Join our Team

Technical Writer

Documentation to support Vitrana Products function.

• Manage documentation workflows and schedules and proofread drafts for adherence to established document design and Vitrana Quality Management System standards.
• Establish strong working relationships with key internal stakeholders and business partners
• Critique and improve accuracy and flow of technical documentation through interaction with product development, product quality, and architecture teams.
• Ensure proper grammar and proofing of all documents
• Schedule and lead discussions around needed documentation changes.
• Support the QMS Head, Quality Head and Product Teams during customer audits
• Collaborate and provide QMS inputs and documentation support to New Product teams, including developing/refining technical and process documentation.
• Collaborate on investigations and troubleshooting (e.g. CAPA, NCR, deviations).
• Recognize internal and external continuous improvement opportunities and drives them to the desired state.

Requirements:

• Degree in Life Sciences, Engineering, Computer Science, or a related field.
• 3+ years of experience in technical writing or developing, editing and maintaining Quality System Documentation in the Life Sciences/Pharmaceutical industry environment.
• Solid experience in writing, reviewing, and editing SOPs
• Excellent communication, time management, and organization skills with high emphasis on attention to detail
• Strong technical aptitude – ability to quickly learn new concepts and tools
• Advanced working knowledge of MS Word, MS Excel
• Good working knowledge of MS Visio, MS PowerPoint
• Strong problem-solving skills and willingness to roll up one’s sleeves to get the job done
• Excellent written and verbal communication skills