Senior Technical Writer, cGMP Lab Documentation

A leading IT staffing company is seeking experienced professionals for a role focused on cGMP laboratory operations. You will review QCRM documents, ensure compliance with quality systems, and provide training on analytical methodologies. The ideal candidate has at least 5 years of lab experience and a Bachelor's degree in a related field. This position involves coordination of equipment management and regulatory readiness, making it critical for maintaining high-quality standards in laboratory testing. #J-18808-Ljbffr