India's DMPLOI - Jobs & Networking AppMacleods Pharmaceuticals has announced a Walk-in Drive for experienced professionals in Quality Control (Peptide API) and Production (Peptide). The walk-in interview will be conducted in Ahilyanagar, Maharashtra, for positions based in Indore. Candidates with relevant pharmaceutical manufacturing experience are invited to attend.
Overview
Particulars Details
Company
Macleods Pharmaceuticals Ltd.
Job Type
Walk-in Interview
Work Location
Indore
Walk-in Venue
Hotel Paradise, New Tilak Road, Near Sarkar Chowk, Maliwada, Ahilyanagar, Maharashtra – 414001
Walk-in Date
5 July 2026 (Sunday)
Reporting Time
09:00 AM onwards
Vacancy Details
1. Quality Control – Peptide (API)
Position: Officer / Sr. Officer
Qualification: B.Pharm / M.Pharm / M.Sc. (Chemistry)
Experience: 3–8 years
Required Expertise: RM/FG section
2. Production (Peptide)
Executive / Sr. Executive
Qualification: B.Sc. / M.Sc. (Chemistry)
Experience: 9–12 years
Skills Required:
Peptide Production
QMS
Purification
Synthesis
HPLC
Officer / Sr. Officer
Qualification: B.Sc. / M.Sc. (Chemistry)
Experience: 3–8 years
Skills Required:
Peptide Production
Purification
Synthesis
HPLC
Documents Required
Candidates should carry:
Updated CV/Resume
Current Salary Structure (CTC Break-up)
Aadhaar Card
Other relevant educational and experience documents (recommended)
Registration
Interested candidates are advised to register through the official Macleods registration link or QR code provided in the notification before attending the interview.
Why Join Macleods?
Macleods Pharmaceuticals is one of India’s leading pharmaceutical companies with a strong presence in APIs, formulations, and global regulated markets. The company offers opportunities to work with advanced manufacturing facilities while following cGMP, quality systems, and regulatory compliance.
Selection Process
Registration
Document Verification
Technical Interview
HR Discussion
Final Selection
Technical FAQs
1. What is RM/FG testing in Quality Control?
RM (Raw Material) testing verifies the quality of incoming materials, while FG (Finished Goods) testing ensures the final pharmaceutical product meets all quality specifications before release.
2. Why is HPLC important in peptide manufacturing?
HPLC (High-Performance Liquid Chromatography) is used to determine peptide purity, identify impurities, and ensure product quality according to regulatory standards.
3. What does peptide purification involve?
Peptide purification removes unwanted impurities and by-products after synthesis using chromatographic techniques to achieve the required purity.
4. What is the role of QMS in pharmaceutical production?
A Quality Management System (QMS) ensures compliance with GMP requirements through documentation, deviation management, CAPA, change control, and continuous quality improvement.
5. What technical skills are expected for peptide production roles?
Candidates should have knowledge of peptide synthesis, purification processes, HPLC analysis, GMP documentation, equipment operation, process monitoring, and pharmaceutical safety practices.
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