4 Research Teams jobs in London

The School has secured multi-million-pound research funding and maintains strong partnerships with UK and international universities, the NHS, charitable organisations, and industry partners. The vision is to establish the School as a world leader in healthcare engineering.

The Research Development Manager is a senior role within the School of Biomedical Engineering & Imaging Sciences, responsible for driving large-scale, high-profile healthcare engineering grants that deliver real-world patient benefits and measurable impact. Working closely with the Head of School, Heads of Research Departments, academic and research staff, and external stakeholders, this role will play a pivotal part in securing funding, fostering strategic collaborations, and facilitating the translation of healthcare engineering innovations into clinical applications.

The Research Development Manager will be instrumental in realizing the School’s vision by providing strategic and operational support, they will support the development and submission of competitive grant applications, fellowships, and funding proposals to governmental agencies, Charities, and industry sponsors. The role requires a strong scientific background, exceptional writing skills, and the ability to translate complex research concepts into clear, compelling narratives tailored to funder priorities.

This is a full time (35 Hours per week), and you will be offered an indefinite contract.

• Lead the design, synthesis, and optimization of complex organic molecules for pharmaceutical applications.
• Develop innovative and scalable synthetic routes, addressing challenges in process chemistry.
• Direct research efforts in medicinal chemistry to identify and improve lead compounds.
• Utilize advanced analytical techniques (e.g., NMR, MS, X-ray crystallography) for structural elucidation and purity assessment.
• Collaborate with cross-functional teams, including biologists, toxicologists, and formulation scientists, to advance drug candidates.
• Oversee and mentor junior research chemists, guiding their technical development and project execution.
• Develop and implement robust quality control measures for chemical synthesis and intermediates.
• Contribute to intellectual property generation through patent filings and scientific publications.
• Stay abreast of cutting-edge research, emerging technologies, and industry best practices in organic and medicinal chemistry.
• Prepare detailed scientific reports, presentations, and regulatory documentation.
• Ensure compliance with all laboratory safety regulations and ethical guidelines.
• Manage research project timelines, resources, and budgets effectively.

• Ph.D. in Organic Chemistry, Medicinal Chemistry, or a closely related field.
• Minimum of 8 years of relevant industrial experience in pharmaceutical research and development.
• Demonstrated track record of successfully leading complex synthetic chemistry projects.
• Extensive experience in modern synthetic methodologies, reaction optimization, and process development.
• Expertise in analytical characterization techniques for organic compounds.
• Strong understanding of drug discovery principles, pharmacokinetics, and toxicology.
• Proven ability to interpret complex data and provide strategic insights.
• Excellent leadership, communication, and interpersonal skills.
• Experience with computational chemistry and molecular modeling is advantageous.
• Ability to thrive in a collaborative, fast-paced, hybrid research environment.

• Lead the development and optimization of robust, scalable, and cost-effective manufacturing processes for small molecules and biologics.
• Design and execute laboratory experiments to define critical process parameters and develop comprehensive process understanding.
• Utilize advanced analytical techniques and Process Analytical Technology (PAT) to monitor and control manufacturing processes.
• Translate laboratory-scale processes to pilot and commercial-scale manufacturing, ensuring successful technology transfer.
• Collaborate closely with discovery research, formulation development, analytical development, and regulatory affairs teams.
• Ensure all process development activities comply with Good Manufacturing Practices (GMP) and relevant regulatory guidelines (FDA, EMA).
• Troubleshoot manufacturing issues and implement effective corrective and preventive actions (CAPAs).
• Develop and manage project plans, timelines, and resources for process development initiatives.
• Stay abreast of emerging technologies, scientific advancements, and industry best practices in pharmaceutical manufacturing.
• Author, review, and approve technical reports, development protocols, and regulatory submission documents.
• Mentor and guide junior scientists and engineers within the process development team.
• Contribute to the strategic direction of the R&D organization regarding manufacturing capabilities.
• Manage intellectual property and contribute to patent filings related to novel processes.
• Maintain a high level of scientific rigor and ethical conduct throughout all research activities.

• PhD in Organic Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline.
• Minimum of 10 years of experience in pharmaceutical process development, with a strong emphasis on API manufacturing.
• Extensive experience in process scale-up, optimization, and validation.
• In-depth knowledge of synthetic organic chemistry, reaction kinetics, and purification techniques.
• Proven experience with GMP regulations and regulatory filing requirements (IND, NDA, BLA).
• Familiarity with Process Analytical Technology (PAT) and Quality by Design (QbD) principles.
• Strong analytical and problem-solving skills, with a meticulous attention to detail.
• Excellent leadership, communication, and project management skills.
• Ability to work independently and effectively lead cross-functional teams in a remote setting.
• Demonstrated track record of successfully bringing pharmaceutical products from development to market.
• Experience with biologics manufacturing processes is a plus.