Mechanical Drafter

About the role

The Mechanical Drafter/Designer plays a key role in supporting engineering change activities for ongoing product rebranding initiatives within a regulated medical device environment. This is a documentation-driven position that requires strong hands-on proficiency in SolidWorks, disciplined execution of engineering change orders (ECOs/CEOs), and a high level of attention to detail.

Responsibilities

• Generate, manage, and release engineering change orders (ECOs/CEOs) from initiation through final approval.
• Update and modify existing SolidWorks models and production drawings to support product rebranding initiatives.
• Execute detailed design updates, including:
• Geometry and layout modifications
• Placement, centering, and orientation of lettering and logos
• Shape changes
• Color, labeling, and branding updates
• Apply appropriate mechanical tolerances and GD&T in manufacturing drawings.
• Ensure all design changes follow formal design control and change management processes.
• Maintain accurate revision control, documentation integrity, and compliance with internal standards.
• Prepare and route design updates through internal review, approval, and release workflows.
• Collaborate closely with mechanical engineers, quality, regulatory, and other cross-functional stakeholders to ensure timely and accurate implementation of changes.
• Support ongoing documentation cleanup and consistency efforts as part of broader rebranding and portfolio integration activities.

Requirements

• 3–5 years of experience working as a Mechanical Drafting/Design.
• Strong proficiency with SolidWorks, including model and drawing updates.
• Demonstrated experience executing and managing engineering change orders (ECOs).
• Working knowledge of mechanical tolerances and GD&T for manufacturing environments.
• Proven ability to work with detailed documentation and maintain accuracy under change-driven workloads.
• Strong organizational skills and attention to detail.
• Able to collaborate effectively in cross-functional teams and follow structured release processes.

Preferred Qualifications

• Experience in the medical device industry or other regulated environments.
• Exposure to Oracle PLM or similar PLM/ERP systems.
• Familiarity with formal design controls, configuration management, and document release workflows.
• Experience supporting product updates related to branding, labeling, or cosmetic design changes.
• Able to manage multiple change orders concurrently while meeting deadlines.

Work Environment

This role is based at a medical device research and development site supporting ventilator hardware and related systems. The position may initially require 100% onsite work to support close collaboration with engineering, documentation, and quality teams. The environment is structured and compliance-focused, emphasizing traceability, change control discipline, and documentation accuracy. Work is primarily desk-based, centered on CAD modeling, drawing updates, and coordination of engineering change activities within formal release systems.

About the Company

This organization is a global medical technology leader dedicated to developing and manufacturing life-sustaining devices used in critical and emergency care environments. With decades of experience delivering high-reliability medical products, the company is widely recognized for its engineering excellence, commitment to quality, and focus on patient safety. Its ventilator and critical care platforms are used by healthcare providers worldwide, supporting patients in high-acuity settings where performance and reliability are essential. The organization operates within a highly regulated framework and maintains rigorous design controls to ensure consistent, compliant product delivery. Employees work in a collaborative environment that values precision, accountability, and continuous improvement, with opportunities to contribute directly to products that play a vital role in saving lives.

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 - $45.00/hr. Requirements 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 Jul 21, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service. 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.