AM-Engineering

As a part of Jubilant Pharma Limited, you will be an integral part of a global integrated pharmaceutical company that offers a wide range of products and services to customers across various geographies. The business is divided into two segments: **Role Overview:** - Jubilant Generics (JGL), a wholly-owned subsidiary of Jubilant Pharma, has Research & Development units in Noida and Mysore, India. - JGL operates manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, focusing on APIs and Dosage manufacturing. - The Mysore facility is a USFDA approved site manufacturing APIs, with a portfolio that targets Lifestyle driven Therapeutic Areas like CVS and CNS. - The Roorkee facility is a state-of-the-art site approved by multiple regulatory bodies like USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA, and follows a B2B model for EU, Canada, and emerging markets. - Both manufacturing units are supported by around 500 research and development professionals based in Noida and Mysore, working on the development of new products across various formulations. **Key Responsibilities:** - Production and manufacturing of APIs and Dosage forms. - Research and Development of new products in API and Solid Dosage Formulations. - Conducting BA/BE studies in-house at the 80-bed facility with global regulatory accreditations. - Regulatory Affairs and IPR professionals ensuring a unique portfolio of patents and product filings in regulatory and non-regulatory markets. **Qualifications Required:** - Bachelor's or Master's degree in Pharmacy or related field. - Previous experience in pharmaceutical manufacturing and research. - Knowledge of regulatory requirements and compliance. - Strong communication and team collaboration skills. You will be part of a dynamic team driving continuous growth and innovation in the pharmaceutical industry. For more information about the organization, please visit www.jubilantpharma.com.,