We have partnered with a global Medical Device company based in Ireland, which is searching for a Validation/Manufacturing Engineer on a contract basis (1-2 years).
They are rapidly expanding their capabilities onsite and currently introduce a lot of new equipment and technology.
Due to this, they need experts to come in and support the introduction of this onsite, working within the Engineering team to qualify and validate the process and equipment.
Experience required:
Experience with legacy equipment and de/re-commissioning
Managing regulatory documentation/submissions
Liaise with suppliers and internal project teams
Led or been a part of product transfer projects
Understand the technical aspects: EQ, Process validation, IQ, OQ, supplier qualification
The role will be full time onsite in Cork with the occasional home office option based on project needs.
Seniority level
Seniority level
Mid-Senior level
Employment type
Employment type
Contract
Job function
Job function
Engineering, Quality Assurance, and Manufacturing
Industries
Medical Equipment Manufacturing
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