Job Title – Sr. Project Engineer
Location - San Diego, CA
Duration – 12+ Months
Work hours: 8am-5pm, 40 hours/week
Client: Medical Device Company
Job Category: Engineering
Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)
Job Description:
Project engineers are responsible for leading and supporting projects as part of a cross-functional global team. This is a highly collaborative position and requires excellent verbal and written communication skills. Projects will involve requirements remediation, developing test methods, writing test protocols, reports, solving test or design issues, mechanical testing, materials, and other types of mechanical engineering projects. Position will be required to be in the lab and office more than 80% of the time in San Diego, CA.
Job Responsibilities:
• Participate in executing technical and/or cross-functional project work.
• Translate customer needs into design input engineering requirements.
• Engineer robust products through strong understanding and application of engineering fundamentals and DFSS principles.
• Develop and execute test methods which specify measurement equipment, test set-up, measurement systems analysis (MSA), and statistical data analysis.
• Execute design verification testing to confirm design outputs meet design input requirements.
• Write detailed technical reports based on design verification analysis/testing for design changes and product design activities.
• Independently tests, analyzes, and solves technical problems.
• Applies knowledge and skills to a variety of standard activities.
• Works with moderate guidance in own area of knowledge.
Required Qualifications:
• BS – Mechanical Engineering, Materials Engineering or Biomedical Engineering with emphasis on mechanical design and product development. MS preferred.
• Minimum 3 years’ experience as practicing engineer
• SolidWorks or equivalent CAD tool
• Ability to manage multiple projects of varying scopes in parallel
• Ability to work leading or as part of a cross-functional team with members from marketing, sales, clinical, regulatory , medical affairs, quality, manufacturing, etc.
• Experience with medical device design control processes and creating and maintaining design control documentation.
• Ability to work with moderate guidance in own area of knowledge.