Position : Engineering Intern (Must Pursuing a Bachelors degree third year or higher)
Location : San Jose CA
Duration : 12 Months
Total Hours/week : 40.00
1st 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 Bachelors 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 handson 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 multidisciplinary 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 MEs QA Planners Purchasing R&D and managers.
- Ensures that manufacturing procedures and appropriate levels of process control are in place and meet regulatory GMPs. 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: ProE 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 PCAs plastics power systems product packaging turnkey subcontractors hardware labeling bar code systems GMP familiarity 21 CFR part 820 medical device manufacturing experience
Required Experience:
Intern