What Jobs are available for Pharmaceuticals in Guilden Morden?
Showing 46 Pharmaceuticals jobs in Guilden Morden
Senior Formulation Scientist - Pharmaceuticals
CB2 0AW Cambridge, Eastern
£60000 Annually
WhatJobs
Posted 25 days ago
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Job Description
Our client, a leading pharmaceutical company at the forefront of drug development in Cambridge, Cambridgeshire, UK , is seeking an experienced Senior Formulation Scientist to join their dynamic R&D team. This crucial role involves the design, development, and optimisation of innovative drug delivery systems and pharmaceutical formulations. The Senior Formulation Scientist will play a key part in the product development lifecycle, from early-stage research to clinical trial support. This hands-on role requires a deep understanding of pharmaceutics, formulation science, and drug product manufacturing processes.
Key Responsibilities:
The ideal candidate will possess a MSc or PhD in Pharmaceutics, Pharmaceutical Sciences, Chemistry, or a related discipline, with significant experience in pharmaceutical formulation development. Proven experience with various dosage forms (e.g., oral solids, injectables, topical) and drug delivery technologies is essential. Strong knowledge of GMP guidelines and regulatory requirements (e.g., FDA, EMA) is required. Excellent analytical, problem-solving, and experimental design skills are necessary. This is a critical on-site role requiring full-time dedication to our state-of-the-art research facilities in Cambridge .
Key Responsibilities:
- Design and develop novel pharmaceutical formulations for various therapeutic areas, considering drug properties and desired delivery routes.
- Conduct pre-formulation studies, including solubility, stability, and compatibility assessments.
- Optimise existing formulations to improve efficacy, bioavailability, and patient compliance.
- Perform characterisation studies of drug products, utilising techniques such as HPLC, DSC, TGA, and dissolution testing.
- Scale-up formulation processes from laboratory bench to pilot plant production.
- Collaborate closely with analytical development, manufacturing, and regulatory affairs teams.
- Prepare and review formulation development reports, CMC documentation, and regulatory submissions.
- Stay abreast of the latest advancements in formulation science, drug delivery technologies, and relevant regulatory guidelines.
- Troubleshoot formulation and manufacturing issues, providing scientific expertise.
- Contribute to project planning and strategy for drug product development.
The ideal candidate will possess a MSc or PhD in Pharmaceutics, Pharmaceutical Sciences, Chemistry, or a related discipline, with significant experience in pharmaceutical formulation development. Proven experience with various dosage forms (e.g., oral solids, injectables, topical) and drug delivery technologies is essential. Strong knowledge of GMP guidelines and regulatory requirements (e.g., FDA, EMA) is required. Excellent analytical, problem-solving, and experimental design skills are necessary. This is a critical on-site role requiring full-time dedication to our state-of-the-art research facilities in Cambridge .
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0
Senior Chemical Process Engineer - Pharmaceuticals
CB2 1AA Cambridge, Eastern
£70000 Annually
WhatJobs
Posted 18 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical research and manufacturing company, is seeking a highly skilled Senior Chemical Process Engineer to join their vital team in Cambridge, Cambridgeshire, UK . This role is critical in designing, optimizing, and scaling up complex chemical processes for the development and production of novel pharmaceutical products. You will apply advanced chemical engineering principles, ensuring efficiency, safety, and regulatory compliance throughout the process lifecycle. The ideal candidate will possess a profound understanding of chemical reactions, separation techniques, and process control within a regulated pharmaceutical environment.
As a Senior Chemical Process Engineer, you will be involved in all phases of process development, from laboratory scale-up to pilot plant and commercial manufacturing. This includes conducting feasibility studies, developing process flow diagrams (PFDs) and piping and instrumentation diagrams (P&IDs), and performing process hazard analyses (PHAs). You will collaborate closely with R&D scientists, manufacturing teams, quality assurance, and regulatory affairs to ensure seamless process transfer and validation. Your expertise in process simulation, optimization, and troubleshooting will be invaluable in addressing complex challenges and driving continuous improvement. This role offers a unique opportunity to contribute to life-saving medicines from a world-renowned scientific hub.
