Position: Quality Control / Quality Assurance Professional in Pharmaceutical Analysis with FDA regulations
Experience: 2 to 5 Years
Max Budget : Max 9 LPA
Working Days: 5 Days
Shift Timings: 2:00 PM to 10:00 PM
Weekly Off: Saturday & Sunday
Work Location: Hitech City, Hyderabad – Onsite
Required Skills
Excellent written and verbal communication skills
Solid understanding of medical terminology and documentation standards
Familiarity with FDA regulations, documentation requirements, and compliance frameworks
Experience in identifying suspicious activities, conducting investigations, and recommending corrective actions
Ability to analyze complex information, identify root causes, and make sound decisions
Strong attention to detail and problem-solving capabilities
Investigative mindset with strong analytical skills
📌 ("Quality Control" OR "Quality Assurance" ) AND (Pharma OR Pharmaceutical ) AND (USFDA OR USFDA OR FDA OR "FDA regulations" OR "FDA compliance") AND (GMP OR cGMP OR GLP) AND ( CAPA )
🏢 WEBFURTHER INDIA
📍 Hyderabad
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.