Regulatory Affairs Associate : FDA submissions, regulatory documentation, compliance
webfurther india pvt. ltd.- Posted an hour ago
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Job Description
Interview Process: F2F Only at Hyderabad
Manager Round
Technical Round
Client Round
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Client: WebFurther India Pvt. Ltd.
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
Strong 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
More Info
Key Skills
Experience in identifying suspicious activities conducting investigations and recommending corrective actions
Familiarity with FDA regulations documentation requirements and compliance frameworks
Strong attention to detail and problem-solving capabilities
Investigative mindset with strong analytical skills
Ability to analyze complex information identify root causes and make sound decisions
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