Jubilant Pharmova Limited
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Job Description

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 & Allergy Therapy Products, and Generics & APIs, comprising Solid Dosage Formulations & Active Pharmaceutical Ingredients.
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.
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Accountabilities Scope of work
  • Multiple Project Handling
  • Execution of Multiple Projects ongoing, both green field and brown-field projects at site.
  • Responsible for the time, cost, scope, quality and Construction Safety for multiple projects.

  • MIS Reports
  • MIS reports on actual progress / schedules and cost tracking.

  • Liaising
  • Interaction with consultants, contractors, internal and external customers.

  • Ensure proper availability of equipments at the site.
  • To establish effective systems for equipment inspection at suppliers works, FAT and SAT / record / follow up to completion.
  • Unified numbering systems for drawings and ensure as built documentation is completed for every Project as a part of good handing over.
  • Responsible for Installation activities and pre commissioning and commissioning activities.

  • Contractor Management
  • To ensure effective Contractor Management.

  • Procurement and Delivery Planning
  • Co-ordination with SCM for the planned procurement and delivery of equipment / systems at site.

  • Project Execution
  • Effective and timely project closure.
  • Drive the execution management in all engineering discipline and ensuring the design aspects are implemented during execution.

  • Scope, Change Management
  • Scope Management and effective change control management throughout the project execution cycle.

Job Details

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