Career Opportunity: Walk-in Interviews for Quality Professionals in a Leading Pharmaceutical Company
A prominent global pharmaceutical company is conducting a walk-in interview for skilled professionals in Quality Control (QC), Quality Assurance (QA), and In-Process Quality Assurance (IPQA). These full-time positions are based at its advanced manufacturing facility in Pithampur (Indore), Madhya Pradesh. The recruitment drive is specifically seeking experienced individuals to strengthen its quality operations. Interested candidates are invited to attend the interview on July 26, 2026, in Chhatrapati Sambhajinagar (Aurangabad), Maharashtra.
About the Company
The company stands as one of India’s leading global pharmaceutical entities, renowned for delivering integrated solutions across contract development and manufacturing (CDMO), complex hospital generics, and consumer healthcare products. With world-class manufacturing facilities and an unwavering commitment to quality, innovation, and regulatory excellence, it offers exceptional career pathways in manufacturing, quality, research, and operations.
Open Positions and Requirements
Opportunities are available for various roles, requiring a B.Pharm or M.Sc. qualification across all positions:
- QC Executive / Sr. Executive: Minimum 3 years of experience.
- QC Manager – Method Validation / Transfer: Minimum 10 years of experience.
- QC Manager – Stability: Minimum 10 years of experience.
- Lab QA / QC Reviewer – Sr. Executive / Dy. Manager: Minimum 6 years of experience.
- IPQA Manager: Minimum 9 years of experience.
Key Responsibilities Highlighted
Successful candidates will be involved in critical quality functions:
- QC Executives will perform analytical testing using advanced instruments like HPLC, GC, LCMS, and Dissolution apparatus, ensuring GMP compliance and supporting routine quality control.
- QC Managers (Method Validation / Transfer & Stability) will lead specialized teams, overseeing analytical method validation, method transfer activities, or comprehensive stability studies for Oral Solid Dosage (OSD) products, maintaining strict adherence to regulatory guidelines.
- Lab QA / QC Reviewers will be responsible for reviewing analytical and electronic QC data, investigating Out of Specification (OOS) and Out of Trend (OOT) events, and ensuring robust Quality Management System (QMS) compliance.
- IPQA Managers will lead In-Process Quality Assurance activities for the OSD manufacturing unit, ensuring cGMP compliance and driving quality improvement initiatives with their teams.
Essential Skills
Key skills sought include expertise in HPLC, GC, LCMS, Dissolution Testing, Analytical Method Validation, Method Transfer, Stability Studies, Quality Control, Quality Assurance, In-Process Quality Assurance (IPQA), OOS & OOT Investigation, cGMP Compliance, QMS, Regulatory Compliance, Team Leadership, and Pharmaceutical Documentation.
Walk-in Interview Details
Date: Sunday, July 26, 2026
Reporting Time: 9:00 AM – 3:00 PM
Venue: Lemon Tree Hotel, R-7/2, Chikalthana, Airport Road, Chhatrapati Sambhajinagar (Aurangabad) – 431001, Maharashtra
Job Location: Pithampur (Indore), Madhya Pradesh
Documents Required
Applicants should bring an updated Resume/CV, current appointment letter, latest salary slip, educational certificates and marksheets, a government-issued photo ID proof, experience certificates, and passport-size photographs.
Why Join This Company?
This is an opportunity to join a global pharmaceutical leader, working with advanced analytical laboratories and world-class manufacturing facilities. The roles offer significant exposure to comprehensive quality systems, regulatory compliance, and leadership within pharmaceutical operations, promising excellent opportunities for career growth, continuous learning, and professional development in an environment committed to innovation, quality, and excellence in pharmaceutical manufacturing.
