Jubilant Biosys is hiring

QC Officer | Jubilant Generics Ltd | B. Pharma/B.Sc. (Chemistry)

Jubilant Generics Limited has announced a job opening for the position of QC officer. The job is for Roorkee – plant. Please refer to the following details to apply.

Company Profile

Jubilant Pharma Limited is a global integrated pharmaceutical company offering a wide range of products and services to its customers across geographies. We organize 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 focuses 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 the state of the art facility and is audited and approved by USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA. This business focuses on B2B model for the EU, Canada, and emerging markets.

Kindly refer to www.jubilantpharma.com for more information about the organization.

Jobs Details

Position Title: Officer-Quality Control

Department: Quality Control (QC)

Qualification: B. Pharma/B.Sc. (Chemistry)

Work Experience: 3-6 Years

Work Location: Roorkee

Salary: Not Disclosed

Job Context

Sampling and Analysis of Packing material, raw material, semi-finished drugs, finished drugs by ensuring compliance and also to maintain the instruments in calibrated state.


Calibration and Preventive Maintenance of instruments, Preparation of reference/working standards, method development/validation, maintaining cGMP and other compliances in area, correct recording, and measuring of results.


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