Position : Engineering Intern (Must Pursuing a Bachelor’s degree third year or higher)

Location : San Jose, CA

Duration : 12 Months

Total Hours/week : 40.00

1^st Shift

Client: Medical Device Company

Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)

Work hours: Part Time – 1st Shift (hours within 8 AM to 5 PM) – Flexible

3 Must haves on the resume:

• Pursuing a Bachelor’s degree in Engineering (Electrical, Mechanical, Industrial or Manufacturing);
• Some work experience; Proficient with Personal Computers, Office and Good Written & Verbal Skills

Job Description:

• This is a Temporary Internship Position at client.
• Candidates will be students from local universities who are pursuing an applicable degree.
• This position is expected to implement change, contribute new ideas, and find innovative methods to accomplish goals.
• The Intern will work on assignments under the guidance of staff and provide hands-on support for process improvement and or floor layouts associated with the manufacturing of complex life science instruments. The Intern will need to have the ability to work through adverse situations while building and maintaining good personal relationships.

Essentials functions:

• Provides hands on support for process improvements to the manufacturing assembly and test processes for flow cytometry instrument under the supervision of Staff Manufacturing Engineers or Production Managers.
• Must have the ability to solve problems, and determine root cause of technical issues related to (process, time and motion studies, floor or work cell layout, resources capacity, ergonomics and other related improvements).
• Must be able to implement effective solutions in a timely manner. Issues are typically multi-disciplinary in nature: mechanical, optical, electrical, and fluidic.
• Strives to continuously improve processes in order to achieve optimal efficiency for manufacturing operations.
• Will serve as a member of cross functional project teams.
• Major objectives may include: product cost reduction efforts, designing processes to improve manufacturing operational efficiency, optimize product design, qualify replacement components, improve product quality, improve customer satisfaction, and reduce manufacturing costs.
• Supports the introduction of new products into manufacturing.
• Establishes processes and procedures create assembly documentation.
• Reviews engineering designs and documentation for completeness, clarity and manufacturability.
• Develops and implements production tooling, test fixtures, equipment, and work cell layout.
• Participates in setting labor standards.
• Develops and implements strategies to optimize material and workflow.
• Must be able to develop and maintain good working relationships with internal customers, primarily line level production personnel, other ME's, QA, Planners, Purchasing, R&D and managers.
• Ensures that manufacturing procedures and appropriate levels of process control are in place and meet regulatory GMP's. Brings regulatory compliance questions and issues to the attention of management as necessary.
• Keeps abreast of the basic requirements for compliance in own area of work and complies with those requirements.
• Participates as required in training on regulatory issues affecting own area of work.
• Brings regulatory compliance questions/issues to the attention of management.
• Promotes a safe work environment. Provide recommendations on maintaining the safety of the work environment.
• Participates in Environmental, Health and Safety programs.
• Addresses corrective actions whenever a hazard is identified.
• Notifies manager of all observed hazardous conditions or unsafe work practices.

Minimum Requirements:

• Must be currently pursuing a BS degree in Industrial Engineering (third year or higher) or similar BS degree.
• Must be proficient in the use of personal computers.
• Excellent written and verbal communication skills, must have good interpersonal skills: conflict resolution, negotiation, and the ability work in a team environment

Desirable Qualifications:

• Experience implementing LEAN manufacturing processes
• 6 Sigma green or black belt courses
• Project management courses
• Experience with engineering drawings, Bills of Materials, and operational procedures
• Experience writing and reviewing Engineering Change Orders
• Experience implementing continuous improvement solutions
• Experience developing manufacturing processes, writing procedures, and training assembly personnel
• The ability to assess and resolve problems in a timely manner.
• Familiarity with ISO 13485 standards
• Familiarity of the following applications: Pro-E, AutoCAD, MS Access, SAP ERP, Visio.
• Experience supporting some of the following commodities or supplier types: lasers, optical components, fluidic systems, machined parts, sheet metal, cables, PCA's, plastics, power systems, product packaging, turnkey subcontractors, hardware, labeling, bar code systems GMP familiarity 21 CFR part 820, medical device manufacturing experience