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Senior Analytical Chemist

Job in South Yorkshire, York, North Yorkshire, YO1, England, UK
Listing for: Aurora Lifesciences
Full Time position
Listed on 2026-10-30
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 42000 - 52000 GBP Yearly GBP 42000.00 52000.00 YEAR
Job Description & How to Apply Below

An exciting opportunity has arisen for a Senior Analytical Chemistto join a growing and fast paced quality and chemistry laboratory within a regulated life sciences environment.

Overview

An opportunity for an experienced Senior analytical chemist to support Quality Assurance activities within a regulated laboratory environment. This role focuses on HPLC-based analysis, method lifecycle management, and stability studies, ensuring compliance with quality standards and supporting product release. Within this role you will work with multi disciplined teams including Microbiology, Quality & Manufacturing.

Key Responsibilities
  • Lead QA oversight of
    analytical chemistry testing
    (HPLC, chromatography, spectroscopy).
  • Manage method development, validation, and transfer.
  • Design and review stability studies and shelf-life assessments.
  • Support routine analysis and release testing for manufacturing.
  • Ensure compliance with data integrity and documentation standards (cGMP).
  • Perform trend analysis and support quality decision-making.
  • Investigate OOS results, lead root cause analysis, and implement CAPA.
  • Troubleshoot analytical methods and instrumentation issues.
  • Train and mentor staff in
    HPLC and analytical techniques
    .
  • Drive continuous improvement in
    lab processes and workflows
    .
Requirements
  • Degree in
    Chemistry, Analytical Chemistry, or related field
    .
  • 3–5+ years experience in a regulated analytical/QC/QA laboratory.
  • Strong hands-on experience with
    HPLC and analytical instrumentation
    .
  • Experience with
    stability studies
    and method validation.
  • Knowledge of cGMP, quality systems, and regulatory standards.
Skills
  • Strong data analysis and interpretation skills.
  • Experience in investigations and root cause analysis.
  • Clear and effective technical writing and communication.
  • Detail-oriented with strong problem-solving and organisational skills.
Compensation Package
  • 36 Days Holiday Annually
  • Company Pension
  • Bonus Up to 8%
  • Healthcare
  • Half Day Friday
Position Requirements
10+ Years work experience
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