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Job ID: JOB-13547
Manufacturing Engineer II

Location: Cork 

Permanent 

Are Medical Devices your passion?

Do you have experience with metals, plastics, or injection moulding?

Are you interested in catheters, occlusion coils and inflation devices?

This client is a leading innovator in the healthcare industry, and is committed to making a difference in peoples lives around the world. By joining this client company you will bring your experience in a highly regulated manufacturing department, along with your project management and operations skills, to work in the cleanroom as an SME leading improvements, troubleshooting, and supporting, before moving into project areas. 

This company is an Equal Opportunity Employer – Race, Colour, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Disability, Veteran.

Key Roles & Responsibilities:

• To identify and order the key activities utilized in quality, service & cost improvements in the Operations Engineering Cycle to meet key business objectives.
• To apply a prioritised approach in Value Centred Engineering to achieve the key opportunities in quality, service and cost.
• Providing technical leadership on all product and process issues.
• Line performance monitoring and the compilation and execution of structured event plans to remediate systemic issues that drive sub-optimal performance.
• Development and implementation of appropriate supporting documentation, and process work instructions compliant with current Good Manufacturing Practices (GMP).
• Leading technical improvement under the team’s Continuous Improvement Program (CIP).
• Transferring and implementing processes either from development or from another manufacturing facility.
• Participation, where appropriate, in the phase review process with respect to new products.
• Provide technical leadership/guidance for the Process Technicians and Manufacturing Engineers I’s on the team.
• Project planning, in detail, in support of major projects, product/process transfer etc.
• Responsible for other projects (value stream and cross functional) as assigned by the company, including the scoping, approval, budgeting, specification, execution, qualification and handover as appropriate. Observance of the site Equipment and Automated Systems (E&AS) procedures for new equipment.
• Establish and support a work environment of continuous improvement that supports the businesses Quality Policy, Quality System and the appropriate regulations for the area they support. Ensure employees are trained to do their work and their training is documented.
• Continuous monitoring and reporting of variables that feed into the business performance metrics, and pro-active identification and resolution of issues around same.
• Cross functional liaison with support functions in pursuit support for achieving the business targets.
• Adherence to, and enforcement of all Environment Health and Safety (EHS) requirements on site.
• Elimination and/or management of material risks on the production floor in co-operation with Supplier Quality engineers.

Education & Experience:

• Level 8 qualification in a relevant Engineering or Science discipline.
• 3-5 years’ experience in a highly regulated environment.
• Strong communicator with excellent problem solving skills.
• Teamwork & collaboration is a key competency for this role.
• Ideally experience of working in a regulated environment.
• Project Management.

What we offer:

• Healthcare coverage for employees and their families
• Pension
• Long term disability/income protection
• Employee Assistance Programme
• Subsidised onsite restaurant
• Free parking
• Great staff retention and company culture

For further information on this role in please contact on Gavin Moran on 087 410 8620 or connect@hero.ie

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/

Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

Data can only be transferred outside of the EEA on the basis of standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given.  You have supplied us with your personal data in the process of applying for a position.  Our client company may have personnel outside of the EEA who will review your data.  We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.

Gavin Moran

JOB-13547

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