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 beth@accpro.ie
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