Manufacturing Quality Engineer

• Medical Devices (3+ yrs exp. req.) #twiceasnice Recruiting
• 4.4 Waterbury, CT Job Details Full-time $90,000
• $110,000 a year 18 hours ago Benefits Relocation assistance Health insurance Dental insurance 401(k) Paid time off Vision insurance 401(k) matching Qualifications Defect resolution root cause analysis Quality control statistical data analysis Preventive action implementation Production deviation management Corrective and preventive actions (CAPA) High school diploma or GED Statistical analysis Customer complaint resolution Failure analysis Full Job Description Manufacturing Quality Engineer•Medical Devices (3+ yrs exp.

req.)

Location:

Near Waterbury, CT Salary:

$90,000

• 110,000 + Annual Bonus Potential +

Benefits Benefits:

Medical, Dental, Vision, 401(k) w/match,

Holidays, PTO Job Type:

Full-Time |

On-site Typical Hours:

Monday-Friday, 40-45 hours per week

Start Date:

ASAP Sponsorship is not available Relocation assistance is available Manufacturing Quality Engineer

• Medical Devices Description Our client in precision manufacturing is looking for a Manufacturing Quality Engineer near Waterbury, CT.

You will lead customer quality investigations, support process validation, and improve inspection methods for regulated, precision-molded components. You will work closely with engineering, manufacturing, quality, and metrology teams. This hands-on role includes measurement programming, root-cause analysis, statistical studies, and new-product quality support. To qualify, you must have medical-device manufacturing or

ISO 13485

experience. You must also understand injection molding or a comparable precision-manufacturing process. This role offers ownership of varied technical projects and a potential path into quality management, regulatory affairs, or another leadership position. Manufacturing Quality Engineer

• Medical Devices Responsibilities Lead customer complaint, containment, and corrective-action activities Communicate investigation findings and preventive actions to customers Perform root-cause analysis and verify long-term corrective actions Support IQ, OQ, PQ, PPAP, first-article, and product-launch activities Create and analyze CMM or vision-system inspection programs Develop control plans, inspection templates, and measurement methods Apply GD&T when planning measurements, fixtures, and inspection methods Conduct capability studies, GR&R, DOE, and other statistical analyses Support inspectors and metrologists with training and troubleshooting Recommend equipment and automation to improve inspection throughput Design or define gauges, fixtures, and inspection tooling Lead projects that reduce scrap, process variation, labor, and COPQ Manufacturing Quality Engineer•Medical Devices Qualifications 3+ years of quality experience in medical-device or

ISO 13485

manufacturing required Injection-molding or precision-manufacturing experience required Customer complaint, CAPA, root-cause, and defect investigation experience required CMM or vision-system programming experience required IQ/OQ/PQ, PPAP, or process validation experience required Proficiency with GD&T and statistical analysis required About #twiceasnice Recruiting Across industries, roles, and North America, we help clients quickly attract top talent with custom-built searches. With the lowest fee in the industry, the longest guarantee, and commission-free senior recruiters

• we align our interests with the long-term success of every placement.

Need recruiting help? www.twonice.com

Pay:

$90,000.00

• $110,000.

00 per year

Benefits:

401(k) Dental insurance Health insurance Paid time off Vision insurance Application Question(s): Do you live within a commutable distance to Waterbury, CT or willing to relocate? The salary range is $90,000

• $110,000 + Annual Bonus Potential + Benefits.

What is your desired salary range?

Education:

High school or equivalent (Required)

Experience:

quality in medical-device or

ISO 13485

manufacturing : 3 years (Required) injection-molding or precision-manufacturing : 3 years (Required) customer complaint, CAPA, root-cause & defect investigation : 3 years (Required) CMM or vision-system programming : 3 years (Required) IQ/OQ/PQ, PPAP, or process validation : 3 years (Required) GD&T and statistical analysis : 3 years (Required)

Work Location:

In person