Key Responsibilities:
As a Senior Chemical Process Engineer, you will be involved in all phases of process development, from laboratory scale-up to pilot plant and commercial manufacturing. This includes conducting feasibility studies, developing process flow diagrams (PFDs) and piping and instrumentation diagrams (P&IDs), and performing process hazard analyses (PHAs). You will collaborate closely with R&D scientists, manufacturing teams, quality assurance, and regulatory affairs to ensure seamless process transfer and validation. Your expertise in process simulation, optimization, and troubleshooting will be invaluable in addressing complex challenges and driving continuous improvement. This role offers a unique opportunity to contribute to life-saving medicines from a world-renowned scientific hub.
Key Responsibilities:
- Design, develop, optimize, and scale up chemical processes for pharmaceutical manufacturing.
- Create and review PFDs, P&IDs, and other process engineering documentation.
- Conduct process simulations and modeling to evaluate performance and identify improvements.
- Perform Process Hazard Analyses (PHAs) and implement safety measures.
- Collaborate with R&D to transition processes from laboratory to pilot and commercial scale.
- Develop and execute process validation protocols.
- Troubleshoot process deviations and implement corrective and preventative actions (CAPAs).
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements.
- Manage process improvement projects to enhance efficiency, yield, and quality.
- Provide technical expertise and support to manufacturing operations.
- Master's or Ph.D. in Chemical Engineering.
- Significant experience as a Chemical Process Engineer in the pharmaceutical or biotechnology industry.
- Strong knowledge of pharmaceutical manufacturing processes, GMP, and regulatory guidelines.
- Proficiency in process simulation software (e.g., Aspen Plus, HYSYS).
- Experience with process scale-up, validation, and technology transfer.
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong understanding of chemical reaction kinetics, thermodynamics, and separation processes.
- Effective communication and interpersonal skills, with the ability to work in cross-functional teams.
- Familiarity with process safety principles and risk assessment techniques.
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1
Remote Senior Quality Assurance Manager - Pharmaceuticals
Cambridge, Eastern
£60000 Annually
WhatJobs
Posted 21 days ago
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Job Description
Our client is a leading pharmaceutical company dedicated to improving global health through innovative and high-quality medicines. They are currently seeking a highly experienced and meticulous Remote Senior Quality Assurance Manager to oversee their quality management systems. This is a pivotal, fully remote role that requires a deep understanding of pharmaceutical manufacturing, regulatory compliance, and quality assurance best practices. You will be instrumental in ensuring that all manufacturing processes and products consistently meet stringent quality standards and comply with global regulatory requirements, including GMP.
Your responsibilities will include developing, implementing, and maintaining comprehensive quality assurance policies and procedures. You will lead and mentor a team of QA professionals, fostering a culture of quality excellence throughout the organization. This involves conducting internal audits, managing external regulatory inspections, and overseeing the investigation and resolution of quality deviations and CAPAs (Corrective and Preventive Actions). You will also be responsible for reviewing and approving batch records, validation protocols, and other critical quality documentation.
The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, including sterile manufacturing and biologics. You must be proficient in interpreting and applying regulatory guidelines from bodies such as the MHRA, FDA, and EMA. Excellent analytical, problem-solving, and decision-making skills are essential, as is the ability to effectively communicate complex quality issues to various stakeholders, including senior management, cross-functional teams, and regulatory agencies. This remote position requires exceptional organizational skills, a high degree of self-motivation, and the ability to manage workload effectively in a distributed environment.
Essential Qualifications:
Your responsibilities will include developing, implementing, and maintaining comprehensive quality assurance policies and procedures. You will lead and mentor a team of QA professionals, fostering a culture of quality excellence throughout the organization. This involves conducting internal audits, managing external regulatory inspections, and overseeing the investigation and resolution of quality deviations and CAPAs (Corrective and Preventive Actions). You will also be responsible for reviewing and approving batch records, validation protocols, and other critical quality documentation.
The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, including sterile manufacturing and biologics. You must be proficient in interpreting and applying regulatory guidelines from bodies such as the MHRA, FDA, and EMA. Excellent analytical, problem-solving, and decision-making skills are essential, as is the ability to effectively communicate complex quality issues to various stakeholders, including senior management, cross-functional teams, and regulatory agencies. This remote position requires exceptional organizational skills, a high degree of self-motivation, and the ability to manage workload effectively in a distributed environment.
