Scientist, Analytical Quality Control

Overview

In this role you support late-stage development and commercial API programs within Pharmaron’s Analytical Quality Control team. You will perform GMP-compliant analytical testing, contribute to method development and validation, and help maintain robust data integrity in a collaborative lab. The position offers growth in a GMP-regulated environment with hands-on exposure to a wide analytical toolkit. You will work alongside experienced scientists to drive quality and efficiency in drug development workflows.

Pay / Benefits

• Competitive salary
• comprehensive benefits package
• strong opportunities for professional growth
• state-of-the-art onsite working environment

Responsibilities

• Perform analytical testing for batch release, development and scale-up using diverse techniques and instrumentation
• Generate accurate, timely analytical data in line with GMP requirements
• Assist with method development, transfer and validation under guidance
• Interpret data, investigate unexpected results, and support follow-up activities
• Maintain GMP-compliant laboratory documentation
• Contribute to lab housekeeping, equipment maintenance and continuous improvement
• Collaborate with Analytical QC and other site functions

Key requirements

• BSc or MSc in Analytical Chemistry, Pharmaceutical Sciences, Chemistry or a related scientific discipline
• Experience in an analytical laboratory environment (industry, postgraduate, placements, or graduate employment)
• Practical experience using HPLC (essential)
• Experience using GC (advantageous)
• Exposure to method development, validation or troubleshooting (beneficial)
• Understanding of GMP principles or experience in a regulated lab (preferred)
• Strong attention to detail, good organisational skills, willingness to learn
• Ability to work independently and in a team

• attention to detail
• team collaboration
• willingness to learn
• HPLC
• GC (advantageous)
• method development

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