Jubilant Generics Limited
Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organise our business into two segments, namely, Specialty Pharmaceuticals, comprising Radiopharmaceuticals (including Radio pharmacies), Contract Manufacturing of Sterile Injectable, Non-sterile and Allergy Therapy Products, and Generics and APIs, comprising Solid Dosage Formulations and Active Pharmaceutical Ingredients.
Jubilant Generics (JGL) is a wholly - owned subsidiary of Jubilant Pharma. JGL in India has Research and Development units at Noida and Mysore. It has two manufacturing facilities one at Mysore, Karnataka and another at Roorkee, Uttarakhand,
engaged in APIs and Dosage manufacturing, respectively.
The manufacturing location at Mysore is spread over 69 acres and it's a USFDA approved site engaged in manufacturing of APIs, and caters to the sales worldwide. API portfolio focusses on Lifestyle driven Therapeutic Areas (CVS, CNS) and targets complex and newly approved molecules. The company is the market leader in four APIs and is amongst the top three players for another three APIs in its portfolio helping it maintain a high contribution margin. The manufacturing location at Roorkee, Uttarakhand is state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO and Brazil ANVISA. This business focusses on B2B model for EU, Canada and emerging markets.
Both manufacturing units are backward- integrated and are supported by around 500 research and development professionals based at Noida and Mysore. R and D 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.
JGL's full-fledged Regulatory Affairs and IPR professionals ensures unique portfolio of patents and product filings in regulatory and non-regulatory market.
Revenue of Jubilant Pharma is constantly increasing and during the Financial Year 2018 -19 it was INR 53,240 Million as compared to INR 39,950 Million during the Financial Year 2017-18.
Kindly refer www.jubilantpharma.com for more information about organization.
To handle Product Life Cycle management and Product Portfolio planning for Non-US formulations business
- Using Business Analytics to monitor Product life cycle of Formulations business
- Constant tracking of the formulations business/business reports to explore new opportunities to be supported with adequate commercial and medical evaluation
and bull;;;;;;; Managing Product Life Cycle of all Non-US products;;;
- Constantly monitoring market data/information/reports for
- Analyzing the trends and working out future projections
-Identifying future products and Therapies to invest in
-Product improvements plans to extend product life cycle, wherever required
-Constantly monitoring patent scenario for key products
and bull;;;;;;; Periodic review of forecasts
- Periodic review of forecasts and track product development/improvement progress to arrive at continue/drop/modify decision.
- Co-ordination with Regional Managers to capture and analyze various opportunities on a Regional/Global scale
- To keep track of New Product Approvals world-wide
and bull;;;;;;; Prepare overall Portfolio strategy and product identification processes
- Product identification and recommendation to strengthen the product portfolio in chosen countries
- Identify newer therapies ( and Products) to enter in
- Robust commercial and adequate medical evaluation based product identification
Education Qualification(Highest )- Post Graduate / Graduate in Pharma/Life sciences
Experience Range :;;;; 4-8 years
No. of years post Highest Qualification : 3 years with Healthcare consultancy / Pharma industry with business analytics experience
Desirable experience :
and bull;;;;;;; Relevant product and science knowledge
and bull;;;;;;; Understanding of Key Pharma market dynamics
and bull;;;;;;; Business and Financial acumen
and bull;;;;;;; Awareness of Regulatory/IP aspects
and bull;;;;;;; Business forecasting and financial analysis
and bull;;;;;;; Collaborative work - ability to drive CFT's for a common goal