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Business Process Analyst; Regulatory/ Medical Device

Company: Change Healthcare
Location: Richmond
Posted on: January 11, 2021

Job Description:

Transforming the future of healthcare isn---t something we take lightly. It takes teams of the best and the brightest, working together to make an impact.As one of the largest healthcare technology companies in the U.S., we are a catalyst to accelerate the journey toward improved lives and healthier communities.Here at Change Healthcare, we---re using our influence to drive positive changes across the industry, and we want motivated and passionate people like you to help us continue to bring new and innovative ideas to life.If you---re ready to embrace your passion and do what you love with a company that---s committed to supporting your future, then you belong at Change Healthcare.Pursue purpose. Champion innovation. Earn trust. Be agile. Include all. Empower Your Future. Make a Difference.Overview of PositionThe Business Process Analyst leads quality process improvement projects in a multinational, quality-controlled environment.What will be my duties and responsibilities in this job?Actively participates in and leads quality improvement initiatives through CAPA, Quality System Change Control and other means to improve upon, modify, and enhance quality processes and corresponding documentation.Establishes and maintains Standard Operating Procedures, as required; reports on trending and Quality / Process Improvement initiatives to managementFacilitates industry certification projects in different functional groups as required; manages Quality and Process improvement projects, as required.Leading the implementation and adoption of tools that support execution of effective processes; developing tool requirements based on business needs; performing standard tool configuration; administration activities through the application GUIReviews and approves quality records as applicable (including tool validation documents); training employees on internal processes and tools; participation inspections and audits, including the quality provision, as requested.What are the requirements needed for this position?3 years of quality system experience in the medical device industry or ISO 13485:2016 regulated industry, or equivalent.Working knowledge of medical device regulations in Canada, the United States, Australia and the European Union.Proficiency with Microsoft Office applications, project management tools, and/ or electronic document control tools; experience in software development, support/services or implementation environment is preferred.Six-Sigma certification (Yellow Belt level) is desirable; Project Management Professional (PMP) desirable.Bachelor and/or College Degree in Computer Science or Computer Engineering or related discipline; or other related education by training or by work experienceWhat other skills/experience would be helpful to have?Familiarity in working under a quality management system or in an otherwise controlled environment.What are the working conditions and physical requirements of this job? General office demandsJoin our team today where we are creating a better coordinated, increasingly collaborative, and more efficient healthcare system Full time

Keywords: Change Healthcare, Richmond , Business Process Analyst; Regulatory/ Medical Device, Healthcare , Richmond, California

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