Principal Regulatory Affairs Specialist – Diabetes Care (on-site)
Abbott · Alameda, CA
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Abbott seeks a Principal Regulatory Affairs Specialist for its Diabetes Care Division in Alameda, California. This on-site role involves leading global regulatory submissions for medical devices and digital health solutions, managing premarket applications and clinical trials, and providing strategic guidance on complex regulatory matters. The position requires expertise in US, EU, and global submission processes with demonstrated ability to anticipate regulatory challenges and influence organizational strategy.
Where this listing comes from
This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-02 (originally posted 2026-08-19). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.
Key requirements
- Therapeutic area
- Metabolic
Privacy & handoff
This role links to Abbott's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.