QC Laboratory Analyst

Smart4Sciences; Basildon; On-site; GBP 25,000 - 35,000; Full time

Job summary

A leading recruitment agency is seeking a QC Laboratory Analyst to work with a pharmaceutical organization in Basildon, UK. You'll perform laboratory tests and maintain data integrity while supporting production of safe and effective medicines. Ideal candidates should have a background in a regulated environment, hold relevant GCSEs, and ideally a degree in a science-related field. This role is a unique opportunity to contribute to critical health products in a GMP-regulated environment.

Qualifications

• Experience in a pharmaceutical, FMCG or regulated environment.
• Strong commitment to accuracy and data integrity.
• Professional and able to follow procedures with precision.

Responsibilities

• Perform laboratory tests to generate reliable, accurate, and compliant data.
• Record test results in compliance with data integrity standards.
• Prepare samples, reagents, and maintain laboratory areas.

Skills

Laboratory testing

Data integrity

GMP compliance

Documentation

Problem-solving

Education

GCSEs in English, Maths, and Science

Degree in Chemistry, Biology, Pharmacy or related discipline

Tools

Laboratory equipment (titrators, pH meters)

Job description

Overview

Are you a meticulous laboratory professional with a passion for quality and compliance?

Smart4Sciences is supporting a leading pharmaceutical organisation in recruiting QC Laboratory Analysts to join their expanding Quality Control team in Basildon, Essex.

The Role

This is an excellent opportunity to contribute to the testing and release of critical medicines within a GMP‑regulated environment. As a QC Laboratory Analyst, you'll be responsible for carrying out high‑quality laboratory testing, maintaining accurate and compliant data, and supporting investigations such as OOS (Out of Specification) where required. You will play a key part in ensuring products meet regulatory standards and supporting the delivery of safe, effective medicines to patients.

Key Responsibilities

• Perform laboratory tests to generate reliable, accurate and compliant data
• Record test results clearly, permanently and in accordance with data integrity standards
• Participate in internal audits, self‑inspections and regulatory inspections
• Follow internal procedures and maintain strong working knowledge of EU GMP
• Contribute to the control, review and compliance of SOPs
• Plan and prioritise testing workloads under supervision
• Prepare samples, reagents and standards according to procedures
• Maintain laboratory areas in an audit‑ready condition
• Perform method validations and method transfers when required
• Operate and maintain standard laboratory equipment (e.g., titrators, pH meters)
• Assist the Quality team with documentation, investigations and validation activities
• Ensure data integrity is upheld in line with ACOLA+ guidelines
• Support KPI monitoring and general QC operations

About You

• Experience working in a pharmaceutical, FMCG or other regulated environment
• Strong commitment to good housekeeping, accuracy and data integrity
• Flexible, proactive and willing to support team priorities
• Professional, punctual and able to follow procedures with precision
• Enthusiastic, committed and quality‑driven

Qualifications

• GCSEs (A-C or equivalent) in English, Maths and Science
• Ideally a Degree in Chemistry, Biology, Pharmacy or related discipline

You'll be joining a dedicated QC team within a business that values reliability, precision, and continuous improvement.

Apply now and take the next step in your QC career