Senior Executive-Production
Job Summary
We are seeking a skilled Manufacturing Professional to join our team at Jubilant Pharma Limited. In this role, you will be responsible for ensuring the smooth operation of our manufacturing facilities and contributing to the development of new products.
About Us
Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. Our business is organized into two segments: Specialty Pharmaceuticals and Generics APIs.
About Our Team
Jubilant Generics (JGL) is a wholly-owned subsidiary of Jubilant Pharma. JGL has Research Development units at Noida and Mysore, with manufacturing facilities in Mysore and Roorkee, Uttarakhand.
Your Responsibilities
• Preparation of standard operating procedures (system related and equipment related)
• Online completion and reviewing of the batch production records and related documents
• Production planning and target achievement with respect to planned production
• Online completion and review of the log cards of equipment, environment monitoring, balance verification, tablet tooling, filter cleaning etc.
• Process Optimization
• Monitoring and controlling the yield losses during production process
• Planning and execution of the preventive maintenance schedule of the equipments with engineering department before last due dates
About Our Facilities
Our manufacturing location at Mysore is a USFDA approved site engaged in manufacturing of APIs, catering to sales worldwide. Our API portfolio focuses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules.
Our manufacturing location at Roorkee, Uttarakhand is a state-of-the-art facility audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focuses on B2B model for EU, Canada and emerging markets.
About Our Culture
Both manufacturing units are backward-integrated and supported by around 500 research and development professionals based at Noida and Mysore. RD works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids.
All BA/BE studies are done In-house at our 80 Bed facility which is inspected and having approvals/certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services.
About Our Growth
JGL's full-fledged Regulatory Affairs IPR professionals ensure a unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing, with INR 53,240 Million during the Financial Year 2018-1+ compared to INR 3+,+50 Million during the Financial Year 2017-18.
What We Offer
We offer a dynamic work environment, opportunities for growth and development, and a competitive compensation package.
Apply Now
We are seeking a skilled Manufacturing Professional to join our team at Jubilant Pharma Limited. In this role, you will be responsible for ensuring the smooth operation of our manufacturing facilities and contributing to the development of new products.
About Us
Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. Our business is organized into two segments: Specialty Pharmaceuticals and Generics APIs.
About Our Team
Jubilant Generics (JGL) is a wholly-owned subsidiary of Jubilant Pharma. JGL has Research Development units at Noida and Mysore, with manufacturing facilities in Mysore and Roorkee, Uttarakhand.
Your Responsibilities
• Preparation of standard operating procedures (system related and equipment related)
• Online completion and reviewing of the batch production records and related documents
• Production planning and target achievement with respect to planned production
• Online completion and review of the log cards of equipment, environment monitoring, balance verification, tablet tooling, filter cleaning etc.
• Process Optimization
• Monitoring and controlling the yield losses during production process
• Planning and execution of the preventive maintenance schedule of the equipments with engineering department before last due dates
About Our Facilities
Our manufacturing location at Mysore is a USFDA approved site engaged in manufacturing of APIs, catering to sales worldwide. Our API portfolio focuses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules.
Our manufacturing location at Roorkee, Uttarakhand is a state-of-the-art facility audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focuses on B2B model for EU, Canada and emerging markets.
About Our Culture
Both manufacturing units are backward-integrated and supported by around 500 research and development professionals based at Noida and Mysore. RD works on Development of new products in API, Solid Dosage Formulations of Oral Solid, Sterile Injectable, Semi-Solids Ointments, Creams and Liquids.
All BA/BE studies are done In-house at our 80 Bed facility which is inspected and having approvals/certifications from The Drugs Controller General (India) and has global regulatory accreditations including USFDA, EMEA, ANVISA (Brazil), INFRAMED (Portugal Authority), NPRA(Malaysia), AGES MEA (Austria) for GCP and NABL, CAP accreditations for Path lab services.
About Our Growth
JGL's full-fledged Regulatory Affairs IPR professionals ensure a unique portfolio of patents and product filings in regulatory and non-regulatory market. Revenue of Jubilant Pharma is constantly increasing, with INR 53,240 Million during the Financial Year 2018-1+ compared to INR 3+,+50 Million during the Financial Year 2017-18.
What We Offer
We offer a dynamic work environment, opportunities for growth and development, and a competitive compensation package.