Stallion Laboratories Pvt. Ltd., a leading pharmaceutical formulation manufacturer since 1988, is hiring for its USFDA and UK MHRA-approved OSD (Oral Solid Dosage) facility in Ahmedabad, Gujarat. With a WHO GMP-approved production unit and a focus on quality, Stallion Laboratories offers exciting career opportunities in its Unit-II at Gallops Industrial Park. Walk-in interviews are scheduled for October 4, 2025, from 9:00 AM to 2:00 PM, targeting local candidates with experience in USFDA OSD facilities. Explore roles in Production, Quality Control (QC), Quality Assurance (QA), Analytical Development Lab (ADL), Engineering, and IT. Join a company committed to creativity, quality, and regulated market excellence.
Job Responsibilities
Production
- Executive/Sr. Executive (6-10 years): Manage compression and granulation processes, ensuring compliance with USFDA standards.
- Operator (2-5 years): Operate blister packing and compression machines with precision.
- Manager (10-14 years): Lead GLP, raw material (RM), and packing material (PM) sections, ensuring operational efficiency.
Quality Control (QC)
- Officer/Sr. Officer (2-5 years): Perform HPLC analysis, testing, GC, GLP, documentation, and equipment washing.
- Executive/Sr. Executive (5-8 years): Oversee vendor qualification, audits, compliance, QMS, training, and documentation.
Quality Assurance (QA)
- Officer/Sr. Officer (2-5 years): Handle documentation for regulatory compliance.
- Manager/Asst. Manager (8-12 years): Review processes and lead QA teams for USFDA and UK MHRA audits.
Analytical Development Lab (ADL)
- Sr. Officer/Executive (5-8 years): Conduct AMV/AMD and routine analysis.
- Officer (1-3 years): Manage ADL documentation.
Engineering
- Operator (2-5 years): Operate and maintain boilers in the OSD facility.
IT
- FTE/Trainee (0-1 years): Support digitalization initiatives, including PharmaCloud, PC 360, and other software implementations.
Qualifications
- Production: B.Pharm, M.Pharm, M.Sc, or ITI Diploma with 2-14 years of experience in compression, granulation, or blister packing.
- QC: M.Sc, M.Pharm, or B.Pharm with 2-8 years of experience in HPLC, GC, GLP, or vendor qualification.
- QA: M.Pharm or B.Pharm with 2-12 years of experience in documentation, audits, or team leadership.
- ADL: M.Sc, M.Pharm, or B.Pharm with 1-8 years of experience in AMV/AMD or documentation.
- Engineering: ITI Diploma with 2-5 years of boiler operation experience.
- IT: MCA or M.Sc (IT) with 0-1 years of experience in digitalization or software implementation.
- Note: Candidates must have experience in USFDA OSD facilities. Those who interviewed in the last 6 months are ineligible.
Benefits
- Work in a USFDA and UK MHRA-approved facility with a proposed EU GMP certification.
- Opportunities for career growth in regulated pharmaceutical markets.
- Collaborative and innovative work environment focused on quality and creativity.
- Immediate joining for successful candidates, ideal for local Ahmedabad professionals.
Application Instructions
Attend the walk-in interview on October 4, 2025, from 9:00 AM to 2:00 PM at: Stallion Laboratories Pvt. Ltd., Unit-II, Plot No. D-4,5,5,17,18,19, Gallops Industrial Park II, Vasna Chacharwadi, Dist-Ahmedabad-382110, Gujarat, India.
Bring your latest resume, CTC breakup, and a passport-sized photo. If unable to attend, email your resume to:
- aarti.oberoi@stallionlabs.com (+91 9998836672)
- jagdish.mathukiya@stallionlabs.com (+91 9409309964)
For more details, visit www.stallionlabs.com.
FAQs
1. Who is eligible to apply for these roles?
Candidates with experience in USFDA OSD facilities and the specified qualifications (B.Pharm, M.Pharm, M.Sc, ITI Diploma, MCA) are eligible. Local Ahmedabad candidates are preferred, and those who interviewed in the last 6 months are not eligible.
2. What documents are required for the walk-in interview?
Bring a copy of your latest resume, CTC breakup, and a passport-sized photo. Immediate joiners are preferred.
