Stallion Laboratories Pvt. Ltd., established in 1988, is a leading pharmaceutical formulation manufacturer with a strong foothold in regulated markets. The company operates a WHO GMP-approved production facility and GLP-qualified quality control labs. Their Unit-II facility is USFDA and UK MHRA approved and is on track for EU GMP certification. This unit specializes in Oral Solid Dosage (OSD) formulations and aims to expand its presence in global regulated markets.
Job Openings at USFDA OSD Facility – Unit-II
Location: Gallops Industrial Park-2, Sarkhej-Bavla Road, Dist-Ahmedabad 382220
Preference: Local candidates only
| S.No | Department | Qualification | Experience | Designation | Skills | Open Positions |
|---|---|---|---|---|---|---|
| 1 | QC | M.Sc / M.Pharma / B.Pharma | 8 to 10 Years | Sr. Executive / Executive Reviewer | Reviewer | 3 |
| 2 | QC | M.Sc / M.Pharma / B.Pharma | 2 to 5 Years | Officer / Sr. Officer | Analyst HPLC/GC | 6 |
| 3 | QC | M.Sc / M.Pharma / B.Pharma | Fresher | Trainee | Analyst Micro | 3 |
| 4 | QC | M.Sc / M.Pharma / B.Pharma | Fresher | Trainee | Analyst Chemical | 4 |
| 5 | IT / Admin | ITI-COPA / BCA | 2 to 5 Years | Officer / Sr. Officer | Computer Operator | 3 |
Job Description
- Sr. Executive / Executive Reviewer (QC): Responsible for reviewing quality control data, ensuring compliance with USFDA regulations, and maintaining documentation accuracy.
- Officer / Sr. Officer Analyst (HPLC/GC): Conduct analytical testing using HPLC and GC instruments, maintain lab equipment, and ensure data integrity.
- Trainee Analyst (Micro & Chemical): Assist in microbiological and chemical analysis under supervision, learn SOPs, and support quality assurance activities.
- Officer / Sr. Officer Computer Operator: Manage data entry, maintain electronic records, and support IT-related tasks within the OSD facility.
Why Join Stallion Laboratories?
- Work in a USFDA-approved OSD formulation facility.
- Opportunity to grow in a company expanding into regulated global markets.
- Exposure to advanced pharmaceutical manufacturing and quality control processes.
- Immediate joining preferred for selected candidates.
How to Apply
Interested candidates with relevant experience in USFDA OSD facilities only should walk in for the interview with the following documents:
- Updated Resume
- CTC Break-up
- Recent Photograph
Note:
- Candidates who appeared in the last 6 months are not eligible.
- Immediate joining candidates will be preferred.
- If unable to attend the walk-in, share your resume at:
Email: aarti.oberoi@stallionlabs.com
Contact: +91 9409309964
