JOB TITLE:
QC Raw Materials Analyst
LOCATION:
Slough, UK (Onsite)
SCHEDULE:
Standard Working Hours
DURATION:
6-Month Contract
PAY:
20-25 £ per hour
Job Overview
We are seeking a QC Raw Materials Analyst
to join the Quality Control Raw Materials team
within a GMP pharmaceutical manufacturing environment. This role supports the testing, documentation, and release of raw materials used in pharmaceutical production while maintaining strict compliance with GMP, safety, and quality standards.
The successful candidate will work with general guidance, manage their own workload to meet timelines, and support junior team members to ensure consistent quality across the department.
Key Responsibilities
- Perform testing of raw material samples and report results in accordance with GMP procedures
- Accurately enter and review test results generated by other team members
- Ensure compliance with all relevant safety, GMP, and quality requirements
- Identify and implement improvements in GMP compliance, safety, and efficiency
- Manage archiving of assay forms and Raw Material Specifications (RMS)
- Prepare and distribute RMS release packs for internal, customer, and inter-site audits
- Provide vendor certifications upon request
- Own the processing and release of RMS documentation, ensuring accuracy and compliance
- Support monthly retain audits
- Manage personal workload and timelines with direction from Group Leaders and Schedulers
- Escalate delays or issues to QC management as needed
- Coordinate daily activities within the Raw Materials team when required
- Support and train junior staff, maintaining high departmental quality standards
Required Skills & Competencies
- Ability to adapt to change and take initiative in a fast-paced environment
- Basic knowledge of chemical and/or biochemical laboratory techniques
- Strong attention to detail with accurate data reporting and quality record keeping
- Ability to review data and uphold quality standards across the team
- Strong communication skills and ability to work independently and collaboratively
- Professional handling of confidential information
- Ability to meet timelines while maintaining high-quality work
- Team-oriented mindset with a supportive and proactive approach
Qualifications & Experience
- Preferred Education: BSc in Pharmaceutical Sciences, Chemistry, or related field
- Experience Level: Entry-level to early career ( 0–4 years)
- Prior experience in a GMP laboratory or pharmaceutical environment is preferred
...