Postmarket Surveillance Analyst I – Global Compliance

Abbott; Plano (TX); On-site; USD 51,000 - 101,000; Full time

Benefits offered by this job

HIP PPO

Retirement plan

Tuition reimbursement

FreeU education

Diversity awards

Job summary

Abbott in Plano, TX is seeking an Analyst I Postmarket Surveillance to support complaint handling, medical device reporting, and cross-functional investigations across global markets. You will enter data, prepare reports, and coordinate regulatory submissions.

The role requires strong communication, independent work skills, and the ability to collaborate with Quality, R&D, and Legal to ensure compliant processes and timely communications. Training and career growth opportunities are available.

Qualifications

• Strong written and oral communication skills required.
• Ability to work independently and on teams in a busy department.
• Knowledge of global regulations for medical device reporting is a plus.

Responsibilities

• Investigate and manage product complaints across global markets.
• Enter and maintain complaint data in the database.
• Prepare technical reports and regulatory submissions (FDA, EU) as needed.
• Collaborate with cross-functional teams (QEs, R&D) on evaluation trends.
• Support inspections by regulatory agencies.

Skills

Strong written and oral communication

Problem solving

Attention to detail

Team collaboration

Education

Bachelor’s degree in healthcare or science

2-year degree with relevant experience

Tools

Computer skills

Job description

Abbott in Plano, TX is seeking an Analyst I Postmarket Surveillance to support complaint handling, medical device reporting, and cross-functional investigations across global markets. You will enter data, prepare reports, and coordinate regulatory submissions.

The role requires strong communication, independent work skills, and the ability to collaborate with Quality, R&D, and Legal to ensure compliant processes and timely communications. Training and career growth opportunities are available.