Manufacturing Engineer II, Capital Equipment

Imperative Care$102K — $120K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering or related field with at least 2 years of relevant experience.
  • Knowledge of product testing and data collection techniques.
  • Strong written and verbal communication skills.
  • Familiar with quality systems for regulatory compliance, especially FDA QSR, ISO 13485.
  • Experience in setting up pilot/production lines, ideally in a controlled environment.
  • Understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
  • Ability to operate independently or as part of a team. Project management experience is preferred.

Responsibilities

  • Assist in constructing prototypes for new products and enhancements.
  • Support manufacturing activities to ensure compliance with plans and quality standards.
  • Verify availability of raw materials in coordination with Supply Chain.
  • Develop Manufacturing Process Instructions and documentation with R&D and Quality departments.
  • Conduct time studies to identify and drive process improvements.
  • Coordinate with Quality personnel to resolve production yield issues and implement continuous improvements.
  • Manage project timelines and manufacturing specifications to meet production goals.

Benefits

  • Stock options and performance-based bonuses as part of total compensation.
  • 401k plan to support retirement savings.
  • Comprehensive health benefits for employees and their families.
  • Generous Paid Time Off (PTO) to promote work-life balance.
  • Parental leave program to support employees with families.
  • Emotional health resources to assist with mental well-being.
Full Job Description
Title: Manufacturing Engineer II, Capital
This position is based in our Campbell, California offices. This position is on-site & full-time

What You'll Do
An individual in this role uses strong hands-on experience to execute and deliver assigned projects/products to ensure manufacturability, supporting technology transfer from design to manufacturing and ultimately scalability for commercialization for complex electromechanical capital equipment. This position will complete projects related to in-house manufacturing, manufacturing engineering, and equipment planning/engineering in accordance the company's Quality System and customer requirements.
  • Assist in the construction of prototypes for new products/processes or current product enhancements.
  • Provide support to in-house manufacturing activities to verify products are manufactured in accordance with product plans and quality/regulatory requirements.
  • Work with Supply Chain to verify inventory of raw materials and components are available per the planned build schedule, monitor and be accountable for material issued to production/projects.
  • Develop manufacturing processes and Manufacturing Process Instructions (MPI's) and lot history records (LHR's) or Device History record (DHR's) in collaboration with R&D and Quality
  • Conduct time studies for each manufacturing process and identify process development initiatives
  • Work with Quality personnel to define in-process inspections and testing and resolve quality and yield issues through continuous improvement projects
  • Inform and coordinate with multi-functional operations project team activities from early project conceptualization through clinical testing
  • Complete, maintain, and monitor manufacturing tasks of project schedule, and ensure that critical timelines and/or budgets are established and met
  • Participate in manufacturing team meetings to ensure communication between members
  • Build positive proactive working relationships with team members and other staff members
  • Complete manufacturing specifications for products; coordinate all process validation activities with Quality- IQ/OQ/PQ.
  • Determine tooling and equipment needs for the timely and cost-effective manufacture of products
  • Work with R&D staff to facilitate smooth transition of products into manufacturing while assuring manufacturability, achieving cost targets and conformance with regulatory and Company requirements.
  • Collaborate with suppliers to ensure parts/services are properly documented and meet specifications
  • Review specifications for sub and final assemblies
  • Support manufacturing line and approve DCO's for manufacturing engineering
  • Support the training/certification of the MPI Trainer for manufacturing process instructions; may train other staff as needed
  • Using continuous improvement techniques, work with Quality Assurance to identify and implement programs to drive down cost and improve yield and reliability

What You'll Bring
  • Bachelor's degree in Engineering or related discipline and min 2 years of related experience; or equivalent combination of education and work experience.
  • Knowledge of and exposure to product testing and data collection
  • Excellent communications skills (both written and verbal) required
  • Experience working under quality systems designed to meet governmental regulations such as FDA QSR, ISO 13485, and the MDD
  • Experience in pilot/production line set-up, validation in a controlled environment is preferred.
  • Familiar with GMP, GDP procedures and requirements
  • Ability to work independently or in team setting required
  • Project management experience 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.

Join Us! Apply today.
Salary Range: $ 102,000 - $120,000 / 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.

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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