Process Development Engineer II

Posted 11 Days Ago
Be an Early Applicant
Campbell, CA
In-Office
95K-106K Annually
Mid level
Healthtech • Biotech
The Role
The Process Development Engineer II supports product development for neuro-interventional medical devices by optimizing and validating manufacturing processes and collaborating with cross-functional teams.
Summary Generated by Built In
Title: Process Development Engineer II
Location: This position is based in our Campbell, California office. This position is full time and on site
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
 A developing professional in this position will provide input to product development projects related to defining, characterizing, optimizing, and validating stable, robust, and capable processes for neuro-interventional medical devices. This position will analyze and identify opportunities for the improvement of internal equipment and processes. This role uses prior experience, learned engineering principles, critical thinking and creative problem-solving skills to evaluate processes and equipment performance.
  • Collaborate with cross-functional teams to define, characterize, optimize, validate, document, and control manufacturing processes by identifying and measuring critical process parameters (CPP) that impact critical quality attributes (CQA) of a product.
  • Perform process characterization studies to validate, improve, or establish processes or equipment to deliver a quality product consistently.
  • Collect, analyze and interpret data to document equipment performance and process outputs.
  • Define, develop, and qualify new equipment/fixtures or improve existing equipment/ fixtures.
  • May participate in innovating, identifying, and selecting new process technologies.

What You’ll Bring
Excellent analytical and statistical skills (SPC, DOEs) using Excel, Minitab &/or JMP with strong ability to prioritize and provide creative, effective and practical solutions.
  • Exceptional critical thinking skills with strong ability to intuitively identify problems, logically and empirically, and associate cause and effect under a variety of perspectives and constraints.
  • Experience working under quality systems designed to meet governmental regulations such as FDA QSR, ISO 13485, the MDD, and knowledge of relevant standards.
  • Familiar with GMP, GDP procedures and requirements.
  • Excellent project management and communications skills (both written and verbal).
  • Ability to complete routine tasks independently and contribute to initiatives in a team setting.
  • Professional experience in the medical device or related regulated industry is preferred.
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: $95,000 – 106,000/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
 

Top Skills

Excel
Fda Qsr
Iso 13485
Jmp
Minitab
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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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