Quality Documentation Coordinator

SOLVENTUM • Flemington, NJ

9d • Onsite

About The Position

At Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers’ toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue. We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you. The Impact You’ll Make in this Role As a Quality Documentation Coordinator you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: How you will make an impact Perform reviews of Device History Records and product retains to investigate complaints and improve product quality Execute changes to Product Manuals and manufacturing systems to ensure process data is captured during Medical Device Manufacturing Support Quality, Engineering and Planning in their efforts to sustain the supply chain by implementing changes to raw materials and suppliers Coordinate process experiments, document changes and approvals Administer and coordinate support for the documentation control function for quality, engineering, manufacturing or safety business units to ensure compliance with appropriate Solventum or governmental agency regulations

Requirements

• High School Diploma/GED and (5) five years Quality OR Document Control experience in a private, public, government or military environment
• 3 years of Microsoft Office Suite (MS Access nice to have)
• Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).

Nice To Haves

• Ability to complete work independently
• Ability to adapt to different work styles

Responsibilities

• Perform reviews of Device History Records and product retains to investigate complaints and improve product quality
• Execute changes to Product Manuals and manufacturing systems to ensure process data is captured during Medical Device Manufacturing
• Support Quality, Engineering and Planning in their efforts to sustain the supply chain by implementing changes to raw materials and suppliers
• Coordinate process experiments, document changes and approvals
• Administer and coordinate support for the documentation control function for quality, engineering, manufacturing or safety business units to ensure compliance with appropriate Solventum or governmental agency regulations

Benefits

• Medical, Dental & Vision
• Health Savings Accounts
• Health Care & Dependent Care Flexible Spending Accounts
• Disability Benefits
• Life Insurance
• Voluntary Benefits
• Paid Absences and Retirement Benefits

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED