Technical Writer Job at PharmEng Technology in Indianapolis

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About The Job : Technical Writer

Our client, a pharmaceutical manufacturing company, is seeking a detail-oriented Technical Writer with expertise in deviations and change control documentation . This onsite role plays a critical part in ensuring regulatory compliance and supporting quality operations through precise, timely, and accurate technical documentation.

Key Responsibilities

• Write, edit, and review high-quality technical documents including deviations, change controls, CAPAs, and other GMP-related records.
• Collaborate with cross-functional teams (QA, Manufacturing, Engineering, etc.) to gather accurate and complete information.
• Ensure all documentation complies with FDA, EU, and internal GMP guidelines.
• Translate complex technical information into clear, concise, and well-structured documents.
• Assist in audit readiness by maintaining organized, traceable documentation.
• Support investigations and root cause analyses by drafting clear summaries and conclusions.

Qualifications

Applicants must be authorized to work in the United States. Sponsorship is not available for this position.

Additional Details

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