Neuland Laboratories Limited, a global leader in active pharmaceutical ingredients (APIs) since 1984, is urgently hiring for pharmaceutical jobs in the Quality Control (QC) Department at our USFDA-approved facilities in Hyderabad, Telangana.
We seek experienced professionals with 3-6 years in HPLC, GC, and LCMS to join our team immediately and advance their Hyderabad pharma careers. As a publicly listed company, Neuland is renowned for delivering end-to-end chemistry solutions to the pharmaceutical industry.
Why Join Neuland Laboratories?
Headquartered in Hyderabad, Neuland operates three FDA-inspected facilities and supports over 85 countries with 846+ DMFs. With a 4.1/5 AmbitionBox rating based on 595 reviews, our collaborative culture, rated 3.9/5, fosters innovation and work-life balance (3.8/5).
Our 40,000 sq. ft. R&D center, staffed by 300+ scientists, drives cutting-edge API development, making Neuland ideal for quality control jobs. Immediate joiners will work in a cGMP-compliant environment, contributing to high-quality APIs for global biotech and pharma leaders.
Job Details
- Location: Hyderabad, Telangana (Unit-3, Gaddapotharam preferred, based on prior Neuland job postings)
- Department: Quality Control (QC)
- Apply: Send resume via WhatsApp to 8179538447 (mention “QC Application”)
- Website: www.neulandlabs.com
- Note: Immediate joiners highly preferred. Bring updated CV, educational certificates, Aadhaar/PAN, last 3 months’ payslips, and experience letters to interviews. Neuland does not charge recruitment fees; beware of fraudulent agencies.
Open Position: Quality Control (HPLC, GC, LCMS)
- Experience: 3-6 years
- Qualification: M.Sc. (Chemistry)/B.Pharm/M.Pharm (inferred from industry standards and web data)
- Vacancies: Multiple (inferred from “urgent openings”)
Required Skills:
- Proficiency in operating HPLC, GC, and LCMS for API testing
- Expertise in method development, validation, and transfer
- Strong knowledge of cGMP, GLP, and 21 CFR Part 11 compliance
- Experience with EMPOWER data review, SOP preparation, and OOS investigations
- Ability to troubleshoot analytical instruments and handle RM/PM/FP testing
Responsibilities:
- Conduct analytical testing of APIs using HPLC, GC, and LCMS
- Review and document analytical data, ensuring compliance with USFDA standards
- Perform stability studies, impurity profiling, and method verification
- Coordinate with production for timely analysis and release
- Support regulatory audits and maintain laboratory safety norms
Career Path: Opportunities to advance to senior QC roles or cross-functional positions in R&D within 2-4 years.
Why Hyderabad?
Hyderabad, a global hub for pharmaceutical jobs, hosts over 1,700 Neuland employees and offers a thriving pharma ecosystem. With proximity to Jubilee Hills and excellent connectivity, it’s perfect for professionals in quality control jobs. Learn more about India’s pharma industry at India’s Pharmaceutical Industry.
Neuland’s Commitment to Excellence
Neuland’s Hyderabad facilities, including Unit-1 with zero 483 observations in USFDA audits, exemplify our commitment to quality. Our QC team plays a critical role in ensuring API integrity across 10 therapeutic areas, from clinical trials to commercial manufacturing.
Immediate joiners will benefit from hands-on training in advanced analytical techniques and exposure to global regulatory standards. Our focus on teamwork, innovation, and patient health creates a rewarding environment for professionals passionate about precision and quality.
How to Apply
Immediate joiners are strongly preferred. Send your updated CV via WhatsApp to 8179538447 with “QC Application” in the message by May 25, 2025. Alternatively, email careers@neulandlabs.com or visit www.neulandlabs.com for more details. Prepare for interviews with all required documents to expedite the process.
Neuland’s rigorous recruitment ensures a perfect fit for our culture of excellence. Join Neuland Laboratories and excel in Hyderabad pharma careers, contributing to a healthier world through superior APIs!
Be Part of Neuland’s Legacy
Neuland Laboratories is more than a workplace—it’s a platform for innovation and impact. With a 27-year history of USFDA compliance and a non-competitive stance with customers, we prioritize API manufacturing and contract services.
Our QC professionals are integral to our mission, ensuring every product meets global standards. Don’t miss this urgent opportunity to join a leading CDMO and shape the future of pharmaceuticals in quality control jobs. Apply now and turn opportunity into reality with Neuland!
