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BiVACOR

Develops magnetically levitated total artificial heart

Manufacturing Engineer 3

Manufacturing EngineeringConfirmed live in the last 24 hours
Full-timeHuntington Beach, CA, USA

About the Job

Requirements

  • A Bachelor of Science in Mechanical, Electrical, Biomedical, or Manufacturing Engineering is required; a Master of Science is desirable, or equivalent experience.
  • At least five years of engineering experience, including process development, manufacturing engineering, and industrialization, preferably in the medical-device or another highly regulated industry.
  • Expertise in process characterization, process failure mode and effects analyses (pFMEAs), MVP, IQ/OQ/PQ/PPQ, and test method validations (TMVs).
  • Working knowledge of medical-device quality regulations, practices, and standards, including ISO 13485 and FDA quality system regulations.
  • Working knowledge of industry best practices and applicable standards.
  • Advanced problem-solving skills, with Six Sigma Green or Black Belt expertise.

Responsibilities

  • Design, develop, and improve manufacturing processes to enhance efficiency and product quality.
  • Implement Lean and Six Sigma methodologies to reduce waste and optimize workflows.
  • Implement automation and advanced manufacturing techniques where applicable.
  • Design, procure, and validate equipment, tools, and fixtures for manufacturing processes.
  • Ensure proper calibration and maintenance of manufacturing equipment.
  • Conduct process validations (IQ, OQ, PQ) and ensure compliance with FDA, ISO 13485, and GMP standards.
  • Support nonconformance and corrective and preventive action (NC/CAPA) investigations and implement corrective actions.
  • Create and maintain manufacturing documentation, including bills of materials, work instructions, and process flow charts.
  • Prepare technical reports and documentation for audits and regulatory submissions.
  • Analyze and resolve manufacturing issues, including corrective and preventive actions and non-conformances.
  • Identify opportunities for process improvements and implement solutions to enhance productivity and reduce costs.
  • Work with cross-functional teams, including research and development, Quality Assurance, and Supply Chain, to support product development and manufacturing goals.
  • Provide technical support to production teams and train operators on new processes and equipment.

Desired Qualifications

  • A Master of Science degree is desirable.

About the Company

BiVACOR

Develops magnetically levitated total artificial heart

BiVACOR is a clinical-stage medical device company developing the BiVACOR Total Artificial Heart (TAH) to replace a failing heart. The device is a compact, titanium implant that uses a single magnetically levitated rotor to pump blood to the lungs and the rest of the body, eliminating valves and mechanical bearings to reduce blood damage. It serves as a bridge-to-transplant and aims to become a long-term (permanent) alternative to heart transplantation. BiVACOR operates in the cardiovascular medtech space, pursuing regulatory approval through preclinical and clinical trials, including an FDA Breakthrough Device Designation and an Early Feasibility Study. Its strategy includes expanding from Australia to the US, securing funding, and advancing toward commercialization to address the large unmet need in end-stage heart failure.

Company size
51-200
Company stage
Grant
Total funding
$46.7M
Headquarters
Huntington Beach, CA
Founded
2008

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