Medical Staff Credentialing Supervisor oversees day-to-day activities of staff that process credentialing and recredentialing applications for health care providers. Implements department procedures to facilitate organized and up-to-date provider databases. Being a Medical Staff Credentialing Supervisor administers system for tracking license and certification expirations to ensure renewals are submitted in a timely fashion. Ensures that applications are properly verified and accurately uploaded into an online credentialing database system. Additionally, Medical Staff Credentialing Supervisor resolves complex questions regarding credentialing or provider database maintenance and best practices. Prepares reports on applications and credentialing status to identify trends and improve the credentialing process. May require a bachelor's degree. May require Certified Provider Credentialing Specialist (CPCS). Typically reports to a manager. The Medical Staff Credentialing Supervisor supervises a small group of para-professional staff in an organization characterized by highly transactional or repetitive processes. Contributes to the development of processes and procedures. To be a Medical Staff Credentialing Supervisor typically requires 3 years experience in the related area as an individual contributor. Thorough knowledge of functional area under supervision. (Copyright 2024 Salary.com)
Position Summary
The individual in this role will support activities related to the design, development, and manufacturing of our equipment products.
Core Responsibilities
· Lead major projects, or phases of projects
· Resolve advanced and complex technical challenges
· Create software architecture (embedded, O.S., and Application layer) for complex electromechanical devices · Software/sensor algorithm development and optimization and/or Machine Learning Algorithm development.
· Perform Risk Analyses, including Fault Tree Analysis (FTA), Failure Mode and Effects Analysis (FMEA), and Cybersecurity Analysis in compliance with applicable standards
· Lead Risk Management activities to ensure compliance with applicable design- and process-related standards
· Lead the product development team in the adoption and use of best practice software design methodologies
· Debug designs
· Provide technical support for product development, as well as systems integration and testing
· Investigate the feasibility of new projects, systems, or approaches
· Mentor other engineers in good coding practices, debugging techniques, etc.
· Work with Quality Assurance to maintain an approved internal Quality System that meets the requirements of GMP’s, QSR, ISO 13485, and IEC62304
Requirements
· BS in Software Engineering, Electrical Engineering, or equivalent
· MS/ME in relevant disciplines is strongly Preferred
· 10 years of experience in software product engineering and development
· Hands-on technical leader/mentor for a team of senior and mid-level engineers.
· C and/or C Language Skills
· Must have Medical device or other safety critical device development experience
· Able to generate thorough and comprehensible documentation - requirements through software, as well as risk documentation.
· Experience with embedded systems development
· Experience with sensors, CAN, A/D, embedded operating systems, multiple processor systems
· Proven ability to run major software development projects from concept to manufacturing
· Proven advanced technical knowledge in software development methodologies
· Demonstrated expert analytical and design skills
· Proven knowledge of project lifestyles, software development environments, and source control techniques
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