Navitas Lifesciences Hiring PV, SAS, CDM & Regulatory Roles

Mohit April 19, 2026
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Hiring PV, SAS, CDM & Regulatory Roles

🏢 Navitas
📍 Bangalore / Chennai
⏳ 0–8+ Years
💰 ₹3 – ₹20 LPA

Navitas Lifesciences is hiring for multiple roles across Pharmacovigilance, Regulatory Affairs, Clinical Data & SAS. This is a great opportunity for both freshers and experienced candidates.

💊 PV QA Auditor

  • Experience: 5+ Years PV + 3+ Years Auditing
  • GVP/GCP audits & compliance
  • CAPA & audit readiness
  • Global safety system evaluation

📊 Safety Specialist (Aggregate & Signal)

  • Experience: 3–6 Years
  • PSUR, PBRER, DSUR reports
  • Signal detection & risk management
  • Safety data analysis
  • PV Practice Quiz

📈 Clinical Data Analyst

  • Experience: 2.5–3 Years
  • Clinical data review & validation
  • SAS exposure preferred
  • Data reporting & analysis
  • CDM vs SAS Guide

💻 Senior SAS Programmer

  • Experience: 5–8+ Years
  • SDTM & ADaM dataset creation
  • TFL generation
  • SAS macro development
  • SAS PDV Guide

📄 Regulatory Associate / Jr Regulatory Associate

  • Experience: 0–3 Years
  • CTD/eCTD submissions
  • USFDA / EMA compliance
  • Document publishing & validation
  • Regulatory Guide

🎓 Eligibility

  • B.Pharm / M.Pharm / PharmD / MSc / BDS
  • Life Sciences / Engineering
  • Knowledge of ICH, GCP, GVP guidelines

💰 Salary & Growth

  • ₹3 – ₹20 LPA (based on role)
  • Global project exposure
  • Growth in PV, SAS & Regulatory domains
  • Salary Guide

💡 Interview Tips

  • Revise domain basics (PV / SAS / RA)
  • Focus on real project experience
  • Aptitude Practice

📩 Apply via Email

Send your resume to:

  • recruitment.bangalore@navitaslifesciences.com
  • recruitment.chennai@navitaslifesciences.com
  • recruitment.india@navitaslifesciences.com
📌 Tip: Mention role name in subject line to increase response chances.
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