Help Us Build the Future of the Human Heart.
At BiVACOR, we’re developing the world’s most advanced total artificial heart, a technology capable of saving millions of lives around the world. We’re a team united by purpose, working on something truly unprecedented. Every part you track down, every work order you keep moving, and every schedule you protect plays a direct role in giving patients another shot at life. If that’s the kind of work that gets you out of bed in the morning, we think you belong here.
About the Role
The Manufacturing Engineer III plays a crucial role in developing, optimizing, and implementing efficient and scalable manufacturing processes for the BiVACOR total artificial heart (TAH). This position focuses on integrating value engineering principles, ensuring high-quality, cost-effective manufacturing while maintaining regulatory and performance standards for implantable components.
The Manufacturing Engineer III collaborates with engineering teams, management, and external vendors to improve tooling and component quality, evaluate cost-reduction strategies, and implement process improvements that enhance the long-term viability and manufacturability of the device. The role involves testing, troubleshooting, and optimizing production processes to ensure product conforms to specifications.
Key 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 NC/CAPA investigations and implement corrective actions.
Create and maintain manufacturing documentation, including BOMs, work instructions, and process flow charts.
Prepare technical reports and documentation for audits and regulatory submissions.
Analyze and resolve manufacturing issues, including CAPAs and non-conformances.
Identify opportunities for process improvements and implement solutions to enhance productivity and reduce costs.
Work closely with cross-functional teams, including R&D, 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.
What You Bring
BS in Mechanical, Electrical, Biomedical or Manufacturing Engineering, MS desirable (or equivalent)
5+ years engineering experience including skills in process development, Manufacturing Engineering and industrialization preferably in the medical device industry or other highly regulated industry
Expert in process characterization, pFMEAs, MVP, IQ / OQ / PQ / PPQ, and TMVs.
A working knowledge of medical device quality regulations, practices and quality standards, such as ISO 13485 and FDA quality system regulations.
Working knowledge of industry best practices and applicable standards.
Advanced problem-solving (Six Sigma Green / Black Belt)
What We Offer
BiVACOR offers a competitive compensation package and comprehensive benefits, including:
401(k) with company matching
Medical, dental, and vision insurance
Health Savings Account (HSA) & Flexible Spending Account (FSA)
Life insurance & Employee Assistance Program
Generous paid time off
This role is based on-site at BiVACOR’s Huntington Beach headquarters. The expected salary range for this position is $120,000 to $127,000. Actual compensation will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Relocation benefits are not available for this posting.
Apply today and be part of something extraordinary.
BiVACOR is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Skills Required
- BS in Mechanical, Electrical, Biomedical or Manufacturing Engineering (or equivalent)
- MS degree
- 5+ years engineering experience in process development, manufacturing engineering, and industrialization (preferably medical device or highly regulated industry)
- Expertise in process characterization, pFMEAs, MVP, IQ/OQ/PQ/PPQ, and TMVs
- Working knowledge of ISO 13485 and FDA quality system regulations
- Knowledge of GMP and industry best practices/standards
- Advanced problem-solving skills; Six Sigma Green/Black Belt
- Experience implementing Lean methodologies and automation/advanced manufacturing techniques
- Experience with design, procurement, validation of manufacturing equipment, tools, and fixtures
- Experience supporting NC/CAPA investigations and implementing corrective actions
- Ability to create and maintain manufacturing documentation including BOMs, work instructions, and process flow charts
What We Do
BiVACOR is a clinical-stage medical device company pioneering the development of a long-term therapy for patients with biventricular heart failure, aiming to provide life-extending solutions for end-stage heart failure.
