12-Month Contract Opportunity
A Manufacturing Engineer position is available at a Medical Device Manufacturer in Cork. The role involves the introduction and validation of new equipment.
This is a full-time, on-site position with a variety of responsibilities.
Key Responsibilities:
* Develop and implement 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.
Requirements:
* Bachelor's degree in Engineering, Manufacturing, Mechanical or a related field.
* In-depth knowledge of medical device manufacturing and validation processes.
* 2-4 years of experience in the medical device industry.
* Strong interpersonal and communication skills, with a proven ability to work effectively within a team.