Junior QC Analyst — Pharma Lab Testing

Manpower Group (UK); United Kingdom; Remote; GBP 22,000 - 30,000; Full time

Job summary

Manpower Group (UK) is seeking a motivated Junior QC Analyst for a pharmaceutical manufacturing team. This entry-level role supports lab testing of raw materials, in-process samples, and finished products to ensure quality and regulatory compliance.

Responsibilities include performing routine analytical testing, recording results according to GMP and GDP, preparing reagents, maintaining instruments, and assisting with documentation and QC admin.

Qualifications

• Entry-level position ideal for recent graduates or individuals starting a career in Quality Control.
• Basic understanding of laboratory techniques.
• Good communication and organisational skills.
• Willingness to learn and develop in a GMP/GDP environment.

Responsibilities

• Perform routine analytical testing on raw materials, in-process samples, and finished products following established methods and SOPs.
• Accurately record and report test results in compliance with GMP and GDP.
• Prepare laboratory reagents, standards, and solutions.
• Assist in maintenance, calibration, and cleaning of laboratory instruments and equipment.
• Support investigations into out-of-specification (OOS) results under supervision.
• Ensure all work is completed within required timelines to support production.
• Maintain a clean, organised, and compliant laboratory environment.
• Follow all health, safety, and environmental procedures.
• Assist with documentation updates and general QC administrative tasks.

Skills

Attention to detail

Communication skills

Organisational skills

Education

Bachelor's degree in Chemistry, Pharmaceutical Science, or related field

Job description

Manpower Group (UK) is seeking a motivated Junior QC Analyst for a pharmaceutical manufacturing team. This entry-level role supports lab testing of raw materials, in-process samples, and finished products to ensure quality and regulatory compliance.

Responsibilities include performing routine analytical testing, recording results according to GMP and GDP, preparing reagents, maintaining instruments, and assisting with documentation and QC admin.