Essential Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 7 years of experience in Quality Assurance within the pharmaceutical industry, with at least 3 years in a management or supervisory role.
- In-depth knowledge of Good Manufacturing Practices (GMP) and relevant international regulatory requirements (MHRA, FDA, EMA).
- Proven experience in conducting audits, managing deviations, and implementing CAPAs.
- Strong leadership, team management, and interpersonal skills.
- Excellent written and verbal communication skills, with the ability to present complex information clearly.
- Proficiency in quality management software and systems.
- Demonstrated ability to work independently and effectively manage tasks in a remote setting.
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2
Principal Process Engineer - Pharmaceuticals (On-site)
CB2 0GA Cambridge, Eastern
£70000 Annually
WhatJobs
Posted 25 days ago
Job Viewed
Job Description
Our client, a prominent pharmaceutical manufacturing company, is seeking an exceptional Principal Process Engineer to join their state-of-the-art facility in **Cambridge, Cambridgeshire, UK**. This critical on-site role involves leading the design, development, and optimization of manufacturing processes for novel pharmaceutical products. You will be responsible for ensuring process efficiency, product quality, and compliance with stringent regulatory standards. The ideal candidate possesses extensive experience in process engineering within the pharmaceutical or biopharmaceutical industry, with a strong focus on scale-up, validation, and continuous improvement.
Key Responsibilities:
Job ID: PROENG77889
Key Responsibilities:
- Lead the design and implementation of new pharmaceutical manufacturing processes, from laboratory scale to commercial production.
- Optimize existing manufacturing processes to improve yield, reduce costs, and enhance product quality.
- Develop Process Flow Diagrams (PFDs) and Piping and Instrumentation Diagrams (P&IDs).
- Conduct process hazard analyses (PHAs) and implement risk mitigation strategies.
- Author and execute process validation protocols (IQ, OQ, PQ) and process development reports.
- Troubleshoot and resolve complex process-related issues during manufacturing.
- Collaborate closely with R&D, Quality Assurance, Manufacturing, and Engineering departments to ensure seamless project execution.
- Stay current with industry trends, new technologies, and regulatory requirements (e.g., FDA, EMA).
- Mentor junior engineers and provide technical guidance on process development and validation.
- Participate in the selection and qualification of new equipment and technologies.
- Contribute to capital project planning and execution related to process changes and expansions.
- MSc or PhD in Chemical Engineering, Biochemical Engineering, or a related discipline.
- Minimum of 10 years of progressive experience in process engineering within the pharmaceutical or biotechnology industry.
- Deep understanding of GMP (Good Manufacturing Practices) and regulatory requirements for pharmaceutical manufacturing.
- Proven experience in process scale-up, technology transfer, and process validation.
- Proficiency with process simulation software (e.g., Aspen Plus, HYSYS) and statistical analysis tools.
- Strong knowledge of unit operations relevant to pharmaceutical manufacturing (e.g., filtration, drying, chromatography, sterile processing).
- Excellent problem-solving, analytical, and critical thinking skills.
- Exceptional leadership, communication, and project management abilities.
- Experience with single-use technologies and continuous manufacturing processes is a significant advantage.
- Chartered Engineer status is preferred.
Job ID: PROENG77889
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3
Principal Pharmaceutical Research Scientist
CB2 0AW Cambridge, Eastern
£90000 Annually
WhatJobs
Posted 1 day ago
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Job Description
Join a globally recognized leader in pharmaceutical innovation, renowned for its commitment to developing life-changing medicines. Our client is seeking a highly accomplished and forward-thinking Principal Pharmaceutical Research Scientist to be based in the renowned scientific hub of Cambridge, Cambridgeshire, UK . This senior role offers a significant opportunity to lead groundbreaking research initiatives, drive the discovery and development of novel therapeutic agents, and contribute to the company's pipeline of innovative treatments. The ideal candidate will possess a Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life sciences discipline, with a proven track record of research excellence and significant contributions to drug discovery in the pharmaceutical industry. You will be responsible for designing and executing complex research projects, leading multidisciplinary teams, and mentoring junior scientists. Key areas of focus will include identifying novel drug targets, developing and validating preclinical models, characterizing drug candidates, and contributing to regulatory submissions. Expertise in specific therapeutic areas (e.g., oncology, immunology, neurology) is highly desirable. This role demands exceptional scientific rigor, critical thinking, and strategic vision. Strong leadership, communication, and interpersonal skills are essential for collaborating effectively with internal teams and external partners. You will be expected to stay at the cutting edge of scientific literature, present findings at international conferences, and contribute to the intellectual property portfolio. The successful applicant will work within state-of-the-art laboratory facilities in Cambridge, Cambridgeshire, UK , employing advanced technologies and methodologies. This position is critical to our client's mission of advancing healthcare and improving patient outcomes. We are seeking a passionate and dedicated scientist who can inspire innovation, guide research strategy, and make a tangible impact on the future of medicine. Your expertise will be instrumental in navigating the complexities of drug discovery and development.
