Preclinical In-Vitro Toxicology Scientist

Preclinical In-Vitro Toxicology Scientist up to c£70k + Bonus + Benefits Do you have the skills to fill this role Read the complete details below, and make your application today. Hampshire, Full Time ABJ6761 ONSITE - 5 days An exciting opportunity has arisen for an experienced In-Vitro Regulatory Toxicology Scientist to join a leading scientific research and product development organisation focused on in-vitro and pre-clinical assessment. This is an excellent opportunity for an experienced scientist to take a technically influential role within a multidisciplinary environment, contributing to advanced pre-clinical testing capabilities across in-vitro science, product development and regulatory toxicology. You will provide technical expertise and scientific direction across in-vitro Regulatory and Genetic Toxicology, supporting pre-clinical research, product development and regulatory programmes. The role will suit an experienced toxicologist with strong hands-on laboratory expertise who can work independently, lead technical activities and collaborate with internal teams and external partners.

Key Responsibilities

• Provide technical expertise in the development and application of in-vitro Regulatory Toxicology approaches.
• Lead and execute in-vitro studies, delivering robust, reliable and scientifically defensible data.
• Develop, optimise and apply Neutral Red, Ames and in-vitro micronucleus assays.
• Apply complex cell culture, exposure techniques and biological testing methodologies to investigate product safety and potential human health effects.
• Interpret experimental findings and bridge in-vitro data with analytical, human-use and clinical information where appropriate.
• Provide technical direction for new testing capabilities, methodologies and assessment strategies.
• Plan and deliver technical work programmes to agreed timescales, quality standards and objectives.
• Collaborate with multidisciplinary teams across Preclinical Science, Analytical Science, Toxicology, Clinical and Product Development.
• Build relationships with external technical partners, CROs, academic groups and specialist consultants.
• Support method transfer, validation and implementation of new technologies.
• Ensure data is generated and managed in line with appropriate quality and regulatory requirements within controlled, quality-assured laboratory environments. xwwtmva
• Contribute to continuous improvement of laboratory methods, processes and scientific capabilities.
• Prepare, author and peer-review sc...