Company Description Stallion Laboratories, incorporated in 1988, is a distinguished Pharmaceutical Formulation Manufacturer with a WHO GMP approved facility and GLP qualified quality control. The company excels in managing niche products with a focus on creativity and uncompromised quality. With a strong presence in both Indian and international markets, Stallion Laboratories has strategic alliances in regions including South Latin America, Africa, South East Asia, CIS, and Francophone countries. Certified by WHO GMP, GLP, and ISO 9001-2015, Stallion Laboratories is expanding with a new facility aimed at obtaining UK-MHRA, EU GMP, and PICS approvals to enter regulated markets. Role Description This is a full-time, on-site role located in Ahmedabad for a Formulation and Development position at Stallion Laboratories. The successful candidate will be responsible for developing pharmaceutical formulations, ensuring regulatory compliance, performing stability testing, and maintaining detailed records of formulation processes. Additional duties include collaborating with cross-functional teams, staying updated with industry trends, and ensuring adherence to quality standards. Qualifications Analytical SkillsExcellent Communication skillsAbility to work collaboratively with cross-functional teamsStrong understanding of regulatory requirements and quality standardsExperience in pharmaceutical formulation development is highly desirableDegree in Pharmacy, Pharmaceutical Sciences, or related field