Hologic Inc logo

Senior Software Design Assurance Engineer

Hologic Inc

  • Newark, NJ
  • 30+ days ago

    Highlights

    Bachelor's degree in Computer Science, Software Engineering, Electrical Engineering, or related discipline with 5+ years of medical device industry experience, or a Master's degree with 3+ years of experience. The Senior Software Design Assurance Engineer is responsible for ensuring the quality, safety, reliability, and regulatory compliance of medical device software throughout the product lifecycle.

    Numbers & Facts

    LocationNewark, NJ

    Description

    Detail | Hologic Skip to main content Skip to main menu tabs for megamenu Skip to sitemap

    Region

    Choose region

    North America Latin America EMEA APAC

    Language

    EN

    Chinese, SimplifiedDutchEnglishFrenchGermanItalianJapanesePortuguese, PortugalPortuguese, BrazilSpanish

    Search jobs

    Senior Software Design Assurance Engineer

    Newark, DE, United States

    Marlborough, MA, United States

    Join our talent community Share Apply

    The Senior Software Design Assurance Engineer is responsible for ensuring the quality, safety, reliability, and regulatory compliance of medical device software throughout the product lifecycle. This role focuses on establishing and maintaining robust software design controls, driving rigorous verification and validation processes, and collaborating with engineering teams to deliver dependable and compliant software solutions for both standalone and embedded medical devices.

    Knowledge

    • In-depth understanding of medical device regulations (e.g., FDA, EU MDR, ISO 13485, IEC 62304) for Software as a Medical Device (SaMD) and embedded systems.
    • Strong grasp of the software development lifecycle (SDLC) and its application to safety-critical systems.
    • Expertise in risk management per ISO 14971, including Hazard Analysis and FMEA.
    • Familiarity with usability principles and IEC 62366 to enhance product safety and effectiveness.
    • Knowledge of regulatory and safety challenges for AI/ML in medical devices.
    • Proficiency in statistical software (e.g., Minitab) for data analysis.

    Skills

    • Ability to mature Quality Management System (QMS) processes using Agile/iterative design controls.
    • Hands-on experience in full SDLC for safety-critical applications.
    • Defining and executing robust software verification and validation (V&V) strategies.
    • Integrating automated testing into CI/CD pipelines and leveraging data analytics for continuous improvement.
    • Advanced project documentation, requirements management, and version control.
    • Software security skills, including threat modeling, vulnerability assessments, and penetration testing.
    • Excellent communication for cross-functional collaboration and technical presentations.

    Behavior

    • Collaborative approach, working closely with cross-functional teams (R&D, Regulatory, Marketing, Manufacturing Engineering, Quality Engineering).
    • Leadership in guiding teams on best practices for software development and compliance.
    • Proactive in identifying process gaps, recommending improvements, and supporting continuous improvement initiatives.
    • Creative and effective problem-solving, ensuring innovative solutions without compromising quality or compliance.
    • Commitment to maintaining compliance with all regulatory requirements and internal policies.

    Experience

    • Bachelor's degree in Computer Science, Software Engineering, Electrical Engineering, or related discipline with 5+ years of medical device industry experience, or a Master's degree with 3+ years of experience.
    • Proven track record in applying medical device regulations and standards to software projects.
    • Experience in leading design assurance activities, risk management, verification, and validation throughout the product lifecycle.
    • Participation in new product development and sustaining product projects, ensuring clear scope and objectives are met.
    • Involvement in regulatory inspections and remediation initiatives.

    Why join Hologic?

    We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career.

    The annualized base salary range for this role is $97,600-$152,700 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand.

    Agency and Third-Party Recruiter Notice

    Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

    Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans.

    #LI-NK1

    Apply now

    Similar jobs

    Lead Compliance Engineer, R&D Featured

    Newark, DE, United States, US, DE Employee

    Hologic is a global leader in medical device innovation, dedicated to improving lives through advanced technology and rigorous quality standards. As we expand our portfolio and reach, we are looking for a talented Lead ...

    View details

    Product Quality Engineer II Featured

    Newark, DE, United States, US, DE Employee

    Are you passionate about ensuring the quality and reliability of life-saving medical devices? At Hologic, we are seeking a Product Quality Engineer 2 to provide engineering support for on-market medical devices. In this ...

    View details

    Program Director, R&D PMO Featured

    Newark, DE, United States, US, DE Employee

    Are you a seasoned program leader ready to drive large-scale innovation and deliver new medical solutions to market? Join our Business Operations team as a Program Director, R&D PMO and play a pivotal role shaping ...

    View details

    Senior Quality Assurance Engineer Featured

    Newark, DE, United States, US, DE Employee

    Designs, implements and maintains quality assurance protocols and methods for processing materials into partially finished or finished products. Responsible for planning, implementing and managing compliance of ...

    View details

    Back to search result

    • Hologic.com
    • Products
    • About
    • Hiring Scam Warning

    Region

    Choose region

    North America Latin America EMEA APAC

    Region

    Choose region

    North America Latin America EMEA APAC

    Contact

    Privacy Policy

    Terms & Conditions

    Patent Info

    2021 Hologic Ltd. All rights reserved.

    Similar Jobs