Worksite: Cranbury, NJ
Duties and Responsibilities
- Oversee and monitor laboratory workload of routine and non-routine analyses by appropriate chemical test methods such as HPLC, LC-MS, GC, USP Dissolution wet chemistry assays
- Plan and organize analytical projects as per specifications and objectives
- Ensure lab duties including sample coordination lab equipment maintenance, document management, inventory control and reconciliation of sample requests/documents are performed accurately by junior scientists. Supervise up to 5 junior scientists
- Check compiled data and documentation of test results
- Conduct documenta reviews including SOPs protocols and test reports
- Apply cGMP/GLP during execution of all work tasks
- Use scientific expertise and analytical skills in troubleshooting, laboratory investigations and problem resolutions
Required to work in the laboratory that has a certain level of noise and contains hazardous chemicals
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Qualifications:
- Master’s degree in Chemistry, Chemical Engineering, Pharmaceutical Engineering or related field
- One-year experience or training in cGMP/GLP and FDA guidelines; and Analytical methods including HPLC, GC, LC-MS, USP Dissolution
- Demonstrated ability to apply and implement GMP regulations into day to day task
