Stallion Laboratories is conducting a walk-in interview on 18 April 2026 for multiple pharma jobs in Production, QC, QA, Warehouse, Packing, and more at its USFDA & UK-MHRA approved OSD Formulation facility. Explore exciting pharmaceutical careers in India with immediate joining preference.
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About the Company
Stallion Laboratories Pvt. Ltd., incorporated in 1988, is a leading integrated private sector pharmaceutical formulation manufacturer based in Ahmedabad, Gujarat. The company has built an unmatched reputation for managing niche products with a strong focus on creativity and uncompromising quality.
Its WHO GMP-approved facilities and GLP-qualified quality control systems reflect a commitment to excellence. Unit-II, a state-of-the-art USFDA and UK-MHRA approved OSD (Oral Solid Dosage) facility at Gallops Industrial Park, is designed with high-end technology for tablets, capsules, and related forms, with a current capacity of 2.2 billion units and scope for expansion to 4 billion.
Proposed for EU GMP approval, Stallion emphasizes innovation, regulatory compliance, and global standards while nurturing over 400 qualified professionals in a growth-oriented environment.
Job Details
- Company Name: Stallion Laboratories Pvt. Ltd.
- Experience: Varies by role (0 to 9 years)
- Qualification: ITI, Diploma, B.Pharm, M.Pharm, B.Sc, M.Sc, B.Com, M.Sc (Micro), BE/Diploma (IT)
- Location: Unit-II, Gallops Industrial Park II, Vasna Chacharwadi, Dist-Ahmedabad, Gujarat, India
- Work Type: On-site
Job Description
Stallion Laboratories Pvt. Ltd. is hiring experienced and dynamic professionals for its USFDA approved OSD Formulation facility – Unit-II. Openings span Production, Warehouse, Packing, QC (including Microbiology), Engineering, QA, ADL, Project Management, and IT departments. These roles support high-quality oral solid dosage manufacturing in a regulated environment with immediate joining preferred for selected candidates.
Production
- Department: Production
- Experience: 2 to 5 Years (Operator/FTE); 2 to 5 Years (Officer/Sr.Officer)
- Education/Qualification: ITI/Diploma; M.Pharm/B.Pharm
Warehouse
- Department: Warehouse
- Experience: 2 to 5 Years (Sr.Officer/Officer); 1 to 3 Years (FTE)
- Education/Qualification: B.Sc/M.Sc/B.Com; ITI/B.Com
Packing
- Department: Packing
- Experience: 2 to 5 Years (Sr.Officer/Officer); 1 to 3 Years (Operator/FTE)
- Education/Qualification: Diploma/ITI; M.Pharm/B.Pharm/M.Sc
QC
- Department: QC (including QC Micro)
- Experience: 3 to 7 Years (Sr.Officer/Executive)
- Education/Qualification: B.Sc/M.Sc (Micro)
Engineering
- Department: Engineering
- Experience: 0 to 2 Years (Trainee Officer/Officer); 1 to 3 Years (Operator/FTE)
- Education/Qualification: ITI/Diploma
QA
- Department: QA
- Experience: 3 to 8 Years (Officer/Sr.Executive)
- Education/Qualification: M.Pharm/B.Pharm
ADL
- Department: ADL
- Experience: 2 to 5 Years (Officer/Sr. Officer)
- Education/Qualification: M.Sc
Project Management
- Department: Project Management
- Experience: 7 to 9 Years (Executive/Sr.Executive/A.M.)
- Education/Qualification: M.Pharm
IT
- Department: IT
- Experience: 1 to 5 Years (Officer/Sr. Officer)
- Education/Qualification: BE/Diploma – IT
Skills/Qualifications
- Hands-on experience in Compression, Granulation, Capsule, Coating, or Blister/CVC Packing
- Strong knowledge of Warehouse activities and inventory management
- Expertise in HPLC analysis, Microbiology testing (male candidates only for certain QC roles)
- Proficiency in Boiler/Utility/Water System operations
- IPQA, Vendor Qualification, Audit, and Stability studies
- Analytical Development Laboratory (ADL) techniques
- Project Management skills in TT/RA/PM/F&D (male candidates preferred)
- IT skills including GxP, data integrity, 21 CFR Part 11, LIMS, ERP, QMS, E-Logbooks, user access management, and validation (IQ/OQ/PQ)
- Regulatory compliance mindset with focus on USFDA, UK-MHRA, and GMP standards
Key Responsibilities
- Operate and maintain Compression, Granulation, Capsule, and Coating machines
- Handle Warehouse receipt, storage, and dispatch activities
- Perform Blister and CVC Packing operations efficiently
- Conduct HPLC analysis and Microbiology testing as per protocols
- Execute IPQA checks, vendor audits, and stability studies
- Manage utilities including Boiler, Water System, and Engineering support
- Support Analytical Development and Project Management activities
- Ensure data integrity, system validation, and GxP compliance in IT systems
- Troubleshoot equipment and maintain documentation per regulatory requirements
Benefits/Perks
- Career growth in a USFDA and UK-MHRA approved facility
- Opportunities for continuous learning and skill development
- Exposure to stringent regulatory environments and global standards
- Collaborative work culture emphasizing quality and innovation
- Potential for long-term stability in a growing pharmaceutical organization
How to Apply
Interested candidates should attend the walk-in interview with a copy of their latest resume, CTC breakup, and a recent photograph.
Candidates unable to attend may email their resume to paresh.patel@stallionlabs.com or contact +91 9104744518 / 9998836672.
For more pharma jobs across India, visit Pharma Recruiter. Apply promptly as immediate joining is preferred.
Walk-in Interview Details
- Date: 18 April 2026 (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: paresh.patel@stallionlabs.com | +91 9104744518 / 9998836672
Why You Should Join
Joining Stallion Laboratories means becoming part of a quality-driven organization with a legacy since 1988 and recent regulatory milestones in its modern OSD facility. The company fosters creativity, offers a supportive culture with work-life balance focus, and provides excellent learning opportunities in a highly compliant, innovative environment. Build a stable pharmaceutical career while contributing to niche formulations for global markets.
FAQs
Q1: Who can apply for these pharma jobs at Stallion Laboratories?
A: Candidates with relevant qualifications (ITI/Diploma/B.Pharm/M.Pharm/B.Sc/M.Sc etc.) and 0–9 years of experience in OSD or regulated facilities are eligible. Some roles specify male candidates only.
Q2: Is prior USFDA experience mandatory?
A: The posting highlights “Working experience in USFDA OSD Facility only should appear,” so preference will be given to candidates with such background, though other experienced professionals may apply.
Q3: What documents are required for the walk-in interview?
A: Bring your latest resume, CTC breakup details, and a recent photograph. Original and photocopies of educational and experience certificates are advisable.
Q4: What are the growth opportunities at Stallion Laboratories?
A: The company supports employee development through continuous learning, exposure to international regulatory standards, and career progression in a expanding OSD manufacturing setup.
