Principal Regulatory Affairs Specialist – Business Partnerships
Location: Alameda, California, United States
Work Mode: On-site
Employment Type: Full-Time
Experience Required: 5+ Years
Industry: Regulatory Affairs | Medical Devices | Digital Health | Diabetes Care
About Abbott
Abbott is a global healthcare leader dedicated to helping people live healthier, fuller lives. With operations in more than 160 countries and a workforce of over 114,000 professionals, Abbott delivers innovative solutions across diagnostics, medical devices, nutrition, and branded generic medicines. Abbott is consistently recognized as one of the world’s most admired companies and an employer of choice for diversity, innovation, and career growth.
Within Abbott’s Diabetes Care Division, the company is transforming diabetes management through advanced sensing and digital health technologies. Abbott’s FreeStyle Libre continuous glucose monitoring systems are used by millions of people worldwide, enabling better health decisions through accurate and actionable data.
Position Overview
Abbott is seeking a Principal Regulatory Affairs Specialist – Business Partnerships to join its Diabetes Care Division at its Alameda, California site. This senior-level role will lead regulatory strategy for global business partnership initiatives, including cloud-based and sensor-driven external collaborations. The position requires deep regulatory expertise, strong cross-functional leadership, and the ability to influence regulatory outcomes across global markets.
The role is highly visible, with department-level influence, and serves as a recognized regulatory expert both internally and externally. The successful candidate will shape regulatory strategies that support breakthrough innovations in diabetes management and digital health technologies.
Key Responsibilities
Develop and execute global regulatory strategies supporting product development and lifecycle management for business partnership initiatives.
Drive regulatory strategy for cloud-based, sensor-based, and digital health collaborations with external partners.
Analyze regulatory outcomes against initial product concepts and recommend strategic actions to optimize approvals and compliance.
Provide senior technical leadership on complex regulatory issues across business units.
Anticipate regulatory risks, emerging regulations, and policy changes; proactively develop mitigation strategies.
Create and manage project plans, regulatory timelines, and submission strategies.
Support cross-functional teams in generating data required for global regulatory submissions.
Author, review, and approve high-quality regulatory and technical documentation, including labeling.
Interface with global regulatory agencies, trade associations, and internal stakeholders as the regulatory liaison.
Oversee regulatory processes related to business partnerships and drive continuous process improvements.
Ensure post-market compliance, including change management, product event tracking, and regulatory reporting.
Provide regulatory input for product recalls, field actions, and crisis management activities.
Contribute to the development and maintenance of SOPs, regulatory systems, and compliance frameworks.
Education & Experience Requirements
Bachelor’s degree in a scientific discipline such as Life Sciences, Biology, Chemistry, or a related field.
Minimum 5 years of experience in Regulatory Affairs within medical devices, in vitro diagnostics, pharmaceuticals, biologics, or digital health.
Proven experience with global regulatory submissions and on-market product changes.
Strong working knowledge of 21 CFR 820, ISO 13485, and applicable U.S. and international regulatory frameworks.
Preferred Qualifications
Experience supporting Class II and Class III medical devices, biologics, or drug-device combination products.
Hands-on experience with 510(k) submissions, PMAs, PMA supplements, and U.S. FDA device regulations.
Experience with EU MDR, international regulatory submissions, and global market access strategies.
Regulatory Affairs Certification (RAC) is preferred.
Familiarity with quality systems, clinical investigations, and ICH guidelines.
Experience working in a highly matrixed, cross-divisional, and globally distributed environment.
Key Skills & Competencies
Advanced regulatory strategy and risk assessment capabilities.
Strong leadership, negotiation, and stakeholder management skills.
Excellent written and verbal communication skills with executive-level influence.
Ability to manage multiple complex initiatives, prioritize effectively, and meet deadlines.
High attention to detail with strong organizational and documentation skills.
Willingness to travel up to 5%, including international travel.
Compensation & Benefits
Base salary range: USD 98,000 – 196,000 (location and experience dependent).
Comprehensive health, wellness, and retirement benefits.
Tuition reimbursement, student debt assistance programs, and ongoing professional development opportunities.
Career advancement within a globally respected healthcare organization.
Equal Opportunity Statement
Abbott is an Equal Opportunity Employer committed to diversity, equity, and inclusion. All qualified applicants will receive consideration for employment without regard to protected characteristics.
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