Abbott
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans diagnostics, medical devices, nutritionals, and branded medicines. We serve people in more than 160 countries with 114,000 colleagues.
Job Description
At Abbott, you can do meaningful work, grow, learn, care for yourself and your family, and live a full life. We offer: Career development opportunities within an international company. Free medical coverage through our Health Investment Plan (HIP) PPO in the next calendar year. A high-contribution retirement savings plan. Tuition reimbursement, the Freedom 2 Save student debt program, and the FreeU education benefit. A recognized great place to work worldwide, including diversity and inclusion accolades. The Opportunity This role is based in Burlington, MA, within the Heart Failure division, focusing on developing solutions for diagnosing, monitoring, and managing heart failure. The Post Market Surveillance Analyst will handle complaint investigations and product evaluations, including managing complaint files, conducting investigations, preparing reports, and evaluating returned products. Key Responsibilities Manage complaint files and maintain accurate records. Communicate with internal and external stakeholders regarding product complaints. Conduct investigations independently, assess if reports need to be filed with regulatory agencies, and prepare necessary documentation. Support product evaluations through testing, reviewing documentation, and preparing technical reports. Identify trends in complaints and evaluations, and communicate findings to management. Ensure compliance with FDA regulations and company policies. Train new employees and support quality and regulatory systems. Collaborate with teams and external consultants on product evaluations. Perform duties in various environments, including offices, labs, and travel to customer sites. Qualifications Bachelor's degree or equivalent experience. At least 5 years of related work experience. Preferred Skills 3+ years in Medical Device Reporting (MDR). Knowledge of medical device regulations and standards (21 CFR Part 820, 803; ISO 14971, 13485). Six Sigma Green Belt training. Apply Now Learn more about our benefits at
www.abbottbenefits.com . Abbott is an Equal Opportunity Employer and values diversity. Connect with us at
www.abbott.com , Facebook, and Twitter. Compensation : $75,300 – $150,700, depending on location and experience. Additional Details
Location: Burlington, MA; Travel: 5%; Work Shift: Standard. Medical surveillance: Not applicable. Work activities include prolonged sitting, keyboard use, and occasional travel. Abbott is committed to equal employment opportunities.
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At Abbott, you can do meaningful work, grow, learn, care for yourself and your family, and live a full life. We offer: Career development opportunities within an international company. Free medical coverage through our Health Investment Plan (HIP) PPO in the next calendar year. A high-contribution retirement savings plan. Tuition reimbursement, the Freedom 2 Save student debt program, and the FreeU education benefit. A recognized great place to work worldwide, including diversity and inclusion accolades. The Opportunity This role is based in Burlington, MA, within the Heart Failure division, focusing on developing solutions for diagnosing, monitoring, and managing heart failure. The Post Market Surveillance Analyst will handle complaint investigations and product evaluations, including managing complaint files, conducting investigations, preparing reports, and evaluating returned products. Key Responsibilities Manage complaint files and maintain accurate records. Communicate with internal and external stakeholders regarding product complaints. Conduct investigations independently, assess if reports need to be filed with regulatory agencies, and prepare necessary documentation. Support product evaluations through testing, reviewing documentation, and preparing technical reports. Identify trends in complaints and evaluations, and communicate findings to management. Ensure compliance with FDA regulations and company policies. Train new employees and support quality and regulatory systems. Collaborate with teams and external consultants on product evaluations. Perform duties in various environments, including offices, labs, and travel to customer sites. Qualifications Bachelor's degree or equivalent experience. At least 5 years of related work experience. Preferred Skills 3+ years in Medical Device Reporting (MDR). Knowledge of medical device regulations and standards (21 CFR Part 820, 803; ISO 14971, 13485). Six Sigma Green Belt training. Apply Now Learn more about our benefits at
www.abbottbenefits.com . Abbott is an Equal Opportunity Employer and values diversity. Connect with us at
www.abbott.com , Facebook, and Twitter. Compensation : $75,300 – $150,700, depending on location and experience. Additional Details
Location: Burlington, MA; Travel: 5%; Work Shift: Standard. Medical surveillance: Not applicable. Work activities include prolonged sitting, keyboard use, and occasional travel. Abbott is committed to equal employment opportunities.
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