Tap Growth AI is hiring: GMP Technical Writer/ Regulatory Documentation Speciali

Pay Scale: $75,362 — $114,386 (Dependent on Experience) Location: Norton, United States ⏰ Work Mode: Work From Office What You’ll Do: Develop and Update Documentation: Write, edit, and maintain SOPs, batch records, work instructions, and other technical documents to support manufacturing operations, equipment use, and quality control processes. Ensure Regulatory Compliance: Ensure all documentation complies with GMP, FDA, EMA, and other relevant regulatory standards, as well as internal policies. Collaborate with Subject Matter Experts (SMEs): Work closely with manufacturing, quality assurance, validation, safety, and engineering teams to gather technical information and ensure accuracy and clarity in documentation. Streamline Processes: Translate complex technical processes into concise, user-friendly instructions to enhance operational efficiency and reduce errors. Document Control: Manage document lifecycle, including version control, reviews, approvals, and archiving, using electronic document management systems (EDMS). What We’re Looking For: Bachelor’s degree in Technical Writing, Pharmaceutical Sciences, Chemistry, Biology, Engineering, or a related field. 2+ years of technical writing experience in a pharmaceutical, biotechnology, or regulated manufacturing environment. Familiarity with GMP and regulatory requirements is highly preferred. Exceptional technical writing and editing skills with a focus on clarity, accuracy, and conciseness. Strong understanding of pharmaceutical manufacturing processes, equipment, and terminology. Ready to make an impact? Apply now and let’s grow together! #J-18808-Ljbffr