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The role of Laboratory Supervisor involves managing daily laboratory operations, ensuring the delivery of high-quality genomic analysis, and maintaining compliance with all regulatory standards. The successful candidate will play a key role in fostering a
Develop, implement, and maintain the quality management system applicable to R&D activities (SOPs, work instructions, standards, etc.). Ensure compliance of R&D projects assigned to CMO Office with relevant regulations (e.g., GCP, GVP, GMP, GLP, ISO, ICH,
Lead the development & qualification of analytical methods (HPLC/CE related). Serve as project representative for pharmaceutical product development on cross-functional project teams. Transfer of analytical methods to quality control (QC) or external
This role is pivotal in ensuring regulatory compliance, operational excellence, and continuous improvement within a cGMP environment. You will manage a team of 17, fostering a culture of accountability, adaptability, and technical expertise while
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,