Key Responsibilities:
Make a profound impact on global health by joining our cutting-edge research team in Cambridge, Cambridgeshire, UK .
Key Responsibilities:
- Lead and direct complex pharmaceutical research projects.
- Identify and validate novel drug targets for therapeutic intervention.
- Design and execute preclinical studies for drug discovery and development.
- Characterize the efficacy and safety profiles of potential drug candidates.
- Mentor and guide a team of research scientists.
- Collaborate with cross-functional teams, including clinical development and regulatory affairs.
- Develop and optimize assays and experimental methodologies.
- Contribute to the preparation of scientific publications and patent applications.
- Present research findings at scientific meetings and conferences.
- Stay abreast of the latest scientific advancements in relevant therapeutic areas.
Make a profound impact on global health by joining our cutting-edge research team in Cambridge, Cambridgeshire, UK .
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4
Senior Pharmaceutical Research Scientist
CB2 0AA Cambridge, Eastern
£65000 Annually
WhatJobs
Posted 2 days ago
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Job Description
Our client is a world-leading pharmaceutical research organisation at the forefront of medical innovation, seeking a highly skilled and dedicated Senior Pharmaceutical Research Scientist to join their esteemed, fully remote team. This is a unique opportunity to contribute to groundbreaking drug discovery and development programmes from the convenience of your home office, anywhere within the UK. The successful candidate will be instrumental in designing, executing, and analysing complex research experiments to identify and validate novel therapeutic targets and develop innovative drug candidates. You will be responsible for leading specific research projects, mentoring junior scientists, and contributing to the scientific strategy of the organisation. Key responsibilities include developing and optimising experimental protocols, conducting advanced assays, interpreting experimental data, and preparing high-quality scientific reports and publications. Collaboration with internal and external research partners, including academic institutions and biotechnology companies, will be a crucial aspect of this role. The ideal candidate will possess a PhD in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline, with a minimum of 5 years of post-doctoral research experience in the pharmaceutical or biotechnology industry. Expertise in drug discovery, target validation, medicinal chemistry, or specific therapeutic areas (e.g., oncology, immunology) is highly desirable. Excellent problem-solving skills, a rigorous scientific approach, and the ability to work independently and collaboratively in a virtual environment are essential. This is an exceptional chance to join a forward-thinking organisation and make a significant impact on the future of medicine.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Design, conduct, and analyse complex experiments to support drug discovery and development.
- Identify and validate novel therapeutic targets for unmet medical needs.
- Develop and optimise innovative assays and experimental methodologies.
- Interpret experimental data, draw conclusions, and communicate findings effectively.
- Prepare high-quality scientific reports, presentations, and manuscripts for publication.
- Lead and mentor junior research scientists, fostering a collaborative research environment.
- Collaborate with cross-functional teams and external research partners.
- Stay abreast of the latest scientific advancements and emerging technologies in pharmaceutical research.
- Contribute to the development and strategic direction of research programmes.
Qualifications:
- PhD in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 5 years of post-doctoral research experience in the pharmaceutical or biotechnology sector.
- Proven track record in drug discovery, target validation, or medicinal chemistry.
- Expertise in relevant therapeutic areas is a strong asset.
- Extensive experience with various laboratory techniques and assay development.
- Strong analytical and problem-solving skills.
- Excellent scientific writing and oral presentation abilities.
