Job Description
Qualifications
Bachelors Degree (± 16 years) or an equivalent combination of education and work experience
Knowledge and experience of Quality Systems Regulations (21CFR820), as well as, Medical Device Reporting (21CFR803) and ISO standard 13485
Requires experience with complaint handling (21CFR820.1+8)
Minimum 5 years In the medical device field
Minimum 3 years Management, supervisory or team leadership experience required
Benefits
Career development with an international company where you can grow the career you dream of
Free medical coverage for employees via the Health Investment Plan (HIP) PPO
An excellent retirement savings plan with high employer contribution
Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree
Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan
Free coverage applies in the next calendar year
The base pay for this position is $10+,300.00 – $218,500.00
In specific locations, the pay range may vary from the range posted
Responsibilities
The Medical Events Section Manager Provides direct supervision and management to staff responsible for filing Medical Device Reports to the FDA (US), Medical Problem Reports to Health Canada, Medical Incident Reports to the EU/EFTA including France, and Medical Device Incident reports to the rest of world for the division's products
Is proficient with medical event reporting and complaint handling policies and procedures
Manages staff to evaluate potentially reportable complaints in compliance with applicable regulations
Ensures that reportable events are filed with worldwide regulatory agencies in compliance with regulations
Ensures that ADC complaints are reviewed within established timeframes
Elevates complaints requiring ADC Management and Medical Affairs guidance, participates in discussions and decision making process to determine reportability
Ensures compliance is maintained and that employees are trained and following the required site level policies and procedures
Anticipates, recognizes, communicates and manages quality issues within the organization and works with appropriate cross functional areas to recommend actions to resolve the issues
Responsible for scheduling day-to-day activities of medical events group staff to ensure timely review of medical event files
Ensures potentially reportable complaints are assessed against criteria for reportability and reports are filed as necessary in compliance with regulations
Works closely with Customer Service, Complaint Handling, and Complaint Investigation teams to ensure that the appropriate information is obtained from complainants to make sure an accurate and timely assessment of reportability is made
Establishes processes and procedures for medical event reporting within the framework of the complaint handling system
Utilizes good judgment and makes timely decisions considering the facts and data at hand; champions specific projects; knows when to escalate to management
Actively recruits, interviews and participates in the hiring process of Medical Events Group members
Participates as a team member and team leader to monitor the productivity of the group, set priorities, and shift resources as appropriate to meet department goals
Sets standards and monitors staff performance; establishes the motivational climate and productivity goals for the group; provides performance feedback; writes and conducts appraisals for employees
Assists in development of development and training plans
Coordinates changing priorities and organizes process improvement projects
Uses tools effectively to monitor progress and results
Job description
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
• Career development with an international company where you can grow the career you dream of.
• Free medical coverage for employees via the Health Investment Plan (HIP) PPO
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
The Medical Events Section Manager Provides direct supervision and management to staff responsible for filing Medical Device Reports to the FDA (US), Medical Problem Reports to Health Canada, Medical Incident Reports to the EU/EFTA including France, and Medical Device Incident reports to the rest of world for the division's products. Is proficient with medical event reporting and complaint handling policies and procedures. Manages staff to evaluate potentially reportable complaints in compliance with applicable regulations. Ensures that reportable events are filed with worldwide regulatory agencies in compliance with regulations. Ensures that ADC complaints are reviewed within established timeframes. Elevates complaints requiring ADC Management and Medical Affairs guidance, participates in discussions and decision making process to determine reportability. Ensures compliance is maintained and that employees are trained and following the required site level policies and procedures. Anticipates, recognizes, communicates and manages quality issues within the organization and works with appropriate cross functional areas to recommend actions to resolve the issues.
What You'll Work On
• Responsible for scheduling day-to-day activities of medical events group staff to ensure timely review of medical event files.
• Ensures potentially reportable complaints are assessed against criteria for reportability and reports are filed as necessary in compliance with regulations.
• Works closely with Customer Service, Complaint Handling, and Complaint Investigation teams to ensure that the appropriate information is obtained from complainants to make sure an accurate and timely assessment of reportability is made.
• Establishes processes and procedures for medical event reporting within the framework of the complaint handling system.
• Utilizes good judgment and makes timely decisions considering the facts and data at hand; champions specific projects; knows when to escalate to management.
• Actively recruits, interviews and participates in the hiring process of Medical Events Group members.
• Participates as a team member and team leader to monitor the productivity of the group, set priorities, and shift resources as appropriate to meet department goals.
• Sets standards and monitors staff performance; establishes the motivational climate and productivity goals for the group; provides performance feedback; writes and conducts appraisals for employees.
• Assists in development of development and training plans.
• Coordinates changing priorities and organizes process improvement projects.
• Uses tools effectively to monitor progress and results.
Required Qualifications
• Bachelors Degree (± 16 years) or an equivalent combination of education and work experience.
• Knowledge and experience of Quality Systems Regulations (21CFR820), as well as, Medical Device Reporting (21CFR803) and ISO standard 13485.
• Requires experience with complaint handling (21CFR820.1+8).
• Minimum 5 years In the medical device field.
• Minimum 3 years Management, supervisory or team leadership experience required.
Apply Now
• Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is $10+,300.00 – $218,500.00. In specific locations, the pay range may vary from the range posted.
