Job Reference: FRS45277
Job Duration: 12 months
Start date: ASAP
Description:
R&D Engineer
Wexford - 12 month Contract
My client, a leading medical device company based in Wexford is looking for a R&D Engineer to join their team.
The successful candidate will have the experience in R&D or process development preferably within a medical device setting. Within this position you will be required to provide support in developing, optimising, implementing, and validating components/elements of a medical device.
About the Role:
* 12 month Contract
* Attractive Salary & benefits package
*12 months + experience required
Responsibilities:
* Design: Design components of a medical device, translating intangible design inputs into tangible engineering specifications and drawings. Select appropriate materials, processes and vendors to achieve the design, and challenge these designs against design specifications, clinical use scenarios and international standards.Build test parts for engineering evaluation, pre-clinical studies and clinical studies.
* Process Development: assists in thedevelopment and optimization of processes to understand key process inputs and outputs, using statistic methods such as DOE asappropriate. Supports new process equipment and tooling development, including specification development, vendor selection and negotiation.
* Documentation: prepare work instructions and standard operating procedures (SOP), write technical documents andreports. Prepare raw material specifications and drawings. Assist in preparing verification and validation protocols and reports.
* Test Method Development: develop new engineering test methods and clinically relevant simulated use test methods in conjunction with R&D technicians; prepare and assist in the validation of test methods.
* Testing: perform lab bench testing, conduct engineering and competitor evaluations, development unit testing, and execute verification and validation activities.
Requirements:
* S. degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering or other related engineering discipline.
* 1-3 years of industrial experience in R&D or process development, preferably in medical device or other regulated FDA/QSR and ISO environment
* Experience in process validation (IQ, OQ and PQ), writing protocols and reports to support verification and validation activities for product commercialization; ability to assist in executing validation.
Next Steps:
APPLY TODAY! Contact Kerry Rickard for more information and to review the full job description
Industry: Manufacturing and Production
Salary:
Salary Benefits:
Vacancy Type: Contract
Job Skills: R&D, Biomedical Engineering, Testing, Validation
Contact Name: Kerry Rickard
Website: -
Direct Application URL: -