Lupin Limited is conducting a walk-in interview in Panchkula on 26 and 27 September 2026 for experienced pharmaceutical professionals in Quality Control (QC) and Quality Assurance (QA). The selected candidates will be based at Pithampur, Indore, with opportunities across QC Formulation, QC API and QA API functions.
The walk-in interview is open to candidates with B.Pharm or M.Sc. qualifications and relevant pharmaceutical quality experience. Positions are available at Officer and Executive levels, with experience requirements ranging from 2 to 10 years, depending on the position.
Lupin is a pharmaceutical company with operations spanning generics, complex formulations, branded products and other healthcare segments. Its official website confirms its substantial manufacturing and R&D footprint in India.
Lupin Walk-In Interview 2026 – Key Details
| Particular | Details |
|---|---|
| Company | Lupin Limited |
| Interview Type | Walk-In Interview |
| Interview Dates | 26 & 27 September 2026 |
| Days | Saturday & Sunday |
| Interview Time | 9:00 AM – 6:00 PM |
| Interview Location | Panchkula |
| Venue | Hotel KC Cross Road, Panchkula |
| Job Location | Pithampur, Indore |
| Departments | QC Formulation, QC API, QA API |
| Qualification | B.Pharm / M.Sc |
| Experience | 2–10 years for QC; 3–5 years for specified QA/QC API roles |
| Employment Type | Full-time |
| Contact Email | suhailkhanl@lupin.com |
| Contact Number | 9617733913 |
Available Positions at Lupin
1. Officer / Executive – QC Formulation
Experience: 2–10 years
Qualification: B.Pharm / M.Sc
Location: Pithampur, Indore
The role covers quality control activities for pharmaceutical formulations, including finished-product and in-process testing.
Candidates may work with products and analytical requirements involving:
- Nasal formulations
- Dermatological formulations
- MDI products
- DPI products
- Finished-product analysis
- In-process testing
- Pharmaceutical analytical testing
2. QC Formulation – Nasal / Derma / MDI & DPI
Candidates should have experience with analytical testing such as:
- Assay
- Related substances (RS)
- Spray Content Uniformity (SCU)
- Spray pattern
- Aerodynamic Particle Size Distribution (APSD)
- Next Generation Impactor (NGI)
- Delivered Dose Uniformity (DDU)
- Fine Particle Mass (FPM)
- Physical testing
The position also involves operating and maintaining laboratory instruments including:
- HPLC
- GC with Chromeleon
- UV spectroscopy
- pH meter
- Spray View and related analytical equipment
Candidates are expected to follow GMP, data integrity and 21 CFR Part 11 requirements while maintaining accurate QC documentation.
3. QC Formulation – OSD Stability Section
Experience: 2–10 years
Qualification: B.Pharm / M.Sc
Responsibilities include:
- In-process testing
- Holding-time testing
- Stability testing
- API and formulation-product analysis
- HPLC analysis
- UV analysis
- GC analysis
- IR analysis
- Polarimeter analysis
- Dissolution testing
- Stability study documentation
- OOS/OOT investigation support
- Laboratory documentation according to CGMP and GLP
- Compliance with data-integrity requirements
The selected professional will also be responsible for performing stability testing according to approved protocols and ensuring timely completion and reporting of stability studies.
4. QC Formulation – OSD Finished Goods / In-Process
Experience: 2–10 years
Qualification: B.Pharm / M.Sc
Key responsibilities include:
- Finished-product analysis for OSD formulations
- In-process testing
- HPLC, GC and UV analysis
- Operation of pharmaceutical analytical instruments
- Pharmaceutical quality-system activities
- LIMS/QAMS/SAP usage
- OOS investigation
- OOT investigation
- Laboratory deviation handling
- QC documentation and compliance
Experience with pharmaceutical quality systems and computerized laboratory systems can be relevant for this position.
5. QC API / QA API – Officer
Experience: 3–5 years
Qualification: B.Pharm / M.Sc
The QC/QA API position includes responsibilities related to pharmaceutical quality systems and manufacturing-quality activities.
Key responsibilities include:
- QMS activities
- Quality Risk Management (QRM)
- IPQA checks
- Line clearance
- Process validation
- Cleaning-sampling activities
- BPR review
- BMR review
- Cleaning-record review
- Computer System Validation (CSV) verification
- cGMP compliance
- Documentation review and accuracy
Mandatory Regulatory Experience
For the specified QA API position, US FDA (USFDA) and MHRA regulated-market exposure is mandatory.
According to the supplied hiring information, candidates without regulated-market exposure will not be considered.
Educational Qualification
Candidates applying for the Lupin QC and QA vacancies should generally have:
- B.Pharm, or
- M.Sc
Experience requirements vary according to the position, with several QC roles requiring 2–10 years of experience, while the specified QC/QA API opportunity requires 3–5 years.
For candidates with less than five years of experience, the supplied eligibility criteria specify that 60% marks are mandatory.
Skills Required for Lupin QC & QA Jobs
Relevant skills for these pharmaceutical quality roles include:
- Quality Control
- Quality Assurance
- Pharmaceutical formulation analysis
- API analysis
- HPLC
- GC
- UV spectroscopy
- IR
- Dissolution testing
- Stability testing
- OOS investigation
- OOT investigation
- Laboratory deviation management
- GMP
- CGMP
- GLP
- Data integrity
- 21 CFR Part 11
- LIMS
- QAMS
- SAP
- QMS
- QRM
- IPQA
- Process validation
- Cleaning validation/sampling
- BMR/BPR review
- CSV
- USFDA-regulated market exposure
- MHRA-regulated market exposure
Documents Required for the Walk-In Interview
Candidates attending the Lupin walk-in interview in Panchkula should carry the following documents:
- Latest updated resume
- Last three salary slips
- Revision/increment letter
- Relieving letters from all previous organizations
Candidates should ensure that their resume clearly highlights their pharmaceutical QC/QA experience, analytical-instrument exposure, formulation/API experience and regulated-market experience where applicable.
Lupin Walk-In Interview Eligibility
Before attending, candidates should carefully check the following conditions:
- Relevant B.Pharm or M.Sc qualification
- Required years of pharmaceutical experience
- Relevant QC or QA experience
- 60% marks where applicable for candidates with less than five years of experience
- USFDA and MHRA exposure for the specified regulated-market position
- Candidates interviewed by Lupin during the previous six months are not eligible
- Required employment and salary documents should be available
Interview Venue and Schedule
Hotel KC Cross Road
Panchkula
Date: 26 & 27 September 2026
Day: Saturday & Sunday
Time: 9:00 AM to 6:00 PM
Job Location after selection: Pithampur, Indore
Candidates should verify the venue and hiring details before travelling, particularly because the walk-in interview is scheduled for a limited two-day period.
How to Apply for Lupin Walk-In Interview
Eligible candidates can attend the walk-in interview at the specified venue in Panchkula on 26 or 27 September 2026 between 9:00 AM and 6:00 PM.
Candidates should carry their latest resume and the required supporting documents.
Email: suhailkhanl@lupin.com
