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.
Stallion Laboratories Pvt. Ltd. Recruitment– Multiple Openings Across Production, QA, QC, Engineering, F&D, ADL & Supply Chain
The post Stallion Laboratories Pvt. Ltd. Recruitment– Multiple Openings Across Production, QA, QC, Engineering, F&D, ADL & Supply Chain appeared first on The Jobs Post –Job Alerts for Freshers & Experts.
