Overview
In this role you will support the Chemistry department’s operations and development, ensuring data integrity and compliant processes. You will review chemistry data, manage materials and equipment, and contribute to continuous improvements. You’ll work in a regulated environment, collaborating with cross-functional teams to resolve quality issues and maintain laboratory standards. This is a hands-on position at a leading biotech facility with a strong emphasis on safety and quality.
Pay / Benefits
- Pension
- Private Medical Insurance
- Income protection and life assurance
- Annual discretionary bonus
- Birthday Holiday entitlement
- Free parking onsite
Responsibilities
- Data review of chemistry testing data
- Audit trail review
- Chemistry testing activities
- Method verification and method transfer
- Support resolution of quality issues
- Support root cause analysis and quality risk assessments
- Management of chemistry materials
- Management of laboratory glassware
- Registration of standards and reagents
- Review of standards and reagent registration
- Writing and reviewing procedures, protocols, and reports
- Writing exceptions
- Implementation of CAPA
- Implementation of Change controls
- Support with equipment calibration, qualification, and maintenance
- Propose and implement continuous improvements
- Writing of CSV protocols and reports
- H&S representative
- Hosting H&S meetings
Key requirements
- Degree in life sciences (preferred)
- Experience in GMP- or GLP-regulated environment
- Experience in a Chemistry role
- GMP/GLP regulatory experience
- Chemistry data review
- CAPA and Change control processes
- Method verification and transfer
- Calibration, qualification and maintenance of equipment
- Documentation writing (procedures, protocols, reports)
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