Position Details
About this role
This role involves supporting manufacturing processes and equipment at suppliers for medical devices, ensuring quality, cost efficiency, and process validation.
Key Responsibilities
- Support supplier activities for capital equipment
- Collaborate on device issue investigations
- Lead process development projects
- Manage change requests and validation activities
- Ensure product quality and process improvements
Technical Overview
Focus on manufacturing process development, equipment support, validation, and quality assurance within a regulated healthcare environment, utilizing Six Sigma, data analytics, and risk management tools.
Ideal Candidate
The ideal candidate is a mid-level engineer with 3+ years of experience supporting manufacturing processes and equipment in a regulated healthcare or medical device environment. They possess strong problem-solving skills, familiarity with validation and risk management, and experience working with capital equipment and electronics manufacturing.
Must-Have Skills
Nice-to-Have Skills
Required Skills
Hard Skills
Soft Skills
Industry & Role
Keywords for Your Resume
Deal Breakers
Lack of engineering degree, Less than 3 years of relevant experience, No experience in regulated industry, Inability to travel up to 20%
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