Senior Quality Specialist: Medical Device

📋 Description

• Applies GMP/GLP/ISO IEC 17025 in all areas of responsibility
• Perform internal quality assurance audits
• Review client or agency documents and implement changes
• Review and approve SOPs
• Maintain awareness of QA regulatory/industry requirements
• Drive system improvements for quality and productivity

🎯 Requirements

• Strong computer, scientific, quality orientation, and organizational skills
• Excellent communication and attention to detail
• Ability to work independently and in a team
• Learn new techniques, multi-task, keep accurate records, follow policies
• Word, Excel, PowerPoint, and database experience
• GMP, Root Cause Analysis, and technical writing experience

🎁 Benefits

• Full-time benefits including medical, dental, vision
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays