QC Officer

SRG; Stirling; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading quality control organisation in the Central Belt of Scotland is looking for an experienced QC professional to enhance their quality systems. The successful candidate will manage QC activities, approve and release raw materials, and ensure compliance with cGMP standards. Strong communication and teamwork skills, alongside experience with HPLC and microbiological testing are essential for this role.

Qualifications

• Experience in QC release and/or stability testing preferably.
• Knowledge of analytical chemistry techniques such as HPLC.

Responsibilities

• Development of quality systems in QC activities.
• Approve and release incoming Raw Materials.
• Ensure compliance with cGMP guidance.

Skills

Strong communication skills

Teamwork

Attention to detail

Time management

Tools

HPLC

Job description

Overview

Are you an experienced QC professional who has worked within a cGMP environment?

SRG have a fantastic opportunity to join a successful and expanding organisation in the Central Belt of Scotland.

Responsibilities

• Development of quality systems, in particular those relating to QC activities of the Quality Department
• Review and approve data such as Environmental Monitoring and QC testing
• Assist with stability study management
• Approve and release incoming Raw Materials
• Management of QMS for QC investigations
• Support analytical method technical transfer and validation
• Carry out a range of analysis such as Environmental Monitoring, endotoxin, bioburden, pH and analytical chemistry based methods
• Support the ongoing maintenance and management of subcontract facilities
• Trending QC data
• Ensure all QC processes are compliant with cGMP guidance

Skills

• Strong communication skills
• Able to work well as part of a team
• Attention to detail
• Time management and planning

Requirements

• Experience in QC release and/or stability testing would be beneficial or experience of similar techniques and lab work
• Experience working with analytical chemistry techniques such as HPLC and/or microbiological methods such as endotoxin and bioburd​en testing
• Experience of working in a GMP regulated environment would be beneficial
• Experience of helping manage a QMS and assist with investigations