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Jubilant Biosys

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18 Jubilant Biosys Jobs

Executive - Regulatory Affairs

2-6 years

Noida

1 vacancy

Executive - Regulatory Affairs

Jubilant Biosys

posted 15d ago

Job Role Insights

Flexible timing

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.

",


Employment Type: Full Time, Permanent

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Prepare for Executive Regulatory Affairs roles with real interview advice

Top Jubilant Biosys Executive Regulatory Affairs Interview Questions

Q1. How to handle and quench pyrophoric chemical in reaction.
Q2. In vivo models and method related to therapeutic area
Q3. Name reactions based on palladium chemistry and copper chemistry
View all 14 questions

What people at Jubilant Biosys are saying

What Jubilant Biosys employees are saying about work life

based on 292 employees
59%
85%
70%
93%
Flexible timing
Monday to Friday
No travel
Day Shift
View more insights

Jubilant Biosys Benefits

Free Transport
Health Insurance
Cafeteria
Job Training
Team Outings
Soft Skill Training +6 more
View more benefits

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