Documentation Specialist I
Merck & Co. Inc
Work Schedule Monday thru Friday; 7:30am thru 4:00pm Responsibilities Track and review manufacturing batch records to ensure compliance with regulatory requirements. Follow up with Manufacturing Technicians to ensure corrections are completed in a timely manner. Maintain error tracking metrics to address and correct repeated violations of GDP. Coach shopfloor technicians on GDP as applicable. Identify and escape GDP issues that could affect the safety, efficacy and quality of drug substance. Review batch record structure and recommend simplifications to minimize errors. Ensure batch record review cycle time. Participate in deviation investigations and CAPA creation. Qualifications Must be detail oriented and able to work quickly with a high degree of accuracy. Must possess sound interpersonal and information gathering skills, be able to work in a team environment and interact effectively with others. Years of Experience: 0 - 3 Years #J-18808-Ljbffr
Vacancy posted 3 days ago
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