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Imperative Care Principal Manufacturing Engineer in Campbell, California

Job Title: Principal Manufacturing Engineer

Location : This position is based in our Campbell, California offices. This position is on-site. 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

The Principal Manufacturing Engineer will plan and lead projects focused on development and continuous improvement of neuro-interventional medical device manufacturing processes though definition, characterization, optimization and validation resulting in stable, robust and capable sustained commercialization. In this position, the Principal Manufacturing Engineer will lead teams and/or projects to develop, improve and qualify internal equipment and processes and will oversee management and qualification of processes at external suppliers and contract manufacturers. Responsibilities will include strategic creative problem solving and critical thinking and will oversee the planning and execution of DOEs/process characterization studies, analysis, interpretation, and documenting and reporting of data.

  • Lead collaborative efforts to research, define and develop new manufacturing processes and improve existing processes.

  • Individually or collaboratively initiate and contribute to manufacturing process innovation by identifying and selecting new process technologies.

  • Lead aspects/individuals to develop, document and qualify new or improve existing equipment and fixturing.

  • Lead teams in the identification of continuous improvement opportunities, including quantifying opportunity investment cost/ROI.

  • Lead tasks to develop process windows, manufacturing control limits and workmanship standards.

  • Lead projects to define manufacturable product design specifications and visual standards.

  • Lead and mentor the design, execution, test, analysis and interpretation of results from DOEs.

  • Lead and mentor DMAIC principles to make data-driven decisions, solve problems and find root cause.

  • Lead or oversee equipment & process documentation architecture.

  • Collaborate with cross functional teams to develop manufacturing systems and architecture to facilitate efficient workflows, effectivity monitoring control plans, lot history records.

  • Lead cross-functional team members to design, characterize, optimize, document, and control all manufacturing processes through the definition and measurement of critical process parameters (CPP) which impact critical quality attributes (CQA) of the product.

  • Lead and teach analytical techniques and apply engineering principles to understand the impact and interaction of materials and processes on process and product outputs.

  • Provide technical subject matter expertise and oversee management and partnerships with external suppliers by executing due diligence assessments, setting specifications for critical quality and/or manufacturing attributes (CQA, CMA) for materials and components, collaborate on development projects and qualification/validate external processes.

    What You’ll Bring

  • BS in Engineering or related discipline and 12+ years of related experience; or MS in Engineering with 8+ years of related experience; or  equivalent combination of education and work experience in the medical device or related regulated industry

  • Able to perform/oversee computer modeling simulations to determine the effects of design, materials and process on the functional and reliability performance of the final product preferred. 

  • Experience in pilot and production line set-up, validation and scale-up in a controlled environment.

  • Excellent analytical and statistical skills (SPC, DOEs) using Excel, Minitab &/or JMP.

  • Excellent knowledge and experience in FDA Design Control procedures and DFSS/DFM tools.

  • Excellent project management and communications skills (both written and verbal). Agile scrum framework preferred.

  • Exceptional critical thinking – able to intuitively identify problems, logically and empirically associate cause and effect, and under a variety of perspectives and constraints, prioritize and provide creative, effective and practical solutions. 

  • Excellent working knowledge and application of DMAIC methodology. Six Sigma Black Belt preferred.

  • 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.

  • Ability to work independently or in a team setting and mentor/manage.

  • Ability to travel – as required.

    Employee Benefits include a stake in our collective success with stock options, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.

    Salary Range:

$174,000 – 181,000 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.  As part of our total rewards package, Imperative Care offers comprehensive benefits including a 401k plan, health benefits, generous PTO, a parental leave program and emotional health resources.

Join Us! Imperative Care (https://imperativecare.com/careers/)

 

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