Drafting Manager
Listed on 2026-01-14
-
Engineering
Manufacturing Engineer, Mechanical Engineer, Quality Engineering
Engineering Drafting Manager
DescriptionThe Engineering Drafting Manager leads the team of engineers and drafters responsible for producing high-quality technical drawings, BOMs, and datasheets to support Sani Sure’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
- Solid Works
- GD&T (ASME Y14.5)
- Injection molded plastic part design
- PLM
- ERP (Syte Line or equivalent)
- Medical device design
- ISO 13485
- Lean manufacturing
- Kaizen methodologies
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 Solid Works and strong understanding of ASME Y14.5 GD&T and design documentation standards
- Proven experience 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; ability to maintain project schedules and visual timelines (e.g., Gantt charts)
- Familiarity with PLM and ERP systems
- 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:
Experience with in 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
Expert Level
Job Type & LocationPermanent position based out of Camarillo, CA.
Pay And BenefitsPay range: $ – $ per year.
Workplace TypeFully onsite position in Camarillo, CA.
Final date to receive applicationsPosition anticipated to close on Jan 23, 2026.
About ActalentActalent is a global leader in engineering and scientific 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.
EqualEmployment Opportunity
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 actalentaccom for other accommodation options.
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