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Hiring PV QA Principal Scientist
Alphanumeric
Remote
3–5 Years
PV QA
🏢 About Company
Alphanumeric Systems is a global provider of technology-enabled services for pharmaceutical and healthcare companies, focusing on pharmacovigilance, compliance, and digital solutions.
📋 Job Overview
- Role: PV QA Principal Scientist
- Location: Remote (India)
- Experience: 3–5 Years (PV) + QMS
- Domain: Pharmacovigilance Quality & Compliance
- Type: Full-Time
📌 Key Responsibilities
- Manage CAPA, deviations & non-conformances
- Perform Root Cause Analysis (RCA)
- Track quality metrics & risk indicators
- Support audits & compliance activities
- Work on PV systems (Argus, Veeva)
- Ensure data integrity & SOP adherence
🎓 Eligibility Criteria
- B.Pharm / M.Pharm / Life Sciences
- 3–5 years Pharmacovigilance experience
- 1–2 years QMS / CAPA / QA exposure
💻 Skills Required
- CAPA & Root Cause Analysis
- PV QMS & compliance
- ICH-GVP, FDA, EMA guidelines
- Argus / Veeva systems
- Audit readiness & risk management
💰 Salary & Benefits
- ₹12 – ₹22 LPA
- Work From Home
- Global pharma exposure
- Leadership growth in PV QA
📚 Internal Resources
🎯 Interview Tips
- Prepare CAPA & RCA scenarios
- Revise GVP guidelines
- Understand audit workflows
- Focus on PV quality systems
📌 Note Before You Apply:
Ensure you have PV + QMS experience before applying. This is a mid-level QA role.
Ensure you have PV + QMS experience before applying. This is a mid-level QA role.
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile and core expertise align with Pharmacovigilance Quality Assurance (PV QA) auditing, GVP compliance standards, global safety data quality management, corrective and preventive actions (CAPA) tracking, and health authority inspection readiness management before proceeding with your application.
Kindly read the full job description carefully before applying. Ensure your profile and core expertise align with Pharmacovigilance Quality Assurance (PV QA) auditing, GVP compliance standards, global safety data quality management, corrective and preventive actions (CAPA) tracking, and health authority inspection readiness management before proceeding with your application.
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