Stallion Laboratories Pvt. Ltd. is conducting a walk-in interview on 24 October 2026 (Saturday) for multiple positions at its OSD Formulation Facility, Unit-II. The openings are available across Quality Control (QC), Analytical Development Laboratory (ADL), and production planning.
Candidates with relevant pharmaceutical qualifications and experience can attend the interview at the company’s corporate office in Ahmedabad, Gujarat.
Job Details
| Particulars | Details |
|---|---|
| Company | Stallion Laboratories Pvt. Ltd. |
| Interview Type | Walk-in Interview |
| Interview Date | 24 October 2026 (Saturday) |
| Interview Time | 9:00 AM to 2:00 PM |
| Facility | OSD Formulation Facility – Unit-II |
| Location | Ahmedabad, Gujarat |
| Qualification | M.Pharm / B.Pharm / M.Sc. |
| Website | www.stallionlabs.com |
Positions Available at Stallion Laboratories
The company is hiring candidates for the following positions:
| Department | Designation | Experience | Required Skills / Area |
|---|---|---|---|
| QC | Officer / Senior Officer | 2–4 years | AMV / AMT / QC Documentation |
| QC | Officer / Senior Officer | 2–4 years | HPLC Analysis / GC Operations |
| QC | Executive | 6–8 years | GLP Documentation & LIMS Master |
| ADL | AM / DM | 10–14 years | Method Development / Method Validation / Cleaning Validation |
| Production Planning | Executive | 6–8 years | RM/PM Section & FG/FP Planning |
Eligibility and Qualifications
Candidates with the following qualifications can apply:
- Master of Pharmacy (M.Pharm)
- Bachelor of Pharmacy (B.Pharm)
- Master of Science (M.Sc.)
Applicants should have relevant experience for their preferred position, ranging from 2 to 14 years, depending on the role.
Required Skills
Quality Control (QC)
- Analytical Method Validation (AMV) / AMT
- QC documentation
- HPLC analysis
- Gas Chromatography (GC) operations
- GLP documentation
- LIMS Master
Candidates applying for the GLP Documentation and LIMS Master position should have knowledge of Specifications (SPECS), Standard Testing Procedures (STPs), and Test Data Procedures (TDPs).
Analytical Development Laboratory (ADL)
- Method development
- Method validation
- Cleaning validation
Production Planning
- Raw Material (RM) and Packaging Material (PM) section
- Finished Goods (FG) and Finished Products (FP) planning
About Stallion Laboratories
Stallion Laboratories was incorporated in 1988 as an integrated private-sector pharmaceutical formulation manufacturer. The company has a WHO CMP-approved production facility and GLP-qualified quality control operations.
Its Unit-II facility is US FDA and UK-MHRA approved and is proposed to be EU GMP approved.
Walk-In Interview Details
Date: 24 October 2026 (Saturday)
Time: 9:00 AM to 2:00 PM
Venue:
Stallion Laboratories Corporate Office
17, 8th Floor, Devpath, Off C. G. Road,
Behind Lal Bunglow, Near Supermall,
Ahmedabad – 380006, Gujarat.
Documents to Carry
Candidates attending the walk-in interview should bring:
- A copy of their latest resume
- CTC breakup
- Photograph
Immediate joining will be preferred.
Unable to Attend the Walk-In Interview?
Candidates who cannot attend the interview can share their resumes through email:
- Paresh Patel: paresh.patel@stallionlabs.com
- Aarti Oberoi: aarti.oberoi@stallionlabs.com