Job Description
We are seeking an experienced Associate R&D Engineer to join our team.
Responsibilities:
* Plan and execute Design Verification testing in a GxP environment.
* Perform data analysis and test reporting.
* Collaborate on defining evaluation and testing strategies for product/process changes.
* Support regulatory submissions.
* Create and/or update component specifications.
* Investigate product complaints and analyze returned devices.
* Provide support for CAPA and Non-Conformance processes.
* Contribute to the project team to deliver key objectives, meeting performance, time, and cost targets.
* Liaise with external vendors/resources to achieve project goals.
* Write procedures, protocols, specifications, and reports.
* Understand physician techniques and clinical needs to develop product training materials.
Requirements:
* Honours degree in Mechanical or Biomedical Engineering or equivalent.
* Approximately 12 months experience in a medical device design or manufacturing environment.
* Design and technical ability based on fundamental engineering principles.
* Data review and statistical methods skills (e.g., Minitab).
* High level of technical writing and reporting skills.
* Strong work ethic, creative problem-solving, and capable of working on own initiative.