Pharmaceutical Technical Writer

Job Summary

A company is looking for a Technical Writer (Pharma) / Validation Analyst.

Key Responsibilities

• Develop, author, and maintain GxP-compliant laboratory documentation including SOPs, protocols, and reports
• Prepare and format Certificate of Analysis (CoA) documents for biologics and QC test results
• Collaborate with QC scientists and analysts to ensure alignment on technical terminology and lab data representation

Required Qualifications

• 3+ years of experience as a Technical Writer in the pharmaceutical or biotechnology industry
• Proven experience supporting large molecule or biologics and QC-focused lab documentation
• Strong understanding of GxP practices, laboratory operations, and equipment validation
• Familiarity with scientific vocabulary related to analytical testing and lab instruments
• Proficiency in Microsoft Word and document management systems is a plus