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Job Description

Role Overview: Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services across various geographies. The business is organized into two segments, namely Specialty Pharmaceuticals and Generics & APIs. Jubilant Generics (JGL) is a wholly-owned subsidiary of Jubilant Pharma, with research & development units in Noida and Mysore, India. JGL operates manufacturing facilities in Mysore, Karnataka, and Roorkee, Uttarakhand, focusing on APIs and Dosage manufacturing. Key Responsibilities: - Qualification & Management of Stability Chambers - Loading & withdrawal of Stability samples - Storage & destruction of Sample after testing - Stability report compilation - Investigation of deviation, Incidents, OOS & OOT results - Recording of analytical data - Preparation & Review of SOPs - Self-auditing - Adherence of SOPs, STPs & GTPS - cGMP / GLP compliance Qualifications Required: - Experience in handling Stability Chambers - Knowledge of loading & withdrawal procedures for Stability samples - Ability to compile Stability reports - Skilled in investigating deviations, Incidents, OOS & OOT results - Proficiency in recording analytical data and reviewing SOPs - Strong understanding of cGMP / GLP compliance and adherence to SOPs, STPs & GTPS - Self-auditing capabilities to ensure compliance with regulatory standards For more information about the organization, kindly visit www.jubilantpharma.com.,

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