REF 1730069
05.02.2025 | Umm Al Qaiwain | full time
Review documents to ensure they meet GMP and site SOP requirements. Identify, investigate, and prepare reports on quality issues. Perform line clearance, inspections, and physical testing in manufacturing areas.
Applicants 4
REF 1728701
04.02.2025 | Umm Al Qaiwain | full time
responsible for developing and implementing quality standards, policies, and procedures to ensure that pharmaceutical products are manufactured, tested, and released in compliance with regulatory requirements.
Applicants 4
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