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. Provide input for master batch records for clinical batches; perform criticality analysis and define control strategies. Ph.D. in Pharmaceutical Sciences, Chemistry, Bioengineering, Chemical Engineering or relevant field; alternatively, a Master's degree with 3+ years of relevant experience. Openness to utilizing modern digital tools and systems to support data int
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