GMP QC Analyst – Pharma Lab (HPLC & Microbiology)

SRG; England; On-site; GBP 28,000 - 42,000; Full time

Job summary

SRG is seeking a motivated QC Analyst to join its regulated manufacturing environment. You will perform testing on raw materials, intermediates, and finished products, while supporting environmental monitoring and stability studies.

The role offers exposure to a wide range of analytical techniques and opportunities for career development. You will contribute to GMP-compliant records, investigation support, and quality management processes in a collaborative team setting.

Qualifications

• Experience in pharmaceutical, biotechnology, or fine chemical laboratories.
• Good understanding of GMP and Quality Management Systems.
• Experience with analytical testing and laboratory techniques.
• Strong attention to detail and documentation compliance.

Responsibilities

• Perform testing of raw materials, intermediates, in-process samples, and finished products per procedures.
• Support manufacturing and customer delivery schedules with timely analytical testing.
• Carry out environmental monitoring and microbiology testing as part of quality control.
• Review analytical data for GMP compliance and support investigations (OOS, deviations, CAPAs).

Skills

Analytical testing

GMP

Documentation

Quality control

Tools

HPLC

GC

AKTA systems

TLC

Job description

SRG is seeking a motivated QC Analyst to join its regulated manufacturing environment. You will perform testing on raw materials, intermediates, and finished products, while supporting environmental monitoring and stability studies.

The role offers exposure to a wide range of analytical techniques and opportunities for career development. You will contribute to GMP-compliant records, investigation support, and quality management processes in a collaborative team setting.