Biotechnology Jobs

246 jobs for “Analytical Chemical Process Development ”

Results

CureAge Therapeutics logo

CureAge Therapeutics · 1–10 people · Seed

Senior Computational Chemist, LNP Design

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  • London
  • Hybrid
  • Senior
  • Permanent · Part time

Lead the computationally guided design of a lipid nanoparticle delivery platform, applying chemical and biophysical principles to optimise LNP composition and formulation. Use AI-enabled chemistry, cheminformatics, predictive models and molecular modelling to prioritise formulation components, working closely with the experimental team and founding team in a small start-up.

Featured 2 weeks ago
Lypo logo

Lypo · 1–10 people · Seed

Molecular Biologist

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  • Edinburgh
  • Hybrid · 2–3 days in office
  • £31,000 – £36,000 pa
  • Mid-level
  • Contract

Implement high-throughput plasmid assembly, colony PCR, Minipreps and pathway construction to build strains for hypothesis testing and model training. Work across disciplines in a lab-based, cross-pollinating team, with fortnightly research updates, mentorship and organised labbook/data keeping. Golden Gate assembly, Benchling in silico cloning and DNA sequencing are core.

Benchling · QIAgility

Featured 6 days ago

Eurofins

Analytical Chemical Process Development Scientist

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  • Liverpool
  • On-site
  • Permanent

Perform method development and proof-of-concept validation on pharmaceutical raw materials, intermediates and drug substances, mainly APIs, using HPLC, GC and MS. Support technology transfers for novel substances, review data for compliance, investigate OOS/OOE results and document work to client procedures. Based on-site at a client facility as a managed PSS scientist, liaising with client representatives and supporting audits and continuous improvement.

HPLC · GC · MS +7

Last month

Eurofins

Analytical Chemical Development Scientist

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  • Macclesfield
  • Permanent

Provide analytical support for drug substance manufacturing and method development, running project analysis, forced degradation studies and proof-of-concept validation. Author and review Analytical Testing Plans, method protocols and validation protocols, using HPLC and GC within a GMP-regulated lab. Work independently and in a multidisciplinary team, communicating findings to internal and external stakeholders.

HPLC · GC · NMR +4

Today

Platform Recruitment

Research Scientist

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  • London
  • On-site
  • Mid-level

Develops and optimises therapeutic delivery formulations, designing lab experiments to assess stability, physicochemical properties and in vitro performance. Works in a multidisciplinary biotech team, characterising formulations analytically and supporting scale-up and tech transfer towards manufacturing. Distinct for its blend of formulation science, experimental development and translational research.

3 weeks ago
GSK logo

GSK · 10000+ people · Public

Senior, Forward Deployed Engineer (Agentic Automation for CMC R&D)

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  • London
  • Hybrid · 2–3 days in office
  • Senior

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

2 weeks ago
GSK logo

GSK · 10000+ people · Public

Senior, Forward Deployed Engineer (Agentic Automation for CMC R&D)

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  • Stevenage
  • Hybrid · 2–3 days in office
  • Senior

Embedded with Chemical Manufacturing & Control teams, you take high-priority use cases from problem framing to working prototypes at days-to-weeks cadence, then ship first production versions. Work is AI-augmented: agent frameworks, multi-agent orchestration, MCP and AI coding assistants handle routine coding while you supply judgement and validation, coaching BU engineers along the way.

Claude Code · GitHub Copilot · Databricks AI Assistant +3

2 weeks ago

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Agilent

Expert R&D Scientist – Chromatography Materials

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  • Church Stretton
  • Senior

Technical lead role driving innovation in polymeric and silica particle technologies for chromatography, diagnostics and biopharma consumables. Involves independently designing and executing complex polymer synthesis, particle manufacture and surface functionalization, plus technology transfer from lab-scale prototypes to full production. Acts as internal consultant and escalation point for critical materials issues, mentors scientists and shapes long-term technology strategy.

3 weeks ago

Moderna · 1001–5000 people · Late stage

Associate Director, CMC Regulatory Science - UK

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  • London
  • Hybrid
  • Director

Lead CMC regulatory strategy for UK-manufactured and UK-licensed mRNA products across development, registration and post-approval lifecycle. Act as primary point of contact with the MHRA, oversee submissions and manufacturing change assessments, and shape global regulatory approaches across cross-functional matrix teams.

MHRA · Generative AI

Clearance required 2 weeks ago

Moderna · 1001–5000 people · Late stage

Associate Director, CMC Regulatory Science, International

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  • London
  • On-site
  • Director
  • Permanent

Leads CMC regulatory strategy for global submissions including IND, CTA, BLA and MAA, and oversees agency correspondence and compliance for mRNA products. Reviews submissions for readiness, drives health authority interactions, and advises manufacturing and quality teams on change controls and regulatory guidance across vaccines, oncology and rare disease programmes.

IND · CTA · BLA +1

Clearance required 6 months ago

Thermo Fisher Scientific

QC Section Head

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  • Swindon
  • Lead · manages people

Leads a team of scientific officers performing GMP QC Chemistry analysis of incoming goods, in-process, intermediate, stability and finished product samples. Acts as first escalation point for technical, compliance and personnel issues, manages batch release, stability studies, documentation and audits, and deputises for the QC Manager. Requires extensive instrumental and traditional analytical experience plus 2+ years of team leadership.

3 months ago

Thermo Fisher Scientific

QC Scientist I

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  • Loughborough
  • On-site
  • Entry level
  • Permanent

Performs chemical, physical and microbiological testing of raw materials, in-process, finished and stability samples in a GMP pharmaceutical QC lab. Uses wet chemistry techniques, auto titrators, Karl Fischer, FTIR and UV-Vis, plus LIMS, with instrument calibration, COSHH risk assessments and 6S housekeeping duties.

LIMS · Microsoft Office · Auto Titrators +4

3 months ago

LGC

Analytical Chemist

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  • Guildford
  • Mid-level
  • Permanent

Hands-on laboratory role analysing pharmaceutical samples including APIs, medicines, herbal products and packaging for MHRA Laboratories. Uses HPLC, GC, GC/LC-MS, IR, Raman, UV, dissolution and wet chemistry, with responsibility for drafting reports, validating data, equipment calibration and maintaining an ISO/IEC 17025 quality system. Works within a team of around 30 analytical scientists, independently coordinating project workloads.

Microsoft Word · Microsoft Excel

Today

University of Oxford

Postdoctoral Research Associate in Chemical Biology and Synthetic Biology

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  • Oxford
  • On-site
  • £40,178 – £48,700 pa
  • Entry level
  • Contract

Join a Gates Foundation-funded programme developing nanopore-based sensing platforms to detect volatile organic compounds in biological samples, part of the multidisciplinary Decoding Olfaction collaboration. The role combines chemical biology and biophysics to advance single-molecule sensing, with the goal of enabling personalised and continuous health monitoring. Multiple fixed-term postdoc positions are available in a collaborative academic and industrial environment.

2 days ago
Isomorphic Labs logo

Isomorphic Labs · 201–500 people · Series A

Associate Director, Clinical Supply Chain, Cambridge, MA

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  • Cambridge, United States
  • Hybrid · 3 days in office
  • Director

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

Last month

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