Job Description:

RESPONSIBILITIES

This position is responsible for, but not limited to, the following:

Utilization of statistical data analysis for trending and investigation purposesAbility to communicate ideas and information clearly, effectively, and conciselyProvide quality engineering support in the manufacturing of medical devices & hardwareEnsure compliance of manufacturing processes and areas to all applicable quality system regulationsLead Nonconformance (NCMR) process such as inspection methods, containment, correction, closure and CAPAs, and drive continuous improvements through analysis of trend dataMonitor and analyze production information to support risk management and to provide direction for corrective and preventive actions and/or process improvement activitiesPartner with manufacturing engineering to ensure necessary process controls and validations are in place and best practices are followed (GMP)Partner with Manufacturing Engineering to implement and maintain electronic manufacturing and inspection work instructions within a Manufacturing Execution System (MES)Oversee the inspection & testing of raw materials, components & finished products to ensure compliance with specifications & quality standards. Establish and maintain quality control procedures, including inspection methods and test protocols.Support internal and external auditing requirements in manufacturing to ensure compliance with quality system requirementsSupport other Quality Engineering functions as required (supplier quality, service, design QA)Perform other TransMedics task and duties as required

MINIMUM QUALIFICATIONS

BS in Mechanical, Electrical, or Biomedical Engineering or other scientific or related discipline.4-6 years’ experience in a Manufacturing Quality and/or Manufacturing Engineering roleWorking knowledge of Medical Device Regulations: FDA 21 CFR 820, ISO 14971 & 13485 as well other applicable regulations and industry standards pertaining to Medical Devices.Experience with manufacturing of complex medical device productsExperience with formal problem-solving methodologies and deductive skills, root cause analysis & CAPA.Experience with handling non-conforming material and assemblies.Experience with work instruction development and maintenance within an MES environment

PREFERRED QUALIFICATIONS

Practical knowledge and experience using Minitab or other statistical analysis tools. Understanding & application of Gage R&R and Measurement system analysis desired.Experience with process validationExperience with non-product software implementation and validationFamiliarity with Critical Manufacturing MESExperience presenting data and information to management

TransMedics is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, national origin, marital status, age, disability or protected veteran status, or any other characteristic protected by law. We are committed to creating an inclusive environment for all employees.