Stallion Laboratories Pvt. Ltd., a reputed pharmaceutical formulation manufacturing company established in 1988, has announced multiple career opportunities for experienced professionals across various departments. The company operates a WHO-GMP approved manufacturing facility and serves regulated markets with a strong commitment to quality, compliance, and innovation.

Immediate joiners will be given preference.

Company Overview

Stallion Laboratories Pvt. Ltd. is a leading pharmaceutical formulation manufacturer with international regulatory recognition, including:

• UK-MHRA Approved Facility
• Health Canada Compliance
• Proposed EU-GMP Approved Plant
• WHO-GMP Manufacturing Standards
• Strong Quality Assurance & Regulatory Systems

The organization specializes in tablet, capsule, coating, granulation, research & development, analytical testing, and quality management systems.

Available Departments & Positions

1. Production Department

Qualification:

• Diploma / ITI
• B.Pharm / M.Pharm

Experience:

• 2–8 Years

Designation:

• Technician
• Operator
• Officer
• Sr. Officer
• Executive

Required Skills:

• Compression
• Granulation
• Capsule Manufacturing
• Coating Operations
• BMR/BPR Preparation
• QMS Documentation

2. Engineering Department

Qualification:

• ITI / Diploma

Experience:

• 2–5 Years

Designation:

• Operator

Skills Required:

• HVAC Operations
• Boiler Maintenance
• Utility Systems
• Electrical Maintenance

3. EHS (Environment, Health & Safety)

Qualification:

• BE / Diploma (PIDS)

Experience:

• 2–4 Years

Designation:

• Officer / Sr. Officer

Skills Required:

• EHS Compliance
• Safety Management Systems
• Regulatory Compliance

4. Quality Assurance (QA)

Qualification:

• B.Pharm / M.Pharm

Experience:

• 2–8 Years

Designation:

• Officer
• Sr. Officer
• Executive

Skills Required:

• QMS
• Stability Management
• IPQA
• Vendor Qualification
• Documentation Control
• SOP Management
• Audit Support

5. Formulation & Development (F&D)

Qualification:

• B.Pharm / M.Pharm

Experience:

• 2–14 Years

Designation:

• Officer
• Sr. Officer
• Executive
• AM/DM

Skills Required:

• Product Development
• Pharmaceutical Documentation

6. Analytical Development Laboratory (ADL)

Qualification:

• B.Pharm / M.Pharm

Experience:

• 2–4 Years

Designation:

• Officer / Sr. Officer

Skills Required:

• Method Development
• Method Validation
• Cleaning Validation

7. Corporate Quality Assurance (CQA)

Qualification:

• B.Pharm / M.Pharm

Experience:

• 6–8 Years

Designation:

• Executive

Skills Required:

• All Time Readiness (ATR)
• Quality Compliance Programs

8. Quality Control (QC)

Qualification:

• B.Pharm / M.Pharm / M.Sc

Experience:

• 2–14 Years

Designation:

• Officer
• Sr. Officer
• Executive
• AM/DM

Skills Required:

• AMV / AMT
• QC Documentation
• GLP Practices
• LIMS Management
• HPLC Analysis
• GC Operations
• Raw Material & Finished Product Testing

9. Project Management (PPMC)

Qualification:

• B.Pharm / M.Pharm / MBA

Experience:

• 10–14 Years

Designation:

• AM / DM

Skills Required:

• Technology Transfer (TT)
• Regulatory Affairs (RA)
• Project Management
• F&D Coordination

10. Supply Chain

Qualification:

• B.Pharm / M.Pharm / MBA

Experience:

• 10–14 Years

Designation:

• AM / DM

Skills Required:

• Corporate & Plant Supply Chain Operations
• Inventory Management
• Logistics Coordination

11. Project Coordinator

Qualification:

• B.Pharm / M.Pharm / MBA

Experience:

• 8–10 Years

Designation:

• Sr. Executive

Skills Required:

• Calendar Management
• Travel Coordination
• MIS Reporting
• Documentation
• MS Office
• Time Management
• Communication Skills

How to Apply

Interested candidates can share their updated resume through:

Email IDs:

• paresh.patel@stallionlabs.com
• aarti.oberoi@stallionlabs.com

WhatsApp:

• +91 9104744518
• +91 9490309964

Technical FAQs

1. What is BMR and BPR in pharmaceutical manufacturing?

BMR (Batch Manufacturing Record) documents the complete manufacturing process of a batch, while BPR (Batch Packaging Record) records all packaging activities. Both are essential GMP documents ensuring product traceability and compliance.

2. What is IPQA in pharmaceutical production?

In-Process Quality Assurance (IPQA) involves monitoring manufacturing activities during production to ensure processes remain within approved specifications and GMP requirements.

3. What is Method Validation in ADL?

Method Validation is the process of proving that an analytical method consistently produces accurate, precise, specific, and reliable results according to ICH guidelines.

4. Why is HVAC important in pharmaceutical manufacturing?

HVAC systems maintain temperature, humidity, air pressure, and cleanliness levels in manufacturing areas, preventing contamination and ensuring product quality.

5. What is LIMS in Quality Control laboratories?

LIMS (Laboratory Information Management System) is software used to manage laboratory samples, testing data, documentation, compliance records, and analytical reports efficiently.