Senior Software Engineer- Cutting-Edge Medical Device Company

Job Title: Senior Software Engineer

Location: Bedford, Massachusetts

Company Overview:

[Company Name] is a leading medical device company dedicated to advancing healthcare through innovative technologies. Our mission is to improve patient outcomes by developing cutting-edge medical devices that enhance diagnostic accuracy, streamline workflows, and empower healthcare professionals. As we continue to grow, we are seeking a highly skilled and motivated Lead Software Engineer to join our dynamic team in Bedford, Massachusetts.

Position Overview:

We are looking for an experienced Lead Software Engineer to play a key role in our software development team. The ideal candidate will have a strong background in developing software for medical devices and a proven track record of leading successful software projects. The Lead Software Engineer will be responsible for leading a team of software engineers, contributing to the design and development of software applications, and ensuring the delivery of high-quality, regulatory-compliant software solutions for our medical devices.

Responsibilities:

1. Team Leadership:
   
   • Lead and mentor a team of software engineers, fostering a collaborative and innovative working environment.
   • Provide technical guidance and support to team members, ensuring the successful execution of software development projects.
   • Collaborate with cross-functional teams, including hardware engineers, regulatory affairs, and quality assurance, to achieve project goals.
2. Software Development:
   
   • Drive the design and development of software solutions for medical devices, ensuring compliance with regulatory standards and industry best practices.
   • Take ownership of the software development life cycle, from requirements analysis to design, implementation, testing, and documentation.
   • Architect robust and scalable software systems that meet the unique challenges of medical device development.
3. Regulatory Compliance:
   
   • Work closely with the regulatory affairs team to ensure that software development activities comply with relevant regulations and standards (e.g., FDA, ISO).
   • Participate in regulatory submissions and audits, providing documentation and evidence of compliance.
4. Innovation and Continuous Improvement:
   
   • Stay current with industry trends and emerging technologies, incorporating new tools and methodologies into the software development process.
   • Drive continuous improvement initiatives within the software development team to enhance efficiency, quality, and delivery timelines.

Qualifications:

• Bachelor's or Master's degree in Computer Science, Software Engineering, or a related field.
• Minimum of 8 years of professional experience in software development, with at least 3 years in a leadership role.
• Proven experience in developing software for medical devices or other regulated industries.
• Strong proficiency in programming languages such as C++ and Python.
• Familiarity with relevant regulatory standards, such as ISO 13485 and FDA regulations.
• Excellent communication and interpersonal skills.

Benefits:

We offer a competitive salary, comprehensive benefits package, and the opportunity to work on cutting-edge technologies that make a meaningful impact on healthcare.

If you are a passionate and experienced Lead Software Engineer looking to contribute to the advancement of medical technology, we invite you to apply for this exciting opportunity. Join [Company Name] and be a part of a team that is dedicated to making a positive difference in healthcare.