Quality Engineer (Onsite - Columbia, MO)

SOLVENTUM•Columbia, MO

3d•$71,200 - $97,900•Onsite

About The Position

Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers’ toughest challenges. As a Quality Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. You will enable better, smarter, safer healthcare to improve lives by pioneering 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.

Requirements

Bachelor’s Degree or higher in an engineering or science discipline (completed and verified prior to start)
Proficiency in MS Office (Word, Excel, PowerPoint, Access) and writing/using data queries, extracts and analysis
Skills including organization, resilience, collaboration, and curiosity.

Nice To Haves

Experience with quality systems such as Quality Manuals, ISO-13485, 21 CFR Part 210, 211 and 820, metrology, calibration, auditing and supplier management
Working knowledge of root cause analysis tools and techniques
American Society for Quality, Certified Quality Engineer (CQE) certification or willingness to obtain
Proficiency in the use of statistical and quality engineering tools such as exploratory data analysis, basic statistics, Gage R&R, Analysis of Variance, Failure Modes and Effects Analysis, Statistical Process Control and Capability, acceptance sampling, correlation and regression, and experimental design
Excellent verbal and written communication skills

Responsibilities

Providing product assurance engineering support for commercialized products including specification and design control, change management, risk management, investigations, and continuous improvement.
Participating in customer audits, ISO 9001 audits, ISO 13485 audits, internal audits, and other activities to identify improvement opportunities.
Providing quality assurance and control for products used in FDA regulated industries, including control of incoming materials, review of in-process tests and release tests and device history records.
Working with manufacturing engineers and other personnel to solve product quality issues.
Leading investigations, corrective action responses, trending and monitoring for nonconforming materials, complaints, and supplier issues.
Interacting with Division quality personnel and outside suppliers to ensure product quality and performance.
Driving quality improvement using engineering best practice, statistical techniques, and Lean Six Sigma methodologies.
Complying with corporate policies, procedures and security standards while performing assigned duties.