Mechanical Engineer

Mechanical Engineer I – Ventilation R&D

As a Mechanical Engineer I on the Ventilation Research & Development team, you will contribute to the design and development of next-generation mechanical and electro-mechanical systems used in critical care ventilation and life-support products. This role focuses on hands-on mechanical design, analysis, and testing, working closely with a multidisciplinary team to ensure products meet performance, reliability, manufacturability, and regulatory requirements.

You will support both new product development and enhancements to existing systems, contributing to life-saving technologies used in hospitals and emergency care settings worldwide. While the role is primarily technical, it may include limited project coordination responsibilities within larger development programs.

This organization is a global leader in the development of innovative medical technologies dedicated to improving outcomes for patients facing critical cardiopulmonary and respiratory challenges. Its portfolio includes advanced life-support, ventilation, monitoring, and therapeutic solutions used by clinicians, emergency responders, and healthcare professionals around the world. The company operates in a highly regulated environment and is deeply committed to engineering rigor, product quality, and patient safety, with a strong mission-driven culture focused on saving lives and improving care.

Key Responsibilities

• Design and develop mechanical parts, assemblies, and enclosures for ventilation systems and related sub-systems.
• Perform engineering analyses including mechanics, tolerance analysis, thermal analysis, and fluid mechanics / fluid dynamics to support system performance and reliability.
• Support airflow management, pressure regulation, thermal control, ingress protection, EMI isolation, and shock/vibration mitigation to meet defined product requirements.
• Refine designs to meet Design for Manufacturability (DFM) and Design for Assembly (DFA) objectives.
• Create and maintain detailed engineering documentation, including: part and assembly drawings, Bills of Materials (BOMs), technical specifications and procurement documentation.
• Generate and manage Engineering Change Orders (ECOs) in compliance with the Quality Management System.
• Support preparation of documentation for design verification, validation, and regulatory submissions.
• Contribute to risk assessments, hazard analyses, and FMEA activities in support of the Design History File.
• Participate in technical design reviews and present concepts, designs, and trade studies to internal stakeholders.
• Interface with suppliers to communicate design intent, review prototypes, and evaluate production samples.
• Conduct part-level, subsystem-level, and system-level verification and validation testing and document results.
• Plan and execute laboratory testing, including Design of Experiments (DOE), for both new and legacy products.
• Provide technical input to project planning, including schedules, budgets, and progress reporting.

Essential Skills

• Proficiency in SolidWorks, including part design, assemblies, drawings, PDM, and simulation tools.
• Strong understanding of mechanical design principles, including fluid mechanics and fluid dynamics as applied to airflow, pressure control, and thermal management.
• Working knowledge of engineering drawings per ASME Y14.5-2009 (GD&T).
• Experience designing and packaging components for embedded or electro-mechanical systems.
• Excellent written and verbal communication skills, with the ability to clearly document and present technical information.
• Self-directed, detail-oriented, and capable of working effectively with minimal supervision.
• Demonstrated commitment to continuous learning and professional development.

Additional Skills & Qualifications

• Bachelor of Science in Mechanical Engineering required.
• 1–3 years of mechanical engineering and product design experience (minimum of 1 year with a Master's degree).
• Experience in the medical device industry or other highly regulated environments is strongly preferred.
• Familiarity with IEC standards and regulatory design controls is a plus.
• Exposure to lab testing, validation protocols, and quality systems is beneficial.

Work Environment

This role operates in a collaborative, cross-functional R&D environment alongside mechanical, electrical, software, and systems engineers, as well as scientists and quality professionals. The position involves a balance of desktop design work, hands-on prototyping, and laboratory testing. Engineers are expected to adhere to rigorous quality and regulatory standards while developing reliable, high-performance solutions for critical care and life-support applications.

Job Type & Location: This is a Contract position based out of Irvine, CA.

Pay and Benefits: The pay range for this position is $35.00 - $38.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision; Critical Illness, Accident, and Hospital; 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available; Life Insurance (Voluntary Life & AD&D for the employee and dependents); Short and long-term disability; Health Spending Account (HSA); Transportation benefits; Employee Assistance Program; Time Off/Leave (PTO, Vacation or Sick Leave).

Workplace Type: This is a fully onsite position in Irvine, CA.

Application Deadline: This position is anticipated to close on Apr 22, 2026.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

Actalent is an equal opportunity employer.

About Actalent

Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day.

Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.