Date PostedMarch 5, 2022
QualificationBachelor Degree, Master’s Degree
Minimum educationGraduate, Post Graduate
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 MSAT ( Manufacturing Science And Technology ).
Hiring Fresher For MSAT ( Manufacturing Science And Technology ) @ BIOCON BIOLOGICS LIMITED
About the Function: MSAT team in Biocon Biologics plays an important role in achieving the manufacturing excellence by providing technical support to the manufacturing / operations teams to enable consistent manufacturing of safe and high-quality biological/biosimilar products. MSAT team bridge the efforts from process development to successful scale-up, validation and consistent manufacturing of high quality, cost effective therapeutic products of biological origin. MSAT team in Biocon Biologics is working on a mission to enable consistent supply of high-quality biosimilar products accessible and affordable across the globe through building multi-disciplinary expertise.
About the Role:
Scheduling, planning, executing, monitoring and control of manufacturing operations.
Coordinating with other departments for manufacturing activities.
Implementing EHS policies in respective areas and ensuring the compliance.
Ensuring cGMP compliance in respective areas, Investigating the deviations/non-conformities to identify the root-cause and CAPA.
Preparation and review cGMP documents like SOP, batch manufacturing records, protocols and reports.
Assessing and mitigating the risks with respect to product, process, operations, equipment, facility and personnel.
Maintaining the equipment and facility in a state of compliance with effective calibration, preventive maintenance and validation programs.
Working on continuous improvement programs for operational efficiency and better compliance.
Authoring/ review of Continued Process Verification (CPV) protocol. Analysis of batch data and trends and summary of CPV report.
Authoring/ review protocol and technical reports to support process changes, modifications, improvements and scale up to support implementation at manufacturing scale.
Authoring study protocols and reports for any trials to support the same. Small scale purification.
Authoring/ review of comparability protocols and reports.
Qualification: BE / B.Tech /ME / M.Tech /MS
Course: Biotechnology, Chemical, Bio Process Engineering.