R&D Biologics Formulation Lead Biocon Biologics Limited

12.0 - 16.0 years

15 - 25 Lacs

bengaluru

Work from Office

Role & responsibilities: The candidate should be an expert in the area of drug product development. He/she should have high level of experience to be called a subject matter expert in concepts of product stability, role of excipients in protein stability, knowledge of higher order structure and its role on product stability The candidate should be well-versed on drug product formulation development. He/she should have knowledge on the concepts of developing a brand new formulation, evaluation of buffer systems, sugar excipients, role of surfactants such as polyols etc. Having experience of developing new formulations for Biosimilar products is a plus The candidate should have experience in running stability programs which include temperature, forced degradation studies, photo-stability studies etc. for multiple programs and should have demonstrated ability to trouble-shoot and course-correct as required in the development phase of Biosimilar drugs The candidate should have expert knowledge on product quality estimation techniques such as HPLC, CE-SDS etc that are connected to Drug Product development so that he/she should be able to understand the nuances of the data generated and relate it to the conclusions being made in formulation The candidate should have knowledge of particle characterization techniques such as DLS and should have experience in implementing such characterization techniques to drug product development. The candidate should have demonstrated experience in conducting studies for scale down model qualification and process characterization experiments associated with drug product. The candidate should be well-versed in basic statistics and should have experience in using statistical software such as JMP, Minitab etc. The candidate should have basic knowledge of regulatory guidance from USFDA, EMA etc. and should have knowledge of ensuring development is done to meet the regulatory requirement. The candidate should have years of experience in developing drug product related data for Biosimilars. The candidate should have mid-level knowledge of various container closure systems such as vials, pre-filled syringes, auto-injectors etc. that are prevalent in the market. Preferred candidate profile: Design studies for the development of drug products for conducting various types of stability studies including process characterization studies Handling of instrument calibration/maintenance issues, interfacing with Engineering and vendors for instrument maintenance so that lab is functioning smoothly Interpretation (including statistics) of data generated, preparing presentations for project meetings and presenting data to seniors Enable process development activities including filter validation, extractables and leachables Involvement in vendor selection, evaluation, legal and IPR documentation, EHS activities and any ad-hoc trainings as required by the Company; discussions with external consultants Ability to manage a team Educational Requirements: Masters in Biotechnology/Pharmacy/any other related field with 12 to 17 years of relevant industrial experience PhD in Biotechnology/Pharmacy/any other related field with 8 to 12 years of relevant industrial experience Post-doctoral research in relevant field with 2 to 3 years of relevant industrial experience

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