Hiring for BIOCON Hiring Freshers and Experience-Apply Now

Our pioneering spirit paved the way for biotechnology in India, and we continue to apply the same spirit in finding novel approaches to improve patient outcomes today for a better tomorrow. This drives us to continuously find new ways to treat diabetes, cancer and autoimmune diseases. Our R&D focuses on prevention, alleviation and treatment and our medicines improve the lives of millions of patients in over 120 countries, by giving them access to life-saving therapies and relief.


Role Summary

1) To gain knowledge on the subject for an employee based on his/her job profile such as (not limited to) Basics of cGMP, GDP, Data Integrity, GLP, Microbiology, or any other GMP Training, as applicable.

2) Employee who are involved in GMP activities should undergo mandatory cGMP Training.

3) Frequency of mandatory training is once in a year.

4) All employees that involving with GMP environment should undergo a mandatory basic microbiology training.

5) To provides information guidance and recommendations to facilitate compliance with DI, GDP in documentation.

6) To ensure that all documentation is accurate, timely, legible, complete and permanent (ALCOA principle).

Key Responsibilities

1. To monitor the compliance with the requirements of Good Manufacturing Practice

2. To ensure the instructions relating to production operations are strictly followed.

3. To update the real time data entry in BMR, CKL, LS, ECC and other documents inDSP2

4. To execute equipment qualification protocols and validation protocols.

5. To perform and document operations in accordance with cGMP.

6. Maintenance of Production equipment in co-ordination with maintenance department

7. To comply with EHS policies and procedures8 Responsible for OTIF execution of all the activities related to Downstream Purification

Educational Qualifications

Required Education Qualification: BA/ B.Com/ B.Sc

Required Experience: 0 – 1 years

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