Pharma QC Analyst: Growth in Analytics & Microbiology

SRG; United Kingdom; On-site; GBP 28,000 - 36,000; Full time

Job summary

SRG is seeking a motivated QC Analyst in the United Kingdom to join our growing Quality Control team in a regulated manufacturing environment.

The role involves testing raw materials, intermediates, in-process samples and finished products, plus environmental monitoring and stability studies. You will work with HPLC, GC, AKTA systems, and other techniques, contributing to continuous improvement and maintaining robust GMP documentation.

Qualifications

• Minimum 1 year in pharma/biotech/laboratory setting.
• Strong GMP and QA documentation experience.
• Experience with analytical testing and laboratory techniques.

Responsibilities

• Perform QC testing of raw materials, intermediates, in-process samples and finished products.
• Support manufacturing schedules through timely analytical testing.
• Carry out environmental monitoring and stability-related testing.
• Review and interpret analytical data ensuring GMP compliance.

Skills

Attention to detail

Teamwork

Problem solving

Documentation

Tools

HPLC

GC

AKTA systems

TLC

UV-Vis

Titration

FlowCam

Job description

SRG is seeking a motivated QC Analyst in the United Kingdom to join our growing Quality Control team in a regulated manufacturing environment.

The role involves testing raw materials, intermediates, in-process samples and finished products, plus environmental monitoring and stability studies. You will work with HPLC, GC, AKTA systems, and other techniques, contributing to continuous improvement and maintaining robust GMP documentation.