Quality Control

Role Overview: You 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 the 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. Key Responsibilities: - Conduct HPLC analysis of Solid Orals and Nasal products - Perform Quality Control activities related to Raw Materials, Packing, In Process, and Finished Products - Ensure compliance with GMP/GLP practices - Work in a fully automated, world-class manufacturing facility - Work with diverse dosage forms in a multi-product environment Qualifications Required: - Bachelor's or Master's degree in Pharmacy or Science - 3-8 years of relevant experience - 2-8 years of experience preferred - Prior exposure to working in regulated plants approved by USFDA/MHRA Additional Details: You will have the opportunity to 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.,