Full-Time

Quality Vessel Engineer

Solventum

Posted on 9/11/2024

Solventum

Solventum

Compensation Overview

$119.1k - $145.5kAnnually

+ Variable Incentive Pay

Mid

Woodbury, MN, USA

Hybrid position requiring in-office presence in Maplewood, MN.

Category
Healthcare Administration & Support
Medical, Clinical & Veterinary
Required Skills
Communications
Requirements
  • Bachelor’s Degree or higher AND three (3) years of experience in quality or engineering in a private, public, government or military environment OR High School Diploma/GED from AND (7) years of experience in quality or engineering in a private, public, government or military environment
  • Bachelor’s degree in Microbiology, Biochemistry, Biology, Chemistry, Chemical Engineering from an accredited institution
  • (3) years of experience in one or more of the following areas: product engineering, quality engineering, manufacturing engineering, industrial controls design, or equipment installation experience in the medical device or other regulated industry
  • Master's degree in Sciences or Engineering from an accredited institution
  • Medical device and/or Quality Management System (QMS) experience such as Food and Drug Administration (FDA) Quality System Regulation (QSR) and/or International Organization for Standardization (ISO) 13485
  • Statistical knowledge and practice e.g. Design of Experiments (DOE), Sampling Plans, Statistical Process Control (SPC), Process and Product Understanding (PPU), and Lean Manufacturing
  • Aptitude for learning other scientific principles such as biology, chemistry, computer science, hardware, system and industrial engineering, statistical methods to help identify and control multi-discipline variation
  • Strong project management skills and ability to lead cross-functional teams in projects that drive improvement
  • Strong written and verbal communication skills with a focus on technical writing
  • Able to work under only general direction while independently determining the approach to problems and solutions
Responsibilities
  • Running experiments to support plant and division efforts to characterize and standardize test vessel process performance parameters for process/product understanding
  • Leading and executing test method validations and cross-over studies
  • Supporting test vessel projects or process improvements, along with trouble shooting, investigating, and analyzing anomalous product or process performance
  • Assisting with product qualifications and test cycle development
  • Updating internal processes, work instructions, and internal systems to align to global operations best practices of a medical device manufacturing while meeting business objectives

Company Stage

N/A

Total Funding

N/A

Headquarters

N/A

Founded

N/A

INACTIVE