You will be involved in experimental design, formulation engineering, process optimization, scale-up, and technology transfer for clinical trial manufacturing. We value a future oriented mindset with openness to adopting and leveraging modern digital tools for workflow optimization, data integrity, and knowledge management. Apply best practices in formulation, characterization, validation, scale up, transfer, and compliant documentation in electronic lab notebooks and data systems; ensuring compliance with GMP, SHE (Safety, Health & Environment), and internal regulatory standards. Act as PLD functional representative within multidisciplinary project teams, collaborating with in Analytical Development, Pharmaceutical & Material Sciences, Engineering, Quality, Legal, Supply Chain, and external CDMOs. Ph
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