Introduction Paragraph Stallion Laboratories is conducting a walk-in interview on 28 March 2026 for multiple pharma jobs in its USFDA & UK-MHRA approved OSD Formulation facility.
Explore exciting opportunities in Production, QC, QA, Warehouse, Packing, and more. Ideal for candidates seeking pharmaceutical careers in India with a regulated manufacturing leader.
Contents
About the Company
Stallion Laboratories Pvt. Ltd., incorporated in 1988, is a reputed 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 quality and innovation.
Its facilities are WHO-GMP approved, with Unit-II being a state-of-the-art Oral Solid Dosage (OSD) plant approved by USFDA and UK-MHRA, and proposed for EU-GMP compliance. Stallion emphasizes creativity without compromising on quality, delivering high standards in tablets, capsules, and other formulations for global markets.
Job Details
- Company Name: Stallion Laboratories Pvt. Ltd.
- Experience: Varies by role (0–9 years)
- Qualification: M.Pharm, B.Pharm, M.Sc, B.Sc, ITI, Diploma (varies by position)
- Location: Vasna Chacharwadi (Gallops Industrial Park II), Dist. Ahmedabad, Gujarat, India
- Work Type: On-site
Job Description
Stallion Laboratories is hiring experienced and fresher candidates for its USFDA-approved OSD Formulation facility (Unit-II). Openings span Production, Warehouse, Packing, Quality Control, Quality Assurance, Engineering, ADL, and Project Management. Immediate joining is preferred for most roles.
Production – Compression/Granulation/Capsule
- Department: Production
- Role: Officer/Sr. Officer or Operator/FTE
- Experience: 2 to 5 Years
- Education/Qualification: M.Pharm/B.Pharm or ITI/Diploma
Warehouse
- Department: Warehouse
- Role: Sr. Officer/Officer or FTE
- Experience: 1 to 5 Years
- Education/Qualification: B.Sc/M.Sc/B.Com or ITI/B.Com
Packing
- Department: Packing
- Role: Sr. Officer/Officer or Operator/FTE
- Experience: 1 to 5 Years
- Education/Qualification: M.Pharm/B.Pharm/M.Sc or Diploma/ITI
QC (HPLC Analyst)
- Department: Quality Control
- Role: Sr. Officer/Executive
- Experience: 3 to 7 Years
- Education/Qualification: M.Pharm/B.Pharm/M.Sc
QC Micro
- Department: QC Microbiology
- Role: Trainee Officer/Officer (Only Male Candidates)
- Experience: 0 to 2 Years
- Education/Qualification: B.Sc/M.Sc Microbiology
Engineering
- Department: Engineering
- Role: Operator/FTE
- Experience: 1 to 3 Years
- Education/Qualification: ITI/Diploma
QA
- Department: Quality Assurance
- Role: Officer/Sr. Executive (IPQA – Only Male Candidates)
- Experience: 3 to 8 Years
- Education/Qualification: M.Pharm/B.Pharm
ADL
- Department: Analytical Development Lab
- Role: Officer/Sr. Officer
- Experience: 2 to 5 Years
- Education/Qualification: M.Sc
Project Management
- Department: Project Management
- Role: Executive/Sr. Executive/A.M. (TT/RA/PM/F&D – Only Male Candidates)
- Experience: 7 to 9 Years
- Education/Qualification: M.Pharm
Skills/Qualifications
- Hands-on experience in Compression, Coating, Capsule, Granulation, and QMS (for Production roles)
- Expertise in Warehouse operations and material management
- Proficiency in Blister Packing and CVC Packing
- Strong knowledge of HPLC analysis and Microbiology testing
- Experience in Boiler, Utility, and Water System maintenance
- IPQA, Vendor Qualification, Audit, and Stability studies
- Analytical Development Lab skills
- Regulatory compliance knowledge (USFDA, UK-MHRA, WHO-GMP)
- Teamwork, attention to detail, and problem-solving abilities
Key Responsibilities
- Operate and maintain Compression, Granulation, and Capsule machines
- Manage warehouse activities including receipt, storage, and dispatch
- Perform Blister and CVC packing operations efficiently
- Conduct HPLC analysis and Microbiology testing as per standards
- Handle IPQA, vendor audits, and stability studies
- Maintain Boiler, Utility, and Water Systems
- Support Analytical Development and Project Management activities
- Ensure strict adherence to QMS and regulatory guidelines
Benefits/Perks
- Career growth in a USFDA and UK-MHRA approved facility
- Opportunities to work with advanced OSD manufacturing technology
- Exposure to stringent international regulatory standards
- Professional learning and development environment
- Association with a quality-focused organization having global presence
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. For more pharma jobs across India, visit Pharma Recruiter.
Walk-in Interview Details
- Date: 28 March 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: +91 9104744518 / 9998836672
- Email: paresh.patel@stallionlabs.com
Why You Should Join
Joining Stallion Laboratories offers a chance to build your pharmaceutical career in a modern, compliant OSD facility recognized by USFDA and UK-MHRA. The company values quality, innovation, and ethical practices, providing long-term stability and growth opportunities in a supportive environment focused on excellence.
FAQs
What is the experience required for these pharma jobs?
Experience ranges from 0-2 years (Trainee roles) to 7-9 years (Project Management), depending on the position.
Who can apply for the walk-in interview?
Candidates with relevant qualifications in Pharmacy, Science, or ITI/Diploma and matching experience in OSD formulation can apply. Some roles specify male candidates only.
Is immediate joining mandatory?
Immediate joining is preferred for most positions.
What are the growth opportunities at Stallion Laboratories?
Employees gain exposure to international regulatory standards, advanced manufacturing, and career progression in a growing USFDA-approved facility.
