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. Kindly refer www.jubilantpharma.com for more information about organization. JOB DESCRIPTION DETAILS OF THE JOB: Designation & Job: Production Chemist Level: 6/7 Business Unit: Generics Function: Manufacturing Country: India Work Location: Nanjangud Reporting Manager: Executive - Production Manufacturing Manager\'s Manager: Matrix Manager: Team Size: Direct Reportees: PURPOSE OF THE JOB: Job Context : To perform laboratory tests to produce chemicals according to established standards and guidelines. Challenges : To effectively produce quality products and meeting regulatory requirements by utilizing the technical expertise on machine operation & its maintenance. KEY ACCOUNTABILITIES: Accountabilities Scope Of Work Equipment handling Operation and Cleaning of Equipments used in the process area. Trouble shooting of the equipments during process. Calibration and verification of the balances used in the process area. Production Planning Manufacturing and packing of the products as per BMR / BPR. Material Handling Dispensing of Raw and packing material. Documentation Maintaining the daily logs of the process area. BMR / BPR filing during process area. Safety, health and environment On line monitoring of the environment conditions in process area. KEY INTERFACES: External Interfaces Internal Interfaces Vendors and Suppliers Employees, Management and Stakeholders EDUCATION & EXPERIENCE: Education Qualification(Highest) with Target Institute(s): B. Pharma/ M. Pharma/ B.Sc/ M.Sc (only for chemistry and microbiology) Desired Certifications: CGMP certificates, Ms Office Experience Range: 2 - 4 years No. of years post Highest Qualification: 5 years Desirable experience: 3-5 years of experience in relevant industry SKILLS REQUIRED: Skills Description Proficiency Level (General Awareness, Working Knowledge, Functional Expert, Mastery) Functional Skills Handling of production equipment Documentation capabilities like filling of BMR / BPR etc. Knowledge of basic CGMP Working Knowledge/ Functional Expert Behavioral Skills Critical thinker Problem solving attitude Attention to details Working Knowledge General Awareness : Knows the fundamental or has general understanding of concepts. Working Knowledge : Has broad job knowledge, knows to apply the full range of concepts and practices and has broad/working knowledge of the subject. Candidate should use these concept in day to day practices. Functional Expert: Candidate is certified functional expert with strong knowledge on concepts. Mastery: Candidate is subject matter expert and has command over the subject/concepts.

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