Macleods Pharmaceuticals Limited is conducting a Walk-In Drive for experienced professionals in Quality Control (OSD), Quality Assurance (OSD), Engineering Services (Injectable & OSD), and Technical Operations at its Indore facility. This recruitment drive offers excellent career opportunities for candidates with experience in pharmaceutical manufacturing, quality systems, validation, engineering maintenance, utilities, HVAC, calibration, and process engineering.

Company Overview

Macleods Pharmaceuticals is one of India’s leading pharmaceutical companies with a strong presence in regulated and semi-regulated markets. The company is known for its high-quality manufacturing facilities, compliance-driven operations, and global healthcare solutions.

Job Details

Location

Indore, Madhya Pradesh

Departments Hiring

Quality Control (OSD)

Position: Officer / Sr. Officer

Qualification:

• B.Pharm
• M.Pharm
• M.Sc (Chemistry)

Experience: 3–9 Years

Required Skills:

• GLP
• Stability Studies
• QMS
• AMT
• AMV
• Finished Product Testing
• Raw Material Analysis

Quality Assurance (OSD)

Officer / Sr. Officer

• Qualification: B.Pharm / M.Pharm
• Experience: 3–9 Years
• Skills: QMS, IPQA, Stability, AQA, Process Validation, Cleaning Validation

Executive / Sr. Executive

• Qualification: B.Pharm / M.Pharm
• Experience: 10–13 Years
• Skills: AQA, IPQA, AMT, AMV, Validation, Qualification, Training

Engineering Services (Injectable)

Executive / Sr. Executive

• Qualification: B.Tech / B.E
• Experience: 10–13 Years
• Skills: Process Engineering

Officer / Sr. Officer

• Qualification: B.Tech / B.E
• Experience: 3–9 Years
• Skills: HVAC, BMS, Water System, Utility, QMS, Electrical, Calibration

Technical Associate / Sr. Technical Associate

• Qualification: ITI / Diploma (Mechanical/Electrical)
• Experience: 3–9 Years
• Skills: HVAC, BMS, Utilities, Electrical Maintenance, Calibration

Engineering Services (OSD)

Officer / Sr. Officer

• Qualification: B.Tech / B.E
• Experience: 3–9 Years
• Skills: Documentation, Electrical, Plant Maintenance, Water System, QMS

Technical Associate / Sr. Technical Associate

• Qualification: ITI / Diploma (Mechanical/Electrical)
• Experience: 3–9 Years
• Skills: HVAC, BMS, Water System, Electrical, Plant Maintenance

Walk-In Interview Details

Date: 11th October 2026 (Sunday)

Time: 09:00 AM Onwards

Venue:
Phoenix Luxury Inn,
In Front of Nayara Petrol Pump,
Parisar Colony, Chhatra Chhaya,
Pithampur, Madhya Pradesh – 454775

Documents Required

• Updated Resume/CV
• Salary Structure (CTC Breakup)
• Aadhaar Card
• Educational Certificates
• Experience Documents

Technical FAQs

1. What is the role of GLP in Quality Control laboratories?

GLP (Good Laboratory Practices) ensures laboratory activities are performed accurately, consistently, and in compliance with regulatory requirements, improving data integrity and product quality.

2. Why is Process Validation important in pharmaceutical manufacturing?

Process Validation confirms that manufacturing processes consistently produce products meeting predefined quality specifications, ensuring safety and regulatory compliance.

3. What is the purpose of HVAC systems in pharmaceutical facilities?

HVAC systems control temperature, humidity, pressure differentials, and airborne contamination to maintain GMP-compliant manufacturing environments.

4. What is IPQA and why is it important?

In-Process Quality Assurance (IPQA) monitors manufacturing activities during production to ensure products meet quality standards and regulatory requirements.

5. What is calibration and why is it critical in engineering operations?

Calibration verifies that instruments and equipment provide accurate measurements, ensuring product quality, process reliability, and compliance with GMP regulations.

Conclusion

This Macleods Pharmaceuticals Walk-In Drive is an excellent opportunity for experienced pharmaceutical professionals in Quality Control, Quality Assurance, Engineering Services, Utilities, HVAC, Validation, and Process Engineering. Interested candidates should attend the interview with all required documents and relevant experience records.