Process Development Engineer II
Imperative Care
2w ago
Neurology
From $95K/yr(estimated)
Description
<span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><b><span style="font-size:12pt;"><span style="line-height:115%;"><span style="font-family:Roboto;">Title: Process Development Engineer II </span></span></span></b></span></span></span><br><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><b><i><span style="font-size:10pt;"><span style="line-height:115%;"><span style="font-family:Roboto;">Location</span></span></span></i></b><i><span style="font-size:10pt;"><span style="line-height:115%;"><span style="font-family:Roboto;">: This position is based in our Campbell, California office. This position is full time and on site</span></span></span></i></span></span></span><br><br><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><b><span style="font-size:12pt;"><span style="line-height:115%;"><span style="font-family:Roboto;"><span style="color:#ed7d31;">Why Imperative Care?</span></span></span></span></b></span></span></span><br><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><span style="font-family:Roboto;">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</span></span></span></span><br><br><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><b><span style="font-size:12pt;"><span style="line-height:115%;"><span style="font-family:Roboto;"><span style="color:#ed7d31;">What You’ll Do</span></span></span></span></b></span></span></span><br><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><span style="font-family:Roboto;"> 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. </span></span></span></span><ul><li style="margin-right:49px;margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">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. </span></span></span></span></li><li style="margin-right:49px;margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">Perform process characterization studies to validate, improve, or establish processes or equipment to deliver a quality product consistently. </span></span></span></span></li><li style="margin-right:49px;margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">Collect, analyze and interpret data to document equipment performance and process outputs. </span></span></span></span></li><li style="margin-right:49px;margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">Define, develop, and qualify new equipment/fixtures or improve existing equipment/ fixtures. </span></span></span></span></li><li style="margin-right:49px;margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">May participate in innovating, identifying, and selecting new process technologies. </span></span></span></span></li></ul><br><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><b><span style="font-size:12pt;"><span style="line-height:115%;"><span style="font-family:Roboto;"><span style="color:#ed7d31;">What You’ll Bring</span></span></span></span></b></span></span></span><br><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><span style="font-family:Roboto;">Excellent analytical and statistical skills (SPC, DOEs) using Excel, Minitab &/or JMP with strong ability to prioritize and provide creative, effective and practical solutions. </span></span></span></span><ul><li style="margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">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. </span></span></span></span></li><li style="margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">Experience working under quality systems designed to meet governmental regulations such as FDA QSR, ISO 13485, the MDD, and knowledge of relevant standards. </span></span></span></span></li><li style="margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">Familiar with GMP, GDP procedures and requirements. </span></span></span></span></li><li style="margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">Excellent project management and communications skills (both written and verbal). </span></span></span></span></li><li style="margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">Ability to complete routine tasks independently and contribute to initiatives in a team setting. </span></span></span></span></li><li style="margin-left:8px;"><span style="font-size:12pt;"><span style="font-family:'Times New Roman', serif;"><span style="font-size:11pt;"><span style="font-family:Roboto;">Professional experience in the medical device or related regulated industry is preferred. </span></span></span></span></li></ul><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><b><span style="font-family:Roboto;"><span style="color:#ed8b00;">Employee Benefits</span></span></b> <span style="font-family:Roboto;">include </span><span style="font-family:Roboto;">a stake in our collective success with stock options, bonus, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.</span></span></span></span><br><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><b><span style="font-family:Roboto;"><span style="color:#ed8b00;">Salary Range:</span></span></b><span style="font-family:Roboto;"> $95,000 – 106,000/annually </span></span></span></span><br><br><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><span style="font-family:Roboto;">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</span></span></span></span><br><br><span style="font-size:11pt;"><span style="line-height:115%;"><span style="font-family:Calibri, sans-serif;"><b><span style="font-size:10pt;"><span style="line-height:115%;"><span style="font-family:Roboto;">Join Us! </span></span></span></b><a href="https://imperativecare.com/careers/" style="color:#0000FF;text-decoration:underline;"><b><span style="font-size:10pt;"><span style="line-height:115%;"><span style="font-family:Roboto;"><span style="color:#ed7d31;">Imperative Care</span></span></span></span></b></a></span></span></span><br><br> <p>The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.</p>
<p>Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.</p>
Imperative Care
MEDICAL DEVICES
Large Diameter Catheters for stroke care
LocationCA - Campbell
Open Jobs33
NeurologyCardiovascular
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