QC Analyst – Raw Materials
Slough, UK
Schedule:
Standard Office Hours
Duration:
6-Month Contract
Pay Rate Range:
£26/ph - 31/ph
Job Responsibilities
As a QC Analyst within the Raw Materials team, you will support the timely and compliant testing and disposition of raw materials in a GMP-regulated custom manufacturing environment. You will work with minimal supervision on day-to-day tasks while collaborating with colleagues to ensure high-quality standards are upheld across the department.
Key responsibilities include:
- Disposition of raw materials for use in manufacturing processes.
- Testing of samples and accurate reporting of results per GMP procedures.
- Critical review of analytical results, raising concerns to QC management as needed.
- Approval of test results generated by peers, ensuring integrity and compliance.
- Participation in departmental quality records including deviations, CAPAs, investigations, and change controls.
- Preparation and review of protocols, reports, and SOPs.
- Adherence to safety protocols relevant to laboratory work.
- Contribution to continuous improvement efforts in quality, safety, and efficiency.
- Training and mentoring of junior team members to maintain high GMP standards.
- Independent management of workload and timely escalation of issues or delays.
Essential Duties and Job Functions
- Execute testing and documentation with attention to detail and compliance.
- Actively contribute to the improvement of departmental procedures and standards.
- Support the maintenance of a compliant laboratory environment.
- Demonstrate flexibility in adapting to changes in priorities or processes.
- Collaborate across teams to meet organizational goals.
Knowledge & Skills
- Sound understanding of chemical/biochemical analytical techniques.
- Proficiency in reporting data and interpreting laboratory results.
- Familiarity with quality records such as deviations and CAPAs.
- Strong documentation and organizational skills.
- Ability to work independently and as part of a team.
- High attention to detail and problem-solving capabilities.
- Effective verbal and written communication.
- Ability to handle confidential information with discretion.
- Commitment to delivering work within agreed timelines and quality standards.
Other Requirements
- Practical experience in a GMP-compliant laboratory environment (preferred).
- Demonstrated technical laboratory skills.
- Strong analytical, critical thinking, and decision-making skills.
- Willingness to contribute to department goals and team development.
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