Position Details
About this role
This role supports manufacturing quality assurance, process improvements, and regulatory compliance within Abbott’s diagnostics manufacturing facilities.
Key Responsibilities
- Support quality issues
- Ensure regulatory compliance
- Implement process improvements
- Maintain device history records
- Perform verification and validation
Technical Overview
Involves quality system management, adherence to ISO and FDA standards, and documentation of verification and validation activities in a manufacturing setting.
Ideal Candidate
The ideal candidate is an entry-level manufacturing or engineering professional with at least 1 year of experience, familiar with quality systems, FDA regulations, and process improvements in a healthcare manufacturing environment.
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 relevant technical degree, Less than 1 year of manufacturing or engineering experience, Unfamiliarity with FDA or ISO standards
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