What you need to know
A globally-renowned medical device company in Co. Offaly that is a leading manufacturer of highly specialised and cutting-edge medical devices for orthopaedic surgery, neurosurgery, reconstructive and general surgery, and regenerative wound care is currently seeking a driven and diligent Project Engineer to join its team.
As a Project Engineer, you will be responsible for overseeing various engineering and process improvement projects and offer technical support to manufacturing operations.
This is a permanent role with an excellent salary and package that includes pension, bonus, healthcare and opportunities for training and development.
Your new job
Key duties & responsibilities include:
Review obsolete component issues and lead the identification and specification review of alternatives and associated implementation efforts.
CAPA management and generation and adherence to GMP.
Communicate project status and escalate issues to the direct manager, program managers, and internal and external partners in a timely fashion.
To effectively manage the introduction of technology on product lines and process improvements.
Support other departments as required, e.g., assist in the analysis of customer returns, debug, root cause analysis, technical support for customers, conduct tests in the Laboratory, etc.
Actively contribute to the enhancement of compliance initiatives for areas of responsibility.
Develop strong links with the company’s other plants to ensure effective ongoing transfer and sharing of products, processes, and systems.
Develop process improvement projects to achieve the highest quality standards.
Provide technical leadership and a structured approach to problem-solving for operations personnel involved in process engineering and development activities.
What are we looking for?
Honours Degree in Electro-Mechanical, Electronic, Mechanical, or related Engineering discipline.
A minimum of three years' relevant experience in a regulated manufacturing environment.
Strong working knowledge of ISO 13485 and 21CFR820
Familiar with electro-mechanical systems design and debugging.
Innovative thinker that is solutions focused and can propose and deliver initiatives for new developments and continuous improvements.
Excellent communicator (oral and written) and is comfortable producing detailed reports.
A proven track record of leading and executing Process Validations.
Technical competency in reading schematics (both electrical and mechanical)
Strong team player who enjoys working in cross-functional teams to achieve collective company goals.
Excellent planning and organizational skills with the ability to consistently meet deadlines.
MS Office, including MS Project
Interested in this role?
Apply for this job now with a Word version of your CV or get in touch with Oliver at email@example.com
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