80 jobs for “Biotech Research Scientist”
Isomorphic Labs London
Lead pharmacology and translational biology strategy for large molecule therapeutics, designing in vivo efficacy and complex in vitro functional assays. Act as Biology Lead on projects, coordinating internal workflows and external CROs, and collaborate with ML and computational biology teams to feed data into generative AI design loops.
Isomorphic Labs London
Owns safety assessment strategy for drug discovery projects from inception to regulatory submission, working with small molecule and biologics platforms. Designs screening cascades, authors IND packages, and manages CRO relationships for outsourced wet-lab work. Also guides development of an AI predictive toxicology platform with ML researchers.
Newton Colmore Spain
Bridge process biology and advanced sensing by running suspension CHO/HEK293 cultures from bench to pilot scale, building Raman/PLS chemometric models, and translating bioreactor behaviour into requirements for engineering and software teams. Work in a multidisciplinary group developing AI-driven bioprocessing systems for mammalian cell culture and monoclonal antibody production, with direct access to the CEO and CTO.
GSK USA - Pennsylvania - Upper Providence
Lead programming activities for complex and pivotal clinical studies, developing, maintaining and validating analysis packages while ensuring compliance with Good Programming Practices and CDISC standards. Mentor junior programmers, support regulatory interactions with EMA and FDA, and bridge scientific requirements with technical solutions in an agile, squad-based global team.
AstraZeneca London
Finance lead for a designated disease area with full P&L ownership across UK & Ireland in-line and pipeline assets. Drives strategic planning, budgeting, monthly forecasting and pricing/reimbursement business cases, applying AI and advanced analytics, while partnering Commercial, Medical, Market Access and Global Finance. Office-based in London with at least 60% attendance.
Newton Colmore Cambridge
Lead the design and development of next-generation drug delivery devices, guiding multidisciplinary teams of engineers, scientists and designers from early-stage concepts through to manufacturable solutions. The role blends hands-on R&D work — concept generation, prototyping, experimental design, verification planning and risk management — with client-facing consultancy, programme leadership and mentoring of junior colleagues.
Moderna Oxford
Provides scientific and hands-on leadership for immunogenicity and ligand binding assay bioanalysis supporting mRNA-LNP therapeutic programs, spanning assay development, validation, clinical sample testing and regulatory submissions. Ensures GcLP compliance and partners with cross-functional teams, with opportunities to work alongside data and AI-enabled analytical approaches.
SRG Loughborough £14 – £15 ph
Perform analytical testing for batch release, stability studies and complaint investigations in a GMP/GLP-regulated pharmaceutical lab, using techniques such as HPLC and UV spectroscopy. Support OOS/OOT investigations, maintain Good Documentation Practices, review and issue GMP documentation, and help with calibration and equipment maintenance. A 12-month temp contract within a cross-functional QC team.
Autolus London
Designs end-to-end data solutions spanning data integration, data warehousing, master data management, governance and analytics for a biopharmaceutical company. Translates business requirements into data models, data flows and integration patterns, and leads architecture and design reviews across enterprise applications and cloud data platforms.
Vertex Pharmaceuticals London
Leads regional or global regulatory strategy for development programs and marketed products, serving as a regulatory lead and primary contact with health authorities. Manages preparation, submission and approval of regulatory applications, advises teams on approval pathways and expedited routes, and monitors regulatory intelligence to inform strategy.
Genomics London
Client-facing programme manager role setting up and embedding a multidisciplinary delivery team around a major pharma partnership, running the integrated delivery plan, milestones, dependencies, risks and resourcing. Coordinates across Science, Data, Engineering, Finance, Legal and People stakeholders, running status meetings, reporting and escalations with the partner. Structured as a six-month engagement with an immediate start.
Moderna Oxford
Lead the technical maintenance and engineering setup of a brand-new Label and Secondary Packaging operation at the Harwell site, from URS and FMEA through commissioning, qualification and validation. Develop preventative maintenance strategies, manage external vendors and build the site maintenance team, working with GMP equipment and digital/AI-enabled engineering tools.
Parexel Harrow
Acts as principal labelling strategist within Global Regulatory Affairs, driving development and maintenance of dCCDS, CCDS, USPI and EU SmPC documents across an assigned product portfolio. Leads Global Labeling Committee reviews of proposed label exceptions and represents labelling on regulatory strategy teams, working with safety, clinical and commercial stakeholders. Home or office based across European locations.
Relation Therapeutics London
Develops and benchmarks machine learning models for DNA sequence, regulatory elements and genetic variation, including variant effect prediction and representation learning. Integrates sequence-derived representations with transcriptomic, epigenomic and perturbational data to uncover disease mechanisms and support target prioritisation, working within the interdisciplinary Rosalind team.
Bicycle Therapeutics Cambridge
Operational backbone of R&D Quality, administering and optimising a validated eQMS (Veeva, TrackWise, Dot Compliance) for GxP document control, training matrices, deviation/CAPA tracking and inspection readiness. Supports FDA, MHRA and EMA inspections and works across clinical, non-clinical and pharmacovigilance teams.
