Jubilant Generics Job For Quality Control
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| Jubilant Generics Job For Quality Control |
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.
Qualification & Experience
M.Sc / B. Pharma/ M. Pharma - 3-8 Years. Experience in Quality Control department and to handle all Instruments like HPLC, GC, UV etc., from a regulatory reputed Pharmaceutical unit.
Location : Roorkee - Plant, IND
Company : Jubilant Generics Limited
Function : Quality
Summary of Job
To carry out sampling activities & maintenance of reserve samples. To ensure & analyze the Raw Material samples by ensuring compliance
Key Responsibilities
Sampling and analysis of Raw material / water samples / finished products / stability samples and swab samples.
Preparation of specifications, general test procedures, and standard test procedures.
To carry out analytical method transfer and analytical method validation activity.
Maintenance of reagents, volumetric solution.
Recording of analytical data.
Calibration and validation of Instruments and equipments.
Responsible for preparation of records of analysis
To ensure cGMP and GLP compliance.
Ensure good housekeeping in the lab.
Investigation of deviations, incidents and OOS.
Key Competencies
Analytical skills (Operating and trouble shooting skills on all analytical equipment's like HPLC, GC, UV, particle size analyzer etc.,)
Review of Pharmacopoeia & it’s changes to improve the existing documents
Exposure to ERP system preferably SA