Terumo Medical Corporation
Talent Acquisition Manager at Terumo Medical Corporation
Job Summary: This position is responsible for investigating, planning, and implementing improvements in and/or additions to current products and manufacturing processes that directly affect safety, quality, and productivity with the end result of producing a better-quality product more efficiently. Ensure compliance to Terumo2s quality policy, respond to customer complaints, perform audits, develop test methods, and/or write procedures for material characterization. Note:
We are not offering employment sponsorship for this position now or in the future (includes OPT, H1B, and other forms of visa). Responsibilities
Proactively investigates, identifies, and implements best-in-class Quality Engineering practices. Provide focused quality engineering support and assume responsibility for timely and effective coordination and/or execution of assigned development project activities. Establish effective corrective action plans. Lead in implementation of quality assurance plans, process controls, and CAPA systems designed to meet or exceed internal and external requirements. Acts as an effective leader or team member in supporting quality disciplines, decisions, and practices. Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Review and approve product and process qualification and validation and other change control related documentation. Develop product/process assurance plans, which include all required elements. Identify and implement effective process control systems to support the development, qualification, and ongoing manufacturing of products to meet or exceed internal and external requirements. Generate internal quality documentation such as quality plans, standard operating procedures, and inspection procedures. Participate in Product Review Boards. Identify non-conformance trends and develop technical investigation plans. Investigates and analyze customer/internal complaints. Performs analytical measurements and experiments to qualify or resolve product and process issues. Develop and implement strategic quality plans, master validation plans, validation protocols, inspection plans and quality/regulatory compliance operating procedures to meet FDA and ISO requirements. Track quality trends and initiate action items to resolve issues. Manage assigned corrective actions. Monitor field quality and analyze field returns to determine root cause. Provide training and support for quality system processes and quality engineering practices. Internal contacts: All departments, including manufacturing, engineering, marketing/sales. External contacts: Customers and vendor contacts regarding purchases and services. Position Requirements
Knowledge, Skills and Abilities (KSAs) Communication skills both verbal and written. Organizational skills as well as time management skills essential for project work. Prefer certification as a CQA, CQE, or CQM, and member of the ASQ. Strong writing, mathematics, and statistics skills. Requires a minimum of a 4-year degree in engineering, life sciences, or similar discipline. Requires eight years of increasing responsibility. Experience in a medical device quality assurance environment preferred. We believe that the future is bright for everyone at Terumo. We work with the future in mind to generate lasting change, create a bigger impact and produce greater outcomes for today, and for decades to come. At Terumo we believe in the power of personal growth and will encourage you to get in the drivers 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 e 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, sustainable solutions for patients. Join us, and help shape wherever we go next! Advancing healthcare with heart Benefits include competitive and comprehensive options such as paid vacation, paid holidays, health, dental and vision benefits, 401(k) with matching contributions, various savings accounts, life and disability coverage, parental leave, tuition reimbursement, travel assistance, and an employee assistance program. Final compensation packages may vary based on experience, internal equity, skillset, geography, education, business needs and market demand. Salary: $86,000 - $125,000. Salary and Location
Newark, DE or Elkton, MD area (listed salary range above).
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Job Summary: This position is responsible for investigating, planning, and implementing improvements in and/or additions to current products and manufacturing processes that directly affect safety, quality, and productivity with the end result of producing a better-quality product more efficiently. Ensure compliance to Terumo2s quality policy, respond to customer complaints, perform audits, develop test methods, and/or write procedures for material characterization. Note:
We are not offering employment sponsorship for this position now or in the future (includes OPT, H1B, and other forms of visa). Responsibilities
Proactively investigates, identifies, and implements best-in-class Quality Engineering practices. Provide focused quality engineering support and assume responsibility for timely and effective coordination and/or execution of assigned development project activities. Establish effective corrective action plans. Lead in implementation of quality assurance plans, process controls, and CAPA systems designed to meet or exceed internal and external requirements. Acts as an effective leader or team member in supporting quality disciplines, decisions, and practices. Applies sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Review and approve product and process qualification and validation and other change control related documentation. Develop product/process assurance plans, which include all required elements. Identify and implement effective process control systems to support the development, qualification, and ongoing manufacturing of products to meet or exceed internal and external requirements. Generate internal quality documentation such as quality plans, standard operating procedures, and inspection procedures. Participate in Product Review Boards. Identify non-conformance trends and develop technical investigation plans. Investigates and analyze customer/internal complaints. Performs analytical measurements and experiments to qualify or resolve product and process issues. Develop and implement strategic quality plans, master validation plans, validation protocols, inspection plans and quality/regulatory compliance operating procedures to meet FDA and ISO requirements. Track quality trends and initiate action items to resolve issues. Manage assigned corrective actions. Monitor field quality and analyze field returns to determine root cause. Provide training and support for quality system processes and quality engineering practices. Internal contacts: All departments, including manufacturing, engineering, marketing/sales. External contacts: Customers and vendor contacts regarding purchases and services. Position Requirements
Knowledge, Skills and Abilities (KSAs) Communication skills both verbal and written. Organizational skills as well as time management skills essential for project work. Prefer certification as a CQA, CQE, or CQM, and member of the ASQ. Strong writing, mathematics, and statistics skills. Requires a minimum of a 4-year degree in engineering, life sciences, or similar discipline. Requires eight years of increasing responsibility. Experience in a medical device quality assurance environment preferred. We believe that the future is bright for everyone at Terumo. We work with the future in mind to generate lasting change, create a bigger impact and produce greater outcomes for today, and for decades to come. At Terumo we believe in the power of personal growth and will encourage you to get in the drivers 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 e 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, sustainable solutions for patients. Join us, and help shape wherever we go next! Advancing healthcare with heart Benefits include competitive and comprehensive options such as paid vacation, paid holidays, health, dental and vision benefits, 401(k) with matching contributions, various savings accounts, life and disability coverage, parental leave, tuition reimbursement, travel assistance, and an employee assistance program. Final compensation packages may vary based on experience, internal equity, skillset, geography, education, business needs and market demand. Salary: $86,000 - $125,000. Salary and Location
Newark, DE or Elkton, MD area (listed salary range above).
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