SaMD Quality Engineer

SRG, the leader in the Life Sciences human capital industry, is looking for a full-time permanent SaMD Quality Engineer for a medical device company in New Jersey. This role is responsible for ensuring the quality and regulatory compliance of GxP systems used in the production of medical devices/IVDs. WHAT YOU NEED TO HAVE to be successful:Minimum of 5 yrs in quality or regulatory manufacturing of medical devices/IVDs.Bachelor's Degree in Biochemical engineering or related science engineering field.Experience Required:Software as a medical device (SaMD) or software accessory to medical device (You must indicate on your resume the medical devices you have experience with in this capacity).21 CFR Part 820, ISO 13485, EU MDR.Review of UAT and software testing/qualification.** SRG values your application, our team will be in touch to schedule interviews with candidates moving forward in the process.

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

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