Senior Quality Engineer

**Job Function**:Quality**Job Sub Function**:Quality Assurance**Job Category**:Professional**All Job Posting Locations**:Ciudad Juarez, Mexico, MX905 Manuel Talamas Camandari 2849, Lote Bravo, Ciudad Juarez, Chihuahua**About MedTech**Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.**About Cardiovascular**Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients.**We are searching for the best talent for SENIOR QUALITY ENGINEER to be in Ciudad Juarez, Mexico.****You will be responsible for**:- Primary responsibilities include working in Quality Engineering and with other functional groups in support of new product/process development, quality operations or quality assurance.- Utilizing Quality Engineering tools/processes in development and implementation of practices for the effective and efficient development, transfer, and maintenance of products/processes throughout the product lifecycle.- Leading efforts with quality improvement opportunities as appropriate to legacy products, continuous improvement, and customer satisfaction.- Develop and establish effective quality control and support associated risk management plans.- Write, review and/or approve process and product validation protocols and reports, equipment qualifications, engineering change orders.- Use statistical tools to analyze data, make acceptance decisions, and improve process capability (Six Sigma, SPC, DOE).- Determine sterility, biological and packaging test requirements utilizing appropriate industry or agency standards for new products.- Ensure that development activities follow design control requirements, product is tested per applicable standards, European Essential Requirements are met per the MDR, and product is properly transferred to manufacturing.- Provide all planning necessary to ensure effective product acceptance. This includes, but is not limited to, part qualifications, specification development, and sampling plans.- Support vendor audits as technical lead as needed and support Supplier Quality as Quality representative as appropriate.- Initiate and investigate Corrective and Preventative Actions (CAPA) as appropriate.- Assist in complaint analysis as appropriate.- Assist Regulatory Affairs in developing submissions for process changes, inspection changes, and new processes/devices as necessary.- Participate in design reviews and pre-validation assessments to ensure the safe and environmentally sound start-up of new processes.- Makes decisions independently on engineering problems and methods and represents the organization in conferences to resolve important questions and to plan and coordinate work.- Consults with supervisor and provide guidance as needed concerning unusual problems and developments.- Responsible for one or more of the following as needed:- Supervise and/or provide guidance to Inspectors and Technicians in Quality LCM, Quality Operation or Quality Assurance activities.- In a supervisory capacity, plans, develops, coordinates, and directs a medium-sized engineering project or a number of small projects with varying levels of complexity.- As an individual researcher, carries out assignments requiring the development of new or improved techniques or procedures.- Work is expected to result in the development of new or improved techniques or procedures.- Work is expected to result in the development of new or refined equipment, materials, processes, products, and/or methods.- Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment when necessary, data are insufficient or confirmation by testing is advisable.- Responsible for communicating business related issues or opportunities to next management level.- Responsible for ensuring subordinates follow all Company guidelines related to Health, Safetyand Environmental practices and that all resources needed to do so are available and in good condition.- Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.- Performs other duties assigned as needed**Requirements**:**Education**:Bachelor’s degree in a related field, along with a minimum of 4 - 6 years of quality,manufacturing, or research and development experience in a medical device or other regulatedindustry is required. Master’s degree i