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Engr Mechanical

  • ... Posted on: Oct 30, 2025
  • ... MillenniumSoft Inc
  • ... Temecula, California
  • ... Salary: Not Available
  • ... Full-time

Engr Mechanical   

Job Title :

Engr Mechanical

Job Type :

Full-time

Job Location :

Temecula California United States

Remote :

No

Jobcon Logo Job Description :

Position : Mechanical Product Test Engineer I Entry Level (Lab, Medical Device & Pharma Industry Exp)

Location : Temecula, CA

Duration : 6 Months

Total Hours/week : 40.00

1st Shift

Client : Medical Devices Company

Job Category : Engineering

Level of Experience : Entry Level

Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT

Work schedule hours 8:00 a.m. to 5:00 p.m

Job Description:

  • Candidate must have previous LAB experience, whether in college or previous work experience. Please ensure that on the work history portion of the resume, clearly states internship or coop experience. Please submit candidates with previous engineering or science related degrees.

Role Summary:

  • The Combination Product Test Engineer is responsible for executing testing activities accurately and on time, in alignment with project scopes and client requirements.
  • Tasks include sample handling, testing, data analysis, documentation, and equipment use within a laboratory setting.

Key Responsibilities:

  • Receive, label, store, and ship samples; manage sample disposition and hazardous waste.
  • Perform product and equipment testing per protocols, methods, and schedules.
  • Analyze data using tools like Excel, JMP, and Minitab; draft and review reports.
  • Maintain lab supplies and cleanliness; ensure organized storage areas.
  • Follow SOPs and quality systems; report and investigate quality events (e.g., OOS, deviations).
  • Support documentation (e.g., protocols, reports, equipment logs) under supervision.
  • Communicate effectively with team members and clients; escalate issues promptly.
  • Collaborate respectfully and contribute to continuous improvement.
  • Perform other duties as assigned.

Qualifications:

  • Associate's degree with 0 2 years of relevant experience (lab services, medical device, IVD, pharma). REQUIRED.
  • Familiarity with GLP, cGMP, ISO, ASTM standards is a plus.
  • Strong attention to detail, multitasking ability, and communication skills.
  • Proficiency in Excel and data analysis tools. REQUIRED.

Jobcon Logo Position Details

Posted:

Oct 30, 2025

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-CIE-6d7a8b105321204c697003faa156398ed5d6ae95db85e163e7d25f6fb9e32c9c

City:

Temecula

Job Origin:

CIEPAL_ORGANIC_FEED

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Position : Mechanical Product Test Engineer I Entry Level (Lab, Medical Device & Pharma Industry Exp)

Location : Temecula, CA

Duration : 6 Months

Total Hours/week : 40.00

1st Shift

Client : Medical Devices Company

Job Category : Engineering

Level of Experience : Entry Level

Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT

Work schedule hours 8:00 a.m. to 5:00 p.m

Job Description:

  • Candidate must have previous LAB experience, whether in college or previous work experience. Please ensure that on the work history portion of the resume, clearly states internship or coop experience. Please submit candidates with previous engineering or science related degrees.

Role Summary:

  • The Combination Product Test Engineer is responsible for executing testing activities accurately and on time, in alignment with project scopes and client requirements.
  • Tasks include sample handling, testing, data analysis, documentation, and equipment use within a laboratory setting.

Key Responsibilities:

  • Receive, label, store, and ship samples; manage sample disposition and hazardous waste.
  • Perform product and equipment testing per protocols, methods, and schedules.
  • Analyze data using tools like Excel, JMP, and Minitab; draft and review reports.
  • Maintain lab supplies and cleanliness; ensure organized storage areas.
  • Follow SOPs and quality systems; report and investigate quality events (e.g., OOS, deviations).
  • Support documentation (e.g., protocols, reports, equipment logs) under supervision.
  • Communicate effectively with team members and clients; escalate issues promptly.
  • Collaborate respectfully and contribute to continuous improvement.
  • Perform other duties as assigned.

Qualifications:

  • Associate's degree with 0 2 years of relevant experience (lab services, medical device, IVD, pharma). REQUIRED.
  • Familiarity with GLP, cGMP, ISO, ASTM standards is a plus.
  • Strong attention to detail, multitasking ability, and communication skills.
  • Proficiency in Excel and data analysis tools. REQUIRED.

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