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Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

+ Career development with an international company where you can grow the career you dream of

+ Free medical coverage for employees* via the Health Investment Plan (HIP) PPO

+ An excellent retirement savings plan with high employer contribution

+ A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune

+ Abbott offers a dynamic and inclusive work environment, competitive compensation, and the opportunity to make a real difference in the lives of many

About Lingo

Abbott's rich history in developing cutting-edge health technologies is evolving with its new venture into biowearables. The biowearables segment is poised to represent the future of the organization, with the potential to generate over $1 billion in revenue within the next five years, supported by Abbott’s robust R&D and financial resources.

At Lingo, we are committed to transforming health management with our cutting-edge biowearables that monitor glucose levels and other critical metabolic biomarkers. Our products integrate seamlessly with other health indicators such as sleep, exercise, and stress, to provide personalized insights that improve metabolic well-being. This is your opportunity to be at the forefront of health innovation and make a significant impact on people’s lives.

The Opportunity

Lingo is seeking an impactful Global Head of Quality and Regulatory Affairs to lead our innovative biowearables initiative and drive the next phase of our growth in consumer health technology. This role is a strategic leadership position reporting directly to the Lingo Divisional VP. This individual will lead the implementation of a best-in-class digital Quality Assurance and Compliance system optimized for Software as Medical Device. In addition, this individual will play a pivotal role in Lingo's global expansion, leading efforts to achieve successful regulatory clearances and commercial launches in LATAM, Europe, Gulf Countries, and Asia.

Overseeing all aspects of quality and regulatory affairs, from design and development to post-market surveillance, this role ensures Lingo meets the highest standards for safety, efficacy, and compliance. This person will serve as the Management Representative for the division with regulatory/inspectional agencies.

Leading a dynamic team of 20+ Quality and Regulatory professionals, you'll continue to develop, grow, and inspire the team to meet short-term and long-term objectives of the business. Your proven experience managing change and driving transformation in a fast-paced consumer and Med Tech landscape will be integral to our success.

What You'll Work On

+ **Digital-First QMS Leadership:** Design and implement a scalable, software-centric Quality Management System (QMS) optimized for Agile, DevOps, and CI/CD workflows, ensuring compliance with applicable regulatory requirements.

+ **Software Quality Assurance:** Define and enforce robust software quality standards across the development lifecycle, including validation, verification, risk management, cybersecurity, and documentation practices.

+ **Global Regulatory Strategy:** Develop and execute regulatory strategies for software-enabled medical devices, ensuring alignment with FDA, EMA, EU MDR, ISO 13485, and other relevant frameworks. Navigate the nuanced classification of Lingo’s app features across geographies.

+ **Market Expansion Leadership:** Lead regulatory efforts to support Lingo’s entry into global markets, including regions where the product may or may not be classified as a medical device.

+ **Audit & Compliance Oversight:** Drive internal audits, maintain software lifecycle documentation, and lead continuous improvement initiatives to ensure global compliance and readiness for regulatory inspections.

+ **Cross-Functional Collaboration:** Partner closely with R&D, software engineering, clinical, and product teams to embed quality and compliance into every stage of product development and iteration.

+ **Team Building & Leadership:** Build and mentor a high-performing QARA team with deep expertise in software quality, regulatory affairs, and medical device compliance.

+ **Post-Market Surveillance:** Oversee software-related complaint handling, CAPA processes, and real-world performance monitoring to ensure safety, effectiveness, and user satisfaction.

Qualifications

+ Bachelor’s degree in engineering, computer science, or a related technical field.

+ MS, MBA or PhD preferred.

+ 10+ years of experience in Quality Management Systems within a regulated industry, with at least 5 years in a leadership role.

+ Proven experience implementing and managing a digital QMS in a SaMD or software-intensive medical device company is essential.

+ Deep understanding of software quality assurance principles, including software validation, risk management, and lifecycle documentation.

+ Experience with AI/ML-enabled medical devices, digital health platforms, or connected health solutions.

+ Extensive knowledge of global regulatory requirements, including FDA regulations (e.g., 21 CFR Part 820), ISO 13485, and EU MDR/IVDR.

+ Successful track record of preparing and submitting regulatory dossiers for SaMD in international markets.

+ Strong leadership and people management skills, with experience building and developing high-performing teams.

+ Excellent communication, interpersonal, and influence skills.

If you're excited about the opportunity to lead innovation in health technology and help shape the future of personal health management, we would love to hear from you.

Together, let’s create products that empower individuals and redefine self-care.

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com (http://www.abbottbenefits.com/pages/candidate.aspx)

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal

The base pay for this position is $193,300.00 – $386,700.00. In specific locations, the pay range may vary from the range posted.

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email [email protected]