Skip to main content
Search roles

Director, Device Development

Location Boston, Massachusetts, United States Job ID R-250816 Date posted 22/04/2026

Job Title Director, Device Development

Introduction to role

This Director/Senior Director position leads Device Development for Alexion products within the Global Product Development function, with a strong focus on continuous product improvement. The role directs complex projects and device development engineering teams to deliver robust Design Control, Laboratory and Device Engineering support for operational activities. It oversees engineering testing, documentation, and inspection activities to ensure safe, reliable, and compliant drug-device combination products reach patients who need them most. Ready to shape how life-changing medicines are delivered?

Accountabilities

  • Lead and manage complex cross-functional projects involving regional and global teams, ensuring alignment on objectives, priorities, and delivery plans.

  • Build and maintain strong cross-functional relationships, including clear escalation paths with Quality, Regulatory, Manufacturing, and Supply Chain to resolve issues quickly and effectively.

  • Drive senior leader stakeholder communication, updates, and governance committee interactions to secure visibility, endorsement, and resources for key programs.

  • Develop and own project strategies in partnership with CMC, Global Project Leads, and other stakeholders, translating product needs into executable device development roadmaps.

  • Manage strategic external partner relationships for specific technologies, resources, and expertise, ensuring high-quality outcomes and value.

  • Mentor and/or manage a device engineering subteam covering design, design verification testing, and industrialization to support integrated design control from clinical development through registration and commercial supply.

  • Conduct deep technical and compliance reviews with engineers to challenge assumptions, strengthen designs, and protect timelines.

  • Ensure all project timelines and activities comply with company quality assurance standards and applicable global regulatory requirements.

  • Provide clear feedback on performance and ensure development plans are defined, tracked, and executed for team members.

  • Champion a culture of scientific rigor, problem-solving, and continuous improvement across device development activities.

Essential Skills/Experience

  • A minimum of 10 years of experience in drug device combination product/device development and commercialization 

  • Experience of commercialization of mechanical or electro-mechanical injection systems or similar drug delivery presentation.

  • Direct cross-functional program management experience in the development and commercialization of device branded products.

  • Demonstrated success leading multi-site, global or enterprise-wide programs in the biotech/ pharmaceutical industry.

  • Experience in interacting with R&D to understand early Device/Combination product needs and develop roadmaps.

  • Working experience in phase-based design control activities with integrated risk management deliverables and human factors/usability engineering studies, from research through registration, launch, and life cycle management.

  • Demonstrated ability to facilitate the interface between the pharmaceutical company and the medical device vendor base.

  • Strong communication, collaboration, and team building skills; ability to connect with all levels of the organization.  Proficient in writing internal reports, project summaries, and internal/external presentations

  • Deep knowledge of the performance, safety and regulatory compliance (EU and FDA) requirements of medical device and combination products (e.g. ISO 11608 series, ISO 14971, IEC 60601 series, IEC 62304, FDA QSR 21 CFR Part 4 and 820 / ISO13485 quality system requirements, and related FDA guidance). 

  • 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 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.  

Desirable Skills/Experience

  • Bachelor’s, Master’s, or PhD Degree in Engineering (Electrical Engineering, Biomedical, Mechanical, or Chemical), plus 12-18-year experience in medical device development.  

The annual base pay (or hourly rate of compensation) for this position ranges from 175,498.40 - 263,247.60 USD Annual (80% - 120%). 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. ​

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need 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 unique and ambitious world.

AstraZeneca offers the chance to work at the forefront of rare disease biopharma, where complex biology is translated into transformative medicines for people living with devastating conditions. With the resources and reach of a global organization combined with the energy of a biotech environment, teams explore rare opportunities in new areas of unmet need while staying close to patients’ lived experiences. Colleagues are encouraged to innovate, learn fast, collaborate across disciplines, and grow through tailored development that aligns personal ambitions with a powerful shared purpose: changing lives every day.

If this role resonates and the mission inspires action, apply now to take the next step in your journey with us.

Date Posted

23-Apr-2026

Closing Date

07-May-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.

We’ll keep you up-to-date

Sign up to be the first to receive job updates.

Interested In

Lady reading through some files