Engineer III, Device Development Location: Boston, MA (hybrid 3x a week) or New Haven, CT When we put unexpected teams in the same room, we unleash bold thinking with the power to encourage life-changing medicines. In-person working gives us the platform to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our outstanding and ambitious world. Introduction to the role This position will serve the role of Engineer III for device development of Alexion products including continuous product improvement within the Development function of Alexion. The candidate will support technical design and development activities for device and combination products and assist the technology transfer. What you’ll do: Support device development activities with the device engineering team to development and bring to market combination product. Support work with device partners in the creation, evolution, optimization and verification of designs and hardware for drug delivery devices, their associated test equipment precision measurement systems, and other such equipment. Help assess and develop innovative container closure systems. Conduct characterization for device function, assembly, manufacturability, etc. using both CAE and traditional engineering techniques. Test mechanical or electromechanical systems on bench top models or production representative units, during design development and verification. Liaise with third parties such as specialist manufacturers and toolmakers. Communicate effectively, both verbally and in writing, internally across departments and with external suppliers. Align with the Company’s quality assurance requirements as well as applicable regulatory requirements. Requirements: Bachelor’s degree in Engineering (Biomedical, Chemical, Mechanical, or Electrical Engineering) Experience in design control activities. Knowledge of primary containers and drug delivery. Understanding of mold, fixture design and build as well as application of validation processes (IQ/OQ/PQ). Experience collaborating with the medical device vendor and tooling company. Knowledge of the regulatory and compliance requirements of device design controls and combination products (i.e. FDA QSR 21 CFR Part 4 and 820/ISO13485 quality system requirements). The duties of this role are generally conducted in an office environment. As is typical of an office-based role, employees must be able, with or without an accommodation to use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving and non-linear thought, analysis, and dialogue; collaborate with others; maintain general availability during standard business hours. 4-6 year experience in medical device development preferred. Experience with injector-based combination product preferred. At Alexion, you will find a collaborative culture that encourages innovation and a diverse environment where your contributions are valued. You will have the opportunity to be at the forefront of rare disease research and make a meaningful difference in patients' lives. Ready to lead and encourage? Apply now and take the first step towards a fulfilling career at Alexion, AstraZeneca Rare Disease. #LI-Hybrid The annual base pay for this position ranges from 101,643.20 - 152,464.80 USD. Our positions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans. Date Posted 21-Oct-2026 Closing Date 03-Nov-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form. For over three decades, patients and their caregivers have been at the center of everything we do. Every day, we are inspired to follow the science and think differently to create better outcomes for them and their families. Our mission is driven by understanding who they are as unique individuals, not solely defined by their diseases. We’re a leading rare disease company with a diversified projects. Our pioneering legacy in rare diseases is rooted in being the first to translate the complex biology of the complement system into transformative medicines over the past three decades. Today, we continue to push the boundaries of science and deepen our understanding of rare diseases with patient-centricity at the core. This knowledge allows us to innovate and evolve into new areas where needs are unmet and provide an opportunity to help people fully live their best lives.

Engineer III, Device Development.

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