Energy Jobline ZR
Entry-Level Quality Systems and Metrology Engineer in Big Lake
Energy Jobline ZR, Big Lake, Minnesota, United States, 55309
Energy Jobline is the largest and fastest growing global Energy Job Board and Energy Hub. We have an audience reach of over 7 million energy professionals, 400,000+ monthly advertised global energy and engineering jobs, and work with the leading energy companies worldwide.
We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.
Job Description Are You Ready to Turn Curiosity into Quality?
Do you enjoy solving complex problems with precise measurements and clear data? Are you excited to learn how process risk, validation, and CAPA come together to build safe, compliant medical devices? Reporting to the Quality Manager, this role lets you apply hands‑on metrology and analytical thinking to real products in a regulated environment.
Your Impact
Operate and program Vision Systems and CMMs; confidently use calipers, micrometers, depth gages, indicators, and plug/thread Go/No-Go gages to verify features.
Write inspection plans, define process controls, and help create production visual standards and standardized acceptance criteria supporting TOMZ’s manufacturing processes.
Collaborate to define test methods, then execute and evaluate Test Method Validations to ensure repeatable, reliable measurements.
Contribute to risk management documentation with cross-functional teams and assist in building Process Master Validation Plans.
Run process qualifications, analyze outputs, and initiate corrections or corrective actions via CAPA when gaps arise.
Guide Incoming, In-Process, and Final inspection activities and champion FAIs to confirm manufacturability.
Support the review, management, execution, and evaluation of gage calibration activities.
Advance Quality Best Practices and GDP/GMP continuous improvement initiatives.
Track/report inspection data—rejection rates, defect modes, and process trends—across customers and product families.
Generate ECOs to release quality engineering documentation and follow the TOMZ Quality Management System.
Take on additional responsibilities as assigned.
You’ll Thrive Here If You Have
Initiative to excel in a fast-moving environment.
Comfort with Microsoft Office (Outlook, Word, Excel, PowerPoint).
Strong English communication skills—both written and verbal.
Basic familiarity with statistical methods and sampling strategies.
Education & Experience
Bachelor’s degree (or higher) in Engineering, Manufacturing, or Business—or directly relevant industry experience in lieu of a degree.
0–2 years in regulated manufacturing; experience is a plus.
Stand‑Out Credentials
ASQ-CQT, CQE, or CRE.
Certification in GD&T.
DMIS programming certifications.
Experience with Class I, II, and/or III medical devices; or exposure to regulated industries like Aerospace, Defense, or Pharmaceutical.
Logistics
Travel: Up to 15% annually; may involve multiple overnights and occasional weekends.
Physical Demands: Bend, stoop, squat, kneel, and lift to 30 lbs (team lift or mechanical assist above 30 lbs); extended sitting; frequent computer use; exposure to oil, grease, occupational noise, cleaning solvents, dust, metal particles, sparks, coolant, and sharp‑edged materials. PPE (e.g., safety glasses, dust masks, ear plugs, cut‑resistant or chemical‑resistant gloves) and engineering controls may be required.
If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.
#J-18808-Ljbffr
We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.
Job Description Are You Ready to Turn Curiosity into Quality?
Do you enjoy solving complex problems with precise measurements and clear data? Are you excited to learn how process risk, validation, and CAPA come together to build safe, compliant medical devices? Reporting to the Quality Manager, this role lets you apply hands‑on metrology and analytical thinking to real products in a regulated environment.
Your Impact
Operate and program Vision Systems and CMMs; confidently use calipers, micrometers, depth gages, indicators, and plug/thread Go/No-Go gages to verify features.
Write inspection plans, define process controls, and help create production visual standards and standardized acceptance criteria supporting TOMZ’s manufacturing processes.
Collaborate to define test methods, then execute and evaluate Test Method Validations to ensure repeatable, reliable measurements.
Contribute to risk management documentation with cross-functional teams and assist in building Process Master Validation Plans.
Run process qualifications, analyze outputs, and initiate corrections or corrective actions via CAPA when gaps arise.
Guide Incoming, In-Process, and Final inspection activities and champion FAIs to confirm manufacturability.
Support the review, management, execution, and evaluation of gage calibration activities.
Advance Quality Best Practices and GDP/GMP continuous improvement initiatives.
Track/report inspection data—rejection rates, defect modes, and process trends—across customers and product families.
Generate ECOs to release quality engineering documentation and follow the TOMZ Quality Management System.
Take on additional responsibilities as assigned.
You’ll Thrive Here If You Have
Initiative to excel in a fast-moving environment.
Comfort with Microsoft Office (Outlook, Word, Excel, PowerPoint).
Strong English communication skills—both written and verbal.
Basic familiarity with statistical methods and sampling strategies.
Education & Experience
Bachelor’s degree (or higher) in Engineering, Manufacturing, or Business—or directly relevant industry experience in lieu of a degree.
0–2 years in regulated manufacturing; experience is a plus.
Stand‑Out Credentials
ASQ-CQT, CQE, or CRE.
Certification in GD&T.
DMIS programming certifications.
Experience with Class I, II, and/or III medical devices; or exposure to regulated industries like Aerospace, Defense, or Pharmaceutical.
Logistics
Travel: Up to 15% annually; may involve multiple overnights and occasional weekends.
Physical Demands: Bend, stoop, squat, kneel, and lift to 30 lbs (team lift or mechanical assist above 30 lbs); extended sitting; frequent computer use; exposure to oil, grease, occupational noise, cleaning solvents, dust, metal particles, sparks, coolant, and sharp‑edged materials. PPE (e.g., safety glasses, dust masks, ear plugs, cut‑resistant or chemical‑resistant gloves) and engineering controls may be required.
If you are interested in applying for this job please press the Apply Button and follow the application process. Energy Jobline wishes you the very best of luck in your next career move.
#J-18808-Ljbffr