Skip to main content
Automatic Data Processing, Inc. seeks a Quality Specialist II to support the implementation and maintenance of the QMS in line with ISO 13485 and regulatory requirements. The role covers batch record review, incoming inspection, and document control to ensure product quality. Responsibilities include managing change control, material specifications, and quality records, while driving continuous improvement and cross-functional collaboration within a growing biotech manufacturing environment.

Also on the board Same function, level within a rung

Level

Senior

Location

San Diego, CA

Occupation

Quality Control Systems Managers

Industry

Biological Product Manufacturing

Posted

15 days ago

Apply for this role (opens in a new tab)