Skip to main content

Walk in interview for M.Pharm, M.Sc, B.Pharm in Manufacturing, Packing & Medical Device at Biocon Biologics



Pharma courses



pharma courses

Walk in interview for M.Pharm, M.Sc, B.Pharm in Manufacturing, Packing & Medical Device at Biocon Biologics

Biocon Biologics at Chennai is a 56000 sq. ft RND centre equipped with end-to-end cutting-edge infrastructure involving upstream, downstream, formulation, analytical characterization, functional characterization, and pilot facilities. A world-class team is being put together to develop biosimilar therapies all the way through process development, characterization, scale-up, and technology transfer to feed into our large-scale manufacturing facilities at Bangalore. We are looking for passionate science-driven minds at all levels across different functions.

Walk In Drive for Asceptic Manufacturing, Biosimilars Manufacturing, DP Packing & Medical Device.

Asceptic Manufacturing
Job description :
• Acquainted with current Good Manufacturing Practice, pharmacopeia, different regulatory requirements and drug and cosmetic acts.
• Basic knowledge of microbiology, pharmaceutics, pharmaceutical chemistry, Biotechnology, Data Integrity, ALCOA and other related pharmaceutical subjects.
• Ensure quality of drug product at difference stages.
• Ensure data integrity and compliance to quality and regulatory requirements at all times.
• Advanced data analysis; comfort with change, adaptability, and continuous learning; and critical thinking and decision making.
• To coordinate with compliance team and QA-QMS for documents i.e. change controls, CAPA, Deviations, QRA, Technical document, Study Protocols and reports.
• Handling of Internal audits and external audits, and to coordinate for department audits.
• Ensure control on microbial contamination in manufacturing area by effective cleanliness of equipment/area and following aseptic practices.
• Ensuring documents availability for batch activity and its online documentation.
• Following of aseptic techniques, gowning procedures and carry out aseptic area operations with good aseptic area behavior.
• To involve in media filling, qualifications and validations in coordination with cross functional teams.
• Ensure that manufacturing area activities i.e., batch manufacturing, vial washing, filling aseptic area entry / exit, autoclave unloading, CIP, SIP, filtration, filling, lyophilizer loading / unloading are carried out in compliance with the cGMP requirements, SOPs and BMRs.
• Maintain the change parts, spares which are required for all the equipment of aseptic areas.
• Ensuring operation and cleaning of autoclaves, vial washing machine, Depyrogenation tunnel, Filling & sealing, Lyophilizer, Manufacturing vessels, Manufacturing vessels, Filter integrity machine etc. as per respective SOPs. Ensure PMP and qualification of these machines in coordination with validation team and ensure activities are performed as per set validated parameters for the equipment’s.

DP Packing & Medical Device
Role Summary

Looking for a challenging & responsible candidate to excel in field of Pharmaceuticals with good knowledge in Packaging& Medical Device.
Roles & Responsibilities
• Responsible for preparation, review and revision of the batch document s and SOPs
• Responsible for preparation of URS for new equipment and instruments.
• Preparation of the Qualification protocols for the new equipment and Instruments.
• Identification and raising of deviation, change controls and compiling other GMP documents.
• Responsible for implementation and closing of the CAPA related to Facility equipment and process.
• Responsible for taking initiation for improvement in the process and procedure.
• Responsible to ensure QMS is followed in operations.
• Should be responsible for monitoring of the Production activity and output.
• Should have Audit experience (USFDA, MHRA, EMA etc.. )
• Should have experience on Pen Devices, Packing, and handling new projects.

Biosimilars Manufacturing
Roles and Responsibilities :
• Upstream Manufacturing (Microbial & Mammalian)
• Downstream Manufacturing (Microbial & Mammalian)
• Process Engineering (USP & DSP)

Qualification : MSC / BSC / M.Pharm / B.Pharm / BE / B.Tech / M.Tech / Diploma.
Experience : 3 to 15 years

Walk-In Interview
Date : 25 September, 2022
Time : 9.30 AM – 12.00 PM
Venue :
Hotel Avasa, Survey No. 64, 15, 24, 25 & 26, Hitech City Rd, HUDA Techno Enclave, Sector 1,
Hyderabad, Telangana 500081.

See All   Hyderabad Alerts   M.Pharm Alerts   M.Sc Alerts   D.Pharm Alerts

See All   Other Jobs  in our Database

Subscribe to Pharmatutor Job Alerts by Email

Search this website