Technician
- Siri Info Solutions
31 Days Ago
NA
C2C
Irvine-CA
4-6 Years
Required Skills: EIS : Medical Device & Regulations~Documentation Review & Editing
Job Description
Title: Technician
Location: Irvine, CA
Duration: 6 months
Role Descriptions:
Technician Responsibilities Works under direct supervision and independently to construct perform experiments| research and test activities related to product quality and reliability.
Sets up| operates| and maintains mechanical and electronic laboratory instruments and equipment.
Report and follow up on issues| progress and seek help when needed| document progress.
Cleans and maintains laboratory equipment| tools| glassware| and lab areas.
Maintains laboratory inventory of consumables.
Interfaces with Metrology department and ensure that the calibrated instruments are properly documented and submitted for calibration on time.
Use written material to help troubleshoot issues and perform tasks.
Build test experiments and run test programs.
Certification in soldering| crimping| electronics assembly| ESD| quality or reliability is nice to have.
Experience with environmental temperature and humidity chambers or HALT chambers is a plus.
Experience with Medical devices is a plus.
Document Control Responsibilities Initiate Change Orders (COs)| Manufacturing Change Orders (MCOs)| Change Requests (CRs) in Agile PLM. Create| manage| and maintain document control procedures.
Track and monitor change progress to ensure timely review and approval.
Maintain compliance with company standards| documentation procedures| and regulatory requirements.
Essential Skills:
5070 work to be accomplished as per the requirement below Use of electrical instruments| mechanical equipment| environmental chambers| hand tools| operating systems such as medical devices| Phaco console| Benchtop power supplies| DMM| laptop| cameras| drills. Ability to independently carry out tests in medical devices as per SOP.
Define| implement| and monitor inspection methods and sampling plans. Excellent communication and cross functional coordination abilities. Strong analytical and documentation skills.
Capture test results in test book.5030 work to be accomplished as per the requirement below
Strong working knowledge of Document Control.
Preferred platform Agile PLM. Hands on experience with CO MCO CR processes
Experience in quality or engineering documentation standards (ISO| FDA if applicable).
Develop| document| and implement procedures to increase operational efficiency and quality.
Implement| and maintain quality control systems| manuals| and procedures Analyze identify bottlenecks or inefficiencies and recommend optimizations
Desirable Skills:
Keyword:
Skills: EIS : Medical Device & Regulations~Documentation Review & Editing
Experience Required: 4-6
