6 medical device engineer jobs at 4 companies in Berkeley, MO
2d
Save
Mark Applied
Hide
Senior Manufacturing Engineer II
Brentwood, Missouri, United States
OnsiteFull Time
5+ YOEBachelor's degree in engineering or related technical field and 5+ years in cGMP pharmaceutical, biopharmaceutical, or sterile medical device manufacturing, with aseptic processing experience.
SolidWorks, AutoCAD, CAD, PLC, Allen-Bradley, Siemens, HMI, SCADA, Excel, Minitab, JMP, OSIsoft PI, Six Sigma
2mo
Save
Mark Applied
Hide
Supplier Quality Engineer
St. Louis, Missouri, United States
OnsiteFull Time
5+ YOEBS in engineering and 5+ years medical device/pharmaceutical quality experience; expertise in supplier quality, cGMP, CAPA, statistical methods, protocol design, and quality system record ownership.
MINITAB
2mo
Save
Mark Applied
Hide
Sr. R&D Engineer
Hazelwood, Missouri, United States
$81k-$103k/yr HybridFull Time
2+ YOEDesign, develop, test, and refine electromechanical medical devices; firmware/embedded software development (C, C++), tool development with C# and Microsoft Visual Studio; develop test protocols to meet FDA/European standards. 2+ years preferred.
C#, Microsoft Visual Studio, C, C++
1d
Save
Mark Applied
Hide
Senior Software Engineer
St. Louis, Missouri, United States
OnsiteFull Time
5+ YOEBachelor's degree preferred and 5+ years of software development experience preferred. Requires C++ proficiency with Visual Studio, MFC, and Qt, plus object-oriented design, multithreading, STL, embedded systems, and medical device software experience.
C++, Microsoft Visual Studio, MFC, Qt, STL, OpenGL
1mo
Save
Mark Applied
Hide
Regulatory Affairs Manager - Labeling
Waukegan or Hazelwood or Dublin or Illinois or Mansfield
$105k-$150k/yr HybridFull Time
7+ YOEBachelor's in science/engineering/life sciences required, 7+ years regulatory affairs medical device labeling experience, RAC preferred; deep knowledge of global device and environmental labeling regulations; strong attention to detail and project leadership.
1w
Save
Mark Applied
Hide
Program Manager
St. Louis, Missouri, United States
$120k-$180k/yr OnsiteFull Time
8+ YOERequires 8+ years in regulated medical device program management, an M.S. in engineering or related technical field, QMS and FDA expertise, ISO 13485 and 510(k) knowledge, leadership, and hardware-software integration experience.
Agile, Quality Management Systems (QMS), FDA, ISO 13485, 510(k), Design History File (DHF), NeedleVue™ LC1 Ultrasound System