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Quality Engineer I Us

  • Quality Engineer I Us job type Posted on: Oct 23, 2026
  • Quality Engineer I Us experience level Techlink Systems Inc
  • Quality Engineer I Us employment type Irvine, California
  • Quality Engineer I Us salary Salary: $56 per hour
  • Quality Engineer I Us employment type Onsite
  • Quality Engineer I Us salary Full-time
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Job Title :

Quality Engineer I Us

Job Type :

Full-Time

Job Location :

Irvine California United States

Remote :

No

Jobcon Logo Job Description :

Job Title: Quality Engineer I_US
Location (On-site, Remote, or Hybrid?): Irvine, CA (onsite)
Contract Duration: until 02/28/2027

Job Description
The Quality Test Engineer performs investigations relating to root cause of customer complaints, proposes and implements corrective and preventative actions as required.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Under supervision, general direction, and in accordance with all applicable federal, state and local laws/regulations and Corporate client, procedures and guidelines, this position is:
Responsible for investigating customer complaints regarding product design, product manufacture, and product testing
Responsible for communicating quality and business-related issues or opportunities to the next management level.
Participates in projects that improve the complaint process and reduces overall customer issues.
Actively participate and engage in CAPA trending meetings.
Analyzes data and applies knowledge of engineering principles and practices to implement continuous improvement projects.
Provide support during External and Internal Audits of the Customer Quality process
Performs other duties assigned as needed.
Responsible for complying with all Federal, State, local and company regulations, policies and procedures including Health, Safety and Environmental compliance.

DESIRED MINIMUM QUALIFICATIONS:
Bachelor's degree in engineering.
Minimum of two (2) years of experience in an engineering related field
Able to read and understand electrical and mechanical schematics.
Strong integration skills to identify Manufacturing and Supplier related issues of Medical Device Capital Equipment.
Ability to apply technical, regulatory, quality systems, and business knowledge to identify, investigate and resolve customer complaints.
Ability to effectively prioritize and manage multiple activities and responsibilities.
Has an understanding of statistics and how to utilize them in data analysis
Must possess a clear understanding of theoretical and practical fundamentals and experimental engineering techniques. Good written and oral communication skills. Computer literate.
Demonstrated root cause and problem-solving skills.
Demonstrated verbal and written communication skills, and ability to effectively communicate with internal and external personnel.
Ability to apply Six Sigma and Process Excellence tools and methodologies preferred.
Understanding of Failure Modes and Effects Analysis and Fault Tree Analysis are preferred
Understanding of Human Factors and Health Hazard Risks are preferred
Knowledge of design control, risk management, production and process controls and applicable laws (i.e., ISO 13485, FDA Quality System Regulation, ISO 14971) is preferred
Proficiency with quality-related applications such as those for Minitab, QI Macros, etc would be a plus.
Experience with CAPA, NCR and Audit software systems is desired.

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Jobcon Logo Position Details

Posted:

Oct 23, 2026

Reference Number:

53371-6496

Employment:

Full-time

Salary:

$56 per hour

City:

Irvine

Job Origin:

CIEPAL_ORGANIC_FEED

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Job Title: Quality Engineer I_US
Location (On-site, Remote, or Hybrid?): Irvine, CA (onsite)
Contract Duration: until 02/28/2027

Job Description
The Quality Test Engineer performs investigations relating to root cause of customer complaints, proposes and implements corrective and preventative actions as required.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
Under supervision, general direction, and in accordance with all applicable federal, state and local laws/regulations and Corporate client, procedures and guidelines, this position is:
Responsible for investigating customer complaints regarding product design, product manufacture, and product testing
Responsible for communicating quality and business-related issues or opportunities to the next management level.
Participates in projects that improve the complaint process and reduces overall customer issues.
Actively participate and engage in CAPA trending meetings.
Analyzes data and applies knowledge of engineering principles and practices to implement continuous improvement projects.
Provide support during External and Internal Audits of the Customer Quality process
Performs other duties assigned as needed.
Responsible for complying with all Federal, State, local and company regulations, policies and procedures including Health, Safety and Environmental compliance.

DESIRED MINIMUM QUALIFICATIONS:
Bachelor's degree in engineering.
Minimum of two (2) years of experience in an engineering related field
Able to read and understand electrical and mechanical schematics.
Strong integration skills to identify Manufacturing and Supplier related issues of Medical Device Capital Equipment.
Ability to apply technical, regulatory, quality systems, and business knowledge to identify, investigate and resolve customer complaints.
Ability to effectively prioritize and manage multiple activities and responsibilities.
Has an understanding of statistics and how to utilize them in data analysis
Must possess a clear understanding of theoretical and practical fundamentals and experimental engineering techniques. Good written and oral communication skills. Computer literate.
Demonstrated root cause and problem-solving skills.
Demonstrated verbal and written communication skills, and ability to effectively communicate with internal and external personnel.
Ability to apply Six Sigma and Process Excellence tools and methodologies preferred.
Understanding of Failure Modes and Effects Analysis and Fault Tree Analysis are preferred
Understanding of Human Factors and Health Hazard Risks are preferred
Knowledge of design control, risk management, production and process controls and applicable laws (i.e., ISO 13485, FDA Quality System Regulation, ISO 14971) is preferred
Proficiency with quality-related applications such as those for Minitab, QI Macros, etc would be a plus.
Experience with CAPA, NCR and Audit software systems is desired.

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