Job Description
The Quality Engineer II supports product and process quality within regulated environments such as medical device, biotech, or pharmaceutical manufacturing. The role focuses on validating processes, equipment, analytical methods, and facilities to ensure compliance with FDA and ISO regulations. The engineer also supports risk management activities, change controls, regulatory submissions, and cross‑functional product development efforts while maintaining validation documentation and quality systems.
Essential Duties and ResponsibilitiesReady to Apply?
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Submit ApplicationJob Details
- Location San Diego, California
- Job Type Full-time
- Category Engineers
- Posted Date June 19, 2026
- Application Deadline July 29, 2026