Stallion Laboratories Pvt. Ltd. is an established and globally recognized pharmaceutical formulation manufacturer, specializing in Oral Solid Dosage (OSD) forms like tablets and capsules. Founded in 1988 in Ahmedabad, Stallion has consistently demonstrated an uncompromising commitment to quality, enabling its products to reach over 50 countries worldwide.
The company’s modern Unit-II facility is a testament to its global ambition, holding prestigious approvals from the USFDA and UK-MHRA, alongside WHO-GMP certification. This rigorous regulatory compliance confirms its place among the elite manufacturers capable of supplying stringent regulatory markets (SRA). Stallion is currently positioning for an EU-GMP audit, promising even greater global exposure and career growth for its employees.
Joining Stallion means entering an innovative, quality-driven environment where your expertise in regulated manufacturing, particularly OSD, is highly valued and essential for its continued global expansion.
The Opportunity: Walk-in Interview on December 7th
Stallion Laboratories is conducting a mega Walk-in Interview on Sunday, December 7, 2025, in Ahmedabad. This is a prime opportunity for experienced professionals to secure a role within a top-tier, USFDA-approved OSD facility.
The company is hiring across key functions critical for maintaining international quality standards: Quality Control (QC), Analytical Development Lab (ADL), and Human Resources (HR).
Key Positions & Experience Levels:
| Department | Role Category | Experience (Years) | Key Skills/Focus |
| Quality Control (QC) | Deputy Manager/Manager (Analysis) | 8 to 12 | HPLC/GC Analysis, Planning, Review |
| Quality Control (QC) | Deputy Manager/Manager (LIMS) | 10 to 12 | LIMS Integration & Operations |
| Quality Control (QC) | Officer/Executive (Analysis) | 2 to 5 | HPLC/Chemical Analysis, AMV/AMT |
| Analytical Dev. Lab (ADL) | Asst. Manager/Manager (Reviewer) | 8 to 10 | Review, Team Handling, Analytical Methods |
| Analytical Dev. Lab (ADL) | Sr. Officer/Executive (Analysis) | 3 to 6 | AMV/AMD, HPLC Analysis |
| Human Resources (HR) | Asst. Manager/Sr. Manager (Plant) | 8 to 12 | Plant HR, Recruitment, Statutory Compliance, Payroll |
| Human Resources (HR) | Officer (ADL Documentation) | 1 to 3 | Documentation, HR Process Support |
Mandatory Requirement: USFDA OSD Experience
A crucial criterion for all technical roles (QC/ADL) is mandatory, hands-on working experience in a USFDA-approved Oral Solid Dosage (OSD) facility. Candidates without this specific background will not be considered for the walk-in interviews.
Essential Skills & Responsibilities
Success at Stallion is built on a foundation of technical excellence and regulatory compliance:
Technical Expertise: Proven proficiency in operating and managing analytical instruments like HPLC (High-Performance Liquid Chromatography) and GC (Gas Chromatography). Knowledge of LIMS (Laboratory Information Management System) is highly desirable, especially for managerial QC roles.
Regulatory Knowledge: Deep working knowledge of GMP (Good Manufacturing Practices), stringent documentation practices, and experience facing regulatory audits (USFDA, UK-MHRA).
Education: M.Sc/M.Pharm/B.Pharm for QC and ADL roles; MBA/MLW/PGHR/MSW for HR positions.
Leadership (Managerial Roles): Ability to lead teams, coach subordinates, and manage performance within a regulated, high-stakes environment.
Walk-in Interview Details
Don’t miss this opportunity to advance your pharmaceutical career in India’s leading pharma hub, Ahmedabad.
Date: 07.12.2025 (Sunday)
Time: 09:00 AM to 2:00 PM
Venue: Treatotel Hotel, B/h Sterling Hospital, Off. Gurukul Road, L.K Society, Nilmani Society, Ahmedabad-380052
To Carry: Latest resume, CTC break-up, passport-size photo, and proof of your USFDA OSD experience.
If You Cannot Attend:
Candidates unable to attend the walk-in can email their resumes to: darshan.mistry@stallionlabs.com or jagdish.mathukiya@stallionlabs.com. Remember to clearly highlight your USFDA OSD experience.
Why Choose Stallion Laboratories?
Stallion offers a professional environment that prioritizes growth and stability:
Global Exposure: Work directly with processes and documentation that meet the highest standards of the USFDA and UK-MHRA, offering unparalleled exposure to global pharmaceutical quality systems.
Career Advancement: Opportunities for fast-track promotions and professional training in regulatory compliance and analytical techniques.
Competitive Compensation: Attractive salaries and performance incentives, along with health insurance, medical, and on-site amenities.
Secure your role in the highly regulated OSD sector with a company committed to quality and global expansion.
Authoritative Sources
Stallion Laboratories Official Website: Confirms WHO-GMP, GLP, and ISO 9001-2015 certifications, and Unit-II as the OSD facility designed for Stringent Regulatory Authorities (SRA).
USFDA/UK-MHRA Accreditation: Indicates the facility’s approval by major global regulatory bodies, validating the requirement for regulated market experience.
