Key skills
Risk Management
About this role
Role Overview
- Support the design, development, installation, validation and improvement of analytical instruments, methods and technology for the Medical QC laboratories
- Provide expert analytical knowledge and problem-solving support to Orbia Fluor and Energy Materials Medical QC teams and external customers
- Define, source, implement and validate new analytical equipment, instruments, and systems
- Maintain & calibrate QC analytical equipment in line with laboratory procedures & schedules
- Lead or support technical projects to improve the efficiency, effectiveness and/or compliance of laboratory processes, procedures, and IT systems
- Provide training and coaching in analytical techniques, test methods and/or laboratory systems to technical and QC teams
- Manage the complex safety challenges of high hazard chemical analysis including the application of risk assessment / risk management methodology
Requirements
- Minimum: HNC/HND Chemistry
- Desirable: Degree in Chemistry or related subject
- Pharmaceutical cGMP laboratory operations
- Analytical method development to cGMP standards including gas chromatography and associated CDS systems
- Implementation, testing & validation of analytical equipment & methods to pharmaceutical GMP standards
- Creating, reviewing, and approving technical / Quality documentation including procedures, plans, protocols & reports
- Use of laboratory IT systems (LIMS, CDS, EQMS, MS Office etc.) including super user / system administration roles
- Lean / continuous improvement, e.g. VSM, RCA, 5S, etc. would be desirable
- Data integrity processes & procedures would be desirable
Benefits
- Competitive compensation package