Glenmark Pharmaceuticals Ltd., a leading integrated research-led global pharmaceutical company, is hosting a Walk-in Interview on June 22, 2025, at our manufacturing unit in Baddi, Himachal Pradesh.
With a mission to improve lives through innovative and affordable medicines, our USFDA and WHO-GMP-approved facility in Kishanpura invites enthusiastic professionals to join our team in Production, Quality Control, and Quality Assurance departments.
About Glenmark Pharmaceuticals
Founded in 1977 and headquartered in Mumbai, Glenmark Pharmaceuticals is a global innovator with a presence in 50+ countries, including the US, Europe, and Asia. Our Baddi facility specializes in inhalers (MDI/DPI), liquid formulations, and solid oral dosages, adhering to USFDA, EU-GMP, and WHO-GMP standards.
With 18,000+ employees and ₹12,605 crore in revenue (FY23), Glenmark is known for generics, branded formulations, and a robust R&D pipeline. Rated 3.8/5 on AmbitionBox for job security, we focus on quality and innovation.
Walk-in Interview Details
We’re hiring for roles at our Kishanpura, Baddi manufacturing unit. Below are the event details:
| Event Details | Information |
|---|---|
| Date | June 22, 2025 (Sunday) |
| Time | 10:00 AM to 4:00 PM IST (Entry closes at 2:00 PM) |
| Venue | Glenmark Pharmaceuticals Ltd., Village-Kishanpura, Baddi-Nalagarh Road, Tehsil-Baddi, Distt-Solan, Himachal Pradesh 173205 |
| Job Location | Baddi, Solan, Himachal Pradesh |
| Application Contact | Savitor Singh: Savitor.Singh@glenmarkpharma.com |
| Note | Only candidates with relevant experience are eligible |
Job Opportunities
Below are the open positions, qualifications, experience, and roles at our Baddi facility, focusing on liquid, inhaler, and quality operations.
1. Production (Liquid)
- Designation: Officer / Senior Officer
- Qualification: D.Pharm
- Experience: 2–6 years
- Section: Manufacturing & Packaging
- Responsibilities:
- Oversee liquid formulation manufacturing and packaging (e.g., syrups, suspensions).
- Ensure batch record compliance and cGMP standards.
- Operate and maintain production equipment in cleanrooms.
- Skills:
- Hands-on experience with liquid manufacturing processes.
- Knowledge of cGMP, SOPs, and cleanroom protocols.
2. Quality Control (Nasal/MDI/DPI)
- Designation: Officer / Senior Officer
- Qualification: M.Sc. / M.Pharm / B.Pharm
- Experience: 2–6 years
- Section: FG/Stability/RM/Documentation/GLP
- Responsibilities:
- Conduct analytical testing of finished goods (FG), raw materials (RM), and stability samples using HPLC, GC, and dissolution testers.
- Perform inhaler testing (e.g., MDI, DPI) for particle size and delivery efficiency.
- Ensure GLP-compliant documentation for USFDA audits.
- Skills:
- Proficiency in HPLC, GC, and inhaler testing.
- Familiarity with cGMP, stability studies, and regulatory compliance.
3. Quality Assurance
- Designation: Officer / Senior Officer
- Qualification: M.Sc. / M.Pharm / B.Pharm
- Experience: 2–6 years
- Section: IPQA
- Responsibilities:
- Conduct In-Process Quality Assurance (IPQA) checks during liquid and inhaler manufacturing.
- Manage deviations, CAPA, and batch record reviews.
- Support USFDA audit preparation and validation activities.
- Skills:
- Expertise in IPQA, cGMP, and USFDA guidelines.
- Strong documentation and analytical skills.
Why Join Glenmark Pharmaceuticals?
Glenmark offers a rewarding career in a globally respected pharmaceutical leader. Benefits include:
- Competitive Salary: Officers earn ₹3–7 LPA; Senior Officers ₹5–10 LPA in Baddi.
- Global Exposure: Work in a USFDA/WHO-GMP-approved facility serving 50+ countries.
- Career Growth: Training in HPLC, IPQA, inhaler testing, and cGMP.
- Supportive Culture: Rated 3.8/5 for job security and 3.6/5 for work-life balance (AmbitionBox).
- Challenges: Employees note high-pressure timelines and occasional overtime (3.5/5 work-life balance).
Why These Roles Matter
These roles drive Glenmark’s production of liquid formulations and inhalers (MDI/DPI), critical for respiratory and pediatric markets. Your work in manufacturing, QC testing, or IPQA ensures quality and compliance, supporting Baddi’s 1,200+ pharma job ecosystem.
Growth Opportunities
Glenmark invests in training for USFDA compliance, analytical techniques, and inhaler development. The Baddi facility offers exposure to global standards, though employees report moderate career growth (3.4/5) and shift-based work.
Work Environment
The Baddi facility features cleanrooms, HPLC labs, and inhaler testing equipment, fostering a quality-focused culture (3.8/5 job security). Expect shift-based roles for production and a structured schedule with entry closing at 2:00 PM.
How to Attend
Join us on June 22, 2025, from 10:00 AM to 4:00 PM at Village-Kishanpura, Baddi. Bring:
- Updated resume.
- Recent passport-size photograph.
- Last two months’ salary slips.
- Educational certificates.
- Experience letters (if applicable).
For queries, contact Savitor Singh at Savitor.Singh@glenmarkpharma.com. Note: Entry closes at 2:00 PM; arrive early.
Preparation Tips
- Production: Highlight liquid manufacturing or packaging experience.
- QC: Detail HPLC or inhaler testing expertise.
- QA: Emphasize IPQA or cGMP audit knowledge.
- Prepare for questions like “How do you ensure cGMP in liquid production?” or “What are key tests for MDI/DPI?”
Important Disclaimer
Glenmark Pharmaceuticals maintains a transparent recruitment process. We do not charge fees or use free email services (e.g., Gmail, Yahoo) for job offers. Verify opportunities through Savitor.Singh@glenmarkpharma.com or Glenmark Careers. Report suspicious activities to HR.
Stay Safe from Fraud
- Confirm offers through official Glenmark channels.
- Avoid sharing personal or financial information with unverified sources.
- Contact Savitor Singh for clarifications.
Why Baddi?
Baddi, Himachal Pradesh, is a pharma manufacturing hub with 1,200+ jobs, hosting Glenmark’s USFDA-approved facility. Its tax benefits and proximity to Chandigarh (50 km) make it ideal for industrial careers.
Join Glenmark’s Mission
Glenmark Pharmaceuticals is committed to improving lives through innovative medicines. By joining our Baddi team, you’ll contribute to USFDA-compliant liquid and inhaler production for global markets. Attend our walk-in interview on June 22, 2025, to join our 18,000+ strong team!
Next Steps
Arrive early for registration (by 2:00 PM) on June 22, 2025. The selection process may include technical interviews (e.g., HPLC analysis, IPQA checks) and document verification. Selected candidates will receive spot offers or follow-up communication.
Contact Us
For queries, email Savitor.Singh@glenmarkpharma.com or visit Glenmark Contact. Stay updated via Glenmark Careers.
Innovate with Glenmark
Join Glenmark Pharmaceuticals to advance pharmaceutical manufacturing in Baddi. Attend our Walk-in Interview on June 22, 2025, and contribute to global healthcare!
