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Terumo
Complaints Engineer II - TA
Career Insights for Technical Writer
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Based on Florida data
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What they do
A Technical Writer writes product instructions, user manuals or other material that helps to explain complex information or procedures. Writes help information available to customers online, or clear explanations of company policies. Supports internal communication among different technical, engineering and scientific specialists working on a project or product. Creates product documentation, and provides input for improving product design.
$70,677 / year median in Florida
-10% projected decline
Job Description
At Terumo Aortic, our mission is to transform the treatment of aortic disease worldwide. With our comprehensive portfolio of surgical, endovascular and hybrid technologies, we enable physicians to find the right fit for each patient anatomy.
The company has over 1,250 associates around the world with manufacturing facilities in Glasgow, Scotland and Sunrise, Florida.
Terumo Aortic is focused on the continuing development of new and innovative products driving the growth of the business globally. Associates are part of a stimulating and exciting environment in which they can develop their skills and achieve career goals. Working for the company, each associate's role contributes greatly to helping to save or improve the lives of patients in over 100 countries worldwide.
At Terumo we believe in the power of personal growth and will encourage you to get in the driver's seat - progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what's next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, impactful solutions for patients.
Join us and help shape wherever we go next!
Advancing healthcare with heart
www.terumoaortic.comJob Summary
Analyzes, evaluates, and investigates external customer complaints in accordance with FDA, ISO, Quality System, EU MDR, and other applicable regulatory requirements. Drives complaint investigations, returned-product evaluation, adverse-event reporting support, trending, customer responses, and post-market surveillance activities and helps improve complaint processes, procedures, and team capability.
Job Details/Responsibilities Drive timely, accurate, and complete complaint and failure investigations with cross-functional teams; perform retention, decontamination, objective testing, returned-product analysis, simulation, root-cause investigation, and resolution in support of product quality and patient safety. Ensure compliance with applicable US and international complaint and adverse-event regulations, including FDA, Canadian requirements, EU MDR, Medical Device Reporting, and vigilance reporting; collaborate on reportability decisions and timely report generation. Serve as the Post-Market Surveillance subject-matter expert for assigned product lines, maintaining knowledge of product design, manufacturing, complaint rates and trends, reportability, risks, and failure modes. Collect complaint follow-up information from customers, medical professionals, field staff, Sales, Field Service, affiliates, and other stakeholders; investigate field clinical events, coordinate clinical-sample investigations, and prepare customer and field responses. Analyze and trend complaint data, convene trending meetings, present engineering failure analyses and critical information, document minutes, follow action items to closure, compile PSURs, and prepare management metrics and reports. Maintain complaint-handling procedures, support team and organizational performance indicators, provide assistance and training to team members, stay current with required training, and promote continuous improvement of complaint and post-market processes. Provide engineering expertise for complaint-investigation test equipment, including feasibility, installation, validation, qualification, layout, procurement, documentation, user training; support schedules, expenditures, and monthly reports. Job Responsibilities (continued) Working Conditions/Physical Requirements Knowledge, Skills and Abilities (KSA) Thorough knowledge of medical-device standards and regulations, complaint handling, Medical Device Reporting, vigilance reporting, and applicable recordkeeping requirements. Strong analytical and problem-solving skills and knowledge of laboratory procedures used to evaluate returned samples and investigate product failures. Excellent written and oral English communication and technical-writing skills, with strong presentation and training capability. Ability to interact effectively with individuals and groups at all organizational levels and with customers, medical professionals, field personnel, and affiliates. Ability to manage multiple priorities independently with accuracy, sound judgment, and close attention to detail. Proficiency with Microsoft Word, PowerPoint, and Excel; Minitab proficiency is preferred. Knowledge of complaint metrics, data analysis and trending, report preparation, investigation equipment, and validation and qualification documentation. Qualifications/ Background Experiences Bachelor's degree in Engineering, Life Sciences, or a related technical field, or equivalent education and experience. At least three years of experience in medical-device quality assurance or a clinical environment. At least four years of quality, complaint-investigation and resolution, or clinical experience in the disposable medical-device industry. Clinical experience or in-depth knowledge of interventional products and medical procedures is strongly preferred. ASQ certification (CQE or CQIA) is desirable. It is Terumo's policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, sexual orientation, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other category protected by law. As a Company, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment. Final compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We provide competitive and comprehensive benefit options which include: annual bonus, paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program.
Job Details/Responsibilities Drive timely, accurate, and complete complaint and failure investigations with cross-functional teams; perform retention, decontamination, objective testing, returned-product analysis, simulation, root-cause investigation, and resolution in support of product quality and patient safety. Ensure compliance with applicable US and international complaint and adverse-event regulations, including FDA, Canadian requirements, EU MDR, Medical Device Reporting, and vigilance reporting; collaborate on reportability decisions and timely report generation. Serve as the Post-Market Surveillance subject-matter expert for assigned product lines, maintaining knowledge of product design, manufacturing, complaint rates and trends, reportability, risks, and failure modes. Collect complaint follow-up information from customers, medical professionals, field staff, Sales, Field Service, affiliates, and other stakeholders; investigate field clinical events, coordinate clinical-sample investigations, and prepare customer and field responses. Analyze and trend complaint data, convene trending meetings, present engineering failure analyses and critical information, document minutes, follow action items to closure, compile PSURs, and prepare management metrics and reports. Maintain complaint-handling procedures, support team and organizational performance indicators, provide assistance and training to team members, stay current with required training, and promote continuous improvement of complaint and post-market processes. Provide engineering expertise for complaint-investigation test equipment, including feasibility, installation, validation, qualification, layout, procurement, documentation, user training; support schedules, expenditures, and monthly reports. Job Responsibilities (continued) Working Conditions/Physical Requirements Knowledge, Skills and Abilities (KSA) Thorough knowledge of medical-device standards and regulations, complaint handling, Medical Device Reporting, vigilance reporting, and applicable recordkeeping requirements. Strong analytical and problem-solving skills and knowledge of laboratory procedures used to evaluate returned samples and investigate product failures. Excellent written and oral English communication and technical-writing skills, with strong presentation and training capability. Ability to interact effectively with individuals and groups at all organizational levels and with customers, medical professionals, field personnel, and affiliates. Ability to manage multiple priorities independently with accuracy, sound judgment, and close attention to detail. Proficiency with Microsoft Word, PowerPoint, and Excel; Minitab proficiency is preferred. Knowledge of complaint metrics, data analysis and trending, report preparation, investigation equipment, and validation and qualification documentation. Qualifications/ Background Experiences Bachelor's degree in Engineering, Life Sciences, or a related technical field, or equivalent education and experience. At least three years of experience in medical-device quality assurance or a clinical environment. At least four years of quality, complaint-investigation and resolution, or clinical experience in the disposable medical-device industry. Clinical experience or in-depth knowledge of interventional products and medical procedures is strongly preferred. ASQ certification (CQE or CQIA) is desirable. It is Terumo's policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, sexual orientation, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other category protected by law. As a Company, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment. Final compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We provide competitive and comprehensive benefit options which include: annual bonus, paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program.