Quality EngineerWarsaw, IN

Reveille Technologies; Warsaw (IN); On-site; USD 50,000 - 70,000; Full time

Job summary

A technology company in Warsaw, Indiana is seeking a candidate with knowledge of quality tools, ISO and FDA requirements, and Statistical Process Control. The successful applicant will analyze quality metrics, develop monitoring methods, and collaborate on project tasks. Candidates must demonstrate an ability to interpret engineering drawings and execute analytical analysis for process improvements. Strong teamwork skills are essential for this role.

Qualifications

• Knowledge of quality tools, risk analysis, and statistics (SPC).
• Ability to read and understand engineering drawings.
• Knowledge of Quality System requirements, ISO and FDA requirements (preferred).
• Experience with Statistical Process Control and inspection techniques.
• Accountability and ownership of Quality metrics.

Responsibilities

• Analyze/review effectiveness of preventive and corrective actions.
• Develop, interpret and implement process monitoring and control methods.
• Collect data and execute various analytical/statistical analysis.

Job description

Knowledge
of basic
quality tools,
risk analysis,
statistics
(SPC)

Ability to read and understand
engineering
drawings

Knowledge of Quality System
requirements,
ISO and FDA
requirements
(preferred)

Ability to effectively work within a
team to
expedite
completion of
critical
project tasks
with other
functional
groups

Experience
with
Statistical
Process
Control and
inspection
techniques

Analyze/review effectiveness of preventive and corrective actions. Review root cause investigation according to an established process.

Accountability and ownership of Quality metrics including maintenance and reviewing of leading and lagging indicators of quality

Develop, interpret and implement appropriate process monitoring and control methods consistent with the level of process/product risk.

Collect data and execute/conduct various analytical/statistical analysis and interpretation as part of process improvements and day-to-day support.

Document, justify, review or analyze whether a proposed change to a process will not enhance the risk level in some way beyond capability of current controls or whether change will result in potential non-compliance to a required standard such as the QSRs

mation will be kept confidential according to EEO guidelines.