Stallion Laboratories Walk-in / Job Openings for Production, QA, QC, Engineering & IT Roles

Stallion Laboratories Pvt. Ltd. is hiring for multiple positions in Production, Packing, QC Micro, QA, ADL, Engineering, and IT/CSV at its manufacturing plants in Bavia (Bavla), Ahmedabad. Openings range from fresher Helper and Trainee roles to senior Manager, DGM/GM positions.

This is an excellent opportunity for pharma jobs in Gujarat with a WHO-GMP certified formulation manufacturing company.

About the Company

Stallion Laboratories Pvt. Ltd., incorporated in 1988 and headquartered in Ahmedabad, Gujarat, is a well-established integrated pharmaceutical formulation manufacturer. The company operates WHO-GMP approved production facilities in Bavla (Bavia), Ahmedabad, manufacturing a wide range of oral solid dosage forms including tablets, capsules, oral dry powders, and oral liquids.

With a strong focus on quality, creativity, and regulatory compliance, Stallion supplies high-quality, affordable medicines across therapeutic segments such as antidiabetics, cardiovascular, antibiotics, gastrointestinal, and more. The company has a global presence with overseas offices and is committed to stringent quality control under GLP standards.

Job Details

• Company Name: Stallion Laboratories Pvt. Ltd.
• Location: Manufacturing Plants, Bavia (Bavla) – Ahmedabad, Gujarat
• Work Type: On-site

Job Description

Stallion Laboratories is expanding its team across various departments at its Bavla manufacturing units. The company is looking for skilled professionals and freshers to support production, quality assurance, quality control, analytical development, engineering, and IT functions in a WHO-GMP environment.

These roles offer opportunities to contribute to high-volume pharmaceutical manufacturing while maintaining international quality standards.

Helper – Production

• Department: Production
• Qualification: Diploma/ITI
• Experience: Fresher
• Designation: Helper
• Skill: Compression/Granulation/Capsule

Officer / Sr. Officer – Production

• Department: Production
• Qualification: M.Pharma / B.Pharm
• Experience: 2 to 5 Years
• Designation: Officer / Sr. Officer
• Skill: Compression / Capsule / Granulation / Coating

Sr. Executive / Asst. Manager – Computer System Validation (CSV) & IT

• Department: Computer System Validation (CSV) and Infrastructure IT
• Qualification: BE / MCA / BCA / B.Tech
• Experience: 8 to 10 Years
• Designation: Sr. Executive / Asst. Manager
• Skill: Proficient in cGMP, GxP, GDP, and 21 CFR Part 11; Validation protocols (URS, VP, IQ, OQ, PQ, etc.); User management and data backup

Officer / Sr. Officer – Packing

• Department: Packing
• Qualification: M.Pharma / B.Pharm / M.Sc
• Experience: 2 to 5 Years
• Designation: Officer / Sr. Officer
• Skill: Primary / Secondary Packing

Sr. Officer / Executive – QC Micro

• Department: QC Micro
• Qualification: M.Pharma / B.Pharm / M.Sc
• Experience: 3 to 7 Years
• Designation: Sr. Officer / Executive
• Skill: HPLC Analyst

Trainee Officer / Officer – Microbiology

• Department: QC
• Qualification: B.Sc / M.Sc Microbiology
• Experience: 0 to 2 Years
• Designation: Trainee Officer / Officer
• Skill: Microbiology Analyst (Only Male Candidates)

Operator – ETP

• Department: Engineering / ETP
• Qualification: ITI / Diploma
• Experience: 1 to 3 Years
• Designation: Operator

Manager – QA

• Department: QA
• Qualification: M.Pharma / B.Pharm
• Experience: 15 to 18 Years
• Designation: Manager

DGM / GM – IPQA / Quality Assurance

• Department: QA (IPQA)
• Qualification: M.Pharma / B.Pharm
• Experience: 25+ Years
• Designation: DGM / GM
• Skill: Quality Assurance oversight, Regulatory Compliance, QMS Implementation and continuous improvement

Officer / Sr. Officer – ADL

• Department: ADL
• Qualification: M.Sc
• Experience: 2 to 5 Years
• Designation: Officer / Sr. Officer

Officer / Sr. Officer – IT / QA / QC Documentation

• Department: IT / QA / QC
• Qualification: M.Pharma / B.Pharm / MCA / BCA / B.Tech
• Experience: 3 to 5 Years
• Designation: Officer / Sr. Officer
• Skill: Pharma documentation, digital systems, Pharmacloud, PC 360

Skills/Qualifications

• Relevant qualification as per the position (M.Pharma, B.Pharm, M.Sc, B.Sc, BE, ITI, Diploma etc.)
• Hands-on experience in pharmaceutical manufacturing, compression, granulation, coating, packing, or quality control
• Strong knowledge of cGMP, GLP, GDP, ICH guidelines, and 21 CFR Part 11 for CSV roles
• Experience in validation protocols, HPLC, microbiology testing, or ETP operations
• Proficiency in documentation, digital systems, and regulatory compliance
• Good communication, teamwork, and problem-solving skills

Key Responsibilities

• Operate and monitor production equipment (compression, granulation, coating, packing)
• Perform quality control testing including HPLC and microbiology analysis
• Execute computer system validation and IT infrastructure activities
• Handle In-Process Quality Assurance and QMS implementation
• Manage documentation and regulatory compliance
• Support analytical development and stability studies
• Ensure adherence to WHO-GMP and safety standards

Benefits/Perks

• Career growth in a WHO-GMP certified manufacturing company
• Exposure to high-volume pharmaceutical production
• Learning opportunities in regulatory compliance and advanced technologies
• Competitive salary commensurate with experience
• Professional work environment focused on quality and innovation
• Long-term stability with a reputed formulation manufacturer

For more pharma jobs, production jobs, QA jobs, and QC jobs in Gujarat and across India, visit Pharma Recruiter.

How to Apply

Interested candidates are requested to share their updated CV to the HR email ID. Mention the position you are applying for in the subject line.

Email: aarti.oberoi@stallionlabs.com
Contact: +91 94093 09964

Apply now to join a growing pharmaceutical formulation company and build your pharmaceutical careers in India.

Why You Should Join

Stallion Laboratories offers a quality-driven culture with a strong emphasis on creativity, compliance, and continuous improvement. Employees benefit from working in modern WHO-GMP facilities, gaining hands-on experience in oral solid dosage manufacturing, and contributing to affordable healthcare solutions.

The company provides a stable platform for long-term career growth in the pharmaceutical industry with opportunities for skill development and professional advancement.

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