Stallion Laboratories Pvt. Ltd., a USFDA and UK-MHRA accredited pharmaceutical leader since 1988, invites professionals with USFDA OSD facility experience to a walk-in interview on July 26, 2025, at our Unit-II, Ahmedabad. Join our mission to deliver innovative, high-quality formulations globally!
Why Join Stallion Laboratories?
Our WHO-GMP certified facility in Ahmedabad ensures top-tier quality in oral solid dosage (OSD) manufacturing. With USFDA and UK-MHRA approvals, we’re set to enter regulated markets. Stallion offers a dynamic, growth-oriented environment for professionals passionate about pharmaceutical excellence. Be part of our legacy of innovation!
Open Positions at OSD Formulation Facility (Unit-II)
We’re hiring for key roles at our USFDA-approved OSD facility in Ahmedabad. Only candidates with USFDA OSD experience are eligible. Preferred local candidates. Below are the openings:
Packing (OSD)
- Designation: Officer/Sr. Officer
- Qualification: M.Sc/M.Pharma/B.Pharma
- Experience: 3-7 years
- Skills: Primary/secondary packing, line clearance, BPR review, packing activities.
Quality Control (QC)
- Designation: Officer/Sr. Officer
- Qualification: M.Sc/M.Pharma/B.Pharma
- Experience: 2-5 years
- Skills: Routine analysis, QMS, LIMS, GLP compliance.
Quality Assurance (QA)
- Designation: Executive/Asst. Manager (AQA), Officer/Sr. Officer (IPQA)
- Qualification: M.Sc/M.Pharma/B.Pharma
- Experience: 6-10 years (AQA), 3-5 years (IPQA)
- Skills: AQA, APQR, stability, QMS, IPQA.
Analytical Development Lab (ADL)
- Designation: Sr. Officer/Executive
- Qualification: M.Sc/M.Pharma/B.Pharma
- Experience: 5-8 years
- Skills: AMD, AMV, routine analysis, HPLC.
Walk-In Interview Details
Join us for our walk-in interview:
- Date: July 26, 2025
- Time: 9:00 AM to 2:00 PM
- Venue: Stallion Laboratories Pvt. Ltd., Unit-II, Plot No. D-4,5,6,17,18,19, Gallops Industrial Park II, Vasna Chacharwadi, Ahmedabad-382110, Gujarat
- Contact: darshan.mistry@stallionlabs.com (+91 8849396973), aarti.oberoi@stallionlabs.com (+91 9409309964)

Note: Bring latest resume, CTC break-up, photo. Immediate joiners preferred. Candidates interviewed in the last 6 months are ineligible.
Why Work in OSD Manufacturing?
The OSD market is thriving, driven by global demand for generics. Stallion’s USFDA-approved facility in Ahmedabad, with a 2.2 billion tablet/capsule capacity, offers cutting-edge technology and compliance with 21 CFR standards. Contribute to life-changing medicines in a high-growth sector!
Qualifications and Skills
Eligibility:
- Education: M.Sc, M.Pharma, or B.Pharma from recognized institutions.
- Experience: Exclusive USFDA OSD facility experience (2-10 years, role-dependent).
- Skills: Expertise in HPLC, QMS, LIMS, AMV/AMD, or packing operations.
- Note: Only candidates with relevant OSD experience should apply.
How to Prepare for the Interview
To excel at the interview:
- Update your resume highlighting USFDA OSD experience.
- Bring CTC break-up, photo, and relevant certificates.
- Be ready to discuss HPLC, QMS, or packing processes.
- Learn about Stallion’s achievements at Stallion Laboratories.
About Stallion Laboratories
Founded in 1988, Stallion Laboratories is a global pharmaceutical manufacturer specializing in OSD formulations. Our Ahmedabad Unit-II is USFDA and UK-MHRA accredited, with plans for EU GMP approval. We export to over 20 countries, ensuring quality and innovation.
Take the Next Step
Don’t miss the July 26, 2025, walk-in interview at Gallops Industrial Park II, Ahmedabad. Join Stallion Laboratories to advance your career in pharmaceutical manufacturing. Unable to attend? Email resumes to darshan.mistry@stallionlabs.com or aarti.oberoi@stallionlabs.com. We look forward to meeting you!