Quality Control Analyst

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

We are seeking a motivated and detail-oriented QC Analyst to join a growing Quality Control team within a regulated manufacturing environment.

This is an excellent opportunity for someone with experience in pharmaceutical, biotechnology, or fine chemical laboratories who is looking to broaden their technical expertise and develop their career within a quality-focused business.

Working as part of a close-knit team of analysts, you will support manufacturing operations through the testing of raw materials, intermediates, and finished products, while also contributing to environmental monitoring, stability studies, and continuous improvement initiatives.

The role offers exposure to a wide range of analytical techniques and technologies, providing an excellent platform for ongoing development.

What You'll Be Responsible For:

Quality Control Testing

• Perform testing of raw materials, intermediates, in-process samples, and finished products in accordance with approved procedures.
• Support manufacturing and customer delivery schedules through timely completion of analytical testing.
• Conduct testing associated with stability studies and product quality programmes.
• Review and interpret analytical data, ensuring compliance with GMP requirements.
• Generate and analyse data using a variety of analytical methods, including:
• HPLC
• GC
• AKTA systems
• TLC
• Apply strong technical and troubleshooting skills to resolve analytical issues and support investigations.

Microbiology & Environmental Monitoring

• Carry out environmental monitoring activities, including:
• Cleanroom monitoring
• Contact plates
• Viable and non-viable monitoring
• Luminometer testing
• Conduct microbiological testing, including:
• Endotoxin testing
• Support monitoring of purified water systems and controlled environments.

Quality & Compliance

• Maintain accurate and compliant laboratory records in line with GMP and Quality Management System requirements.
• Support investigations relating to:
• Deviations
• Out-of-Specification (OOS) results
• Change controls
• Corrective and Preventive Actions (CAPAs)
• Ensure compliance with pharmacopoeial requirements, ICH guidelines, and laboratory procedures.

About You

You are a quality-focused laboratory professional who enjoys analytical problem-solving, working in a regulated environment, and contributing to the delivery of high-quality products.

You'll bring:

• Prior experience working within a pharmaceutical, biotechnology, or fine chemical laboratory.
• A good understanding of GMP and Quality Management Systems.
• Experience with analytical testing and laboratory techniques.
• Strong attention to detail and an organised approach to documentation and compliance.
• Excellent problem-solving and technical troubleshooting skills.
• Strong IT, analytical, and numerical capabilities.

Particularly Relevant Experience

• HPLC analysis
• Microbiological testing
• Stability studies
• AKTA systems
• Endotoxin and bioburden testing
• Laboratory investigations and GMP documentation

Why Join Us?

• Join a supportive and collaborative team environment.
• Gain exposure to a wide range of analytical and microbiological techniques.
• Work across quality control, manufacturing support, and product development activities.
• Access ongoing training and professional development opportunities.
• Be part of a business that values quality, innovation, and continuous improvement.

Location & Working Pattern

• Monday to Friday, 9:00am - 5:00pm
• Primarily laboratory-based role (approximately 80% lab, 20% office)
• Occasional weekend working on a rotational basis to support business requirements
• Relocation support may be available for the right candidate

The Opportunity

This is an excellent opportunity for an analyst with experience in chemistry, microbiology, or pharmaceutical quality control to join a friendly and highly collaborative team. Whether your strengths lie in HPLC, microbiology, or a broader analytical background, you'll have the opportunity to develop your skills across multiple areas while contributing to the manufacture and release of high-quality products.