Valent BioSciences

Compliance

• Serve as GLP Study Director with full accountability for the scientific integrity, regulatory compliance, and successful execution of environmental fate and metabolism studies and other regulatory studies in accordance with FIFRA and Good Laboratory Practice guidelines
• Lead the design, execution, interpretation, and reporting of regulatory studies, including protocol development and preparation of final reports for submission to regulatory agencies
• Act as a primary technical interface with regulatory authorities, preparing scientifically sound responses to EPA and state agency inquiries
• Provide scientific leadership to internal teams and contract research organizations, ensuring data quality, regulatory acceptability, and adherence to timelines
• Supervise, mentor, and develop Chemists and Associate Chemists; set priorities, provide coaching, and conduct performance evaluations
• Manage multiple projects simultaneously, developing realistic timelines, manpower plans, and cost estimates; communicate status and risks to internal stakeholders
• Maintain deep expertise in environmental fate, metabolism, chromatography, and regulatory guidelines; evaluate emerging scientific and technical advances for application to Valent programs
• Contribute to cross-functional project teams, providing strategic scientific input to meet regulatory and business objectives
• Ensure compliance with safety, regulatory, and waste disposal procedures; participate in required training and safety programs
• May represent Valent at scientific conferences, contribute to publications, and identify patentable innovations

Regulatory Scientist