247 jobs for “Analytical Chemical Process Development ”
Develops and deploys cheminformatics and machine learning models on large proprietary datasets to guide go/no-go decisions across drug-discovery programmes. Embeds predictive models into multidisciplinary teams spanning DMPK, toxicology and safety pharmacology, and prototypes LLM-driven agent workflows for design-make-test-analyse cycles.
ChemAxon · RDKit · Pipeline Pilot +2
GSK · 10000+ people · Public
Embedded forward deployed engineer role in GSK's Enterprise AI team, working within the Chemical Manufacturing & Control area to prototype AI solutions at days-to-weeks cadence. Focuses on document authoring and generation for regulatory filings, agentic workflows, RAG, knowledge systems and LLM evaluation, with heavy daily use of AI coding agents. Proven prototypes are handed off to a Sr. Solutions Engineer for scale-up.
Claude Code · GitHub Copilot · Databricks AI Assistant +3
Eurofins
Perform routine and non-routine analytical testing of pharmaceutical oral drug products and new modalities using HPLC, Karl Fischer, dissolution and mass spectrometry. Review data for GLS and GMP compliance, investigate out-of-specification results, and develop and validate analytical methods while training colleagues and supporting client projects at a Macclesfield pharma facility.
HPLC · Karl Fischer · Mass Spectrometry +1
Eurofins
Perform routine, non-routine and stability testing on finished pharmaceutical products at a client site, using HPLC, Dissolution, Karl Fischer and UV techniques. The role also covers technology transfers, analytical validation, GMP data review and OOS investigations, working within a managed services team embedded at the client's facility.
HPLC · Dissolution · Karl Fischer +4
IQVIA
Shapes and drives end-to-end clinical trial supply strategy, translating study protocols into kit designs, demand forecasts and packaging plans. Oversees vendors, IRT systems, distribution and temperature-excursion management while leading client and vendor meetings. Combines analytical planning with operational leadership across GxP-regulated clinical supply work.
Interactive Response Technology · Microsoft Word · Microsoft Excel +1
Moderna · 1001–5000 people · Late stage
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.
ECL · Gyrolabs · Reporter Gene Assays +3
FIELD
This role involves hands-on troubleshooting, maintenance, calibration, and repair of medical equipment both onsite and remotely within a leading hospital environment. The engineer will perform preventative maintenance, equipment upgrades, and ensure compliance with manufacturer guidelines and contractual KPIs. Strong diagnostic skills and the ability to explain technical issues clearly to non-technical stakeholders are essential.
Nexus Life Sciences
Leads a Clinical Method Development and Validation team, overseeing bioanalytical method delivery for a New Product Development programme. Provides technical leadership in a GLP-compliant lab, acting as expert in extraction techniques and optimising HPLC, UPLC and LCMSMS systems while mentoring the team.
HPLC · UPLC · LCMSMS +1
Moderna · 1001–5000 people · Late stage
Perform routine cGMP Quality Control testing using HPLC, UPLC, GC, UV spectroscopy, DLS and Karl Fischer analysis, supporting raw materials, in-process materials, drug substance, product release and stability programs. Coordinate and execute global GMP stability studies, manage sample lifecycles in LabVantage LIMS, trend data statistically, and author protocols and regulatory documentation. The role is 100% onsite at the Harwell facility and involves collaboration with manufacturing, QA, regulatory and external testing partners.
LabVantage · LIMS · Generative AI
Vertex Pharmaceuticals
Oversees quality control testing for a genetically edited cell therapy, acting as lead point of contact for external CDMOs and QC labs on GMP release, stability and method lifecycle work. Leads OOS/OOT investigations, reference standards and assay controls programmes, authoring and approving SOPs, COAs and protocols. Hybrid role based in London requiring close collaboration with contract test labs and management on compliance risks.
LIMS
Talentmark
Analyse large-scale single-cell, bulk transcriptomics and other omics datasets, and develop new computational methods to extract biological insight. Build scalable, well-tested software and workflows for atlas-scale data (millions of cells) and high-dimensional proteomics, acting as the analytical point of contact in multidisciplinary collaborations from analysis plan through to publication or portfolio decision.
Visium · Xenium · MERFISH +4
Genomics
Staff-level product engineer leading a petabyte-scale analytical data platform built on multi-tenant ClickHouse, spanning database internals through to data-serving systems. Work includes sharding and replication strategy, materialised views, self-healing pipeline automation, and Data-as-a-Service productisation, plus shaping data foundations for an agentic AI layer. The role combines hands-on engineering with line management of a small team and setting platform-wide technical direction.
ClickHouse · Mystra · MystraAI
Thermo Fisher Scientific
Provides technical support and training to customers using mass spectrometry, LCMS and metabolomics platforms across EMEA. Delivers application optimisation, troubleshooting, presentations and product feedback to R&D, combining scientific expertise with customer engagement and up to 50-75% travel.
Thermo Fisher Scientific
Leads the design and implementation of bioanalytical strategies for a client-dedicated global biopharma team, ensuring lab-based activities align with context of use. Manages experimental design, tech transfer and regulatory submissions, interacting with lab scientists, cross-functional groups and Health Authorities in a matrix environment.
ddPCR · qPCR · RT-qPCR +6
Parexel
Leads research design and analytical strategies for clinical trials, developing and reviewing statistical analysis plans and authoring reports, abstracts and manuscripts. Acts as functional lead on study teams, directing biostatistical activities, performing complex analyses in SAS or R, and quality-controlling deliverables while mentoring junior staff and liaising with clients on scope and budget.
SAS · R
