Current Opportunities
Manufacturing Quality Engineer II – Validation
This position is responsible for ensuring compliance with regulatory requirements (FDA, ISO, GMP) by developing, executing, and maintaining validation protocols. This position focuses on Equipment Qualification (IQ/OQ/PQ), Process Validation, and Test Method Validation to ensure product quality, reliability, and regulatory compliance. The ideal candidate will have strong technical expertise in medical devices, leadership skills, and the ability to drive continuous improvement in validation processes.
Location: Huntington Beach, CA
Engineer Technician III
The Engineering Technician is a hands-on role responsible for supporting the development, improvement, and scaling of assembly and test processes for a Class III medical device. The Engineering Technician will help bridge design and production by executing validations, maintaining equipment, documenting processes, and supporting pilot and low-volume manufacturing operations.
Location: Huntington Beach, CA
Manufacturing Engineer III – Clean Processes
The Manufacturing Engineer III plays a crucial role in developing, optimizing, and implementing critical cleaning and contamination-control processes for the BiVACOR total artificial heart (TAH). This engineer serves as the company’s subject-matter expert for cleaning process design, driving process robustness, regulatory compliance, and scalability from prototype through commercialization.
Location: Huntington Beach, CA
Manufacturing Technician (Mechanical)
The Manufacturing Technician is a senior hands-on role responsible for the assembly, testing, packaging, and troubleshooting of Class III medical devices in compliance with documented procedures, quality standards, and regulatory requirements (FDA 21 CFR Part 820, ISO 13485, ISO 14644).
This role requires strong technical skills, a quality-first mindset, and the ability to work independently under minimal supervision.
Location: Huntington Beach, CA
Manufacturing Technician (Electrical)
The Manufacturing Technician is a senior hands-on role responsible for the assembly, testing, packaging, and troubleshooting of Class III medical devices in compliance with documented procedures, quality standards, and regulatory requirements (FDA 21 CFR Part 820, ISO 13485, ISO 14644).
This role requires strong technical skills, a quality-first mindset, and the ability to work independently under minimal supervision.
Location: Huntington Beach, CA
Product Builder / Operator
The Product Builder / Operator is responsible for assembling, testing, and packaging medical devices in compliance with documented procedures, quality standards, and regulatory requirements (FDA 21 CFR Part 820, ISO 13485, ISO 14644).
This role plays a critical part in ensuring each device meets exacting standards before it reaches patients.
Location: Huntington Beach, CA
Our Benefits and Perks
Health and Welfare
- Medical Benefits – Numerous HMO and PPO options, several of which have monthly premiums fully employer funded.
- Dental/Vision, Short-term & Long-term Disability also available at low employee cost.
Vacation and PTO
BiVACOR also has very generous vacation and PTO policies. Vacation policy for first year employees is 80 hours per year. Increasing yearly up to 136 hours upon 7th year of employment. In addition to vacation, we also have a PTO policy equaling an additional 80 hours of time off per year.
401(k)
BiVACOR proudly offers both Non-Elective and Elective 401(k) plans.
Our Non-Elective 401(k) is a 4% employer only contribution, made on your behalf each pay period and immediately vested upon 90-day qualification.
Our Elective 401(k)-employer match is up to 6%. That means that for every dollar you contribute to your 401 (k), you will receive a matching dollar-for-dollar contribution in your account up to 6% of your pay.
Incentives
Short-Term and Long-Term Incentives are also part of our current benefit package.

