We’re currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Limerick. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.

Duties

− Assist in determining the budget to support requirements
− Evaluate or assist in evaluating technology necessary to support requirements
− Propose options to Management/Customer/Stakeholders
− Provide technical support for projects
− Support and/or develop and execute equipment or process related validations in accordance with IML requirements, processes and procedures
− Assist in negotiation with equipment suppliers
− Utilize necessary project tools, i.e. URS, Microsoft Project, etc. to manage projects successfully
− Measure/evaluate equipment efficiencies, downtime and assist in the development of maintenance requirements
− Propose and implement improvement projects that improve compliance, improve efficiencies, yields or throughputs
− Define root cause and implement solutions to equipment and process related non-conformances utilising the NCMR and CAPA processes
− Actively interfacing with cross-functional team members, always practicing good team work in support of day to day operating requirements
− Ensure effective closure on quality system documents (Audit Action, NCR’s, CAPA’s, Maps, etc.)
− Implementation of safety/environment requirements on purchase and changes of all new and existing equipment.

Education & Experience

− Hold a relevant degree or equivalent qualification in production, manufacturing or mechanical engineering.
− Experience in relevant engineering role
− Prior experience in a GMP or medical device manufacturing environment
− Prior experience in equipment and process validation activities
− Process development experience


If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie for further information.