Senior Device Engineer – Device Platform – Combination Product Operations

HOW MIGHT YOU DEFY IMAGINATION?

Youve earned your degree.

How will you use that achievement to reach your goals?

Do more with the knowledge youve worked hard to acquire and the passion you already have.

At Amgen, our shared missionto serve patientsdrives all that we do.

It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide.

Become the professional you are meant to be in this meaningful role.

Senior Device Engineer
– Device Platform Combination Product Operations Live What you will do Lets do this.

Lets change the world.

The senior device engineer will lead and/or participate in the design, development and lifecycle management related activities for drug delivery devices.

This includes technical operations support for design control activities, contract manufacturing, failure investigation, leading and assessing design changes, development test procedures, scale-up and global launch, supplier development, and continuous improvement.

Scope includes mechanical and electro-mechanical delivery devices such as fluid transfer devices, automatic pen injectors, and micro-infuser delivery pump systems.

The qualified candidate will be part of a sustaining device engineering team that ensures design history files of the mechanical and electro-mechanical delivery devices are maintained.

The engineer will participate in multi-functional teams, leading device design activities such as developing product improvements, analytical failure analysis and implementing design solutions, assessment of proposed changes, product launches, and defending inspection and follow through of commitments.

Be responsible for applying all conventional aspects of the subject matter, functional area, and assignments.

This individual will plan and conduct work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures and criteria and devise innovative approaches to problems encountered.

Accountability of developing and maintaining technical records within design history file associated with assigned products.

Develop Test Method, generate and maintain design specification, protocol & report writing, prototyping, DOE/SPC product optimization, design verification & validation, FMEA, etc.

Lead system level root cause investigation, coordinate design improvements with development partners, strategic planning and implementation of design changes and improvements.

Works with Scientists and Engineers internally and externally to assess and develop appropriate design and manufacturing specifications.

Individual contributor with Leadership attributes to optimally represent device engineer within a large network/matrix organization.

This position will be located in Cambridge, MA or Thousand Oaks, CA and requires up to 10% domestic and international travel.

Win What we expect of you We are all different, yet we all use our unique contributions to serve patients.

The dynamic professional we seek is an individual with these qualifications.

Basic Qualifications: Doctorate degree OR Masters degree & 3 years of Engineering and/or Operations experience OR Bachelors degree & 5 years of Engineering and/or Operations experience OR Associates degree & 10 years of Engineering and/or Operations experience OR High school diploma / GED & 12 years of Engineering and/or Operations experience Preferred Qualifications: Bachelor’s degree in engineering or other science-related field with 7 years of relevant work experience with 5 years of experience in operations/manufacturing environment Medical device industry experience and regulated work environment experience A background in developing and commercialization of medical devices and knowledge of manufacturing processes At a minimum familiar with the following standards and regulations: Quality System Regulation 21CFR820 Risk Management ISO 14971 EU Medical Device requirements Council Directive 93/42/EEC Strong understanding and experience in design controls, failure investigation, initiating and bringing complex projects to conclusion Excellent communication and technical writing skills Ability to work independently and across functional teams Thrive Some of the vast rewards of working here As we work to develop treatments that take care of others, we also work to care for our teammates professional and personal growth and well-being.

Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act Generous Total Rewards Plancomprising health, finance and wealth, work/life balance, and career benefitswith compensation and benefits rated above 4 stars (out of 5) on Glassdoor Apply now for a career that defies imagination Objects in your future are closer than they appear.

Join us.

careers.amgen.com 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.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.

Please contact us to request accommodation.

Amgen requires all staff in the United States, Puerto Rico and Canada to be vaccinated from COVID 19 as a condition of employment.

In accordance with applicable law, Amgen will provide reasonable accommodations to staff members who qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance.

Such accommodation may not pose an undue hardship to Amgen, its operations, or its staff.

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