Stallion Hiring QA QC Production

Stallion Labs Hiring QA QC Production | Ahmedabad

Stallion Laboratories hiring QA, QC, ADL, Production, Warehouse, Engineering & IT professionals. ITI, BSc, MSc, BPharm, MPharm. Ahmedabad.

Pharmaceutical professionals looking for career opportunities in Quality Assurance, Quality Control, Production, Packing, Analytical Development Laboratory (ADL), Warehouse, Engineering, and Information Technology can explore the latest recruitment drive announced by Stallion Laboratories Pvt. Ltd. The company is expanding its operations and inviting applications from qualified candidates for multiple positions at its Unit-I manufacturing facility in Ahmedabad, Gujarat.

This hiring initiative offers opportunities for both freshers and experienced professionals across pharmaceutical manufacturing, quality systems, formulation development support, engineering operations, warehouse management, and information technology functions. Candidates with experience in formulation manufacturing, GMP-regulated environments, validation activities, analytical testing, microbiology, plant maintenance, and pharmaceutical compliance are encouraged to apply.

For job seekers searching for pharma jobs in Ahmedabad, Quality Assurance jobs, Production Officer vacancies, Quality Control careers, ADL analyst positions, warehouse jobs, engineering opportunities, and pharmaceutical manufacturing careers, this recruitment drive presents multiple openings within a growing pharmaceutical organization.

Company Overview

About Stallion Laboratories Pvt. Ltd.

Stallion Laboratories Pvt. Ltd. is a pharmaceutical manufacturing company engaged in the development and production of high-quality pharmaceutical formulations. The organization operates with a strong focus on quality management systems, regulatory compliance, manufacturing excellence, and continuous improvement.

The company manufactures pharmaceutical products in accordance with industry standards and emphasizes GMP compliance, quality assurance, operational efficiency, and patient safety. With ongoing expansion and increasing business requirements, Stallion Laboratories continues to strengthen its workforce across technical, operational, and support functions.

Its Ahmedabad facility provides professionals with opportunities to work in a regulated pharmaceutical environment while gaining exposure to quality systems, manufacturing processes, analytical operations, and engineering functions.

Job Role & Responsibilities

Quality Assurance (Validation)

Designation

• Officer
• Senior Officer

Qualification

• B.Pharm
• M.Pharm

Experience

• 2 to 4 Years

Key Responsibilities

• Validation protocol preparation and execution.
• Process validation activities.
• Equipment qualification support.
• Cleaning validation documentation.
• Regulatory compliance monitoring.
• Review of validation reports.
• GMP documentation management.

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Quality Assurance (IPQA)

Designation

• Officer
• Senior Officer

Qualification

• B.Pharm
• M.Pharm
• M.Sc

Experience

• 2 to 4 Years

Key Responsibilities

• In-process quality monitoring.
• Batch manufacturing record review.
• Line clearance activities.
• GMP compliance verification.
• Process monitoring and documentation.
• Investigation support and CAPA implementation.

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Production & Packing

Areas

• Granulation
• Compression
• Coating
• Packing

Designation

• Officer
• Senior Officer

Qualification

• B.Pharm
• M.Pharm

Experience

• 2 to 4 Years

Key Responsibilities

• Manufacturing and packing operations.
• Batch execution and documentation.
• Equipment operation and monitoring.
• Process optimization activities.
• Production planning support.
• Compliance with GMP requirements.

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Analytical Development Laboratory (ADL)

Areas

• Documentation
• Analytical Method Validation (AMV)
• Analytical Method Development (AMD)
• Routine Analysis

Designation

• Officer
• Senior Officer

Qualification

• B.Pharm
• M.Pharm
• M.Sc

Experience

• 2 to 4 Years

Key Responsibilities

• Analytical method development.
• Method validation activities.
• Stability sample testing.
• Routine analytical testing.
• Documentation review and compliance.
• Laboratory investigation support.

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Quality Control & Microbiology

Areas

• HPLC
• GLP
• Microbiology

Designation

• Officer
• Senior Officer

Qualification

• M.Sc
• M.Pharm
• B.Pharm

Experience

• 2 to 4 Years

Key Responsibilities

• Raw material and finished product testing.
• HPLC analysis and laboratory operations.
• Microbiological testing activities.
• GLP compliance monitoring.
• Data review and documentation.
• Stability studies and quality investigations.

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Warehouse (Dispensing)

Designation

• Officer
• Senior Officer

Qualification

• B.Sc
• M.Sc
• B.Pharm

Experience

• Fresher to 2 Years

Key Responsibilities

• Material dispensing operations.
• Inventory management.
• Warehouse documentation.
• Material reconciliation.
• GMP-compliant storage practices.

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Engineering Department

Project Manager

Qualification: B.E.

Experience: 12 to 15 Years

Responsibilities

• Project planning and execution.
• Utility and facility management.
• Engineering compliance monitoring.
• Budget and resource management.

