Quality Control

The ideal candidate for this role should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of relevant experience. Immediate joiners are preferred for this position. As a member of our team, your responsibilities will include conducting HPLC analysis of Solid Orals and Nasal products, hands-on experience in Quality Control activities related to Raw Materials, Packing, In Process, and Finished Products, as well as ensuring compliance with GMP/GLP practices. The preferred candidate will have 2-8 years of experience and prior exposure to working in regulated plants, specifically those approved by USFDA/MHRA. In return, you will have the opportunity to work in a fully automated, world-class manufacturing facility. You will be involved in working with diverse dosage forms in a multi-product environment. Additionally, you will receive attractive attendance bonuses, special allowances, and unparalleled opportunities for learning and growth. This is a full-time position with benefits such as Provident Fund, yearly bonus, and day shift schedule. The ability to commute or relocate to Tirupati, Andhra Pradesh is required for this role. If you are ready to join immediately and have at least 3 years of experience in 10-key typing, we encourage you to apply. The application deadline for this position is 14/07/2025.,