About the role
We are seeking a detail-oriented QC Materials Technician to support the inspection, sampling, and release of incoming materials within a GMP-regulated environment. This role is critical to ensuring the quality and availability of materials used in advanced aseptic manufacturing processes.
Please read the following job description thoroughly to ensure you are the right fit for this role before applying.
You will play a key role in maintaining compliance, supporting material release activities, and ensuring high standards across documentation, inspection, and environmental monitoring.
Key Responsibilities- Perform inspection and sampling of incoming raw materials in line with SOPs and GMP standards
- Monitor and support the incoming material inspection programme
- Ensure materials meet required quality standards for use in manufacturing
- Maintain accurate and compliant GMP documentation
- Coordinate testing of incoming materials where required
- Manage material status control (release/reject)
- Conduct environmental monitoring activities in sampling areas
- Ensure equipment is calibrated and maintained per procedures
- Identify, report, and support resolution of deviations and procedural issues
- Support planning of daily activities to ensure on-time material availability
- Contribute to quality systems including CAPAs, change controls, and audit actions
- Minimum 1 year experience in a GxP or GMP environment
- Experience with quality documentation and compliance processes
- Strong attention to detail and commitment to data integrity xwzovoh
- Strong written and verbal communication skills
- Comfortable working across multiple warehouse/storage locations
- Proficiency in Microsoft Office (Word, Excel, PowerPoint)
You’ll be part of a forward-thinking organisation working at the cutting edge of advanced therapies, where quality, innovation, and patient impact are at the heart of everything we do. This is an opportunity to contribute to meaningful work in a highly regulated and rewarding environment.
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