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Aurobindo Pharma Ltd (APL). APL is a growing Indian multinational pharmaceutical manufacturing firm with turnover of over US$650Mn, with presence in more than 22 countries across the globe. APL produces a wide range of Active Pharmaceutical Ingredients (API’s) and Finished Formulations which is marketed in more than 108 countries across the globe
Job Title: Purification Sciences – Downstream Process Development Biologics R&D
No of Posts: 6
Location: Hyderabad / Secunderabad
Eligibility: B.Tech/B.E, M.Tech – Life science, Biotechnology, Immunology
Experience: 2 – 7 Years
Job Description:
- Candidate should have effective verbal and written communication skills, Masters in Technology with 2-5 years of experience in purification process development for Biologics. MTech candidates with BTech in Chemical
- Engineering or biotechnology from top institutes in the country are preferred.
- AM/DM in downstream is responsible for purification process development of at least one to two monoclonal antibodies, development and optimization of chromatography/filtration/viral inactivation/formulation steps, process integration to meet desired product quality requirement.
- Support in planning, lead in detailed experimental plans and execution of day-to-day activities with the support of research executives to develop the processes producing high quality products and suitable for large-scale commercial production. Experience in end to end process development, characterization, scale up and validation at clinical or commercial scale for at least one product is preferred.
- Perform activities to select/evaluate buffers, resins, chromatography/filtration systems, fill finish, concentration and devices to deliver materials to support characterization and pharmacological profiling of the products.
- Coordinate cross functionally to get the results and other supports from cross functional teams for completing the assigned tasks.
- Recording raw data and ensuring proper recording of experimental details, procedures, observation and results in Laboratory note books.
- Deriving conclusion after summarizing results, literature search and evaluation of novel technologies. Data monitoring, trending and statistical analysis using JMP or SIMCA P tools is expected.
- Preparing and discussing clear regular updates on accomplishment and progress of the tasks assigned via presentations and reports.
- Maintain well-organized, clear and complete records of all activities across areas of responsibility including preparation of SOPs, development reports, technology transfer documents execution documents suitable for rapid adoption by manufacturing.
