Jubilant Pharma Limited is actively hiring for Executive-QC and Research Trainee (Regulatory Affairs) roles at its advanced manufacturing and R&D facilities in India. This is a strong opportunity for B.Pharm, M.Pharm, MSc candidates looking to build careers in Quality Control (QC) and Regulatory Affairs (RA) within a USFDA-approved pharma environment.
With global regulatory approvals (USFDA, MHRA, PMDA, WHO), Jubilant Generics offers exposure to API manufacturing, analytical validation, and global regulatory filings—making it a high-value career move for pharma professionals.
🔍 Job Overview
1. Executive – Quality Control (QC)
- Location: Roorkee, Uttarakhand
- Department: Quality Control
- Experience: 1–5 Years (Typical Industry Range)
2. Research Trainee – Regulatory Affairs
- Location: Greater Noida, Uttar Pradesh
- Department: Regulatory Affairs
- Experience: Freshers / Entry-Level
🧪 Key Responsibilities
QC Executive Role
- Technology transfer from ARD to QC
- Analytical method development & validation
- Cleaning validation as per regulatory standards
- Review of analytical raw data & records (In-process & Finished Products)
- Preparation of validation protocols
- Ensure cGMP & GLP compliance
- Maintain error-free documentation
Regulatory Affairs Trainee Role
- Assist in regulatory documentation & submissions
- Support dossier preparation (CTD/eCTD basics)
- Exposure to global regulatory guidelines (USFDA, EMA)
- Work with cross-functional R&D and QA teams
🎓 Qualifications Required
- B.Pharm / M.Pharm / MSc (Chemistry / Life Sciences)
- Strong understanding of:
- cGMP / GLP guidelines
- Analytical techniques (HPLC, GC – for QC role)
- Regulatory frameworks (for RA role)
- Freshers can apply for Research Trainee role
💰 Salary & Benefits (Estimated)
- QC Executive: ₹3.5 – ₹7 LPA
- RA Trainee: ₹2 – ₹3.5 LPA
Additional Benefits
- Work in USFDA-approved facility
- Exposure to global regulatory audits
- Career growth in QC / RA domain
- Training in analytical & regulatory systems
🌍 Why Join Jubilant Generics?
- Global presence in APIs & formulations
- Strong R&D ecosystem (500+ scientists)
- Regulatory approvals across US, EU, Japan
- High-growth pharma manufacturing company
📩 How to Apply
Application Link For Executive – Quality Control (QC)
Application Link For Research Trainee – Regulatory Affairs

