Manufacturing Engineer
Cork
Contract
€32 - €36 p.h
€32 - €36 p.h
Are you looking to further your career in Manufacturing within the Medical Device industry?
The ideal candidate possesses a high level of technical expertise. You will play a critical role in creating and refining processes in order to improve manufacturing safety, quality, and productivity.
Note: No sponsorship is provided for this contract role, a Stamp 1G or Stamp 4 is necessary.
Education & Experience:
The ideal candidate possesses a high level of technical expertise. You will play a critical role in creating and refining processes in order to improve manufacturing safety, quality, and productivity.
Note: No sponsorship is provided for this contract role, a Stamp 1G or Stamp 4 is necessary.
- 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.
- Hands on technical expertise, 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 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 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