Ginny Lyke

Technical Writer | Supporting GxP Documentation & Quality Systems | SAP • Veeva Vault • JIRA

Role
Technical Writer at BioMarin Pharmaceutical Inc.
Location
Boise, ID, US
LinkedIn followers
500 followers
Writing/EditingView LinkedIn profile

About Ginny Lyke

Technical Writer and documentation specialist with experience supporting…

Experience

  1. Technical Writer

    BioMarin Pharmaceutical Inc.

    Apr 2025 — Present · US

    As a Technical Writer supporting GxP/GMP-regulated documentation within Quality Management Systems (QMS), I collaborate with cross-functional teams across Quality, Manufacturing, and IT to maintain clarity, consistency, and compliance throughout controlled document workflows.My work focuses on supporting system transitions, ensuring documentation alignment, and managing updates within established change control processes.Key responsibilities:• Maintain and edit GxP/GMP-regulated documentation and controlled records to ensure clarity, compliance, and consistency across departments.• Support the ERP transition from Oracle EBS to SAP by aligning and updating controlled documents within Veeva Vault and JIRA-based workflows.• Partner with SMEs, document owners, and process leads to manage document lifecycles and maintain accuracy across Quality Systems.• Contribute to workflow coordination, template maintenance, and document routing efficiency through proactive communication and attention to detail.

Education

  • Boise State University

    BA, English, Technical Writing Emphasis

    1996 — 2000

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Ginny Lyke — Technical Writer at BioMarin Pharmaceutical Inc. in Boise, ID, US | Unifers