Job Description:Senior Quality Systems Engineer POSITION SUMMARYWe are seeking a dynamic, analytical thinking individual to join our Quality team, focusing on Quality Systems, CAPA, Internal Audit, metric reporting and process improvement initiatives. The ideal candidate will possess a strong background in medical devices or IVD, with a proven track record in managing quality-related activities in a fast-paced dynamic environment. QMS experience is essential.RESPONSIBILITIESThis position is responsible for, but not limited to, the following:Supports the overall QMS processes for the organization. Responsible for activities required to ensure compliance of Quality Management Systems (QMS), specifically regarding CAPA and internal/external audits. Additional responsibilities include supporting other QMS functions such as NCMRs, Supplier Controls, Management Review, Risk Review, etc.Execution and coordination of activities associated with CAPA program, including administration and record management, providing quality input to investigations, reporting, as well as metrics and trendingSupport CAPA Owners in quality-related technical principles, including but not limited to Problem Solving tools and techniques (Root Cause Analysis, DOE, FMEA, etc.)Manages the Internal Audit program, including scheduling audits, ensuring timely response to findings, as well as metrics and trendingSupport external audits and inspections by providing subject matter expertiseDevelopment of Quality Metrics, and coordination of quality data collection and analyses for use in monthly metrics meetings and Management ReviewsProvide quality assurance support cross-functionally across the organizationLead/participate in Risk Management and FMEA initiativesDevelop, implement, and manage Quality Control/Quality System process improvements.Identify opportunities for improvement within the Quality System to ensure compliance and efficiency. Correct or improve gaps/opportunities in an independent fashion by writing and releasing new or revised Quality System documentationUnderstand how and when to escalate quality issues to leadership team within the organization, presenting data and information necessary to draw conclusions and take actionProvide training and support to employees on quality processes and proceduresSupport work on quality plans, quality processes and special projects, as requiredPerform other TransMedics tasks and duties as assigned/required MANAGEMENT RESPONSIBILITIESThis position will not have management responsibilitiesPHYSICAL ATTRIBUTESMust be able to lift 50lbs MINIMUM QUALIFICATIONSBachelor's Degree in Engineering, Biomedical Science, or other technical discipline preferred, with 5-7 years of relevant experience in medical device industry, including responsibility for Product Quality and/or Quality SystemsA working knowledge of Quality System Standards and regulations, including 21 CFR Part 820, ISO 13485, EU MDRAbility to multi-task, handling multiple projects and changing prioritiesExperience in the creation and documentation of procedures and processesMust be results-driven and exhibit a sense of urgencyProficiency with Microsoft Office - Word, Excel, PowerPoint and Access experience requiredPREFERRED QUALIFICATIONS:Experience participating in internal and external audits, preferably serving as qualified internal auditorAbility to communicate ideas and information clearly, effectively, and frequently (both oral and written)Ability to exercise independent judgment in methods, techniques, and evaluation criteria for obtaining resultsAbility to act independently to determine methods and proceduresProblem-solving skills and the ability to resolve issues as they ariseStrong interpersonal skills, with the ability to assimilate with various cross-functional teamsTransMedics is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, national origin, marital status, age, disability or protected veteran status, or any other characteristic protected by law. We are committed to creating an inclusive environment for all employees.