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Mechanical Engineer

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Actalent

Irvine, CA (In Person)

$109,200 Salary, Full-Time

Posted 2 days ago (Updated 12 hours ago) • Actively hiring

Expires 6/13/2026

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Job Description

Mechanical Engineer Position Overview This role combines mechanical product design with hands-on verification and validation (V&V) testing within a regulated environment. The Mechanical Engineer is responsible for developing, documenting, and supporting mechanical designs while contributing to laboratory-based testing to ensure product performance, quality, and regulatory compliance. Working under general supervision, this individual will collaborate cross-functionally with Engineering, Quality, Operations, and external suppliers to deliver robust, cost-effective, and high-quality products that meet stringent industry standards. Key ResponsibilitiesMechanical Design & Development + Design and develop mechanical components and assemblies for new and existing products using SolidWorks + Create comprehensive engineering documentation, including: + Part drawings + Assembly drawings + Bills of Materials (BOMs) + Purchasing specifications + Apply knowledge of materials and manufacturing processes (e.g., plastics, sheet metal, gaskets, cables) + Generate and manage Engineering Change Orders (ECOs) to support design control and product release + Participate in design reviews and support prototype development with suppliers Verification & Validation (V&V) Testing + Develop, execute, and support V&V test protocols for new and existing designs + Set up and operate laboratory equipment and test fixtures + Conduct product testing and system validation using established methodologies + Collect, analyze, and document test data in accordance with regulated processes + Perform basic statistical analysis and present findings to engineering teams Documentation & Compliance + Author test reports, technical documentation, and validation summaries + Ensure compliance with Good Documentation Practices (GDP) and quality system requirements + Maintain accurate and traceable records for audits, inspections, and regulatory submissions Collaboration & Communication + Partner with cross-functional teams (Engineering, Quality, Operations, and Suppliers) to ensure design robustness and manufacturability + Present design concepts, test results, and technical findings in formal reviews + Support supplier engagement for prototyping and component validation + Provide regular updates on project progress and key deliverables Lab & Process Support + Maintain lab equipment, calibration records, and organization + Support internal and external audits by ensuring complete and compliant documentation + Contribute to continuous improvement of testing methods and development processes Required Qualifications + Bachelor's degree in Mechanical Engineering or related engineering/science field + 1-3 years of relevant experience in engineering or product development + Proficiency in SolidWorks for part modeling and drawing creation + Experience with verification and validation testing concepts + Strong technical documentation and communication skills + Ability to work within structured processes in a regulated environment Preferred Qualifications + Experience in regulated industries such as medical devices, aerospace, or automotive + Familiarity with: + Injection molding and sheet metal design + Laboratory testing methods and equipment + Statistical tools (e.g., Minitab) + Understanding of design controls and product lifecycle management Key Skills & Attributes + Strong attention to detail and organizational skills + Problem-solving mindset with creativity in design solutions + Ability to work both independently and collaboratively + Effective written and verbal communication skills + Hands-on approach with a balance of design and testing responsibilities Company Overview The organization is a global leader in advanced medical technologies focused on improving outcomes for patients in critical and acute care environments. Its portfolio includes innovative devices, software, and integrated solutions designed to support the diagnosis and treatment of serious cardiopulmonary and respiratory conditions. Serving healthcare providers across hospitals, emergency medical services, public safety agencies, and military environments worldwide, the company is driven by a mission to deliver life-saving technologies with precision, reliability, and clinical impact. With a strong emphasis on research and development, employees work at the intersection of engineering innovation and patient care. The culture promotes collaboration, continuous improvement, and a shared commitment to making a meaningful difference in people's lives. This is an environment where individuals can grow their careers while contributing to technologies that directly impact patient survival and recovery. Job Type & Location This is a Contract position based out of Irvine, CA. Pay and Benefits The pay range for this position is $40.00 - $65.00/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 May 20, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
San Francisco Fair Chance Ordinance:
Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector:
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.

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