GMP Technical Writer – Pharma Documentation Expert

A pharmaceutical company in New Jersey is seeking a detail-oriented GMP Pharmaceutical Technical Writer. This role involves creating and maintaining controlled documentation to meet GMP regulations. The ideal candidate will collaborate with internal teams to ensure the accuracy and clarity of technical documents crucial for manufacturing. Qualifications include a Bachelor's degree in a relevant field and at least 2 years of experience in technical writing within a GMP-regulated environment. Proficiency in document management systems is required. #J-18808-Ljbffr