Pharmaceutical Analyst – GMP Lab (HPLC & Dissolution)

RXinsider LTD.; Liverpool; On-site; GBP 28,000 - 42,000; Full time

Benefits offered by this job

Perkbox access

Life Assurance

Company Pension

Health Cash Plan

Volunteer days

Free on-site parking

Job summary

Eurofins is seeking a Pharmaceutical Analyst to perform analysis of pharmaceutical raw materials, drug substances and finished products within a GMP framework. The role involves using traditional and modern techniques such as HPLC, dissolution, Karl Fischer, and UV spectroscopy.

You will review data, investigate OOS results, document records, and contribute to workflow improvements while ensuring compliance and timely reporting.

Qualifications

• Degree in Chemistry or related discipline with strong pharma knowledge.
• Experience in a pharmaceutical testing laboratory, preferably with solid dose products.
• Competent with traditional analytical techniques and modern instrumentation (HPLC, Dissolution, Karl Fischer, UV).
• Ability to interpret raw data, troubleshoot methods, and follow GMP requirements.

Responsibilities

• Perform routine and non-routine analysis using traditional and modern analytical techniques within GMP.
• Review analytical data for compliance with GMP standards and approved methods.
• Investigate and document OOS results and action limits per client procedures.
• Document data in accordance with client policies to ensure traceability.
• Monitor productivity and report test volumes, cycle times, and issues.

Skills

Analytical thinking

Data interpretation

GMP knowledge

Education

Bachelor's or Master's degree in Chemistry

Tools

HPLC

Dissolution

Karl Fischer

UV spectroscopy

Gas chromatography

Mass spectrometry

Job description

Eurofins is seeking a Pharmaceutical Analyst to perform analysis of pharmaceutical raw materials, drug substances and finished products within a GMP framework. The role involves using traditional and modern techniques such as HPLC, dissolution, Karl Fischer, and UV spectroscopy.

You will review data, investigate OOS results, document records, and contribute to workflow improvements while ensuring compliance and timely reporting.