation in conjunction with validation activities.
• Liaise within a cross functional team, to provide and drive validation inputs and initiatives into the overall operational activities of the company.
• Liaise with external vendors for validation plans and requirements.
• Development of validation projects, master validation plans.
• Support the implementation of Company Policies and GMP.

Experience and Qualifications:

• Degree in Engineering/Science discipline.
• 3 to 5 years’ experience in a Validation or Quality engineering role.
• Strong working knowledge of process validation and capability. Experience in method validation and process characterization is an advantage.

What's on offer?

• A Permanent Role with a great benefits package and shift allowance!

Next Steps:

• The role looks like something you might be interested in? Hit the “Apply Now” button
• If this job isn’t suited to your skills but you are looking for a new opportunity please get in touch by sending an email to [email protected]