Apply now for Lupin Quality Assurance Executive role in Indore. High-paying pharma QA job with 10 LPA salary, USFDA & MHRA compliance, SAP, QUMAS expertise.
Lupin Limited Hiring Executive for Quality Assurance (Documentation Cell Management) – Apply Now for High Paying Pharma QA Jobs
In 2025, the Indian pharmaceutical sector continues its global dominance, with Lupin Limited leading the charge in delivering high-quality, compliant, and innovative pharmaceutical solutions. Lupin is now hiring experienced professionals for its Quality Assurance (Documentation Cell Management) department at Pithampur, Indore, Madhya Pradesh.
This is a golden opportunity for experienced pharma QA professionals looking to advance their careers with one of India’s most respected multinational pharmaceutical giants. With lucrative salary packages, global regulatory exposure, and professional growth, this position offers everything pharmaceutical quality assurance professionals desire in a high-paying, stable career.
🌟 About Lupin Limited
Lupin Limited is a global pharmaceutical leader known for its consistent commitment to innovation, patient-centric solutions, and regulatory excellence. With operations spanning across over 100 countries and robust regulatory approvals from top global agencies like USFDA, MHRA, EMA, and TGA, Lupin stands as a beacon of trust and compliance.
The company is deeply invested in cutting-edge research, stringent quality standards, and a corporate culture that emphasizes continuous learning, professional growth, and ethical excellence. Joining Lupin means becoming part of a globally recognized organization at the forefront of pharmaceutical manufacturing, compliance, and regulatory leadership.
📍 Job Position Details
-
Position: Executive – Quality Assurance (Documentation Cell Management)
-
Department: Quality Assurance
-
Location: Pithampur, Indore, Madhya Pradesh
-
Industry: Pharmaceuticals / Life Sciences / Biopharma
-
Salary: Up to ₹10 LPA
-
Experience Required: 8–10 Years
-
Qualification: B. Pharma / M.Sc
🎯 Key Responsibilities
📄 Master Documentation Preparation
-
Prepare, review, and issue master documents including:
-
Site Master Files (SMF)
-
Batch Manufacturing Records (BMR)
-
Batch Packaging Records (BPR)
-
-
Upload and manage documents using advanced electronic document management systems (e-DMS) such as SAP, QUMAS, and Artwork Management tools.
-
Coordinate document sharing with regulatory authorities, external partners, and internal departments ensuring full traceability.
🗄 Document Distribution & Archival
-
Control distribution of master documents across departments, vendor sites, and cross-functional teams.
-
Oversee archival processes, ensuring secure storage of documents per regulatory requirements.
-
Manage document lifecycle from issuance to secure destruction, maintaining full traceability.
🔍 Regulatory Compliance & Submission Support
-
Ensure full compliance with USFDA, MHRA, EMA, and other international regulatory standards.
-
Support Regulatory Affairs in dossier preparation by collecting, scanning, and submitting all necessary documentation.
-
Participate in internal audits, self-inspections, and regulatory inspections, ensuring inspection readiness at all times.
💻 Electronic Document Management
-
Operate advanced e-DMS platforms:
-
SAP Document Management System
-
QUMAS Document Control
-
Artwork Management Tools
-
-
Manage document revision cycles, controlled issuance, labeling, and record uploads.
-
Maintain audit trails for full data integrity compliance.
🔬 Data Integrity & ALCOA++ Principles
-
Enforce Good Documentation Practices (GDP).
-
Implement ALCOA++ principles ensuring all data is:
-
Attributable
-
Legible
-
Contemporaneous
-
Original
-
Accurate
-
Complete
-
Consistent
-
Enduring
-
Available
-
🔐 Logbooks & Certificates Management
-
Issue and control department-wise logbooks.
-
Prepare and release Certificates of Analysis (CoA) and Certificates of Conformance (CoC) for commercial and exhibit batches.
-
Control reprint annexures for executed batch documentation.
🏷 Retention Sample Room Management
-
Oversee the Retention Sample Room ensuring compliance with all sample storage protocols.
-
Manage inventory records and ensure availability for regulatory audits.
🏆 Why Choose Lupin Limited for Your QA Career?
Lupin offers more than just a job — it offers a future:
-
Global Regulatory Exposure: Work directly with international regulatory bodies including USFDA, MHRA, EMA, WHO-GMP.
-
Cutting-Edge Technology: Hands-on experience with top-tier document management platforms like SAP, QUMAS, and advanced LIMS systems.
-
Competitive Compensation: Earn up to ₹10 LPA with performance-based growth opportunities.
-
High Job Security: Pharma QA remains one of the most stable, recession-proof industries.
-
Continuous Learning: Internal training, certifications, and professional development programs to enhance your expertise.
-
Work-Life Balance: Ethical work culture, supportive leadership, and a collaborative environment.
-
Global Pharma Career Launchpad: Opportunities to grow into international regulatory, compliance, and leadership roles.
💡 Who Should Apply?
If you meet the following criteria, apply today:
✅ Minimum 8 years experience in regulated pharma QA
✅ Hands-on experience with document control systems (SAP/QUMAS)
✅ Exposure to international regulatory bodies (USFDA/MHRA/EMA)
✅ Strong knowledge of GDP, ALCOA++, and data integrity principles
✅ B. Pharma / M.Sc degree holders
📧 How to Apply
Qualified candidates are invited to submit their updated resume along with all relevant experience and relieving documents to:
Email 1: suhailkhan1@lupin.com
Email 2: parichayindore@lupin.com
Official Website: www.lupin.com
