Description
Lonza is hiring a Process Technical Writer in Portsmouth, New Hampshire, to create, edit, and manage manufacturing batch records and cGMP documentation for life sciences manufacturing. The role supports production, quality, regulatory compliance, and patient safety by coordinating document revisions, review meetings, stakeholder feedback, documentation schedules, and manufacturing readiness risks. A bachelor’s degree is required, while biotechnology, life sciences, regulated manufacturing, and cGMP technical writing experience are preferred; the position is onsite Monday through Friday.
