Technical Writer I - Process Development

Catalent seeks a Technical Writer I to author and maintain scientific and manufacturing documentation for biologics development programs at its Madison, Wisconsin facility. The role involves creating protocols, development reports, and client-facing documents while ensuring accuracy and compliance with GMP standards.

Responsibilities

• Author, edit, and maintain technical reports, protocols, certificates of testing, and scientific documentation
• Review documents for accuracy, consistency, completeness, formatting, and quality compliance
• Collaborate with scientists, manufacturing personnel, and quality teams to gather information and resolve documentation questions
• Identify and escalate discrepancies to ensure accurate reporting and minimize downstream impacts
• Support client-facing technical reports and manage multiple documentation projects simultaneously

Requirements

• Bachelor's degree in STEM with minimum 1 year relevant experience, or associate's degree with 4+ years
• Strong written communication, editing, proofreading, and organizational skills
• Exceptional attention to detail and ability to identify inaccuracies and inconsistencies
• Cross-functional collaboration and professional stakeholder communication skills
• Proficiency with Microsoft Office applications including Word, Excel, and Outlook
• Comfort in documentation-focused, desk-based environment supporting scientific operations