Analyst I (Quality Control Technician III)

About the Company

An exciting opportunity has arisen for an Analyst I (Quality Control Technician III) to join a Quality Analytical Laboratory supporting the manufacture and release of sterile pharmaceutical products. Working within a GMP-regulated environment, you will play a critical role in analytical testing activities that help ensure medicines meet the highest quality standards before reaching patients. This position offers exposure to a broad range of laboratory techniques and testing activities within a collaborative, fast-paced pharmaceutical manufacturing environment.

About the Role

As part of a multi-skilled analytical team, you will:

Responsibilities

• Perform GMP analytical testing across in-process, release, stability, raw material and validation samples.
• Conduct environmental monitoring testing, including conductivity, TOC and wet chemistry analyses.
• Evaluate, review and document analytical results in line with GMP requirements.
• Support laboratory investigations, deviations and troubleshooting activities.
• Contribute to efficient laboratory operations and continuous improvement initiatives.
• Help support timely product release and manufacturing activities.

Qualifications

• An MLO or HLO qualification in Analytical Chemistry, Chemistry, Life Sciences or a related scientific discipline.

Required Skills

• Strong attention to detail and commitment to quality.
• The ability to work effectively in a GMP-regulated environment.
• A practical, hands-on and collaborative approach.
• Fluent English communication skills.
• Flexibility to work a 24/5 rotating shift schedule.

Preferred Skills

• GMP laboratory experience.
• HPLC, UPLC or GC experience.
• Experience using LIMS or chromatography data systems such as Empower.

Pay range and compensation package

Competitive Rate + 25% Shift Allowance

6-12 Months