Position Details
About this role
This role involves providing quality engineering support for new medical device development, ensuring compliance with industry standards, and supporting product lifecycle activities.
Key Responsibilities
- Support product development
- Ensure regulatory compliance
- Review development activities
- Support post-market surveillance
- Maintain quality standards
Technical Overview
Technical scope includes quality assurance, design control, verification and validation, and regulatory compliance for medical devices.
Ideal Candidate
The ideal candidate is a quality engineer with experience in medical device development, supporting product launches, and ensuring compliance with GMP and ISO standards. Strong leadership and regulatory knowledge are essential.
Must-Have Skills
Nice-to-Have Skills
Tools & Platforms
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of experience with medical devices, No knowledge of GMP or ISO standards, Unable to support product development lifecycle
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