Job Details

****3 Month contract****

SUMMARY OF POSITION:

The CAD Drafter is part of the Research and Development team working on the design of a Medical Device and is responsible for detailed design and development of design documentation in compliance with quality system requirements. The CAD Drafter must be proficient with AutoCAD and SolidWorks.

JOB RESPONSIBILITIES:

• Contributes to engineering efforts to meet strategic objectives.
• Designs and models Medical Device components and assemblies.
• Uses established CAD standards to prepare electronic drawings from marked-up plans and/or verbal instruction by Engineers, Designers, or Manager.
• Interacts with Oracle Agile PLM document vault and other document vault products.
• Organizes workload to accomplish project goals within established timelines.
• Coordinates and communicates with Engineers and other R&D team members.

JOB SPECIFICATIONS:

• Proficient with 3D & 2D CAD (AutoCAD, SolidWorks), GD&T.
• Minimum 2 years of experience producing Mechanical and/or Electrical design documentation.
• Effective verbal and written communication skills.
• Proficient with Microsoft Office software: Word, Excel, and Outlook
• Experience in medical product development and commercialization, or in an ISO or similarly regulated and design-controlled, quality-system driven environment, desired.
• Physical demand/ Work Environment:
• The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk or hear, stand and walk. The employee is frequently required to sit in a stationary position for extended periods.
• Specific visual acuity required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. The employee is required to perform activities such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving small parts; using measurement devices; and/or assembly or inspection of parts at distances close to the eyes.
• This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, and photocopiers.

ACCOUNTABILITIES:

• Meet deadlines on multiple concurrent projects.
• Understand and comply with applicable medical device quality regulations (ISO, FDA) and Company operating procedures, processes, and policies.

RELATIONSHIPS:

• Reports to Manager, R&D Mechanical Engineering.
• Takes direction from Manager or R&D Engineers.
• Works closely with a broad range of team member disciplines and experience levels.