Responsibilities:
• Collaborate with subject matter experts to support the creation of technical documentation and extract information to translate to documents
• Analyze existing documentation to identify content gaps or inconsistencies.
• Effectively translates processes into easily comprehensible documentation.
• Orchestrates, coordinates documentation project to ensure accuracy, consistency, completeness, and delivery within the specified project deadline.
• Initiates and tracks document change orders.
• Perform other duties as assigned.
• Technical Writing experience.
• Applied Knowledge of the requirements of FDA QSR, ISO13485:2016 and ISO 14971:2012 for medical devices preferred.
• Strong written and verbal communication skills.
Qualifications
• Strong written and verbal communication skills.
• Understanding of technical product support documentation.
• Project management experience.
• Bachelor\'s degree or equivalent experience.
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