Quality Control Chemist

RBW Consulting; Woking; On-site; GBP 35,000 - 55,000; Full time

Job summary

A pharmaceutical organization in Woking is seeking a Quality Control (QC) Radiochemist to ensure compliance in radiopharmaceutical production. The role involves hands-on QC operations, testing, and analysis while adhering to GMP standards. Candidates should have experience in QC analytical testing and familiarity with instruments like HPLC and Gas Chromatography. Flexibility for shift work is crucial. Competitive salary and benefits offered.

Qualifications

• Strong understanding of GMP and GLP standards.
• Experience in QC analytical testing within a pharmaceutical or radiopharmacy environment.
• Familiarity with QC instrumentation essential for testing.

Responsibilities

• Conduct routine QC testing and analysis for radiopharmaceuticals.
• Maintain and troubleshoot QC equipment.
• Manage raw material sampling and release systems.
• Support SOP updates and quality system improvements.

Skills

Understanding of GMP and GLP standards

Experience in QC analytical testing

Familiarity with HPLC

Familiarity with Gas Chromatography

Commitment to safety and quality standards

Tools

HPLC

Gas Chromatography

Job description

Quality Control (QC) Radiochemist – Woking

We’re partnering exclusively with a growing pharmaceutical organization embarking on an exciting phase of transformation and investment. This role is integral to ensuring the highest standards of quality and compliance in the production of radiopharmaceuticals for patient use.

As QC Radiochemist, you will take ownership of QC operations, ensuring that every batch meets stringent regulatory and safety requirements. This is a hands‑on position suited to a detail‑oriented professional who thrives in a fast‑paced, GMP‑compliant environment.

This position involves shift work, so flexibility is key. The shifts would be rotating weekly; 3am‑11am, 6am‑2pm and 8am‑4pm.

Key Responsibilities

• Conduct routine QC testing and analysis for radiopharmaceuticals in compliance with GMP and EU standards.
• Maintain and troubleshoot QC equipment such as HPLC and Gas Chromatography.
• Manage raw material sampling and release systems.
• Support SOP updates and quality system improvements.
• Ensure adherence to regulatory and safety protocols, including radioactive waste handling.

Requirements

• Strong understanding of GMP and GLP standards.
• Experience in QC analytical testing within a pharmaceutical or radiopharmacy environment.
• Familiarity with HPLC, Gas Chromatography, and other QC instrumentation.
• Ability to manage documentation and adhere to regulatory requirements.
• Commitment to safety and quality standards.
• Flexibility to work shifts.