Bachelors Degree (± 16 years) or an equivalent combination of education and work experience
Knowledge and experience of Quality Systems Regulations (21CFR820), as well as, Medical Device Reporting (21CFR803) and ISO standard 13485
Requires experience with complaint handling (21CFR820.1+8)
Minimum 5 years In the medical device field
Minimum 3 years Management, supervisory or team leadership experience required
Benefits
Career development with an international company where you can grow the career you dream of
Free medical coverage for employees via the Health Investment Plan (HIP) PPO
An excellent retirement savings plan with high employer contribution
Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree
Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan
Free coverage applies in the next calendar year
The base pay for this position is $10+,300.00 – $218,500.00
In specific locations, the pay range may vary from the range posted
Responsibilities
The Medical Events Section Manager Provides direct supervision and management to staff responsible for filing Medical Device Reports to the FDA (US), Medical Problem Reports to Health Canada, Medical Incident Reports to the EU/EFTA including France, and Medical Device Incident reports to the rest of world for the division's products
Is proficient with medical event reporting and complaint handling policies and procedures
Manages staff to evaluate potentially reportable complaints in compliance with applicable regulations
Ensures that reportable events are filed with worldwide regulatory agencies in compliance with regulations
Ensures that ADC complaints are reviewed within established timeframes
Elevates complaints requiring ADC Management and Medical Affairs guidance, participates in discussions and decision making process to determine reportability
Ensures compliance is maintained and that employees are trained and following the required site level policies and procedures
Anticipates, recognizes, communicates and manages quality issues within the organization and works with appropriate cross functional areas to recommend actions to resolve the issues
Responsible for scheduling day-to-day activities of medical events group staff to ensure timely review of medical event files
Ensures potentially reportable complaints are assessed against criteria for reportability and reports are filed as necessary in compliance with regulations
Works closely with Customer Service, Complaint Handling, and Complaint Investigation teams to ensure that the appropriate information is obtained from complainants to make sure an accurate and timely assessment of reportability is made
Establishes processes and procedures for medical event reporting within the framework of the complaint handling system
Utilizes good judgment and makes timely decisions considering the facts and data at hand; champions specific projects; knows when to escalate to management
Actively recruits, interviews and participates in the hiring process of Medical Events Group members
Participates as a team member and team leader to monitor the productivity of the group, set priorities, and shift resources as appropriate to meet department goals
Sets standards and monitors staff performance; establishes the motivational climate and productivity goals for the group; provides performance feedback; writes and conducts appraisals for employees
Assists in development of development and training plans
Coordinates changing priorities and organizes process improvement projects
Uses tools effectively to monitor progress and results
Job description
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
Working at Abbott
At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:
• Career development with an international company where you can grow the career you dream of.
• Free medical coverage for employees via the Health Investment Plan (HIP) PPO
• An excellent retirement savings plan with high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.
The Opportunity
The Medical Events Section Manager Provides direct supervision and management to staff responsible for filing Medical Device Reports to the FDA (US), Medical Problem Reports to Health Canada, Medical Incident Reports to the EU/EFTA including France, and Medical Device Incident reports to the rest of world for the division's products. Is proficient with medical event reporting and complaint handling policies and procedures. Manages staff to evaluate potentially reportable complaints in compliance with applicable regulations. Ensures that reportable events are filed with worldwide regulatory agencies in compliance with regulations. Ensures that ADC complaints are reviewed within established timeframes. Elevates complaints requiring ADC Management and Medical Affairs guidance, participates in discussions and decision making process to determine reportability. Ensures compliance is maintained and that employees are trained and following the required site level policies and procedures. Anticipates, recognizes, communicates and manages quality issues within the organization and works with appropriate cross functional areas to recommend actions to resolve the issues.
What You'll Work On
• Responsible for scheduling day-to-day activities of medical events group staff to ensure timely review of medical event files.
• Ensures potentially reportable complaints are assessed against criteria for reportability and reports are filed as necessary in compliance with regulations.
• Works closely with Customer Service, Complaint Handling, and Complaint Investigation teams to ensure that the appropriate information is obtained from complainants to make sure an accurate and timely assessment of reportability is made.
• Establishes processes and procedures for medical event reporting within the framework of the complaint handling system.
• Utilizes good judgment and makes timely decisions considering the facts and data at hand; champions specific projects; knows when to escalate to management.
• Actively recruits, interviews and participates in the hiring process of Medical Events Group members.
• Participates as a team member and team leader to monitor the productivity of the group, set priorities, and shift resources as appropriate to meet department goals.
• Sets standards and monitors staff performance; establishes the motivational climate and productivity goals for the group; provides performance feedback; writes and conducts appraisals for employees.
• Assists in development of development and training plans.
• Coordinates changing priorities and organizes process improvement projects.
• Uses tools effectively to monitor progress and results.
Required Qualifications
• Bachelors Degree (± 16 years) or an equivalent combination of education and work experience.
• Knowledge and experience of Quality Systems Regulations (21CFR820), as well as, Medical Device Reporting (21CFR803) and ISO standard 13485.
• Requires experience with complaint handling (21CFR820.1+8).
• Minimum 5 years In the medical device field.
• Minimum 3 years Management, supervisory or team leadership experience required.
Apply Now
• Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
The base pay for this position is $10+,300.00 – $218,500.00. In specific locations, the pay range may vary from the range posted.
💡 Quick Summary
Seeking a career-building opportunity? The Medical Events Section Manager position is now open for candidates interested in the Event Management Jobs sector. This role in Alameda offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Event Management Jobs is a plus.
