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Job type: Permanent

Discipline: Design, Project Engineering, Project Management

Location: United States

Device Engineer - Software - Permanent - Concord, CA

Proclinical is partnered with a medical device organization that needs to expand its engineering capabilities in efforts to product new therapeutics products.

Skills & Requirements:

Bachelor of Science or higher degree in Computer Science, Computer Engineering, Electrical Engineering, or similar
Minimum 5 years of relevant product development experience, including software development and testing experience per IEC 62304
Good experience throughout the product development lifecycle and with developing and sustaining embedded devices
Good leadership skills with a capability to lead distributed technical teams
Excellent problem-solving skills with a preference to be hands-on
Excellent verbal and written communication skills
Preferred experience and working knowledge of medical device development, including a thorough understanding of and familiarity with 21 CFR Part 820, EU MDR, and ISO 13485 guidelines and standards
Preferred experience and working knowledge of Cybersecurity guidance and best practices
Preferred experience in software design and implementation in relevant programming languages (e.g., C, C++, C#, Python)
Results driven and highly motivated self-starter that can work independently with minimal supervision
Flexible with the ability to manage simultaneous tasks and adapt to changing priorities
Some travel required (<20%)

The Device Engineer will:

Lead and support design and development of new medical device technologies and solutions
Lead and support design transfer, manufacturing and sustaining activities for commercial medical devices
Engage and collaborate with cross-functional teams to gather and define product requirements, define high-level design, evaluate technical concepts, and contribute to technical decisions
Act as a systems and software subject matter expert to provide technical guidance to project teams that accomplishes tasks and achieves company objectives
Plan and coordinate detailed design, implementation, verification, and design transfer across external development teams and vendors
Design, setup, and conduct laboratory experiments to characterize the performance of new technical solutions and interactions with biologics and chemistry
Support in-vitro studies and early-stage clinical trials for new products
Define and maintain medical device software lifecycle processes and instructions per IEC 62304
Define and maintain a software development environment and supporting tools
Prepare clear and concise technical reports and documentation in accordance with quality system requirements
Stay current with relevant developments in academia and industry through literature review and training

If you are having difficulty in applying or if you have any questions, please contact Victoria Kroon at (+1) 929-387-4315 or v.kroon@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.