6,376 Experimental Scientist jobs in the United Kingdom

• Design and execute complex research projects focused on identifying and validating novel drug targets for various diseases.
• Lead multidisciplinary research teams, providing scientific direction, technical guidance, and mentorship to junior staff.
• Develop and implement innovative experimental methodologies and assays to assess compound efficacy and safety.
• Interpret complex experimental data, draw sound conclusions, and communicate findings effectively to senior management and project teams.
• Author high-quality scientific publications and present research findings at international conferences.
• Collaborate closely with colleagues in chemistry, pharmacology, toxicology, and clinical development to advance projects through the R&D pipeline.
• Contribute to the strategic planning and prioritization of research initiatives, ensuring alignment with company objectives.
• Maintain a thorough understanding of the latest scientific literature, emerging technologies, and competitive intelligence in relevant therapeutic areas.
• Ensure all laboratory operations adhere to stringent safety, quality, and regulatory standards (e.g., GLP, GMP).
• Manage external collaborations with academic institutions and contract research organisations.
• Develop and present research proposals and progress reports to internal stakeholders and external partners.
• Oversee the budget and resource allocation for assigned research projects.
• Champion scientific excellence and innovation within the R&D organisation.
• Contribute to the intellectual property strategy through invention disclosures and patent filings.
• Foster a collaborative and high-performance research environment.

Who are we?

Specialists in providing engineered above ground drainage and water supply systems,Polypipe Building Services leverages offsite fabrication to design and deliver solutions to mechanical and public health engineers, M&E contractors as well as local authorities. Polypipe Building Services houses well-known industry brand Terrain and has been delivering systems to commercial, high rise residential, healthcare, education and leisure projects for over 50 years.

About the role: You will be responsible for the research and development of

• New products

• Product iterations

• Process improvements

All to deliver business strategy while maximising value of our portfolios to timescale and cost, either as a project lead or part of a wider multi-functional project team. Identifying new opportunities, validating into tangible opportunities managing them through the NPD process.

Your day to day:

• Responsible for design, prototyping and material selection for the product portfolio

• Working to a brief to deliver key projects and initiatives, ensuring that you are on budget and on time

• Measuring project progress, and reporting by exception on constraints and challenges

• Bringing innovative concepts together into tangible solutions and products

• Working alongside the Marketing team to support campaigns

• Working with engineering & manufacturing innovations to monitor technological advances and explore new development strands as well as process improvements

• Participate in continuous improvement of R&D by identifying efficiencies

• Build a working knowledge of all our products and systems, whether manufactured, fabricated or bought in

• Delivery of added value on products

• Support occasional external conferences and site meetings

• Keep abreast of market and competitor changes

Skills & Experience we require:

The essentials:

Strong track record in product design, generally equivalent to around two years experience.

In-depth knowledge of 3D and 2D CAD design software

In-depth knowledge of the MS suite of office software

Basic knowledge of polymer materials and their properties

Experience of design for additive manufacturing

The desirables:

Mechanical Engineering product design experience

Knowledge of BIM

Knowledge of FMEA and DfMA concepts and relevant software

Experience with CFD

Knowledge of project management software

Minimum of HND qualified within a relevant engineering discipline, Degree qualified in an engineering/design discipline is preferred

3D printing

Experience of protecting a product with IP

Benchwork practical skills

Plastics processing skills

Knowledge of toolmaking techniques

What we can offer you:

A great team whilst working alongside another R&D Engineer

Monday - Friday work only with flexible start/finish times including early finish Fridays at 3:00pm!

Competitive salary

25 days of annual leave plus the bank holidays (with a holiday purchase scheme that starts in January 2026!)

Matched pension contributions up to 8%

Sharesave scheme

Team days and events

Life assurance

Want to know more? Apply now or call to speak to our Resourcing Business Partner on (phone number removed). We can't wait to hear from you!

• Design and conduct experiments to support the discovery and development of new drug candidates.
• Investigate molecular mechanisms of disease and identify potential therapeutic targets.
• Develop and optimize in vitro and in vivo assay systems relevant to drug efficacy and safety.
• Analyze experimental data, interpret results, and draw scientifically sound conclusions.
• Prepare detailed reports, presentations, and contribute to scientific publications and patent applications.
• Collaborate effectively with multidisciplinary teams, including chemists, biologists, pharmacologists, and toxicologists.
• Maintain meticulous laboratory notebooks and adhere to Good Laboratory Practice (GLP) standards.
• Troubleshoot experimental issues and proactively seek solutions.
• Stay current with the latest scientific literature and technological advancements in relevant therapeutic areas and drug development.
• Contribute to project planning and strategy discussions within the research team.
• Operate and maintain specialized laboratory equipment.
• Ensure a safe and compliant laboratory environment.
• Assist in the characterization of drug candidates and the development of preliminary pharmacokinetic and pharmacodynamic profiles.
• Present research findings at internal meetings and potentially at external scientific conferences.

