387 jobs for “Technician In Molecular Microbiology”
Leads analytical strategy for late-phase small molecule products, owning comparability studies, characterisation strategies and post-approval change submissions. Partners across R&D, manufacturing sites and regulatory in a matrix, embedding method knowledge into tech transfers and defending strategies during health authority inspections.
PAT
GSK · 10000+ people · Public
Embedded with Chemical Manufacturing & Control teams, you take high-priority use cases from problem framing to working prototypes at days-to-weeks cadence, then hand proven solutions to a Solutions Engineer for scale-up. Work is AI-augmented: agent frameworks, multi-agent orchestration, MCP, and AI coding assistants are the default mode of building, turning manual lab and process workflows into agentic automation.
Claude Code · GitHub Copilot · Databricks AI Assistant +3
Isomorphic Labs · 201–500 people · Series A
Lead the hardening and scaling of an inference platform serving fleets of cutting-edge ML models for scientific applications. Set strategy and roadmaps, architect next-generation services to solve scaling limits, and partner with research, product and operations teams to align infrastructure with biotech R&D cycles.
Kubernetes · Google Cloud Platform · NVIDIA GPU +1
Isomorphic Labs · 201–500 people · Series A
Lead end-to-end clinical trial material planning, vendor management, packaging, labeling, inventory and global distribution for an AI-first drug discovery company. Act as the clinical supply authority within a lean Pharmaceutical Sciences & CMC team, building scalable systems and vendor networks while partnering closely with Clinical Operations and CROs.
IRT · RTSM
Autolus · 101–500 people · Series C
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.
SaaS · APIs · Cloud Data Platforms
Autolus · 101–500 people · Series C
Hands-on senior role owning the computerised-system lifecycle for GxP systems, from impact and supplier assessments through validation, release, operation and retirement. Authors and executes CSV documentation, performs data integrity and 21 CFR Part 11 assessments, manages change controls and CAPAs, and supports regulatory inspections as a CSV subject matter expert.
SaaS · Cloud
Eurofins
Responsible for managing a pathology laboratory's day-to-day operations, ensuring compliance with ISO 17025, UKAS and retail quality standards. Duties include safety and COSHH compliance, equipment calibration, audit leadership, KPI monitoring, and developing Team Leaders while maintaining 7-day shift coverage.
LIMS · Microsoft Excel · Microsoft Word
LGC
Hands-on role independently developing, optimising and validating analytical methods using LC-MS, troubleshooting complex analytical challenges and building new testing solutions for specialist laboratories. You own method development projects from feasibility through validation and implementation, working across the business in a busy commercial testing environment under ISO 17025.
LC-MS · GC-MS/MS · HRAM
Thermo Fisher Scientific
Support the QC Chemistry team by performing routine analytical testing of incoming goods, intermediates and finished products under cGMP conditions. Duties include stock control of reagents and reference standards, equipment checks, calibration and preventative maintenance, reagent preparation, glassware washing, waste disposal and maintaining technical documentation and training records.
pH Meters · Balances
Eurofins
Manages a team of laboratory staff in a food microbiology lab, ensuring analytical procedures meet ISO17025 and UKAS standards. Responsibilities include training, appraisals, holiday and sickness management, quality assurance, equipment calibration, HSE compliance and reporting KPIs to the Laboratory Manager.
LIMS
Vertex Pharmaceuticals
A one-year PhD fellowship within an International Regulatory Affairs team, supporting development programs and marketed products. The fellow helps build and implement regulatory strategy, prepares and submits applications to local health authorities under supervision, and reviews regulatory intelligence to keep submissions compliant. Based at the London headquarters with hybrid or on-site working options.
IQVIA
Serves as subject matter expert in COA endpoint strategy, instrument development and regulatory strategy, advising pharma and biotech sponsors and representing the company as an external scientific thought leader. Leads qualitative research supporting content validity, oversees internal project teams, mentors consultants and supports business development through proposals and client presentations.
Vertex Pharmaceuticals
Leads statistical work for post-marketing clinical trials, observational studies and real world data investigations, serving as Statistics lead on assigned projects. Develops protocols, analysis plans and TFL specifications, collaborating with clinical development, medical affairs, health economics and real world evidence teams. Requires strong SAS and R skills with a drug developer mindset.
SAS · R
Moderna · 1001–5000 people · Late stage
Lead development, qualification, validation and execution of complex cell-based immunoassays generating clinical trial data across therapeutic areas. Act as scientific point of contact within the Immuno-assays group, performing GCP/GLP-compliant sample testing, authoring validation reports, and mentoring junior lab staff. Fully onsite at Harwell, reporting to the Associate Director, Immuno-assay UK.
GraphPad Prism · Microsoft Word · Microsoft Excel +2
Fortrea
Technical lead for all data management activities on late phase (IIb-III) clinical trials, from start-up through completion. Develops Data Management and Quality Management Plans, designs CRF/eCRF and database structures, and coordinates edit checks and discrepancy management. Acts as client liaison, tracking cycle times and metrics while overseeing data review staff.
RAVE · EDC
