Senior Design Quality Engineer

There are 64 million patients struggling with Heart Failure worldwide. When these Heart Failure patients continue to decline despite being on optimum pharmaceutical therapy, they lose hope. The only options down the road are extremely invasive. CCM therapy is an FDA Breakthrough designated solution that is minimally invasive and gives hope back to these patients. This is not a job, It is a MISSION to help the nearly one million patients (in the United States alone) who are struggling with heart failure and qualify for CCM therapy. The Sr QE is Responsible for providing QA leadership and partnering with product development with planning, coordinating, and managing the quality assurance (QA) activities associated with PD projects to ensure compliance to internal and external requirements during the development and commercialization of new products and changes for existing products. Responsible for providing technical leadership in establishing, implementing, and maintaining quality system processes and documentation in compliance with domestic and international regulatory/quality requirements How You'll Add Value

• Design Control expert who: works with product development engineering to ensure proper completion of required documentation for design control phases according to the design controls SOP.
• Quality lead on product development teams to ensure adherence to company quality procedures and applicable US and OUS regulatory requirements and standards.
• Assure that all applicable elements and product technical standards that are applicable to a design category are effectively incorporated into new designs and into changes to designs
• Complete Risk Management activities for new and/or modified products and processes which includes risk assessment occurs in the appropriate phase of the project, authoring risk management plans and reports, facilitating risk assessment activities with no guidance required
• Author and maintain all risk documentation required for Impulse Dynamics products
• Complete and own design history file verifications during and at the end of each design control phase.
• Review and approve all external Engineering Change Orders provided by the contract manufacturer and assesses risk documentation.
• Assist in writing, updating and/or reviewing of procedures and other quality assurance related technical data forms and quality documents.
• Adhere to QMS requirements outlined in procedures and work instructions.
• Review validation protocols and reports for GMP compliance
• Assist in carrying out internal quality audits on company systems and documentation
• Authors non-conformance reports and corrective actions
• Perform investigations of non-conformances, customer complaints and corrective actions
• Ensures the timely and effective follow-up of all identified or assigned quality issues
• Assists in the maintenance of the Quality Management System
• Acts as an effective leader or team member in supporting quality disciplines, decisions, and practices
• Provide training and support for quality system processes and quality engineering practices
• Maintains and demonstrates understanding of global standards, regulations, and regulatory bodies to include but not limited to ISO 13485:2016, 21 CFR part 820, 21 CFR part 812, MDSAP and MDR
• Develop, conduct, and document Quality design engineering procedures, including equipment repair, failure analysis, and product deployment.
• Write clear and detailed technical reports and procedures in English.

Do you have experience in Productivity software?, * BS in Engineering or Life Science Field

• 10 years of experience in medical device industry or regulated environment (e.g., ISO 13485:2016, 21 CFR Part 820 and MDSAP) in one of the following functions: Quality Assurance/Quality Engineering or Product Development Engineering
• Educational/work background that includes work with medical instrumentation is required.
• Work experience in the Medical Device Industry, Defense Industry or the Armed Forces in highly desirable.
• Strong communication and organizational skills.
• Intermediate to advanced knowledge of MS Office Suite (e.g., Word, Excel)
• Self-starter with high attention to detail and ability to work on multiple projects
• Demonstrated ability to participate in cross-functional team environment
• Strong written and verbal communication skills
• Ability to work independently with little to no supervision
• Excellent organizational abilities and superior attention to detail
• Must have high level of interpersonal skills
• Possesses strong analytical and problem-solving skills
• Excellent time management skills and project management skills
• Capability of objective analysis
• Proactive attitude to address problems

4.04.0 out of 5 stars Marlton, NJ 08053 $120,000 - $130,000 a year, Pulled from the full job description

• Health insurance
• 401(k) matching
• Paid holidays
• Opportunities for advancement, Our hiring process lets you show off the very best version of yourself while learning all about us at the same time. Our recruiting promise is a candidate experience that's enjoyable, thorough, and fair. That's our way of inspiring the innovative brightest minds. Impulse Dynamics has been built by the efforts of great people from diverse backgrounds. We believe great ideas can come from anywhere-we strive to foster an inclusive culture built around a diversity of thought and mutual respect. We lead with inclusion and empower our team members to do their best work as their most authentic selves. We strive to foster an inclusive and diverse team, committed to making a difference. Equal Opportunity Employer Statement: Impulse Dynamics is an equal opportunity employer. Impulse Dynamics is committed to the spirit and letter of all federal, state, and local laws and regulations pertaining to equal opportunity. To provide equal employment and advancement opportunities to all applicants, employment decisions at the company will be based on merit, qualifications, and abilities. The company does not unlawfully discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, genetic information, or other protected status. This policy extends to all terms, conditions, and privileges of employment, as well as the use of all Impulse Dynamics facilities. Compensation & Benefits

Annual Base Salary Range: $ 120,000 - $ 130,000

• Full Coverage Medical Benefits - Employee + family contribution is 100% covered by Impulse Dynamics.
• Paid Vacation, floating holidays, and sick time.
• Paid Holidays
• 401k Match (up to 6%)
• Annual bonus eligibility

Unless specifically indicated communicated otherwise in writing, all employees are "at-will" employees. The Company reserves the right to modify the aforementioned terms with appropriate notice and under no circumstance do the above described compensation and benefits constitute a promise to continue them for the duration of an employee's employment.

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, which is 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 across the globe. With global headquarters in Marlton, N.J., the company has additional offices in Frankfurt, Germany.