**Rewritten Job Title:**

Lead Design Assurance Engineering Manager - Revolutionizing Medical Device Development **Rewritten Job Description:** About the Role: Join our team as a Lead Design Assurance Engineering Manager and play a pivotal role in shaping the future of medical device development. As a key member of our team, you will be responsible for leading the design assurance engineering function, ensuring the development of safe, effective, and high-quality medical devices that meet regulatory requirements. Key Responsibilities: Lead the design assurance engineering function, ensuring compliance with regulatory requirements and industry standards. Develop and implement design control processes, including design input, output, and verification. Collaborate with cross-functional teams, including R&D, regulatory, and quality assurance, to ensure seamless integration of design assurance activities. Provide technical leadership and guidance to design engineers, ensuring they have the necessary skills and knowledge to develop high-quality designs. Develop and maintain technical documentation, including design specifications, test plans, and reports. Participate in design reviews and audits to ensure compliance with regulatory requirements and industry standards. Identify and mitigate design risks, ensuring the development of safe and effective medical devices. Stay up-to-date with regulatory requirements and industry standards, ensuring our designs meet the latest requirements. Requirements: Bachelor's degree in Computer Engineering, Software Engineering, Computer Science, Electrical Engineering, or related technical field. Minimum of 5 years of relevant technical experience, or advanced degree with 3 years of technical experience. Strong knowledge of software design, development, debug, and test practices. Experience using unit test frameworks, such as Google Test / Mock, and following a Test-Driven Development software practice. Familiarity with using static analysis tools. Experience developing software within the medical device industry. Experience using Git for source control and experience in a pull-request based workflow. Familiarity with CI/CD tools such as Jenkins, GitLab CI/CD, or Travis CI to automate the build, test, and deploy software products. Experience with medical device design controls (e.g. ISO 13485), risk analysis (e.g. ISO 14971), and IEC62304 and SDLC. What We Offer: A competitive salary and flexible benefits package. A dynamic and inclusive culture that welcomes the challenge of life-long learning. The opportunity to work on cutting-edge medical device development projects. A collaborative and supportive team environment. The chance to make a meaningful impact on the lives of patients and healthcare professionals. How to Apply: If you are a motivated and experienced design assurance engineering professional looking for a new challenge, please submit your application, including your resume and a cover letter, to [insert contact information]. Apply for this job