Plant Maintenance (Senior Executive / Assistant Manager)

Qualification: B.E.

Experience: 8 to 12 Years

Responsibilities

• Preventive and breakdown maintenance.
• Utility management.
• Equipment reliability improvement.
• Maintenance planning and execution.

ETP Operator

Qualification: ITI

Experience: 2 to 4 Years

Responsibilities

• Effluent Treatment Plant operations.
• Environmental compliance monitoring.
• Utility system management.
• Safety compliance activities.

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Information Technology (IT) Manager

Qualification

• B.Tech
• M.Tech

Experience

• 12 to 15 Years

Additional Requirement

• Pharmaceutical Formulation Experience Mandatory

Key Responsibilities

• IT infrastructure management.
• ERP and system administration.
• Data security and network management.
• Technology support for manufacturing operations.

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Production & Packing (ITI Freshers)

Qualification

• ITI

Experience

• Freshers Welcome

Responsibilities

• Support manufacturing and packing operations.
• Learn pharmaceutical production processes.
• Follow SOP and GMP requirements.
• Assist production teams in routine activities.

Eligibility / Qualifications

Educational Qualification

Candidates with any of the following qualifications are eligible based on role requirements:

• B.Pharm
• M.Pharm
• B.Sc
• M.Sc
• B.E.
• B.Tech
• M.Tech
• ITI

Relevant Courses

B.Pharm, M.Pharm, Pharmaceutical Technology, Industrial Pharmacy, Pharmaceutical Analysis, Quality Assurance, Quality Control, M.Sc Chemistry, M.Sc Microbiology, Analytical Chemistry, Biotechnology, B.Sc Chemistry, B.Sc Microbiology, Mechanical Engineering, Electrical Engineering, Instrumentation Engineering, B.Tech Information Technology, M.Tech Information Technology, Industrial Engineering, Environmental Engineering, Utility Management.

Experience Required

• Freshers
• 2 to 4 Years
• 8 to 12 Years
• 12 to 15 Years

(Depending on the department and position)

Why Join Stallion Laboratories?

Pharmaceutical manufacturing continues to offer strong career opportunities for professionals in quality systems, production, engineering, and analytical functions. Stallion Laboratories provides exposure to regulated manufacturing operations, quality-focused work environments, and structured career growth opportunities.

Career Benefits

• Opportunities across multiple departments.
• Exposure to GMP-compliant pharmaceutical operations.
• Learning and development opportunities.
• Career growth in quality, manufacturing, engineering, and IT.
• Experience in formulation manufacturing environments.
• Supportive and quality-driven workplace culture.
• Long-term career prospects within the pharmaceutical industry.

Location & Salary

Location: Kerala Bavla, Ahmedabad

Estimated Salary: ₹2.5 LPA – ₹24 LPA (Approximate salary based on role, qualification, experience, and pharmaceutical industry standards)

Application Process

Interested candidates should share their updated resume along with the following details:

• Current CTC
• Expected CTC
• Notice Period

Email Application

Email: aarti.oberoi@stallionlabs.com

Subject Line Format

Department Name – Position Applied For

Candidates are advised to clearly mention their experience, qualification, and preferred department while applying.

Frequently Asked Questions (FAQs)

1. Are freshers eligible for Stallion Laboratories vacancies?

Yes. Freshers with ITI qualifications can apply for Production & Packing positions, and Warehouse roles are open for candidates with Fresher to 2 years of experience.

2. Which departments are currently hiring?

The company is hiring for QA, QC, Microbiology, ADL, Production, Packing, Warehouse, Engineering, and IT departments.

3. What qualifications are accepted?

B.Pharm, M.Pharm, B.Sc, M.Sc, B.E., B.Tech, M.Tech, and ITI candidates can apply depending on the position.

4. Is pharmaceutical experience required?

Yes. Relevant pharmaceutical formulation experience is preferred, and it is mandatory for certain senior positions such as IT Manager.

5. What is the experience range required?

The company is hiring candidates ranging from freshers to professionals with 15 years of experience.

6. How can candidates apply?

Interested candidates can email their updated resume to aarti.oberoi@stallionlabs.com with the required details and subject line format.

Summary

Stallion Laboratories Pvt. Ltd. is hiring for multiple departments including QA Validation, IPQA, Production, Packing, ADL, Quality Control, Microbiology, Warehouse, Engineering, and IT at its Ahmedabad facility. Freshers and experienced professionals with qualifications ranging from ITI, B.Sc, M.Sc, B.Pharm, M.Pharm, B.E., B.Tech, and M.Tech are eligible to apply.

Company	Stallion Laboratories Pvt. Ltd.
Department Vacancies	QA Validation, IPQA, Production, Packing, ADL, QC, Microbiology, Warehouse, Engineering, IT
Qualification	ITI, B.Sc, M.Sc, B.Pharm, M.Pharm, B.E., B.Tech, M.Tech
Experience	Freshers to 15 Years
Location	Ahmedabad, Gujarat