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)

26 Oct
|
GC Technologies
|
Hyderabad

26 Oct

GC Technologies

Hyderabad

Interview Process: F2F Only in Hyderabad Manager Round Technical Round Client Round Share ur CV on WhatsApp: (phone hidden) 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 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 robust 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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