JOB REQUIREMENTS: Help us change lives At Exact Sciences, we\'re helpingchange how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you\'re working to help others. Position Overview The Senior Bioinformatics Quality Engineer I is responsible for ensuring the quality of the medical device software for IVD, IUO and LDT products. This entails executing verification and validation processes to ensure quality and compliance, as well as development and maintenance of software design controls for the products. The Sr Bioinformatics Quality Engineer I will be involved in testing, verification, and validation of the bioinformatics pipelines in all phases of system development. This position is responsible for ensuring the creation, update and timely delivery of design controls and aiding in the development of verification and validation protocols. Working in a team setting, this role will contribute to the implementation of new software solutions that process and interpret Next Generation Sequencing (NGS) data for cancer diagnostics. This role will work with software and bioinformatics teams to ensure development satisfies requirements, also guiding software changes to ensure adequate testing and compliance for IVD, IUO and LDT products. This position will be responsible for supporting software queries in audits. With extensive science and/or engineering background, this role requires a strong focus on quality and attention to detail, and places high value on peer review, software testing and documentation. This position will join a geographically distributed team of highly motivated bioinformatics engineers at the forefront of cancer diagnostics and will be required to collaborate closely with scientists, IT and others creating these solutions. This position may be remote. Essential Duties Include, but are not limited to, the following: Be accountable for design controls for medical device software and best practices for LDT software and create and manage all applicable documentation. Participate in creation and management of software requirements. Participate in design feasibility assessments of medical device software. Participate in risk assessments and hazard analysis for software products, including... For full info follow application link. We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. Applicable portions of the Company\'s affirmative action program are available to any applicant or employee for inspection upon request. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/F13DD47746464FD9