India's DMPLOI - Jobs & Networking AppLupin Limited, one of India’s leading pharmaceutical companies, has announced a Walk-In Interview Drive for experienced professionals in Production, Packing, Quality Control, QA Environmental Monitoring, and Microbiology QA functions. The recruitment drive is focused on candidates with experience in Nasal, Dermatology, MDI/DPI, and Sterile Ophthalmic formulations for its manufacturing facility located at Pithampur, Indore.
This is an excellent opportunity for candidates seeking career growth in a USFDA and MHRA-regulated pharmaceutical environment.
Walk-In Interview Details
Details
Company
Lupin Limited
Interview Type
Walk-In Interview
Interview Date
14 June 2026 (Sunday)
Timing
09:00 AM to 06:00 PM
Job Location
Pithampur, Indore
Interview Venue
Novotel Ahmedabad, Iscon Cross Roads, SG Highway, Ahmedabad, Gujarat – 380015
Contact Email
suhailkhan1@lupin.com
Mobile Number
9617733913
Open Positions
1. Production Filling Operator (Nasal & Derma)
Qualification: ITI / B.Sc / Diploma
Experience: Minimum 2 Years
Key Responsibilities
Handling nasal and topical formulation filling operations.
Operating bottle filling, capping, tube filling, and soft bag filling machines.
Working with equipment such as DARA, PKB, Marchesini, NORDEN, and IMA-PG systems.
Maintaining GMP-compliant production records.
2. Production Packing Operator (Nasal & Derma)
Qualification: ITI / B.Sc / Diploma
Experience: Minimum 2 Years
Key Responsibilities
Packing operations for nasal formulations.
Operating labeling, cartoning, printing, and scanning systems.
Managing batch packaging activities for nasal sprays, solutions, and suspensions.
Working in PAS-X based Electronic Batch Manufacturing Record (EBMR) systems.
3. Quality Control Officer/Executive (Nasal, Derma, MDI & DPI)
Qualification: B.Pharm / M.Sc
Experience: 2–10 Years
Key Responsibilities
Analysis of finished products using Assay, Related Substances, Spray Pattern, APSD, DDU, and FPM tests.
Operation and maintenance of HPLC, GC, UV Spectrophotometer, pH Meter, and Spray View systems.
Ensuring compliance with GMP, Data Integrity, and 21 CFR Part 11 requirements.
4. Quality Control Officer/Executive (Sterile Ophthalmic)
Qualification: B.Pharm / M.Sc
Experience: 2–10 Years
Key Responsibilities
Testing ophthalmic products for Assay, Related Substances, Dissolution, and Particle Size Distribution.
Operation of HPLC, GC, UV-Visible Spectrophotometer, Dissolution Apparatus, and Malvern Particle Size Analyzer.
Calibration and maintenance of analytical instruments.
Compliance with regulatory and quality standards.
5. QA Environmental Monitoring Officer
Qualification: M.Sc Microbiology
Experience: 2–6 Years
Key Responsibilities
Environmental monitoring in sterile manufacturing areas.
Review of microbiological data and media preparation records.
Autoclave cycle reconciliation and aseptic area monitoring.
Electronic data review and quality documentation management.
6. Microbiology QA Officer
Qualification: M.Sc Microbiology
Experience: 2–6 Years
Key Responsibilities
Trend analysis of microbiological data.
Environmental monitoring in aseptic and controlled areas.
Investigation of microbiological OOS events.
Review of sterility, BET, method validation, and stability study data.
Release and validation of analytical and microbiological studies.
Eligibility Criteria
Candidates must possess:
Updated Resume/CV
Last three salary slips
Latest increment/revision letter
Experience and relieving letters from previous organizations
Minimum 60% marks if total experience is below 5 years
Hands-on experience in Nasal, Derma, MDI, DPI, or Ophthalmic formulations
Note: Exposure to USFDA and MHRA regulated environments is mandatory.
Why Join Lupin?
Work in a globally recognized pharmaceutical organization.
Exposure to advanced manufacturing technologies.
Opportunity to work under USFDA and MHRA regulatory standards.
Career growth in specialized formulation and sterile manufacturing domains.
Learning opportunities with modern analytical and quality systems.
Technical FAQs
1. What is APSD testing in MDI/DPI products?
Aerodynamic Particle Size Distribution (APSD) measures the particle size distribution of inhalation products using instruments such as the Next Generation Impactor (NGI). It helps ensure efficient drug delivery to the lungs and compliance with regulatory requirements.
2. Why is 21 CFR Part 11 compliance important in pharmaceutical QC?
21 CFR Part 11 governs electronic records and electronic signatures. Compliance ensures data integrity, traceability, security, and acceptance of electronic records by regulatory authorities such as the USFDA.
3. What is Environmental Monitoring (EM) in sterile manufacturing?
Environmental Monitoring involves routine assessment of cleanroom conditions through viable and non-viable particle monitoring, surface monitoring, and personnel monitoring to ensure aseptic manufacturing conditions.
4. What is the purpose of Related Substances (RS) testing?
Related Substances testing identifies and quantifies impurities and degradation products in pharmaceutical formulations, ensuring product safety, efficacy, and compliance with pharmacopeial specifications.
5. What is BET testing in microbiology laboratories?
Bacterial Endotoxin Testing (BET) detects endotoxins from Gram-negative bacteria in sterile pharmaceutical products. It is critical for ensuring patient safety, especially for injectable and ophthalmic products.
Interested candidates meeting the eligibility criteria can attend the walk-in interview on 14 June 2026 at Novotel Ahmedabad and explore rewarding career opportunities with Lupin Limited.
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