Executive-Packing Jubilant Generics Limited
Jubilant Generics Limited
Office Location
Full Time
Experience: 2 - 2 years required
Pay:
Salary Information not included
Type: Full Time
Location: Saharanpur
Skills: manufacturing, APIs, RD, Regulatory Affairs, IPR, SOPs, production planning, Process optimization, Preventive Maintenance, QMS, Training, Solid Dosage Formulations, cGMP Standards, Audits
About Jubilant Generics Limited
Job Description
As a member of Jubilant Pharma Limited, you will be part of a global integrated pharmaceutical company that offers a diverse range of products and services to customers worldwide. Our business is structured into two segments - Specialty Pharmaceuticals and Generics & APIs. Jubilant Generics (JGL), a wholly-owned subsidiary of Jubilant Pharma, operates Research & Development units in Noida and Mysore, India. We have manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, focusing on APIs and Dosage manufacturing. Our Mysore facility is a USFDA approved site with a strong API portfolio catering to global sales, particularly in Lifestyle driven Therapeutic Areas. The Roorkee facility is a state-of-the-art site approved by multiple regulatory bodies for B2B models in various markets. Our manufacturing units are supported by a team of around 500 research and development professionals working on developing new products in API and Solid Dosage Formulations. Our R&D facilities have global regulatory accreditations and conduct BA/BE studies in-house. Your role will involve the following responsibilities: - Preparation of standard operating procedures for both system-related and equipment-related processes - Completion and review of batch production records and related documents online - Production planning and target achievement - Process optimization and monitoring of yield losses - Planning and execution of preventive maintenance schedules - Monitoring and controlling equipment and environment parameters - Online entries in SAP system - Procurement and approval of change parts and tablet tooling - Handling of Quality Management System activities - Compliance with SOPs and audit observations - Manufacturing and market investigation reviews - Maintaining cGMP standards throughout the process - Ensuring readiness for audits or visits - Managing consumable stocks and cleaning activities - Providing on-the-job training and demonstrations to employees - Allocating tasks to subordinates Join us at Jubilant Pharma Limited and be a part of our growth story. For more information about our organization, visit www.jubilantpharma.com.,