Preclinical In-Vitro Toxicology Scientist

Hudson Shribman
United Kingdom
Last week
£55,000 – £70,000 pa

Salary

£55,000 – £70,000 pa

Posted
21 Aug 2026 (Last week)

Preclinical In-Vitro Toxicology Scientist up to c£70k + Bonus + Benefits

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.

* Contribute to continuous improvement of laboratory methods, processes and scientific capabilities.

* Prepare, author and peer-review scientific reports, technical documentation, regulatory materials, presentations and publications.

* Support external scientific collaborations, including method transfer and inter-laboratory validation.

Experience & Skills Required

* Degree, MSc or PhD in Biological Sciences, Toxicology, Pharmacology, Biomedical Sciences, Cell Biology, Molecular Biology or a related discipline.

* Significant practical experience in in-vitro Regulatory Toxicology, Genetic Toxicology or pre-clinical area.

* Hands-on experience with Neutral Red, Ames and/or in-vitro micronucleus testing.

* Strong experience in complex cell culture, exposure techniques, biological assays and data interpretation.

* Experience developing, optimising, transferring or validating in-vitro testing methodologies.

* Understanding of relevant regulatory toxicology guidelines, including OECD, ECVAM and ICCVAM.

* Experience within a controlled, quality-assured laboratory environment, ideally with GMP, GLP or GxP.

* Ability to assess complex biological datasets using appropriate data analysis, computational or bioinformatics.

* Experience contributing to regulatory submissions, scientific reports, technical documentation or external scientific communications.

Desirable

* Experience in disease modelling, molecular toxicology or adverse outcome pathway frameworks.

* Knowledge of bioinformatics, computational biology or advanced biological data analysis.

* Experience with high-content screening, high-throughput assays or innovative in-vitro platforms.

* Experience managing CROs, suppliers or scientific collaborations.

Benefits: Up to £70k + up to 30% bonus + 20% pension

To Apply: Please contact Alison Basson on (phone number removed) / (phone number removed) or apply quoting ABJ6761 to

Related Jobs

View all jobs

Project Manager

GxPeople Global London, United Kingdom
£80,000 – £90,000 pa

Manager, Serious Breach Office

Johnson & Johnson MedTech High Wycombe, United Kingdom
Hybrid

Manager, Serious Breach Office

Johnson & Johnson MedTech Belgium
Hybrid

Manager, Serious Breach Office

Johnson & Johnson MedTech
Hybrid

Endomech Sales Specialist|Johnson & Johnson MedTech | Surgery| West Midlands

Johnson & Johnson MedTech Birmingham, United Kingdom
Hybrid

Commercial Business Manager NORTH|Johnson&Johnson MedTech| North UK

Johnson & Johnson MedTech Leeds, United Kingdom

Industry Insights

Discover insightful articles, industry insights, expert tips, and curated resources.