Process Development Engineer I

Reposted 5 Days Ago
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Campbell, CA, USA
In-Office
90K-95K Annually
Entry level
Healthtech • Biotech
The Role
The Process Development Engineer I will optimize and validate processes for medical devices, support cross-functional teams, and ensure manufacturing quality standards.
Summary Generated by Built In
Title: Process Development Engineer I
Location: This position is full time and on-site in Campbell, CA
Why Imperative Care?
Do you want to make a real impact on patients? Imperative Care is changing the way stroke and vascular diseases are treated. As part of our team, you’d be supporting 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 new professional in this field, a Process Development Engineer I will participate in defining, characterizing, optimizing, and validating processes for product development of intravascular medical devices. This role will use basic professional knowledge, critical thinking, and creative problem-solving skills to assist in improving internal equipment, applying engineering principles, conducting process studies, analyzing project data, and documenting equipment/processes.
  • Assist cross-functional teams in designing, characterizing, optimizing, documenting, and controlling all manufacturing processes through the definition and measurement of critical process parameters (CPP) which impact critical quality attributes (CQA) of the product.
  • Participate in Design of Experiments (DOEs) and DMAIC projects to help design, execute, test, analyse, problem-solve and find root cause when evaluating changes/improvements to a process or design.
  • Collaborate effectively and work independently to complete tasks after receiving detailed instructions.
  • Support teams that create process windows, manufacturing control limits, and workmanship standards.
  • Participate in projects to define manufacturable product design specifications and visual standards.
  • Monitor equipment and documentation processes.
  • Build relationships with cross functional teams that develop manufacturing workflows, monitor control plans effectivity and lot history records.
  • Maintain professional knowledge of analytical techniques and engineering principles applications to collect and analyze data and understand the impact and interaction of materials and processes, on process and product outputs.

What You’ll Bring
  • Bachelor’s degree in engineering or related field, and less than 2 years of any other professional experience; or equivalent combination of education and work experience.
  • Professional experience in the medical device industry is preferred.
  • Excellent analytical and statistical skills (SPC, DOEs) using Excel, Minitab &/or JMP.
  • Ability to identify problems, logically and empirically, and associate cause-effect relationships under a variety of perspectives and constraints. 
  • Ability to prioritise and provide creative, effective and practical solutions.
  • Strong communications skills (both written and verbal).
  • Experience in pilot/production line set-up, validation in a controlled environment is preferred.
  • Knowledge of quality systems design to meet governmental regulations such as FDA QSR, ISO 13485, the MDD, and knowledge of relevant standards is desired.
  • Basic knowledge or experience with FDA Design Control procedures and DFSS/DFM tools a plus.
  • Ability to perform computer modelling simulations on material, process & properties a plus.
  • Familiar with GMP, GDP procedures and requirements.

Employee Benefits include a stake in our collective success with stock options, bonus, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.
Salary Range: $90,000 – 95,000 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

Join Us! Imperative Care

The posted salary range reflects compensation for employees based in the local Bay Area market. For candidates hired outside of this geographic area, compensation may vary and be adjusted based on location, local market conditions, and other factors
 

Skills Required

  • Bachelor's degree in engineering or related field
  • Professional experience in the medical device industry
  • Excellent analytical and statistical skills using Excel, Minitab &/or JMP
  • Experience in pilot/production line set-up, validation
  • Knowledge of quality systems design to meet regulations
  • Familiar with GMP, GDP procedures and requirements

Imperative Care Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Imperative Care and has not been reviewed or approved by Imperative Care.

  • Fair & Transparent Compensation Posted salary bands for multiple roles are explicit and compare favorably to U.S. norms in several functions. Publicly listed ranges help anchor expectations and indicate a market‑competitive stance.
  • Equity Value & Accessibility Stock options are consistently included as part of offers and total rewards. Equity is positioned as a meaningful component alongside base pay and, in some roles, bonus.
  • Leave & Time Off Breadth Company materials highlight generous PTO and a parental leave program as standard benefits. Multiple postings reiterate these time‑off elements across roles.

Imperative Care Insights

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The Company
HQ: Campbell, CA
193 Employees
Year Founded: 2015

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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