Short Description : Stallion Laboratories Recruitment 2026 : Stallion Laboratories Pvt. Ltd. is inviting applications for multiple openings in Production, Packing, Warehouse, Engineering, Quality Control (QC), Quality Assurance (QA), Analytical Development Laboratory (ADL) and Corporate Quality Assurance (CQA) departments at its USFDA-approved pharmaceutical manufacturing facility in Ahmedabad, Gujarat. Candidates with relevant pharmaceutical industry experience are encouraged to apply.
Stallion Laboratories Recruitment 2026Production, QC, QA, ADL & Warehouse Jobs |
Recruitment Overview |
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| Organization | Stallion Laboratories Pvt. Ltd. |
| Job Type | Private Job |
| Industry | Pharmaceutical Manufacturing |
| Departments | Production, Packing, Warehouse, Engineering, QC, QA, ADL & CQA |
| Experience | 1–12 Years |
| Qualification | ITI, Diploma, B.Pharm, M.Pharm, B.Sc, M.Sc, B.Com |
| Work Location | Ahmedabad, Gujarat |
| Application Mode | Email |
Vacancy Details |
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| Department | Designation | Experience | Qualification | Key Skill |
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| Production | FTE / Officer | 1–4 Years | ITI / Diploma / B.Pharm / M.Pharm | Compression, Granulation, BMR, BPR |
| Packing | Officer / Sr. Officer | 2–4 Years | B.Pharm / M.Pharm | Blister Packing, CVC Packing |
| Warehouse | Technician / Operator / Manager | 2–12 Years | ITI / Diploma / B.Sc / M.Sc / B.Com / B.Pharm | RM, PM, FG, Export Documentation |
| Engineering | Operator | 1–3 Years | Second Class Boiler Operator | Boiler, ETP |
| Quality Control (QC) | Officer / Sr. Officer / AM / DM | 2–10 Years | M.Pharm / B.Pharm / M.Sc | HPLC, AMV, AMT, QMS, OOS, OOT |
| Quality Assurance (QA) | Officer / Sr. Officer / Executive | 2–8 Years | B.Pharm / M.Pharm | IPQA, Stability, Doc Cell, AQA |
| ADL | Officer / Sr. Officer | 2–4 Years | M.Pharm / B.Pharm / M.Sc | Method Validation, Method Development |
| CQA | Executive | 5–7 Years | B.Pharm / M.Pharm | GMP Compliance, QMS |
Key Skills |
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- Pharmaceutical Manufacturing
- Compression & Granulation
- Blister & CVC Packing
- Warehouse Management
- HPLC Analysis
- AMV / AMT
- Method Validation
- Method Development
- IPQA Activities
- GMP / GLP Compliance
- QMS Documentation
- OOS / OOT Investigation
- CAPA & Change Control
- Regulatory Compliance
- Documentation & Audit Support
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Department-wise Job Responsibilities |
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Production- Compression & Granulation activities.
- BMR/BPR preparation and documentation.
Packing- Blister Packing and CVC Packing operations.
Warehouse- RM, PM, FG handling and warehouse management.
- Export documentation and dispatch coordination.
Engineering- Boiler operation and ETP activities.
Quality Control (QC)- HPLC analysis, AMV/AMT testing.
- QMS, OOS, OOT, CAPA, Change Control.
Quality Assurance (QA)- IPQA, Stability, Documentation Control.
- BMR/BPR issuance and audit support.
Analytical Development Laboratory (ADL)- Method Development and Method Validation.
Corporate Quality Assurance (CQA)- GMP compliance and Quality Management Systems.
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How To Apply |
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| Interested candidates can send their updated CV to the official email address along with the required documents. Email ID : paresh.patel@stallionlabs.com Application Mode : Email |
Documents Required |
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- Updated Resume / CV
- Last Three Months’ Salary Slips
- Appointment Letter with CTC Structure
- Educational Certificates & Mark Sheets
- Aadhaar Card / PAN Card
- Experience Certificates (If Applicable)
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About Stallion Laboratories |
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| Stallion Laboratories Pvt. Ltd. is a leading pharmaceutical manufacturing company with a USFDA-approved manufacturing facility located in Ahmedabad, Gujarat. The company specializes in pharmaceutical production, quality systems, analytical development, regulatory compliance and warehouse operations while maintaining global quality standards. |
Who Can Apply |
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- ITI and Diploma holders.
- B.Pharm and M.Pharm graduates.
- B.Sc. and M.Sc. candidates.
- B.Com graduates for Warehouse roles.
- Candidates having relevant pharmaceutical industry experience.
- Professionals with experience in Production, Packing, Warehouse, Engineering, QC, QA, ADL or CQA.
- Candidates with GMP, QMS, HPLC, IPQA, Validation and Documentation experience.
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Career Growth at Stallion Laboratories |
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| Stallion Laboratories provides professionals with excellent opportunities to build careers in pharmaceutical manufacturing, quality assurance, quality control, analytical development, warehouse management and engineering. Employees gain practical exposure to GMP-compliant manufacturing, regulatory requirements, documentation systems, audits, validation and quality management, supporting long-term career growth. |
Stallion Laboratories Recruitment 2026 FAQs |
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| Q1. Which departments are hiring at Stallion Laboratories? Production, Packing, Warehouse, Engineering, Quality Control (QC), Quality Assurance (QA), Analytical Development Laboratory (ADL) and Corporate Quality Assurance (CQA). |
| Q2. What qualifications are required? Depending on the position, candidates with ITI, Diploma, B.Pharm, M.Pharm, B.Sc., M.Sc. and B.Com qualifications can apply. |
| Q3. What experience is required? Relevant pharmaceutical industry experience ranging from 1 to 12 years is required depending on the position. |
| Q4. Where is the job location? The positions are based at Stallion Laboratories’ manufacturing facility in Ahmedabad, Gujarat. |
| Q5. Can candidates apply by email? Yes. Interested candidates should send their updated CV and required documents to paresh.patel@stallionlabs.com. |
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