• Ph.D. in Pharmacology, Molecular Biology, Biochemistry, or a closely related life science discipline.
• Minimum of 3 years of postdoctoral research experience or equivalent industry experience in pharmaceutical R&D.
• Proven expertise in designing and executing complex biological assays (e.g., cell-based assays, biochemical assays, enzyme kinetics).
• Strong understanding of drug discovery and development processes.
• Experience with relevant analytical techniques (e.g., HPLC, LC-MS, ELISA, Western Blotting).
• Excellent data analysis and interpretation skills.
• Proficiency in scientific software for data analysis and presentation.
• Strong written and verbal communication skills, with the ability to clearly articulate scientific concepts.
• Ability to work effectively both independently and as part of a collaborative research team.
• Experience in (mention specific therapeutic area, e.g., oncology, immunology, neuroscience) is a plus.
• Familiarity with small molecule drug discovery is highly desirable.
• Commitment to working full-time at the Wolverhampton facility.

• Design and conduct preclinical research experiments.
• Develop and validate biological assays.
• Investigate drug efficacy, safety, and mechanisms of action.
• Characterise novel drug targets and molecules.
• Perform molecular and cellular biology techniques.
• Analyse and interpret complex experimental data.
• Prepare scientific reports and presentations.
• Collaborate with multidisciplinary research teams.
• Maintain accurate laboratory records and documentation.
• Stay abreast of scientific literature and industry trends.

• PhD in Pharmacology, Biochemistry, Molecular Biology, or related field.
• Proven research experience in drug discovery/development.
• Expertise in relevant experimental techniques (assay development, cell culture, molecular biology).
• Strong data analysis and interpretation skills.
• Excellent written and verbal communication skills.
• Ability to work independently and manage projects.
• Experience with relevant therapeutic areas is a plus.

• Design, execute, and optimise in vitro and in vivo experiments to evaluate the efficacy and safety of drug candidates.
• Develop and validate new assays and methodologies relevant to drug discovery and development.
• Conduct detailed analysis of experimental data, interpret results, and draw meaningful conclusions.
• Prepare comprehensive scientific reports, presentations, and publications for internal and external stakeholders.
• Collaborate effectively with cross-functional teams, including medicinal chemists, pharmacologists, toxicologists, and clinical scientists.
• Maintain accurate and detailed laboratory records in accordance with company and regulatory guidelines.
• Stay abreast of the latest scientific literature, technologies, and trends in pharmaceutical research.
• Troubleshoot experimental issues and propose solutions to ensure project progression.
• Contribute to the intellectual property strategy through patent applications and scientific publications.
• Operate and maintain laboratory equipment, ensuring a safe and efficient working environment.
• Present research findings at internal and external scientific meetings.
• Contribute to the identification of new drug targets and development candidates.
• Ensure adherence to Good Laboratory Practice (GLP) and other relevant regulatory standards.

• PhD in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
• Proven track record in pharmaceutical research and development, with hands-on experience in assay development and preclinical studies.
• Expertise in (mention a relevant area, e.g., small molecule drug discovery, biologics development, specific disease area).
• Strong understanding of drug discovery and development processes.
• Proficiency in data analysis software (e.g., GraphPad Prism, R) and molecular biology techniques.
• Excellent laboratory skills and experience with relevant instrumentation.
• Strong written and oral communication skills, with the ability to present complex scientific information clearly.
• Demonstrated ability to work collaboratively in a team environment and manage multiple projects.
• Critical thinking and problem-solving abilities.
• Experience with GLP and regulatory compliance is a significant advantage.
• A proactive approach and a passion for scientific innovation.

• Design and conduct complex experiments to investigate biological pathways, identify potential drug targets, and develop novel therapeutic compounds.
• Execute a variety of laboratory techniques, including cell culture, molecular biology assays, protein biochemistry, and high-throughput screening.
• Analyse experimental data, interpret results, and draw scientifically sound conclusions.
• Prepare detailed reports, present findings at internal meetings and external scientific conferences, and contribute to publications.
• Collaborate effectively with interdisciplinary teams, including medicinal chemists, pharmacologists, and clinicians, to advance drug discovery projects.
• Develop and validate new experimental assays and methodologies.
• Maintain accurate and comprehensive laboratory records, ensuring compliance with Good Laboratory Practice (GLP) standards.
• Manage laboratory resources, including ordering supplies and maintaining equipment.
• Stay abreast of the latest scientific literature, research trends, and technological advancements in the relevant therapeutic areas.
• Contribute to intellectual property generation through patent applications.
• Mentor and guide junior scientists and research assistants.
• Troubleshoot experimental issues and devise creative solutions to overcome scientific challenges.
• Ensure a safe working environment by adhering to all laboratory safety protocols.

