Engineer

Join Amgens Mission of Serving Patients At Amgen, if you feel likeyourepart of something bigger,itsbecause you are. Our shared missionto serve patients living with serious illnessesdrives all that we do. Since 1980,wevehelped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year.

Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rarediseases, andobesity and obesity-related conditions.

As a member of the Amgen team,youllhelp make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them,youllthrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Engineer What you will do Letsdo this.

Letschange the world. In this vital role you willjoin ourDeviceEngineering group to supportchange control, engineering robustness, anddevice development. In support of Amgens mission to serve patients, the Device Engineering group at Amgen is a diverse team working toidentify, develop, commercialize, and continuously improve drug delivery devices tooptimizethepatientexperience. The role willbe responsible fordriving and coordinating complex, cross-functional product development efforts, with clear ownership for managing interactions, dependencies, and interfaces to ensure program execution. The successful candidate will be a key member of the technical team that progresses towards the design, development, and transfer of drug delivery devices. The role ensures that the quality targets are satisfied,identifiestechnical risks and coordinates risk retirement activities on the program. The position is based at our Amgen Massachusetts site with the possibility of a flexible working arrangement meeting business and private needs. You will be joining Amgens device development team consisting of 50+ engineers.

Responsibilities:

The Engineer will be primarily responsible for end-to-end execution of Change Controls, withadditionalresponsibilities supportingrobustnessengineering and design transfer activities. Specifically, the Engineer will: Lead end-to-end preparation and execution of Change Controls, including defining scope, rationale, and supporting documentation Partner with Change Owners, Document Owners, and SMEs to align timelines, impact assessments, and approvals Author and/or support redlining and finalization of controlled documents Ensure completeness, accuracy, and compliance of change records within the Quality Management System Support presentation of changes at Change Control Boards (CCBs) Support development and maintenance of the Design History File Supporttasks withinone or more of theDesign forRobustness disciplines:

KinematicDesign, ToleranceDesign, Structural StrengthDesign, MaterialDesign, DFA, DFM Collaborate across robustness disciplines toidentifyrisks and mitigations, opportunities,and best trade-off solutions Collaborate closely with manufacturing, quality, and suppliers to improve product robustness and reduce variation-driven failures Apply systems-level thinking toanticipatehow design decisionsimpact downstreammanufacturability andperformance What we expect of you We are all different, yet we all use our unique contributions to serve patients. Thedynamicprofessional weseekis an individualwith these qualifications.

Basic Qualifications:

Masters degree OR Bachelors degree and 2 years ofEngineerexperience OR Associates degree and 6 years ofEngineerexperience OR High school diploma / GED and 8 years of

Engineerexperience Preferred Qualifications:

2+ years of progressive experience as an engineer or scientist within a research & development, manufacturing, or engineering environment Experience with change control and configuration management in regulated environments Experience authoring technical documentation and working within a QMS Experience in medical device or combination product development under DesignControls Understanding of manufacturing processes (e.g., injection molding, assembly processes) Familiarity with technical drawings and specifications Working knowledge of relevant standards (21 CFR 820, ISO 13485, ISO 14971) Strong communicationand cross-functional collaboration skills Ability to work with teams across functional areas, cultures, and time zones Fluent in English language What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture,wellsupport your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility,comprisingof health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies. Apply now and make a lasting impact with the Amgen team. careers.amgen.com In any materials yousubmit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline Amgen does not have an application deadline for this position; we will continue accepting applications until we receivea sufficient numberor select a candidate for the position. Sponsorship Sponsorship for this role is not guaranteed. 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 and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against seriousdisease. 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, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation toparticipatein 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.