Planning and Execution of all Microbial and mammalian upstream related processes and lab activities.
Designing and executing experiments for yield and Quality improvement and process intensification of current commercial microbial and mammalian products and protocol based batches execution.
An executive with extensive expertise in Biologics (Upstream) Development & Manufacturing: Product Technical Life Cycle Management.
Collaborate with cross-functional teams to facilitate the transfer of upstream processes from development to manufacturing.
Provide technical expertise in upstream bioprocessing, to optimize manufacturing processes.
Work closely with development teams to gather and document critical process parameters and data for successful transfer.
Collaborate with Quality Assurance to ensure compliance with cGMP and other regulatory standards.
Participate in process validation activities and support the resolution of deviations or discrepancies.
Qualification & Experience
Education: Master’s in Biotechnology, or related field.
Relevant professional / Educational background
3+ years in biopharma manufacturing in MSAT or process improvement roles.