- Ability to work independently, manage projects, and collaborate effectively in a remote setting.
- Publication record in peer-reviewed journals.
- Must be eligible to work in the UK.
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5
Senior Pharmaceutical Research Scientist
CB2 1AA Cambridge, Eastern
£65000 Annually
WhatJobs
Posted 3 days ago
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Job Description
Our client, a leading biopharmaceutical company, is seeking an accomplished Senior Pharmaceutical Research Scientist to join their innovative R&D department in Cambridge, Cambridgeshire, UK . This role offers an exceptional opportunity to contribute to the discovery and development of novel therapeutics. You will be responsible for designing and executing complex research projects, leading experimental design, and interpreting results within the context of drug discovery and development pipelines. Your expertise will be crucial in areas such as medicinal chemistry, pharmacology, molecular biology, or a related discipline. You will be involved in the identification of new drug targets, the synthesis and characterization of potential drug candidates, and the assessment of their efficacy and safety in preclinical models. This position requires a deep understanding of scientific principles, advanced laboratory techniques, and data analysis methodologies. You will collaborate closely with a multidisciplinary team of scientists, clinicians, and project managers to advance projects from discovery through to clinical development. A significant part of your role will involve staying abreast of the latest scientific literature, identifying emerging trends, and proposing innovative research strategies. You will be responsible for documenting experimental procedures, analyzing data, and presenting findings at internal meetings and potentially at scientific conferences. The ideal candidate will possess a Ph.D. in Pharmaceutical Sciences, Chemistry, Biology, or a related field, with a minimum of 5-7 years of post-doctoral or industry experience in drug discovery. Proven experience in leading research projects and a strong publication record are essential. Expertise in specific therapeutic areas (e.g., oncology, immunology, neuroscience) and experience with relevant assays and technologies are highly desirable. Excellent critical thinking, problem-solving, and communication skills are required. The ability to work effectively in a collaborative, fast-paced environment is paramount. This role offers a competitive salary, excellent benefits, and the chance to make a significant impact on human health through groundbreaking pharmaceutical innovation.
Key Responsibilities:
Key Responsibilities:
- Design and lead innovative drug discovery research projects.
- Conduct experiments using advanced molecular and cellular biology techniques.
- Synthesize, characterize, and test novel small molecules or biologics.
- Analyze and interpret experimental data, drawing sound scientific conclusions.
- Collaborate with cross-functional teams to advance R&D projects.
- Prepare research reports, manuscripts, and presentations.
- Mentor junior research staff and provide scientific guidance.
- Stay current with scientific literature and emerging technologies in drug discovery.
- Contribute to the strategic direction of the R&D department.
- Ensure compliance with all laboratory safety and regulatory guidelines.
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6
Senior Pharmaceutical Research Scientist
CB2 0QQ Cambridge, Eastern
£60000 Annually
WhatJobs
Posted 4 days ago
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Job Description
Our client, a leading pharmaceutical company, is seeking a highly motivated Senior Pharmaceutical Research Scientist to join their dynamic R&D team. This lab-based role is situated in the prestigious scientific hub of Cambridge, Cambridgeshire, UK . You will be responsible for designing and executing complex research projects, contributing to the discovery and development of novel therapeutics. This position offers a fantastic opportunity to work on groundbreaking projects and collaborate with world-class scientists.
Key Responsibilities:
Required Qualifications:
Key Responsibilities:
- Design and conduct experimental studies to investigate biological targets and pathways relevant to disease.
- Develop and validate novel assays for drug discovery and characterization.
- Perform detailed data analysis, interpretation, and reporting of experimental results.
- Contribute to the development of preclinical drug candidates.
- Collaborate closely with internal teams (e.g., medicinal chemistry, pharmacology, DMPK) and external partners.
- Stay abreast of the latest scientific literature and technological advancements in the pharmaceutical industry.
- Present research findings at internal meetings and external scientific conferences.
- Mentor and guide junior research scientists and technicians.
- Manage laboratory resources and ensure compliance with safety and ethical guidelines.
- Contribute to the preparation of patent applications and regulatory submissions.
- Identify and evaluate new technologies and methodologies to enhance research capabilities.
- Troubleshoot experimental challenges and propose innovative solutions.
