The Role
Lead product and process development for neuro-interventional medical devices, focusing on manufacturing process improvement, characterization, and compliance with standards.
Summary Generated by Built In
Job Title: Staff Process Development Engineer
Location: This position is based in our Campbell, California offices. This position is onsite and full time.
Why Imperative Care?
Do you want to make a real impact on patients? Imperative Care is changing the way stroke is treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.
What You’ll Do
As a member of our organization, you will take the lead on product and process development projects for neuro-interventional medical devices, with a focus on building stable, robust, and capable manufacturing processes. The scope includes defining, characterizing, optimizing, and validating processes, as well as driving equipment development and improvements internally and at supplier/contract manufacturer sites.
The position requires someone who thrives on solving complex problems, applying structured engineering approaches, and translating design requirements into practical, manufacturable solutions. Work will span from early concept development through scale-up, with heavy emphasis on process characterization (DOEs, data analysis), equipment and fixturing design, and rigorous documentation.
What You’ll Bring
Join Us! Apply Today.
Salary Range: $157,000 – 167,000/annually
Please note that the salary information is a general guideline only. Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer.
Location: This position is based in our Campbell, California offices. This position is onsite and full time.
Why Imperative Care?
Do you want to make a real impact on patients? Imperative Care is changing the way stroke is treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.
What You’ll Do
As a member of our organization, you will take the lead on product and process development projects for neuro-interventional medical devices, with a focus on building stable, robust, and capable manufacturing processes. The scope includes defining, characterizing, optimizing, and validating processes, as well as driving equipment development and improvements internally and at supplier/contract manufacturer sites.
The position requires someone who thrives on solving complex problems, applying structured engineering approaches, and translating design requirements into practical, manufacturable solutions. Work will span from early concept development through scale-up, with heavy emphasis on process characterization (DOEs, data analysis), equipment and fixturing design, and rigorous documentation.
- Process Development: Own the development of new processes and improvement of existing ones—driving definition, characterization, optimization, and validation.
- Technology Innovation: Identify, evaluate, and implement new process technologies that advance our manufacturing capabilities.
- Equipment Development: Lead the design, qualification, and improvement of manufacturing equipment and fixturing.
- Process Characterization: Plan, design, and mentor execution of DOEs to establish process windows, control limits, and workmanship standards.
- Data-Driven Problem Solving: Apply DMAIC and other analytical methods to identify root cause, reduce variation, and drive robust solutions.
- Cross-Functional Collaboration: Partner closely with R&D, QA/RA, and Operations to define manufacturable product specifications, visual standards, and workflows that ensure smooth transfer into production.
- Documentation & Control: Lead documentation of equipment and processes, ensuring compliance with best practices, quality system requirements, and regulatory standards.
- Supplier Engagement: Participate in the management, development, and qualification of external supplier processes.
- Culture & Quality: Actively support our Quality Management System and promote a culture of rigor, safety, and continuous improvement.
What You’ll Bring
- BS in Engineering with 8+ years of related experience, or MS with 6+ years (medical device or other regulated industry preferred).
- Strong background in process characterization, validation, and scale-up in a controlled environment.
- Skilled in analytical/statistical methods (DOE, SPC) with proficiency in Excel and Minitab.
- Solid knowledge of FDA Design Control, DFSS/DFM tools, GMP/GDP, and relevant standards (ISO 13485, FDA QSR).
- Excellent critical thinking — able to connect cause and effect, prioritize under constraints, and deliver practical solutions.
- Experience in pilot and production line setup, validation, and scale-up.
- Proven ability to work independently and to lead/mentor others.
- Strong communication and project management skills.
- Molding experience is desirable.
- Ability to travel as required.
Join Us! Apply Today.
Salary Range: $157,000 – 167,000/annually
Please note that the salary information is a general guideline only. Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer.
Top Skills
Dfm
Dfss
Excel
Fda Design Control
Fda Qsr
Gdp
Gmp
Iso 13485
Minitab
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The Company
What We Do
Imperative Care is a Silicon Valley-based medical technology company focused on developing the next generation of innovative solutions to address the vast and urgent needs in stroke intervention and peripheral thrombectomy. With a physician-driven approach and a culture of rapid innovation, we are working to improve every aspect of the stroke procedure with the goal of bringing patients the best care possible. We have two 510(k) cleared product platforms, as well as an expansive technology development pipeline. Follow us for updates as we work to change the way stroke is treated.
For important safety and risk information, visit bit.ly/3yWkfEJ.
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