GMP Documentation Specialist: Regulatory Docs & eQMS Expert

A leading life sciences recruitment firm is seeking a GMP Documentation Specialist/Technical Writer in Pennsylvania. The role involves authoring and revising GMP documents, ensuring compliance with cGMP and GxP standards. Candidates should have several years of experience in GMP documentation, knowledge of industry regulations, and a detail-oriented approach. This position is ideal for those with expertise in eQMS systems and a solid understanding of document control processes. #J-18808-Ljbffr