• Responsible for and maintaining and improving the Quality Management System (QMS).
• Support R/D and production areas by documenting lab experiments, production information and records; writing and compiling Standard Operating Procedures (SOP), Design History Files (DHF), Master Records (MaF), and FDA submissions; processing Engineering Change Requests (ECR).

• 1-2 years of experience in Quality Assurance, Quality control, or other fields with an emphasis on Technical Writing
• A clear understanding of logic and the scientific method.
• Critical thinking
• Detail oriented. Seriously.
• Good communication skills- interpersonal, writing, verbal, electronic
• Excellent writing and formatting skills.
• Microsoft Word and Excel fluency.
• Strong problem solving and issue resolution skills

• Option for Health and Dental with a portion of company contribution
• Paid sick and vacation
• Team Building Events

We are a R&D company whose mission is to extend the duration and quality of human life through advanced neurotechnology.