Join over 250+ passionate scientists, chemical engineers, and regulatory specialists advancing life-saving therapies across India and 50+ global markets.
We combine the entrepreneurial speed of a fast-growing pharma leader with the stability, safety, and governance of an established global supplier.
Over 1,420+ continuous days without a lost-time injury. Automated process safety systems, high-spec personal protective equipment (PPE), and continuous industrial hygiene monitoring protect our team 24/7.
Every employee undergoes an average of 24+ hours of annual technical, cGMP, and EHS training. We sponsor higher education, certifications, and international scientific conferences.
With 4 major manufacturing units and a rapid expansion pipeline across Kopparthi and Bidar, high performers enjoy rapid promotions, cross-functional lateral moves, and direct executive mentorship.
Explore immediate openings across our Central R&D center in Hyderabad and manufacturing plants in Bidar and Kadapa.
Lead route scouting, QbD parameter design, and biocatalytic chiral resolution for upcoming CNS and antiviral generic APIs. Collaborate with Kilo lab teams for tech transfer.
Perform chromatographic method validation, forced degradation studies, and finished API batch release under strict 21 CFR Part 11 and WHO-GMP data integrity standards.
Author Module 3 CTD dossiers for Regulatory Type II DMFs and European CEP filings. Coordinate with regulatory agencies for deficiency responses and customer technical audits.
Supervise multi-ton batch reactor trains, centrifugation, and cleanroom vacuum drying blocks. Ensure complete BMR compliance, safety interlocks, and solvent recovery adherence.
Oversee continuous operation of the 150 KLD ETP, Multiple Effect Evaporator (MEE), and hazardous waste co-processing programs. Maintain ISO 14001 / 45001 compliance.
Even if your specific role is not listed above, we actively review resumes for exceptional chemists and engineers.
