Attend Piramal Pharma’s walk-in interview on 20th July 2025 for Quality Control and Quality Assurance roles in Pithampur, Indore. Join a USFDA-compliant OSD facility. Apply now for QC/QA pharma jobs with 3–8 years of experience.
💼 Piramal Pharma Walk-In Interview July 2025 – Hiring for QC & QA Roles in Pithampur, Indore
Piramal Pharma Limited, a globally renowned Contract Development and Manufacturing Organization (CDMO), is organizing a walk-in interview on 20th July 2025 (Sunday) at its Pithampur, Indore facility. This hiring drive is for experienced professionals in Quality Control (QC) and Lab Quality Assurance (Lab-QA) roles, offering a golden opportunity to work in a USFDA and MHRA-compliant plant with cutting-edge technology and global reach.
🏢 About Piramal Pharma Limited
Piramal Pharma Solutions is a division of Piramal Enterprises Limited, operating in over 30 countries, with manufacturing facilities across North America, Europe, and Asia. With a turnover nearing $1.9 billion, Piramal has earned a strong reputation for its end-to-end drug development services. The Pithampur facility is a specialized hub for oral solid dosage (OSD) forms, capable of producing 4.5 billion units annually, and has been inspected and approved by major global regulatory bodies like USFDA, MHRA, and EU GMP.
📋 Job Openings at Pithampur Plant – QC & QA Roles
🔬 Quality Control (QC) – Sr. Executive / Deputy Manager
- Experience: 3–5 Years
- Qualification: B.Pharm / M.Pharm / M.Sc. (Chemistry)
- Core Responsibilities:
- Perform analysis of Raw Materials (RM), Finished Goods (FG), Stability, and Packaging Materials (PM)
- Execute stability studies aligned with ICH guidelines
- Ensure data integrity, proper documentation, and method validation
- Skills Required:
- Proficient in HPLC, GC, Dissolution Testers, Malvern 3000, and LCMS
- Good knowledge of instrument calibration, troubleshooting, and compliance protocols
🧪 Lab Quality Assurance (Lab-QA) – Sr. Executive / Deputy Manager
- Experience: 5–8 Years
- Qualification: B.Pharm / M.Pharm / M.Sc. (Chemistry)
- Core Responsibilities:
- Conduct electronic data review of analytical instruments (HPLC, LCMS, GC, Dissolution, etc.)
- Handle lab incidents, OOS/OOT investigations, and maintain quality oversight
- Ensure compliance with USFDA, MHRA, and EU GMP audit requirements
- Skills Required:
- Strong understanding of analytical data integrity and regulatory guidelines
- Experience in handling audit queries and supporting regulatory inspections
📅 Walk-In Interview Details – Mark Your Calendar!
- 🗓 Date: Sunday, 20th July 2025
- ⏰ Time: 9:00 AM to 3:00 PM
- 📍 Venue: Piramal Pharma Limited,
Plot No. 67–70, Sector-2,
Pithampur, Indore, Madhya Pradesh – 454775 - 📞 Contact: Anuj Yagik – +91 6260600524
- 📧 Email: Anuj.Yagik@piramal.com
📑 Documents to Carry
To be considered for these roles, bring the following:
- Updated Resume
- Educational Certificates
- Government-issued ID (Aadhar/PAN)
- 3 Passport-size Photos
- Latest Salary Proof (Payslips/Offer Letters)
❓ Can’t Attend the Walk-In?
If you’re unable to make it to the venue on the specified date, email your resume to Anuj.Yagik@piramal.com with the role you’re applying for. You can also explore more opportunities on:
🌟 Why Work at Piramal’s Pithampur Facility?
Piramal’s Pithampur site is among India’s leading OSD production plants, equipped with modern infrastructure and a fully functional in-house analytical laboratory conducting 99.5% of QC testing. With a 3.6/5 employee satisfaction rating, the site offers:
- Exposure to global regulatory standards
- Access to Piramal Learning University
- Opportunities to move into regulatory affairs, validation, and global project teams
🎓 Interview Preparation Tips
- Highlight experience with analytical equipment like HPLC, LCMS, and GC
- Emphasize any regulatory audit exposure (e.g., USFDA, MHRA)
- Mention your role in data integrity, investigation handling, or SOP implementation
🚀 Career Growth at Piramal
With internal mobility and structured learning pathways, Piramal supports continuous professional development. Employees have the chance to work on cross-functional projects and move across verticals such as QA, Regulatory Affairs, and Project Management.
✅ Apply Now!
If you are passionate about quality in pharmaceuticals and ready to make a global impact, don’t miss this opportunity to join a world-class pharma leader. Attend the walk-in interview on 20th July 2025 or send in your resume to begin your journey with Piramal Pharma Limited.
🔗 Apply Today and Take the Next Step Toward a Rewarding Career in Pharma!
