Regulatory Affairs Associate : FDA submissions, regulatory documentation, compliance (Hyderabad)

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 solid analytical skills