A leading IT staffing firm is looking for an experienced professional to oversee QCRM document creation and ensure compliance with cGMP regulations. You will work in a laboratory environment, supporting the validation, optimization, and management of lab equipment. The ideal candidate holds a relevant Bachelor's degree and has at least 5 years of experience in laboratory operations. This position is on-site in Northborough, Massachusetts and involves significant client interaction.
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Senior Technical Writer – cGMP & Lab Quality • Northborough, MA, United States
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