Quality Control Analyst

RBW Consulting; Croydon; On-site; GBP 29,000 - 38,000; Full time

Job summary

RBW Consulting partners with a pharmaceutical manufacturer to recruit a QC Analyst for their South London site. The role focuses on testing raw materials, in-process samples and finished products within a GMP environment to ensure product quality and data integrity.

You will perform analytical testing using HPLC and GC, support laboratory validation and maintenance, conduct environmental monitoring and water sampling, investigate out-of-spec results, and maintain GMP-compliant documentation

Qualifications

• Degree in a Scientific discipline or equivalent.
• Experience in an analytical laboratory environment.
• Strong understanding of GMP and Data Integrity requirements.
• Hands-on experience with HPLC and GC, including troubleshooting instrumentation.
• Excellent documentation and report-writing skills.
• Strong attention to detail and a proactive approach to quality.

Responsibilities

• Testing raw materials, packaging components, in-process samples, and finished products.
• Performing analytical testing using HPLC and GC techniques.
• Supporting laboratory validation, calibration, and maintenance activities.
• Conducting environmental monitoring and water sampling.
• Investigating OOS results and supporting quality investigations.
• Maintaining GMP-compliant documentation and data integrity standards.
• Performing in-process quality inspections and production line checks.
• Working closely with Quality, Production, and other cross-functional teams.

Skills

GMP knowledge

Data Integrity

Attention to detail

Education

Degree in a Scientific discipline or equivalent

Tools

HPLC

GC

Job description

QC Analyst | South London | Pharmaceutical Manufacturing

Looking for your next opportunity in Quality Control?

We're partnering with a pharmaceutical manufacturer seeking a QC Analyst to join a busy and growing Quality team. This is a fantastic opportunity for someone with analytical laboratory experience who enjoys working in a GMP-regulated environment and wants to contribute to product quality, compliance, and continuous improvement.

What you’ll be doing:

• Testing raw materials, packaging components, in-process samples, and finished products
• Performing analytical testing using HPLC and GC techniques
• Supporting laboratory validation, calibration, and maintenance activities
• Conducting environmental monitoring and water sampling
• Investigating OOS results and supporting quality investigations
• Maintaining GMP-compliant documentation and data integrity standards
• Performing in-process quality inspections and production line checks
• Working closely with Quality, Production, and other cross-functional teams

What we’re looking for:

• Degree in a Scientific discipline or equivalent
• Experience working within an analytical laboratory environment
• Strong understanding of GMP and Data Integrity requirements
• Hands-on experience with HPLC and GC, including troubleshooting instrumentation
• Excellent documentation and report-writing skills
• Strong attention to detail and a proactive approach to quality

This role would suit candidates from pharmaceutical, biotech, medical device, FMCG, food, or other regulated manufacturing environments who are looking to further develop their career within Quality Control.

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