Discover lucrative pharma jobs in Ahmedabad! Attend Stallion Laboratories walk-in interview on 22nd November 2025 for Production and QC roles in a USFDA-approved OSD unit.
Contents
About the Company
Stallion Laboratories Pvt. Ltd., established in 1988, is a prominent pharmaceutical formulation manufacturer with WHO-GMP certified facilities and a strong commitment to quality excellence. Its Unit-II is a state-of-the-art USFDA and UK-MHRA approved oral solid dosage (OSD) facility, with EU-GMP certification in progress.
Renowned for innovation, niche generics, and zero-compromise regulatory compliance, Stallion Laboratories offers rewarding pharmaceutical careers in India focused on global regulated markets.
Job Details
- Company Name: Stallion Laboratories Pvt. Ltd.
- Experience: 2 to 5 Years
- Qualification: B.Sc, Diploma, ITI, M.Sc (Chemistry)
- Location: Gallops Industrial Park-2, Vasna Chacharwadi, Sarkhej-Bavla Road, Ahmedabad, Gujarat – 382220
- Work Type: On-site
Job Description
Stallion Laboratories Unit-II, a fully USFDA & UK-MHRA approved OSD formulation plant, is conducting urgent hiring for experienced professionals in Production and Quality Control departments. These production jobs and QC jobs demand proven expertise in regulated environments and offer immediate opportunities in one of India’s leading pharmaceutical companies.
Production Operator / FTE
- Department: Production (OSD)
- Market: Regulated (USFDA, UK-MHRA, EU-GMP)
- Role: Operator / Fit-for-Execution (FTE)
- Experience: 2–5 years in USFDA-approved OSD facility
- Education/Qualification: B.Sc / Diploma / ITI
Quality Control Officer / Sr. Officer
- Department: Quality Control
- Market: Regulated (USFDA, UK-MHRA, EU-GMP)
- Role: Officer / Senior Officer – HPLC Analysis
- Experience: 2–5 years in USFDA-approved OSD facility
- Education/Qualification: M.Sc (Chemistry)
Skills/Qualifications
- Mandatory 2–5 years hands-on experience only in USFDA-approved OSD facilities
- Expertise in Tablet Compression, Coating, Capsule Filling, or Packing (CVC Line) – Production roles
- Proficiency in HPLC analysis and finished product testing – QC roles
- In-depth knowledge of USFDA, UK-MHRA, and EU-GMP guidelines
- Strong documentation practices and cGMP compliance
- Immediate joining capability preferred
- Preference for local candidates from Ahmedabad/Gujarat
Key Responsibilities
- Operate compression, coating, capsule filling, and packing lines
- Perform in-process checks and troubleshooting
- Execute HPLC analysis and stability testing
- Maintain accurate batch records and logbooks
- Ensure strict regulatory and cGMP compliance
- Support validation activities and audit readiness
Benefits/Perks
- Work in cutting-edge USFDA & UK-MHRA approved facility
- Fast-track career growth in regulated markets
- Exposure to upcoming EU-GMP operations
- Competitive salary with timely appraisals
- Stable, professional, and recognition-driven work culture
- Valuable global market experience and long-term stability
How to Apply
Eligible candidates are requested to carry an updated resume, latest CTC break-up, and a passport-size photograph. You can also email your profile to darshan.mistry@stallionlabs.com or jagdish.mathukiya@stallionlabs.com.
For quick application, submit your resume through India’s leading pharma job portal – Pharma Recruiter. Don’t miss this chance to advance your pharmaceutical career in India!
Walk-in Interview Details
- Date: 22 November 2025 (Saturday)
- Time: 09:00 AM to 02:00 PM
- Venue: Stallion Laboratories Pvt. Ltd., Unit-II, Plot No. D-4,5,6,17,18,19, Gallops Industrial Park II, Vasna Chacharwadi, Dist-Ahmedabad-382 110, Gujarat, India
- Contact/Email:darshan.mistry@stallionlabs.com | jagdish.mathukiya@stallionlabs.com | +91 9998836672
Why You Should Join
With over 35 years of excellence in pharmaceutical manufacturing, Stallion Laboratories provides a culture of learning, innovation, and strict compliance. Employees gain unparalleled exposure to highly regulated markets, rapid career progression, and the pride of contributing to global healthcare. Joining Stallion means securing long-term stability and becoming part of an organization poised for strong growth in the US, UK, and EU markets.
FAQs
Is experience from non-USFDA plants acceptable?
No. Only candidates with 2–5 years in USFDA-approved OSD facilities are eligible.
Can freshers apply for these pharma jobs?
No. Minimum 2 years and maximum 5 years of relevant regulated experience is mandatory.
I attended an interview at Stallion in the last 6 months. Am I eligible?
Candidates who appeared for an interview in the last 6 months are not eligible.
Is relocation support provided for candidates outside Gujarat?
Preference is strictly for local Ahmedabad/Gujarat candidates; relocation candidates may not be considered.
Take the next step in your pharmaceutical career – mark your calendar for 22nd November 2025 and walk in to join Stallion Laboratories today!