• PhD in Molecular Biology, Biochemistry, Pharmacology, or a closely related life science discipline.
• Minimum of 3-5 years of post-doctoral or industry research experience in drug discovery or pharmaceutical R&D.
• Proven track record of designing and executing complex experiments and generating high-quality data.
• Expertise in at least one of the following areas: oncology, immunology, neuroscience, or infectious diseases.
• Hands-on experience with key laboratory techniques such as qPCR, Western blotting, ELISA, flow cytometry, and recombinant protein expression/purification.
• Proficiency in data analysis software (e.g., GraphPad Prism, R) and scientific literature databases.
• Excellent written and verbal communication skills, with the ability to present complex scientific information clearly.
• Strong problem-solving abilities and a critical thinking mindset.
• Ability to work independently and collaboratively within a fast-paced research environment.
• Strong organisational skills and meticulous attention to detail.
• Experience with CRISPR/Cas9 gene editing or small molecule drug discovery is highly desirable.

• Design, develop, and implement bioinformatics pipelines for the analysis of high-throughput sequencing data (e.g., RNA-Seq, ChIP-Seq, WGS, WES).
• Perform sophisticated statistical and computational analyses of complex biological datasets to identify patterns, generate hypotheses, and extract meaningful insights.
• Develop and maintain custom scripts and algorithms for data processing, quality control, and visualization.
• Collaborate closely with biologists, geneticists, and other researchers to define research questions and provide tailored bioinformatics support.
• Contribute to the interpretation of results and the preparation of manuscripts for publication in peer-reviewed journals.
• Stay current with the latest advancements in bioinformatics, genomics, and related fields, evaluating and implementing new tools and methodologies.
• Manage and organize large datasets, ensuring data integrity and accessibility.
• Provide guidance and training to junior members of the research team on bioinformatics techniques and best practices.
• Contribute to grant proposals and foster collaborations within the scientific community.
• Ensure reproducible research practices through robust documentation and version control.

• A PhD or Master's degree in Bioinformatics, Computational Biology, Statistics, Computer Science, or a related field.
• A minimum of 4 years of hands-on experience in bioinformatics analysis, preferably in a research setting.
• Strong programming skills in Python and/or R, essential for script development and data analysis.
• Proficiency with standard bioinformatics tools and databases (e.g., BLAST, SAMtools, GATK, Ensembl).
• Experience with command-line environments (Linux/Unix) and high-performance computing clusters.
• Solid understanding of statistical methods applicable to biological data analysis.
• Experience with various sequencing technologies and data types.
• Excellent analytical and problem-solving skills, with a meticulous approach to data.
• Strong communication and collaboration skills, with the ability to explain complex technical concepts to non-experts.
• Demonstrated ability to work independently and manage multiple projects effectively in a remote setting.

• Design, execute, and interpret complex experiments related to drug discovery and development, focusing on target validation, lead optimization, and preclinical studies.
• Develop and implement novel assays and methodologies to assess drug efficacy, safety, and pharmacokinetic profiles.
• Analyze and critically evaluate experimental data, generating comprehensive reports and presenting findings to internal teams and external collaborators.
• Lead research projects, providing scientific direction, mentoring junior scientists, and managing timelines and resources effectively within a remote setting.
• Collaborate closely with cross-functional teams, including medicinal chemistry, biology, pharmacology, and regulatory affairs, to advance projects through the pipeline.
• Stay abreast of the latest scientific literature, technological advancements, and industry trends in pharmaceutical research.
• Contribute to the preparation of scientific publications, patents, and regulatory submissions.
• Ensure strict adherence to laboratory safety standards and good experimental practices.
• Actively participate in team meetings and scientific discussions, contributing valuable insights and fostering a collaborative research environment.

• Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
• Minimum of 5 years of post-doctoral or industry experience in pharmaceutical research and development.
• Demonstrated expertise in one or more therapeutic areas and associated research methodologies.
• Strong track record of successful experimental design, execution, and data interpretation.
• Excellent understanding of drug discovery processes and regulatory requirements.
• Proven ability to lead projects and mentor scientific staff.
• Exceptional written and verbal communication skills, with the ability to present complex scientific information clearly and concisely.
• Proficiency in relevant scientific software and data analysis tools.
• Ability to work independently, manage priorities effectively, and thrive in a remote, collaborative environment.
• Experience with in vivo models and preclinical development is highly desirable.