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Supervisor, Medical Events Group

3+ years
$98,000 – $196,000 annually
10 June 20, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Supervisor, Medical Events Group – On-site (Alameda, CA)

Job Summary

Abbott’s Diabetes Care Division is hiring a Supervisor for the Medical Events Group in Alameda, CA. This role leads vigilance reporting activities, ensuring global compliance with medical device safety regulations. The ideal candidate will supervise complaint handling processes, provide subject matter guidance, and monitor reporting efficiency and accuracy, directly impacting product safety and regulatory adherence worldwide.


Key Responsibilities

  • Supervise personnel handling vigilance reporting and global complaint assessments.

  • Ensure timely completion and submission of vigilance reports per regulatory requirements.

  • Coordinate with Customer Service, Complaint Evaluations, and Investigation teams for accurate documentation and regulatory submissions.

  • Provide training, guidance, and subject matter expertise to the Medical Events Group and other relevant departments.

  • Monitor processes and staff performance to improve reporting efficiency and resolve issues.

  • Identify complaint trends and communicate findings promptly to management.

  • Verify vigilance reports and related data for metrics, risk assessments, CAPAs, and other activities.

  • Assist the Associate Director with performance evaluations and administrative functions.


Required Skills & Qualifications

  • Bachelor’s Degree in Science, Medicine (Physician, Nursing, Pharmacy), or related technical discipline.

  • Minimum 3 years’ experience in a quality-related role or equivalent clinical/medical/nursing setting.

  • Strong analytical, problem-solving, and critical-thinking abilities.

  • Proficient in written and verbal communication at all organizational levels.

  • Knowledge of FDA and international medical device safety and vigilance reporting guidelines preferred.


Perks & Benefits

  • Salary Range: $98,000 – $196,000 annually.

  • Free medical coverage through Health Investment Plan (HIP) PPO.

  • Excellent retirement savings plan with substantial employer contributions.

  • Tuition reimbursement, Freedom 2 Save student debt program, and FreeU education benefits.

  • Career growth opportunities in a globally recognized, award-winning healthcare organization.


Company Description

Abbott is a global healthcare technology leader specializing in diagnostics, medical devices, nutrition, and branded pharmaceuticals. With a presence in 160+ countries, Abbott pioneers innovations that transform lives, particularly in diabetes care with cutting-edge glucose monitoring technologies.


Work Mode

On-site – Alameda, California, United States


Call to Action

If you are passionate about healthcare safety and regulatory excellence, apply now to join Abbott’s Medical Events Group and make a global impact in medical device vigilance.