At MicroPort, the business problem is to ensure the quality and integrity of medical solutions by mastering every detail, with the purpose of prolonging and reshaping the lives of patients everywhere.
Requirements
- A working knowledge of basic computer skills
- Database management knowledge
- Ability to apply skills in a manner to ensure proper decisions for acceptance or rejection of goods is imperative.
- Visual acuity requirements apply to the role, including peripheral, color, and depth perception.
- Ability to work independently
- Ability to interface with peers, engineers, and Regulatory auditors.
- Ability to accurately record data results
Responsibilities
- Assure inspection is performed in accordance with FDA, ISO, and other applicable regulations / guidelines.
- Follow written instructions with engineering-based content.
- Apply attention to detail in documentation.
- Accurately record data results to ensure proper segregation of accepted and rejected products.
- Develop, update, and maintain Device History Record database
- Provide Certificate of Conformance (CoC) upon request
- Operate under the direction of QC Management team
Other
- Ability to follow instructions, both written and oral.
- Ability to work in a team environment.
- Professional communication skills.
- High School Diploma or GED required
- One year of related experience required for Technician role
