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Laboratory testing of household chemical products and raw materials, in a regulated environment where GMP/GLP standards apply. Formulation of laboratory samples for stability and consumer testing. Participation in industrial trials, supervising compliance
Responsible for providing Regulatory CMC expertise into the development and implementation of the global regulatory strategy, operations and planning for the CMC aspects of assigned projects/products. Responsible for preparing and managing CMC regulatory
Lead, plan, and coordinate daily cell and tissue culture activities in compliance with GMP standards. Supervise and mentor a team of (Senior) Biotech Associates, ensuring quality and efficiency in manufacturing. Initiate and follow up on deviations,
In this role, you’ll provide global scientific and technical leadership, contribute to innovation strategies, and act as a thought leader - both within Lonza and the wider biopharmaceutical industry. Guide development of mammalian USP/DSP processes for
Responsible for all tasks and resources including cross functional co-ordination required to complete relevant QC microbiology activities within regulated environment in the required timeframe. Management of QC Microbiology team to carry out tasks.