Gland Pharma Limited, one of India’s most trusted pharmaceutical companies, is hiring experienced Quality Assurance professionals for its sterile injectables division. The company will conduct a walk-in interview on 17th October 2025 at its Pashamylaram facility (Unit-II) near Hyderabad.
This opportunity is ideal for candidates with 5–8 years of QA experience in injectable manufacturing who aspire to grow in a global, regulatory-compliant CDMO environment.
About Gland Pharma
Founded in 1978 and headquartered in Hyderabad, India, Gland Pharma Limited is a global leader in injectables and a contract development and manufacturing organization (CDMO). The company specializes in generic and complex injectables, supplying high-quality, affordable medicines to 100+ countries, including the USA, Europe, Canada, and Australia.
With USFDA- and EMA-approved facilities, Gland Pharma ensures the highest standards of quality, innovation, and regulatory compliance. Its consistent focus on sterile manufacturing excellence makes it one of the top pharma employers in India.
Job Details – QA Executive (Sterile Injectables)
Department: Quality Assurance
Designation: Executive / Senior Executive
Experience: 5–8 years
Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc
Work Location: Unit-II, MPSF Plant, Pashamylaram (On-Site)
This position involves batch release and quality assurance activities for sterile injectable products. Candidates should have a strong foundation in regulatory audits, process validation, and documentation control.
Key Responsibilities
Review Master Batch Production Records (MBPR) and media fill reports
Compile and verify Batch Production and Control Records (BPCR) for release
Issue BPCRs and monitor production requisitions
Report deviations and maintain executed documentation
Prepare and review process validation and cleaning validation protocols
Ensure compliance with cGMP, SOPs, and global regulatory standards
Skills & Qualifications
Deep understanding of sterile injectable manufacturing processes
Proficiency in batch release, deviation reporting, and documentation
Hands-on experience with media fill, validation protocols, and regulatory compliance
Strong communication and teamwork skills
Walk-In Interview Details
📅 Date: Friday, 17th October 2025
⏰ Time: 09:30 AM – 11:30 AM
📍 Venue:
Gland Pharma Limited (Unit-II)
Plot No. 42–52, Phase III, TSIC Industrial Area,
Pashamylaram, Telangana
What to Bring:
Updated Resume
Educational Certificates
Experience Letters
Latest Salary Slips / CTC Proof
Photo ID (Aadhar / PAN)
Outstation Candidates:
Email your resume to Suryateja.velaga@glandpharma.com. (No walk-in required; virtual screening will be scheduled.)
Important: Gland Pharma does not charge any recruitment fees. Beware of unauthorized job agencies.
Why Join Gland Pharma?
Working at Gland Pharma means joining a global pharmaceutical powerhouse known for its strong compliance culture and innovation in injectables.
Employee Benefits:
Comprehensive health insurance
Transport facilities and hybrid work support
Performance-based incentives
Training and development opportunities
Retirement benefits and long-term stability
This QA role offers a strategic career path in sterile manufacturing with exposure to regulated international markets.
Background Context
As the demand for sterile injectables continues to rise globally, Gland Pharma remains at the forefront of manufacturing excellence. With cutting-edge facilities and a workforce committed to precision, the company continues to drive India’s leadership in global pharma exports.
According to the USFDA and EMA regulatory database, Gland Pharma maintains a strong record of compliance, making it a preferred partner for major international pharmaceutical brands.
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