Sr Process Development Engineer

Job Title: Sr Process Development Engineer
Location
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
This position will participate in product development projects defining, characterizing, optimizing, and validating stable, robust, and capable processes for neuro-interventional medical devices. They will participate/lead improvement and development of internal equipment and processes and may participate in qualification of processes at external suppliers/contract manufacturers. Responsibilities will include creative problem solving, strategic critical thinking, application of engineering principles to design process characterization studies, analyzing, interpretation and documenting/reporting data, and documenting equipment/processes.

• Work collaboratively but act autonomously to develop new processes and improve existing processes and may participate in innovating, identifying, and selecting new process technologies.
• Will work on/lead defining, developing, and qualifying new equipment/fixturing or improving existing equipment/ fixturing.
• Will participate/lead in various stages of process design including definition, selection, characterization, optimization, and validation.
• Will work/lead project teams to develop process windows, manufacturing control limits &workmanship standards and will define manufacturable product design specifications and visual standards.
• Will participate/lead in the design, execution, test, and analysis of results from DOE's and will plan and apply DMAIC principles to make data-driven decisions
• Will collaborate with 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.

What You’ll Bring

• BS in Engineering or related discipline and 5+ years of related experience; or MS in Engineering with 3+ years of related experience; or equivalent combination of education and work experience in the medical device or related regulated industry. Able to perform computer modelling simulations on material, process & properties a plus.
• 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.
• Exceptional critical thinking – able to intuitively identify problems, logically and empirically associate cause and effect, and under a variety of perspectives and constraints, prioritise and provide creative, effective, and practical solutions.

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.
Join Us! Apply Today.
Salary Range: $119,000 – 130,000 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.