Biocon Biologics Limited Walk In Drive For Asceptic Manufacturing ( Injectables ) on 13th Mar 2022

Biocon Biologics Limited Walk In Drive For Asceptic Manufacturing ( Injectables ) on 13th Mar 2022

Biocon Biologics Limited, a subsidiary of Biocon Limited, is a fully integrated global biosimilars organization. It is leveraging cutting-edge science, innovative tech platforms and advanced research & development capabilities to lower treatment costs while improving healthcare outcomes. It has a strong research pipeline of biosimilar molecules across diabetes, oncology, immunology, and other non-communicable diseases.

Walk In Drive For Asceptic Manufacturing ( Injectables )

Experience: 3 – 8 Years

Job location : Bangalore/Bengaluru

Education

B.Pharma in Pharmacy, B.Tech/B.E. in Bio-Chemistry/Bio-Technology

MS/M.Sc(Science) in Biotechnology, Bio-Chemistry, Chemistry, M.Pharma in Pharmacy, Post Graduation Not Required

Job description

• Responsible for all sections of production area and plan and execute production to meet business requirements within timelines.
• Ensure data integrity and compliance to quality and regulatory requirements at all times. Also ensure that entry/exit, preparation and autoclave, CIP, SIP, formulation, filtration, vial washing, depyrogenation, filling, sealing, Lyophilized loading/unloading activities are carried out in compliance with the cGMP requirement and as per respective SOPs. Maintain the change parts, spares which are required for all the equipment’s of the production areas.
• Ensure continuous monitoring of BMS i.e. temperature, differential pressure, relative humidity, PMS and their compliance.
• Handling of manpower and allocating defined responsibilities to the team in production areas. Micro planning of shift activities of the day, conveying the work flow to the team and taking follow ups for progress of assigned work. To ensure discipline in the team and aseptic practices are compliant always.
• To coordinate with compliance team and QA-QMS for documents i.e. change controls, CAPA, Deviations, QRA, Technical document, Study Protocols and reports.
• To coordinate with supporting departments i.e. QA, QC, Engineering & Maintenance, for achieving the day to day production targets and compliance.
• To ensure facility is following EHS requirements.
• Handling of Internal audits and external audits, and to coordinate for department audits. To involve in media filling, qualifications and validations in coordination with cross functional teams.
• To assist to production head and any new assessment shall be done as assigned by the production head.

Time and venue

13th Mar, 9.00 AM – 12.00 PM

Hotel Avasa, Survey No. 64, 15, 24, 25 & 26, Hitech City Rd, HUDA Techno Enclave, HITEC City, Hyderabad, Telangana 500081

Contact – Jyothirmai