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Integra LifeSciences Staff Engineer - Design Assurance and Reliability Engineering in Irvine, California

Changing lives. Building Careers.

Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes.

SUMMARY DESCRIPTION

This is a key functional role within the Design and Reliability Assurance Engineering team. The role involves the process of planning, organizing, leading and reporting all risk management activities through collaboration with cross functional teams. This role is responsible to also lead and coordinate process, practice, procedures and technology adoption for the continuous improvement of risk management work product and deliverables for projects and programs.

The role is also responsible for support of New Product Development (NPD), Sustaining Engineering and Continuous Improvement projects of varying scope and complexity. This individual will collaborate with internal customers and external design and development partners, participating on cross-functional project teams through all phases of the product and process development through commercialization, and support technical teams with planning, execution, reporting and communication of Design and Reliability Assurance work products and deliverables.

ESSENTIAL DUTIES AND RESPONSIBILITIES

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily:

  • Provide Risk Management and Human Factors leadership, expertise, guidance and supervision during all project phases from initiation through end of life.

  • Development of efficient and robust processes, procedures, practice, tools and technology to support continuous improvement in risk management.

  • Leads development and implementation of key performance indicators (KPI’s) and metrics for the risk management process and metrics.

  • Leads and conducts SWAT assessments in risk management to support continuous improvement across business processes

  • Lead the process of planning, organizing, leading and reporting all risk management activities through collaboration with cross functional teams.

  • Lead and support New Product Development (NPD), Sustaining Engineering and Continuous Improvement projects of varying scope and complexity.

  • Collaborates with internal customers and external design and development partners, participating on cross-functional project teams through all phases of the product and process development through commercialization, and supports technical teams with planning, execution, reporting and communication of Design and Reliability Assurance work products and deliverables.

QUALIFICATIONS/EXPERIENCE REQUIRED

The requirements listed below are representative of the knowledge, skill, and/or ability required for this position.

  • Bachelor’s Degree in Engineering (Mechanical, Systems, Chemical or Electrical) or Science (Biology, Chemistry) with 10 years of experience working within a Medical device or other regulated industry with knowledge of Risk Management (ISO 14971 2019), MDD (Medical Device Directive), IEC 62366, ISO 13485 (Quality Management Systems), FDA QSR and cGMP.

  • Master's Degree in Engineering (Mechanical, Systems, Chemical or Electrical) or Science (Biology, Chemistry) with 8 years of experience working within a Medical device or other regulated industry with knowledge of Risk Management (ISO 14971 2019), MDD (Medical Device Directive), IEC 62366, ISO 13485 (Quality Management Systems), FDA QSR and cGMP.

  • Strong analytical skills and a working knowledge of problem solving methodologies

  • Working knowledge of DFSS techniques

  • 8 years of experience in a Quality Assurance role for medical device or pharmaceutical product development

  • Knowledge of industry best practices and advances in Risk Management practices, process, tools and technology

  • Demonstrates excellent knowledge of statistical sampling and analysis tools/methods to support data-driven decision making

  • Demonstrates excellent organizational, verbal and written communication skills

  • Proficient with the MS Office Suite, and statistical software.

  • Must be able to work independently with minimal supervision.

  • Able to prioritize projects and manage assigned Design Assurance resources to meet organizational goals and objectives

Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:

EEO Is the Law (https://www.eeoc.gov/laws/index.cfm) | EOE including Disability/Protected Veterans (https://www.eeoc.gov/eeoc/publications/ada_veterans_employers.cfm)

Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA (https://www.eeoc.gov/eeoc/publications/fs-ada.cfm) . If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.

Integra - Employer Branding from Integra LifeSciences on Vimeo (https://player.vimeo.com/video/265760526)

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