Supplier Quality Engineer

Job Overview

Impulse Dynamics (USA), Inc. is a fast‑growing medical device company that has pioneered a new form of therapy for heart failure called Cardiac Contractility Modulation, or CCM TM, delivered by the company’s Optimizer® Smart System. CCM is a first‑of‑a‑kind, proprietary, life‑changing treatment alternative for a vast population of heart failure patients worldwide. With global headquarters in Marlton, NJ, the company also has offices in Frankfurt, Germany.

This role is part of our mission to help nearly one million patients in the United States alone who qualify for CCM therapy, providing hope through minimally invasive treatment.

$95,000.00/yr – $/yr

• Maintain and oversee purchasing controls compliance, ensuring proper documentation of supplier performance and continuous monitoring files.
• Lead supplier qualification initiatives, assess ongoing performance, and ensure adherence to regulatory and company standards.
• Provide training and education to company personnel and suppliers on purchasing control applications to sustain long‑term compliance.
• Collaborate with engineering teams to guide supplier selection and documentation of requirements for new materials and components.
• Ensure selected suppliers meet regulatory requirements and possess recognized credentials and competency for intended purchasing needs.
• Manage and analyze supplier corrective action reports, monitor performance trends, and provide insights for site‑level management reviews.
• Conduct remote and onsite supplier audits to verify compliance, identify risks, and drive continuous improvement.
• Engage in continuous improvement activities within the function and areas of responsibility, focusing on enhancing processes and identifying opportunities for efficiency.
• Work closely with Product Development teams to support pre‑market activities, ensuring supplier selection, qualification, and documentation align with regulatory and business requirements.

• Bachelor’s degree in engineering, supply chain management, or a related field (background in electronics/electrical engineering is preferred).
• Experience in supplier quality management, auditing, and regulatory compliance.
• Strong understanding of purchasing controls, supplier qualification processes, and corrective action management, particularly with contract manufacturing.
• Excellent communication, problem‑solving, and analytical skills.
• Ability to collaborate effectively with cross‑functional teams and external suppliers.
• ISO 13485 Certified Lead Auditor or CQA required.

• Excellent written and verbal communication skills, with the ability to interact with all levels of the organization and suppliers.
• Superior organizational abilities and the ability to maintain deadlines.
• Ability to take initiative and build team relationships in a multi‑disciplinary environment.
• Ability to translate technical requirements and specifications to external suppliers.
• Working knowledge of software programs:
  Microsoft Word, PowerPoint, Excel, Project.
• Position requires some travel, international and domestic (up to 50 %).

Impulse Dynamics is an equal‑opportunity employer. The company is committed to the spirit and letter of all federal, state, and local laws and regulations pertaining to equal opportunity. Employment decisions are based on merit, qualifications, and abilities, with no discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, genetic information, or other protected status.

Annual base salary range: $100,000 – $115,000.

• Full coverage medical benefits – employee and family contributions fully covered by Impulse Dynamics.
• Paid vacation, floating holidays, and sick time.
• Paid holidays.
• 401(k) match up to 6 %.
• Annual bonus eligibility.

All employees are “at‑will” employees unless otherwise communicated in writing. The company reserves the right to modify the aforementioned terms with appropriate notice, and the described compensation and benefits do not constitute a promise to continue for the duration of employment.

Entry level

Full‑time

Quality Assurance (Medical Equipment Manufacturing)