Position: QA Validation Associate II
Location: Central Islip, New York, USA
Job Type: Full-Time | On-Site
Experience Required: 35 years
Shift: Monday to Friday, 8:30 AM 5:00 PM
Position Overview
We are seeking a highly detail-oriented QA Validation Associate II to join our Quality Assurance team. The successful candidate will support GMP documentation review, ensure compliance with regulatory and industry standards, and assist with continuous quality improvements for manufacturing and release processes of drug substances and products.
Key Responsibilities
Qualifications
Physical Requirements
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