12 month contract opportunity for Cork based Manufacturing Engineer with a Medical Device Manufacturer. Responsible for the introduction and validation of new equipment. This is a full time onsite role
Key Responsibilities
- Lead the development and implementation of manufacturing processes for various projects, ensuring compliance with quality standards and regulatory requirements.
- Collaborate with stakeholders to implement technical, validation, and regulatory strategies while managing risks and maintaining compliance.
- Coordinate project plans and communicate effectively with internal and external partners to ensure smooth execution.
- Design mechanical systems from concept to implementation, ensuring alignment with project requirements and industry standards.
- Work with cross-functional teams (e.g., electrical engineering, manufacturing, quality assurance) for seamless project execution.
- Conduct equipment testing and simulations to validate designs and ensure performance.
- Analyse test results and make necessary modifications to improve functionality and reliability.
- Ensure compliance with safety standards and regulatory requirements in all designs.
- Contribute to continuous improvement initiatives through active participation in quality assurance processes.
Skills & Experience
- Level 8 degree in Engineering, Manufacturing, Mechanical or a related field.
- In-depth knowledge of medical device manufacturing and validation processes.
- 2-4 years experience in the medical device industry.
- Strong interpersonal and communication skills, with a proven ability to work effectively within a team.
Morgan McKinley is acting as an Employment Agency and references to pay rates are indicative.
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