- Maintain detailed and accurate laboratory notebooks and records.
Required Qualifications:
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 5 years of post-doctoral or industry research experience in drug discovery.
- Proven track record of designing and executing complex biological experiments.
- Extensive experience in developing and validating assays for target identification and validation.
- Strong understanding of disease mechanisms and drug discovery processes.
- Proficiency in relevant laboratory techniques (e.g., cell culture, molecular biology, biochemical assays, flow cytometry).
- Experience with data analysis software (e.g., GraphPad Prism, R) and statistical analysis.
- Excellent written and verbal communication skills, with the ability to present complex scientific data.
- Strong leadership, teamwork, and problem-solving abilities.
- Ability to work independently and manage multiple research projects simultaneously.
- Experience with small molecule or biologic drug development.
- Knowledge of bioanalytical techniques and their application is a plus.
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7
Senior Pharmaceutical Research Scientist
CB2 0GG Cambridge, Eastern
£55000 Annually
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical innovator, is seeking a highly motivated and experienced Senior Pharmaceutical Research Scientist to join their dynamic R&D team in Cambridge, Cambridgeshire, UK . This role is pivotal in driving forward groundbreaking research in drug discovery and development, focusing on novel therapeutic areas. The ideal candidate will possess a strong scientific background, exceptional problem-solving skills, and a proven track record in laboratory-based research.
Responsibilities:
Qualifications:
This is an exciting opportunity to make a significant impact on the future of medicine within a supportive and innovative company culture. The role offers a competitive salary, comprehensive benefits, and opportunities for professional growth.
Responsibilities:
- Design, execute, and interpret complex experiments to identify and validate new drug targets.
- Develop and optimize in vitro and in vivo assay systems to support drug candidate screening and characterization.
- Collaborate effectively with cross-functional teams, including medicinal chemistry, pharmacology, and toxicology, to advance projects from discovery through to preclinical development.
- Analyze and present experimental data at internal project meetings and external scientific conferences.
- Contribute to the preparation of research reports, patents, and regulatory submissions.
- Mentor and guide junior scientists, fostering a collaborative and high-performance research environment.
- Stay abreast of the latest scientific literature and emerging technologies in relevant therapeutic fields.
- Ensure compliance with all laboratory safety regulations and company policies.
Qualifications:
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 5 years of post-doctoral or industry research experience in pharmaceutical R&D.
- Extensive experience with assay development, molecular biology techniques, and data analysis software.
- Strong understanding of drug discovery processes and relevant therapeutic areas.
- Excellent written and oral communication skills.
- Ability to work independently and as part of a team in a fast-paced environment.
- Demonstrated leadership potential and mentorship capabilities.
This is an exciting opportunity to make a significant impact on the future of medicine within a supportive and innovative company culture. The role offers a competitive salary, comprehensive benefits, and opportunities for professional growth.
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8
Principal Pharmaceutical Research Scientist
CB2 1TN Cambridge, Eastern
£75000 Annually
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
Our client, a leading innovator in the pharmaceutical industry, is seeking a highly accomplished Principal Pharmaceutical Research Scientist to join their fully remote R&D department. This senior position will lead cutting-edge research projects focused on drug discovery and development. You will be responsible for designing and executing complex experiments, analyzing biological data, and contributing to the strategic direction of our research pipeline. The ideal candidate will possess a Ph.D. in a relevant scientific discipline (e.g., Pharmacology, Biochemistry, Molecular Biology) and a minimum of 8 years of post-doctoral research experience in the pharmaceutical or biotechnology sector. Proven expertise in specific therapeutic areas and a strong publication record are highly desirable. You will mentor junior scientists, collaborate with cross-functional teams (including clinical, regulatory, and manufacturing), and contribute to patent applications and regulatory submissions. This is a remote-first role, requiring a self-motivated individual with excellent analytical, problem-solving, and communication skills. You must be adept at working independently, managing multiple projects, and presenting complex scientific findings clearly and concisely. Experience with cutting-edge technologies and assay development is essential. This is a unique opportunity to drive innovation and make a significant impact on patient health from anywhere in the UK, supporting our world-class research efforts based in Cambridge, Cambridgeshire, UK .
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