Glenmark Pharmaceuticals Ltd., a research-driven global pharmaceutical company headquartered in Mumbai, has announced a walk-in interview in Indore for multiple pharmaceutical jobs. The hiring drive is for its USFDA-approved formulation facility at Pithampur, Indore, focusing on OSD (Oral Solid Dosage) and SSD (Semi Solid Dosage) manufacturing.
The Glenmark walk-in interview 2026 will be conducted from 16 March to 20 March 2026, offering opportunities for freshers and experienced pharma professionals (0–9 years experience) in Quality Control, Quality Assurance, Production, and Warehousing departments.
This hiring event is ideal for candidates seeking pharmaceutical jobs in Indore, QC analyst jobs, QA officer roles, and production jobs in pharma manufacturing plants.
Job Details
- Company: Glenmark Pharmaceuticals Ltd.
- Job Type: Walk-in Interview
- Industry: Pharmaceutical / Formulation Manufacturing
- Experience Required: 0–9 Years
- Location: Pithampur, Indore, Madhya Pradesh
- Interview Dates: 16 – 20 March 2026
- Interview Time: 02:00 PM – 04:00 PM IST
Department & Position Details
1. Quality Control (QC)
Sections: RM / PM / Compliance / FG / Stability / QMS / Lab Support
Designation: Trainee, Officer, Senior Officer, Executive
Experience: 0–9 Years
2. Quality Control – LIMS
Designation: Senior Officer
Experience: 4–7 Years
3. Quality Assurance (QA/IPQA)
Designation: Officer
Experience: 2–4 Years
4. Semi Solid Dosage Manufacturing
Sections: SS Manufacturing / SS Filling
Designation: Junior Officer
Experience: 2–4 Years
5. Solid Dosage Manufacturing
Sections: Granulation / Compression / Packaging / Coating / Capsule Filling
Designation: Junior Officer / Officer / Senior Officer
Experience: 2–8 Years
6. Warehousing
Sections: FG / RM / QMS
Designation: Officer
Experience: 3–6 Years
Key Responsibilities
Quality Control
- Perform RM, PM, FG, and stability testing using validated analytical methods.
- Maintain quality documentation and compliance with regulatory standards.
- Ensure adherence to USFDA, GMP, and GLP guidelines.
- Operate and maintain analytical instruments and LIMS systems.
Quality Assurance / IPQA
- Conduct in-process quality checks during manufacturing.
- Review batch manufacturing records (BMR) and compliance documentation.
- Ensure production processes comply with GMP and regulatory standards.
Production (OSD & SSD)
- Operate manufacturing equipment for granulation, compression, coating, capsule filling, and packaging.
- Monitor semi-solid and oral solid dosage production processes.
- Maintain equipment cleaning and documentation as per SOPs.
Warehousing
- Handle raw materials, finished goods, and inventory documentation.
- Maintain warehouse compliance and quality management systems.
Qualifications
- B.Pharm / M.Pharm / B.Sc / M.Sc / Diploma in Pharmacy / relevant science degree
- Experience in pharmaceutical manufacturing or quality functions preferred
- Knowledge of GMP, GLP, and regulatory compliance
- Freshers may apply for trainee and entry-level QC roles
Benefits of Working at Glenmark
- Opportunity to work in a USFDA-approved pharmaceutical manufacturing facility
- Exposure to global regulatory standards and advanced pharma manufacturing technologies
- Competitive salary packages and career growth opportunities
- Professional development within a global pharmaceutical company
Walk-in Interview Details
Venue:
Glenmark Pharmaceuticals Limited
Plot No. 2, Phase II, Pharma Zone
I SEZ, Pithampur, Indore, Madhya Pradesh – 454775
Interview Date: 16 – 20 March 2026
