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Sr. Quality Systems Specialist LinkedIn Twitter Email Message Share Why Join Bracco Medical Technologies? At Bracco Medical Technologies, every employee has an impact on our Mission to empower lifesaving decisions. We create medical devices that give healthcare providers the insights they need to confidently and safely diagnose patients. Our unique line of products includes Intravascular Ultrasound (IVUS), Fractional Flow Reserve (FFR), Cardiovascular Imaging contrast delivery (CVi), and CT and MRI contrast delivery systems. Position Description Position Summary: The Senior Quality System Specialist will be responsible for developing and maintaining a robust quality system in compliance with all relevant standards and regulations. This role will create, deploy and improve quality system processes in support of corporate objectives, and will be directly involved in shaping strategies that will support on-going improvement and effectiveness of the quality system. Primary Duties & Responsibilities: Quality Management System Compliance: * Initiate, facilitate and/or manage projects to expand, enhance and improve the quality system. * Create, review and maintain quality system SOPs, work instructions and other documents. * Act as liaison for global corporate QMS with counterparts from other facilities. * Support Notified Body audits, customer/partner audits and FDA inspections. * Provide quality system training for the organization. * Lead special projects to enhance and extend the effectiveness of the QMS * Support or coordinate field action investigations and related activities * Facilitate the creation and assignment of training requirements within the Learning Management System * Manage document change control within our PLM system * May supervise or provide work direction, training, and mentoring for junior team members Monitoring of External Standards: * Monitor the release of new standards that may affect Product or the Quality Management System * Lead efforts to ensure compliance of emerging standards and regulations * Conduct gap assessments of new regulations and standards, and drive resolution of the gaps to ensure ongoing QMS and Product Compliance. * Coordinate with Regulatory and other teams to communicate and educate staff on emerging standards that may affect the QMS and the business. * May lead the External Standards Review Board, as assigned. Internal Audit Team: * Serve as a Lead Auditor for internal audits at the corporate site. * Support internal audits and supplier audits at domestic and international sites. * Initiate and execute audits, including developing and documenting the audit plan, leading the audit, generating the audit report, and tracking subsequent actions. * Approve corrective action plans and verify effective and timely implementation of corrective actions for audit nonconformities. * Work with SME's to ensure audit record content is accurate, well documented, and meets the requirement of the process. * May lead the Corporate Internal Audit Team, as assigned. Corrective and Preventive Action: * Ensure that all CAPAs are entered into the CAPA system, assigned to the appropriate personnel, and completed according to CAPA procedures and within specified time periods. * Develop metrics and perform trend analysis of the CAPA process to identify areas for improvement. * Mentor and coach CAPA owners toward effective investigation and root cause analysis, resulting in CAPA content that is accurate, well documented, meets the requirement of the process, and is completed in a timely manner. * Own and lead Quality Management System CAPAs, as needed * May lead the corporate CAPA Board, as assigned Qualifications (Knowledge, Skills & Abilities): Minimum * Bachelor's degree required. * 5+ years medical device experience including at least 3 years in Quality Management Systems. * Strong knowledge and hands-on experience with FDA QSR/QMSR, ISO 13485, EU Medical Device Regulation (MDR), and other national and i ternational regulations (Canada, Japan, China, Brazil, etc.). * Able to build relationships and work effectively with individuals at all levels of the organization in a collaborative and congenial manner. * Ability to clearly and concisely articulate ideas both verbally and in writing. * Proven organizational skills, planning skills and ability to work effectively within teams * Proven ability to take initiative and ownership in order to move projects or tasks forward to completion * Ability to shift priorities based on the current business needs and to make progress on multiple, concurrent projects. * Independent decision-making and problem-solving skills; ability to analyze information, evaluate results and choose the best solution. Preferred: * Experience with EU MDR assessment and implementation * Experience supporting field action activities * ISO 13485 Lead Auditor certification Other: * Mental demands - work is detail oriented, often with multiple priorities. The environment is deadline sensitive and may be exposed to high-pressure situations. * Hybrid role - this position requires in-office attendance for at least two days each week * Travel requirements are moderate. Travel to domestic facilities would be about 2 - 3 days duration each trip, and travel to international facilities would be a week. Total travel expected to be 10% - 15%. Job Location 7905 Fuller Road, Eden Prairie, Minnesota Tracking Code 1338-432 ACIST Medical is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.