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Supervisor, Medical Events Group

3+ years
$98,000 – $196,000
10 July 29, 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 – Medical Devices

Location: Alameda, CA
Company: Abbott – Diabetes Care Division
Work Mode: On-site (Monday–Friday)
Job Type: Full-Time
Salary Range: $98,000 – $196,000 (location-dependent)


Job Summary

Abbott is hiring a Supervisor for the Medical Events Group (MEG) within its Diabetes Care Division in Alameda, California. This role ensures timely global vigilance reporting and medical device safety compliance in accordance with FDA and international regulations. Ideal for professionals with experience in complaint handling, pharmacovigilance, or regulatory affairs, this role leads reporting teams and collaborates cross-functionally with customer service, evaluation, and investigation groups.


Key Responsibilities

  • Supervise personnel responsible for vigilance report review and submission

  • Ensure compliance with global medical device reporting regulations

  • Oversee accurate documentation and on-time regulatory submissions

  • Provide SME guidance and training to MEG team and other departments

  • Monitor process efficiency and implement improvements

  • Analyze trends and escalate safety signals or reporting anomalies

  • Verify data accuracy for metrics, CAPAs, and risk assessments

  • Support performance reviews and administrative activities for the MEG team


Required Skills & Qualifications

  • Bachelor’s degree in Science, Nursing, Pharmacy, or equivalent technical field

  • Minimum 3 years of experience in a quality, clinical, medical, or lab setting

  • Strong communication, problem-solving, and decision-making skills

  • Knowledge of FDA and international vigilance reporting requirements


Preferred Skills

  • Background in medical device complaint handling

  • Experience supervising in a regulatory or QA environment

  • Familiarity with risk evaluation and safety data tracking systems


Perks & Benefits

  • Base salary range: $98,000 – $196,000

  • Free HIP PPO medical coverage eligibility

  • High-contribution retirement savings plan

  • Tuition reimbursement and student debt repayment programs

  • FreeU bachelor’s degree education path

  • Career growth with a Fortune-ranked global medical technology leader

  • Inclusive workplace recognized for diversity and innovation


Company Description

Abbott is a world-renowned leader in healthcare and medical technologies. With products spanning diagnostics, medical devices, branded generics, and nutrition, Abbott helps over 10,000 people improve heart health, treat chronic pain, and manage diabetes daily. The Diabetes Care Division is revolutionizing blood glucose monitoring with cutting-edge sensing technology.


Work Mode

On-site – Alameda, California (Monday–Friday)


Call to Action

Be a critical part of advancing medical device safety globally. Apply today to lead Abbott’s Medical Events Group and make a meaningful impact in patient health and compliance.