Staff Supplier Quality Engineer

Imperative Care$150K — $167K *
Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • BS in Engineering or related discipline with 8+ years of supplier quality experience, or MS in Engineering with 6+ years in a related field; or equivalent experience in medical devices.
  • Experience with catheters, endovascular, or neurological devices is mandatory.
  • Proven ability to manage multiple tasks with precision and timeliness.
  • Experience in leading corrective action processes for suppliers (CAPAs, NCMR/NCRs, SCARs).
  • Strong understanding of FDA 21 CFR Part 820, ISO 13485, ISO 14971, and good manufacturing practices.
  • Excellent written and verbal communication skills, capable of clear technical documentation.

Responsibilities

  • Provide Supplier Quality Engineering support for medical device development and manufacture.
  • Ensure compliance with quality assurance standards and regulatory guidelines such as ISO 13485 and FDA regulations.
  • Collaborate with suppliers to establish robust materials, products, and processes.
  • Implement supplier change management processes to oversee material qualifications and change notifications.
  • Analyze and monitor supplier performance metrics for quality issues and risk management.
  • Drive supplier quality audits and facilitate the development of quality risk management processes.
  • Lead and execute Supplier Quality projects with minimal supervision.

Benefits

  • Stock options and competitive salaries that reward collective success.
  • 401k retirement savings plan with company contributions.
  • Comprehensive health benefits package including medical, dental, and vision.
  • Generous paid time off (PTO) policy.
  • Parental leave program to support family needs.
Full Job Description
Title: Staff Supplier Quality Engineer
This position is based in our Campbell, California offices. This position is on-site, full-time.

What You'll Do
Provide Supplier Quality Engineering support in the development, manufacture, and distribution of Imperative Care's medical device products consistent with the Company's Quality Policy and Quality Objectives. Establish and maintain quality assurance standards that adhere to ISO 13485, FDA and other governmental regulations.
  • Collaborate with suppliers and business partners to ensure robust materials, products, processes, and systems.
  • Implement supplier change management process including change notification, dissemination of information, impact assessment, approval of changes, and supports material/supplier qualifications.
  • Lead component qualification change projects in collaboration with key business partners and the supplier's applicable functional groups.
  • Manage and raise supplier issues when intervention or a change at a supplier.
  • Monitor and analyze supplier performance metrics, identify areas of opportunity, communicate supplier risks, and drive the resolution of supplier quality issues and risk control processes.
  • Support internal and supplier related NCMR and CAPA. Drive corrective actions for supplier process by assisting suppliers to true root cause analysis and CAPA
  • Plan, conduct, report and follow-up on supplier quality system audits
  • Drive and execute supplier quality agreements
  • Partner with Procurement, R&D, Operations, and Suppliers in the timely investigation, resolution/prevention of supplier-related issues to minimize/prevent business disruptions.
  • Own, drive, and lead the assigned Supplier Quality related projects, activities, initiatives with limited supervision.
  • Apply Project Management methodologies to plan, organize, connect, shape, lead, and deliver results for supplier quality management (SQM) projects.
  • Apply analytical and problem-solving skills to develop and optimize supplier performance.
  • Analyze quality data and identify trends impacting risk benefits requirements of product and quality systems for external suppliers. Lead discussions to drive resolution.
  • Develop/implement Quality Risk Management process for supplier-related matters with partnerships of subject-matter-experts (SME)
  • Responsible for presenting supplier-related issues or opportunities to next management level

What You'll Bring:
  • BS in Engineering or related discipline and 8+ years of supplier quality experience; or MS in Engineering with 6+ years of related experience; or equivalent combination of education and work experience in the medical device or related regulated industry Lead development and validation of test methods to comply with recognized standards
  • Must have experience with catheters, endovascular or neurological devices
  • Must have demonstrated ability to perform multiple tasks concurrently with accuracy
  • Experience leading supplier or process issues (CAPAs, NCMR/NCRs, SCARs, etc.)
  • Must have strong knowledge of quality system requirements (FDA 21 CFR Part 820, ISO 13485), risk management standards (ISO 14971) and good manufacturing practices
  • Excellent communications skills (both written and verbal)
  • Must be able to provide thorough and meticulous review of documents
  • Must be able to write clear, concise, and well thought out technical documentation.
  • Proficiency with Microsoft Office products
  • Ability to communicate effectively, both orally and in writing, with all organizational levels
  • Strong attention to detail and ability to function in a fast-paced dynamic environment

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! Imperative Care
Salary Range: $150,000 - 167,000
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.

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.

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.

About Imperative Care

Imperative Care is a medical device company that develops and commercializes devices for the treatment of ischemic stroke. The company was founded in 2016 by Fred Khosravi and Vikram Janardhan. Imperative Care's flagship product is the Zoom Aspiration System, which is used to remove blood clots from the brain during a stroke. The company's mission is to improve patient outcomes and reduce the burden of stroke on healthcare systems. Imperative Care has raised over $85 million in funding from investors such as Ascension Ventures, Bain Capital Life Sciences, and Rock Springs Capital.
Learn more about Imperative Care
Size
50 employees
Industry
Net Income
-$2 million
Founded
2016
5 Year Trend
+60%
Revenue
$10 million

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