USFDA, Pharmaceutical QA, Quality Complaints, Complaint Investigation, Risk Assessment, Regulatory Compliance, CAPA, Healthcare BPO, International Clients, US Clients, UK Clients. (Hyderabad)

USFDA, Pharmaceutical QA, Quality Complaints, Complaint Investigation, Risk Assessment, Regulatory Compliance, CAPA, Healthcare BPO, International Clients, US Clients, UK Clients. (Hyderabad)

27 Oct
|
GC Technologies
|
Hyderabad

27 Oct

GC Technologies

Hyderabad

Interview Process: F2F Only in Hyderabad

Manager Round

Technical Round

Client Round

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Client: MNC

Position: USFDA, FDA Guidelines, Pharmaceutical QA, Quality Complaints, Complaint Investigation, Risk Assessment, Regulatory Compliance, CAPA, Root Cause Analysis, Healthcare BPO, International Clients, US Clients, UK Clients.

Experience: 1 to 5 Years

Max Budget : Max 8 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

📌 USFDA, Pharmaceutical QA, Quality Complaints, Complaint Investigation, Risk Assessment, Regulatory Compliance, CAPA, Healthcare BPO, International Clients, US Clients, UK Clients. (Hyderabad)
🏢 GC Technologies
📍 Hyderabad

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