Worksite: Cranbury, NJ
Duties and Responsibilities
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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
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Plan and organize analytical projects as per specifications and objectives
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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
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Check compiled data and documentation of test results
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Conduct documenta reviews including SOPs protocols and test reports
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Apply cGMP/GLP during execution of all work tasks
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Use scientific expertise and analytical skills in troubleshooting, laboratory investigations and problem resolutions
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Required to work in the laboratory that has a certain level of noise and contains hazardous chemicals
Qualifications:
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Master’s degree in Chemistry, Chemical Engineering, Pharmaceutical Engineering or related field
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One-year experience or training in cGMP/GLP and FDA guidelines; and Analytical methods including HPLC, GC, LC-MS, USP Dissolution
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Demonstrated ability to apply and implement GMP regulations into day to day task
