Jubilant Generics (JGL) is a wholly – owned subsidiary of Jubilant Pharma. JGL in India has Research & 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&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 & 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.
Job Context:
Procurement of Raw materials, packing materials & revenue items as per laid procedures and within budgets at the unit level in coordination with planning & corporate procurement divisions
Challenges:
Safety and quality products, Shorter lead time, less inventory and better throughput, Supplier base consolidation, Access to latest technology, risk management, unforeseen delays, Fast changing markets
Accountabilities
Effective scheduling of RM / PM to avoid stock outs and excess inventory.
Monthly MIS related to purchase and inventory
Ensure procurement in line with budget outlay
Cost reduction through value analysis/value engineering
Identification and development of new vendors for cost effectiveness
Vendor Evaluation and Vendor Audits as per QA requirements
Perform periodic vendor performance rating to measure the vendor performance w.r.t. quality, delivery and price
Responsible for addressing the requirements of internal/external customers.
Ensuring compliance to SOPs & as per cGMP related RM & PM procurement.
Responsible for effective co-ordination with logistics and accounts for to ensure smooth flow of material.
Education Qualification :Graduation from any stream, Preferable MBA (Supply Chain Management)
Experience Range : 10-15 years’ of experience in the procurement of RM/PM in Pharma company.
Functional Skills :
Vendor Development Skills,
Negotiation and Bargaining Skills
Knowledge of Regulatory guidelines such as USFDA, MHRA, TGA, ANVISA etc.,
Knowledge of ERP system preferably SAP
Behavioral Skills :
Good Communication & Management skills
Inspiring and Influential leadership skills
Negotiation and Interpersonal skills
Systems Thinker and Technical Savvy
Sound judgement and decision making