Sr Device Engineer

Position: Sr Device Engineer I
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Every member of Gilead’s team plays a critical role in the discovery and development of life‑changing scientific innovations. Our employees are our greatest asset as we work toward bold ambitions, and we’re seeking passionate, ambitious people ready to make a direct impact. We believe every employee deserves a great leader. People leaders are the cornerstone of the employee experience, evolving culture and creating an environment where every employee feels included, developed, and empowered to achieve their aspirations.

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Job Description

We are seeking a highly skilled and proactive Senior Device Development Engineer to lead technical development efforts for parenteral drug‑device combination products, including autoinjectors, prefilled syringes, and needle safety systems. This individual‑contributor role is ideal for an engineer with deep technical expertise, strong cross‑functional collaboration skills, and a passion for delivering innovative, patient‑centric solutions. The role may include oversight of contractors or matrixed resources but does not include direct people management.

Key Responsibilities

• Lead technical development activities for combination products from concept through commercialization, ensuring robust design and performance.

• Develop and execute design control documentation, including design inputs/outputs, verification, validation, and risk management.

• Author and review technical reports and contribute to regulatory submissions (IND, NDA, etc.).

• Collaborate cross‑functionally with Regulatory, Quality, Clinical, and Manufacturing teams to align on development strategy and execution.

• Support technology transfer to clinical and commercial manufacturing sites, including process development and troubleshooting.

• Drive technical problem‑solving, root cause analysis, and continuous improvement initiatives.

• Represent the device development function in internal and external technical discussions, including with suppliers and partners.

• Stay current with industry standards and regulatory expectations, including FDA, EMA, ISO 13485, ISO 14971, and cGMP.

Basic Qualifications

• Doctorate OR

• Master’s and 4+ years of relevant experience OR

• Bachelor’s and 6+ years of relevant experience

Preferred Qualifications

• Bachelor’s or Master’s degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, or related field.

• Minimum of 6+ years (BS) or 4+ years (MS) of relevant experience in combination product development.

• Strong understanding of design control, risk management, and regulatory standards for combination products.

• Demonstrated ability to solve complex technical problems and contribute to strategic project decisions.

• Excellent communication and collaboration skills; able to work effectively across functions and with external partners.

The salary range for this position is: $ - $. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. This position may also be eligible for a discretionary annual bonus, discretionary stock‑based long‑term incentives (eligibility may vary), paid time off, and a benefits package. Benefits include company‑sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit Gilead Compensation & Benefits.

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without…