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Description

The Engineering Drafting Manager leads the team of engineers and drafters responsible for producing high-quality technical drawings, BOMs, and datasheets to support SaniSure’s sales, operations, and customer service functions. This role ensures all drawings are accurate, complete, and released on time while serving as the link between Engineering, Sales Representatives, Customer Service, and Operations. The Engineering Drafting Manager is a highly independent team leader and technical expert, guiding drafters, resolving complex issues, and fostering a proactive, data-driven culture focused on zero errors, fast turnaround, and continuous improvement.

Skills

iso 9001, solidworks, gd&t, injection molded plastic part design, plm, erp, syteline, medical device, ISO 13485, lean manufacturing, kaizen

Top Skills Details

iso 9001,solidworks,gd&t,injection molded plastic part design,plm,erp,syteline

Additional Skills & Qualifications

Bachelor of Science in Mechanical Engineering or related technical field 10+ years of experience in mechanical design or drafting, with at least 4 years in a leadership or supervisory role. Experience in ISO 9001 or higher-tier quality system environments. Expert proficiency in SolidWorks with a strong understanding of ASME Y14.5 GD&T and design documentation standards. Proven experience in creating and reviewing technical drawings for injection-molded and assembled products. Strong understanding of manufacturing methods, material selection, and tolerance stack-ups. Demonstrated success in managing teams to deliver against strict deadlines and quality metrics. Proficient in Microsoft Office tools, including Excel, PowerPoint, and Teams, with the ability to maintain project schedules and visual timelines (e.g., Gantt charts) to track progress and communicate milestones effectively. • Familiarity with PLM and ERP systems (experience with SyteLine or equivalent preferred). • Excellent communication skills with the ability to collaborate across Engineering, Operations, and Customer-facing teams. • Highly independent, detail-oriented, and comfortable working in a fast-paced, cross-functional environment. Preferred Qualifications • Experience within bioprocessing, medical device, or other highly regulated industries. • Working knowledge of ISO 13485 or IATF 16949 requirements. • Prior success leading or contributing to Lean, Kaizen, or process optimization initiatives. • Experience transitioning to a new drafting software package

Experience Level

Expert Level

Job Type & Location

This is a Permanent position based out of Camarillo, CA.

Pay and Benefits

The pay range for this position is $135000.00 - $145000.00/yr.

Internal benefits provided

Workplace Type

This is a fully onsite position in Camarillo,CA.

Application Deadline

This position is anticipated to close on Jan 23, 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 due to a disability, please email [email protected] (%[email protected]) for other accommodation options.