| Requirements: |
- Requires Bachelors Degree in Chemistry, Biochemistry or related Science discipline with a minimum 5 years experience in a senior analytical supervisory role in a Quality Control Analytical Laboratory within the pharmaceutical industry. Masters degree preferred
- Previous experience in the setting up of a cGMP/GLP analytical Laboratory essential
- Previous participation in FDA, ISO and other regulatory audits
- Thorough knowledge and hands-on experience of HPLC, GC, FTIR & UV/Visible spectrophotometer, Dissolution apparatus and wet chemistry techniques
- Excellent interpersonal and communication skills with good leadership abilities
- Ability to generate reports and present technical presentations to QC Laboratory management
- The QC Laboratory Supervisor must have demonstrated the required technical competence as a supervisor and must be capable of effectively coaching, guiding and managing employee development
- Computer literacy with good working knowledge of statistical tools, statistical process control, Excel, Word and PowerPoint computer packages
- Handles multiple tasks and programs concurrently.
- Conforms to Company policies and procedures, Quality Systems, cGMP and FDA requirements. |
