24 days old

Senior Engineer - Combination Product & Medical Device Risk Manager

Amgen
Thousand Oaks, CA 91360
  • Job Code
    114880299
Amgen

Job ID: R-86022
Location: Thousand Oaks, CA, US 91360

Amgen is currently seeking a Senior Engineer for our Design and Development group. In support of Amgen's mission to serve patients, our diverse team is working to continuously develop and improve drug delivery devices and combination products to ensure supply and to optimize patient experience.

The Sr Engineer maintains Risk Management Files (RMF) for Amgen products including all development and post-market requirements. Additionally, supports regulatory medical device reporting requirements for agencies such as FDA and European Competent Authorities.

Additional Responsibilities:
  • Collaborate with development and change management teams to assess risk (design/user/system/process) for manual, mechanical and electromechanical devices and create or update the RMF
  • Partner with the complaints and safety teams to support life cycle management
  • Provide feedback to product development teams regarding observed design-related and user-related failure modes
  • Maintain close interaction with the engineering, human factors and quality functions to contribute to product development and improvement.
  • Ensure Quality Risk Management Files are in alignment with 21CFR Part 820 design control and risk management requirements of ISO 14971:2012 for all Amgen commercialized combination products.
  • Conduct risk assessments and create/revise risk management documents as required by Standard Operating Procedures, FDA, EU and other medical device and combination product regulations.
  • Management of hazard analyses, design risk assessments, use risk assessments, system risk assessments, and process risk assessments for combination products with manual, mechanical or electromechanical device constituent parts.
  • Work with design engineers to assess design changes from systems perspective, identifying risks, driving design mitigations and evaluating effectiveness of the risk control measures
  • Lead periodic and event driven risk reviews of the RMF's for commercialized products
  • Advise the complaints intake teams with assessment of risks related to reported complaints
  • Support the medical safety teams with assessment and responses to regulatory agencies and competent authorities related to medical device reporting requirements
  • Successfully influence outcomes, communicate with all levels of the organization, facilitate development of solutions to critical business issues, and effectively define objectives to enable effective metrics generation and reporting
  • Understand manufacturing processes for Amgen's packaged and/or distributed products
  • Provide root cause analysis of complaint investigations


Basic Qualifications
  • Doctorate degree; OR
  • Master's degree and 3 years of risk management or engineering experience OR
  • Bachelor's degree and 5 years of risk management or engineering experience OR
  • Associate's degree and 10 years of risk management or engineering experience OR
  • High School diploma/GED and 12 years of risk management or engineering experience


Preferred Qualifications
  • Master's Degree in Engineering, preferred Mechanical, Electrical, or BioMed
  • 6+ years of experience with risk analysis methods such as PrHA and FMEA for medical devices
  • 5+ years of experience in a Medical Device Development or Device Risk Management role
  • 3+ years of experience with Medical Device Reporting requirements, preferably for the European Union
  • Experience with risk management per ISO 14971
  • Experience working with complaints intake and complaints investigation teams
  • Ability to read, analyze and interpret general business periodicals, professional journals, technical procedures, or governmental regulations
  • Ability to converse technically with mechanical, electronic, software, and quality engineers
  • Capable of managing multiple projects in a deadline driven environment
  • Working knowledge of DOORs Next Generation requirements management software
  • Strong technical writing and interpersonal skills


Amgen strives to serve patients by transforming the promise of science and biotechnology into therapies that have the power to restore health or save lives. In everything we do, we aim to fulfill our mission to serve patients. And every step of the way, we are guided by the values that define us.

Amgen leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

Join Us

If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.

Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

PI114880299

<b>Amgen</b><br/><br/><b>Job ID: </b>R-86022<br/><b>Location: </b>Thousand Oaks, CA, US 91360<br/><br/>Amgen is currently seeking a Senior Engineer for our Design and Development group. In support of Amgen's mission to serve patients, our diverse team is working to continuously develop and improve drug delivery devices and combination products to ensure supply and to optimize patient experience.<br><br>The Sr Engineer maintains Risk Management Files (RMF) for Amgen products including all development and post-market requirements. Additionally, supports regulatory medical device reporting requirements for agencies such as FDA and European Competent Authorities.<br><br><b>Additional Responsibilities: </b><br><ul><li>Collaborate with development and change management teams to assess risk (design/user/system/process) for manual, mechanical and electromechanical devices and create or update the RMF</li><li>Partner with the complaints and safety teams to support life cycle management</li><li>Provide feedback to product development teams regarding observed design-related and user-related failure modes</li><li>Maintain close interaction with the engineering, human factors and quality functions to contribute to product development and improvement.</li><li>Ensure Quality Risk Management Files are in alignment with 21CFR Part 820 design control and risk management requirements of ISO 14971:2012 for all Amgen commercialized combination products.</li><li>Conduct risk assessments and create/revise risk management documents as required by Standard Operating Procedures, FDA, EU and other medical device and combination product regulations.</li><li>Management of hazard analyses, design risk assessments, use risk assessments, system risk assessments, and process risk assessments for combination products with manual, mechanical or electromechanical device constituent parts.</li><li>Work with design engineers to assess design changes from systems perspective, identifying risks, driving design mitigations and evaluating effectiveness of the risk control measures</li><li>Lead periodic and event driven risk reviews of the RMF's for commercialized products</li><li>Advise the complaints intake teams with assessment of risks related to reported complaints</li><li>Support the medical safety teams with assessment and responses to regulatory agencies and competent authorities related to medical device reporting requirements</li><li>Successfully influence outcomes, communicate with all levels of the organization, facilitate development of solutions to critical business issues, and effectively define objectives to enable effective metrics generation and reporting</li><li>Understand manufacturing processes for Amgen's packaged and/or distributed products</li><li>Provide root cause analysis of complaint investigations</li></ul><br><br><b>Basic Qualifications</b><br><ul><li>Doctorate degree; OR</li><li>Master's degree and 3 years of risk management or engineering experience OR</li><li>Bachelor's degree and 5 years of risk management or engineering experience OR</li><li>Associate's degree and 10 years of risk management or engineering experience OR</li><li>High School diploma/GED and 12 years of risk management or engineering experience</li></ul><br><br><b>Preferred Qualifications</b><br><ul><li>Master's Degree in Engineering, preferred Mechanical, Electrical, or BioMed</li><li>6+ years of experience with risk analysis methods such as PrHA and FMEA for medical devices</li><li>5+ years of experience in a Medical Device Development or Device Risk Management role</li><li>3+ years of experience with Medical Device Reporting requirements, preferably for the European Union</li><li>Experience with risk management per ISO 14971</li><li>Experience working with complaints intake and complaints investigation teams</li><li>Ability to read, analyze and interpret general business periodicals, professional journals, technical procedures, or governmental regulations</li><li>Ability to converse technically with mechanical, electronic, software, and quality engineers</li><li>Capable of managing multiple projects in a deadline driven environment</li><li>Working knowledge of DOORs Next Generation requirements management software</li><li>Strong technical writing and interpersonal skills</li></ul><br><br>Amgen strives to serve patients by transforming the promise of science and biotechnology into therapies that have the power to restore health or save lives. In everything we do, we aim to fulfill our mission to serve patients. And every step of the way, we are guided by the values that define us. <br><br>Amgen leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.<br><br>Join Us <br> <br> If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. <br> <br> Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. <br> <br> As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. <br> <br> Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.<br/><br/> <img src="https://analytics.click2apply.net/v/7eRDb8tYlANOtZ1NF7Y5y"> <p>PI114880299</p>

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Posted: 2019-10-25 Expires: 2019-11-25

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Senior Engineer - Combination Product & Medical Device Risk Manager

Amgen
Thousand Oaks, CA 91360

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