> Markdown version of [/jobs/ext/4629240-principal-quality-systems-engineer-cardiac-rhythm-management-diagnostics-crmdx](https://www.wearedevelopers.com/jobs/ext/4629240-principal-quality-systems-engineer-cardiac-rhythm-management-diagnostics-crmdx). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Principal Quality Systems Engineer - Cardiac Rhythm Management & Diagnostics (CRMDx) - **Company:** Boston Scientific Corporation - **Location:** Saint Paul, MN, United States - **Experience:** Expert - **Salary:** $102,100.0 - $194,000.0 - **Contract:** Permanent contract - **Skills:** Microsoft Word, Microsoft Excel - **Published:** November 7, 2026 - **Apply:** https://www.juju.com/job/7_5315A9E458E6D3C1014AA10FAA06B673 ## About the Role Establish or maintain CRM design control procedures, templates, and tools Required Qualifications:Bachelor's degree in science, Engineering, Health, or related fields Minimum of 8 years of work experience in the medical device or other regulated industrySolid computer skills required including Excel, Word, and PowerPointStrong communication skills (verbal and written) Preferred Qualifications:Working knowledge of US and International regulations and standards applicable to BSC including 21 CFR 806 & 820, ISO 13485:2016Project management experienceExperience within BSC quality systemsExperience with Design Control processExperience working with cross functions teams such as Regulatory, Research and Development, Clinical, and QualityStrong presentation skillsTravel is very limited, maybe up to 10%Requisition ID: 636093Minimum Salary: $ 102100Maximum Salary: $ 194000The anticipated compensation listed above and the value of core and optional employee benefits offered by ## Description About the role:This Principal Quality Systems Engineer serves as a Design Control representative leading awareness, visibility, and communication of quality initiatives in support of global and CRM quality goals. This role is responsible for compliance of the CRM Design Control to BSC Global Quality System and applicable regulatory requirements and standards. Work Mode:At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Relocation Assistance:Relocation assistance is not available for this position.Visa Sponsorship:Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position.Your responsibilities will include:Deliver and manage completion of CRM divisional deliverables, including updates to procedures, Work Instructions, and knowledge sharing documentsActive membership of Global Procedural and Design Control Community of PracticeDrive and provide guidance to team members regarding quality strategies driven by BSC Global Quality SystemProvide project direction, coaching, and mentoring for engineering and technical team personnelWork cross-functionally in identifying and resolving procedural issuesDrive continuous improvement initiatives to enhance CRM Design Control Process and its efficiency while maintaining or improving product qualityApply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.Advise management on potential improvements or enhancements to quality systems and processes in the company. Promote a culture of quality and compliance within the organization through regular communication and training.Provide essential support during internal and external audits by presenting Design Control storyboard in front room and addressing questions related to CRM DC process. Provide back room support by supplying necessary documentation and leading DC backroom stream.