Biocon Biologics Limited Hiring Freshers & experience

Biocon Biologics Limited Walk-in Interview 2025.Biocon Biologics Limited Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue..

Vacancy details:

  • Department: Multiple
  • Experience: Freshers & experience
  • Salary: ₹Not Disclosed

Important Details :

  • Work Location: Multiple
  • Selection Process: The selection will be on the basis of Interview.
  • Mode of Interview: Face to face
  • Interview Rounds of Interview: HR

Job Description: Greeting from Biocon Biologics Limited !!!

 

Key Responsibilities

1. Driving new facility design; Concept, Basic and Detailed engineering design with focused effort on Upstream and Downstream Unit operations.

2. Support 2KL SU and 6 KL SS mAb manufacturing facility Scale up and technology transfer.

3. Upstream and Downstream equipment and process trouble shooting; Bioreactors, Centrifuge, chromatography skid, Filtration systems, UFDF/TFF, Filling station, Freeze Thaw etc.,

4. Knowledge on Monoclonal antibody manufacturing process and support production operations.

5. Handle CAPEX requirements for multiple drug substance facilities – 2KL and 6 KL scale.

6. Key driver to bring new technology and systems into production facility.

7. Active support in Process and Cleaning validation.

8. Drive process automation for equipment’s – Handling recipes/phases etc.,

9. Drive process trouble shooting and investigation with CAPA identification.

10. Perform Technology transfer/facility fitment assessment for new products.

11. Handle software tools like SuperPro/SchedulePro (Process simulations).

12. Perform process analytics/model creation using SIMCA and other standard analytical tools.

13. Drive the equipment Qualification: (review of FAT, SAT protocol and preparation of in-house DQ, IQ, OQ and PQ protocol and report)

14. Basic Automation knowledge for recipe (Siemens PCS7, CCP, Unicorn and other platforms) and MES support

15. Complying with EHS policies.

16. Complying with cGMP practices as per SOP, batch records and protocols.

17. Preparation and review of cGMP documents like SOP, batch records, checklists, registers, protocols and reports

SWARNALATHA B

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