A leading Indian pharmaceutical company, renowned for its commitment to innovation, quality, and patient care across domestic and international markets, is hosting a walk-in interview. The company, which develops and manufactures a broad spectrum of pharmaceutical products from world-class, globally compliant facilities, offers significant career growth opportunities. This recruitment drive specifically targets experienced Quality Control (QC) professionals for its Injectable Manufacturing Unit.
Walk-In Interview Event:
Interested candidates are invited to attend a walk-in interview for Quality Control positions at the company’s Injectable Manufacturing Unit in Sanand, Ahmedabad, Gujarat.
- Date: Friday, 26th June 2026
- Time: 10:00 AM to 04:00 PM
- Venue: Plot No. SM-14-15-16/1, GIDC II, Sanand, Ahmedabad, Gujarat
Available Positions and Candidate Requirements:
The company is recruiting for Officer and Executive level roles within Quality Control, focusing on profiles with expertise in HPLC, GC, and LIMS.
- Designation: Officer / Executive
- Qualification: Applicants must hold a B.Pharm, M.Pharm, B.Sc, or M.Sc degree.
- Experience: A proven track record of 3 to 7 years of relevant experience in pharmaceutical Quality Control is essential.
Core Responsibilities:
Successful candidates will be integral to maintaining the highest quality standards, with responsibilities encompassing:
- Analytical Testing: Performing comprehensive analysis of Raw Materials, Packing Materials, In-process samples, Finished Products, and Stability Samples. This involves operating advanced analytical instruments such as HPLC, GC, UV, and FTIR, along with preparing and standardizing reagents.
- Documentation and Compliance: Rigorous review and documentation of analytical data in accordance with GMP (Good Manufacturing Practices) and GLP (Good Laboratory Practices). Ensuring strict adherence to data integrity guidelines, regulatory requirements, and efficient management of laboratory records.
- Quality Management: Handling Out of Specification (OOS) and Out of Trend (OOT) investigations, managing deviations, and implementing Corrective and Preventive Actions (CAPA). Contributions to method validation, verification, and stability studies, as well as collaboration with Quality Assurance and Production teams, are also key.
- Laboratory Upkeep: Conducting environmental and water monitoring, calibration, and routine maintenance of laboratory instruments to ensure operational readiness and regulatory compliance.
Desired Regulatory Experience:
Candidates with experience in regulated pharmaceutical settings are highly valued, particularly those familiar with:
- USFDA, EU GMP, and WHO GMP guidelines
- Strong Data Integrity Practices
- Operations within Injectable Manufacturing Facilities
Why Consider This Opportunity?
Join a leading pharmaceutical firm offering exposure to global regulatory frameworks and a state-of-the-art injectable manufacturing environment. This role promises professional growth, continuous learning, and a collaborative, quality-driven work culture.
Required Documents for Interview:
All applicants are requested to bring the following to the interview:
- Updated Resume/CV
- Educational Certificates
- Proof of Current CTC and Salary Slips
- Experience Certificates
- Government Identity Proof
- Recent Passport Size Photographs
Eligible and enthusiastic professionals are encouraged to attend this significant recruitment event with all necessary documentation to explore a rewarding career path.
