Full Time

Quality Control Officers

Macleods Pharmaceuticals
Indore
₹4 - ₹9 LPA
Posted 04/02/2026

About the Role

Role & Responsibilities
• Perform analysis and testing of raw materials (RM), in-process samples, finished goods (FG), and stability samples
• Execute analytical method validation (AMV), analytical method transfer (AMT), and related documentation
• Conduct stability studies including sample storage, testing, data compilation, and reporting
• Operate and maintain analytical instruments such as HPLC, GC, UV, and FTIR with proper calibration
• Maintain laboratory records in compliance with GLP and GMP requirements
• Investigate and document OOS, deviations, and laboratory incidents
• Support regulatory inspections and audits ensuring section-wise compliance
• Ensure adherence to pharmacopoeial standards (IP, USP, BP) and data integrity principles

Qualification
• B.Pharm
• M.Pharm

Experience
• 2–8 years of experience in Quality Control
• Experience in OSD and/or API QC preferred
• Exposure to FG, Stability, RM testing, AMT/AMV sections

Skills
• Strong knowledge of analytical techniques and pharmacopoeial standards
• Hands-on experience with HPLC, GC, UV, FTIR
• Good documentation practices and data integrity awareness
• Ability to troubleshoot laboratory and analytical issues

Salary & Benefits
• Estimated CTC: ₹4.0 – ₹9.0 LPA (based on experience and interview performance)
• Health insurance and mediclaim coverage
• Provident Fund and gratuity
• Performance-based incentives
• Professional development opportunities

Walk-In Interview Details
• Date: 8 February 2026 (Sunday)
• Time: 09:00 AM onwards
• Venue: Macleods Pharmaceuticals, Plot No. M50 to M54A, Indore SEZ Phase-II, Pithampur, Dist. Dhar, MP – 454774

About the Company
• Macleods Pharmaceuticals is one of India’s fastest-growing pharmaceutical companies
• Operates multiple GMP-compliant manufacturing facilities including a state-of-the-art Indore SEZ plant
• Strong presence in formulations and API manufacturing

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