Salary: Part-time, hourly rate contract
Job description:
This role involves leading quality assurance activities on projects, providing guidance on documentation and planning for product development. You will ensure that project teams follow quality systems and regulations, investigate material biocompatibility, and conduct risk assessments.
Required skills and qualifications:
* Minimum Bachelor's degree in Engineering or related field
* 6+ years of medical device design and development/quality assurance experience
* Ability to lead product verification & validation activities
Benefits:
Hybrid working arrangement, with the opportunity to work from home part-time.
Others:
You will interact with customer and supplier companies in a professional manner, proactively communicate to ensure an ongoing two-way exchange of information, and intervene in technical issues when they arise.