Quality Control Inspector 3rd Shift

Brunk Industries, Inc.; Lake Geneva (WI); On-site; USD 40,000 - 60,000; Full time

Job summary

Brunk Industries, Inc. is seeking a Quality Control Inspector for the 3rd shift. This role involves inspection and testing of high precision metal components to ensure quality standards are met. Candidates should have a high school diploma and experience in the quality field, especially within the medical device industry. Join a team that values innovation and excellence in a flexible work environment.

Benefits

Competitive salary

Attractive benefits

Flexible work environment

Qualifications

• High School Diploma or GED required.
• Previous experience in Quality Field in Medical Device preferred.
• Educated in 21 CFR 820 regulatory requirements & TS13485.

Responsibilities

• Perform inspections and testing to ensure components meet specifications.
• Execute in-process inspections and document results.
• Coach and mentor Press Stamping Operators on inspection techniques.

Skills

Data analysis

Inspection techniques

Teamwork

Statistical interpretation

Education

High School Diploma or GED

Tools

Minitab

Microsoft Office

OGP Flash

Keyence IM

Job description

Brunk Industries, Inc., a globally recognized company specializing in high precision metal components for the Medical Device Industry as well as other high-tech applications, is currently seeking a Quality Control Inspector on 3rd shift. If you are motivated by new opportunities and business growth, seek a stimulating and rewarding career, we invite you to join our diverse team of talented professionals. Brunk offers a competitive salary, a wide range of attractive benefits, a flexible work environment and a culture built on innovation and excellence.

Job Function:

The Quality Control Inspector will perform inspection and testing responsibilities in accordance to Brunk Quality System to ensure that all manufactured components meet customer specifications.

Job Responsibilities:

This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.

• Complete documented training and fully understand all SOP/WI that apply to the Inspector duties as deemed by QA Manager
• Execute visual, mechanical, physical inspection and record results to incoming material and sub-tier component operations per documented inspection plan.
• Perform / document final inspection on required components and compile accurate quality documentation package to accompany shipment.
• Execute in-process inspections & monitor each manufactured component during every operation.
• Perform first article, verification, validation inspections as deemed necessary by the Quality Supervisor and/or Quality Manager and document accordingly.
• Execute required inspections per documented plan by use of, but not limited to, micrometers, calipers, comparators, CMM, Automated vision systems, indicators, height gauges, profilometer and force gauges.
• Apply collected inspection data to SPC format as directed per documented inspection plan, analyze and follow reaction plan.
• Coach / Mentor in process Press Stamping Operators on the proper use and technique of inspection gauging or measurements.
• Actively participate in Yellow Belt projects or corrective and preventative action teams.
• Execute visual or dimensional sorting operations.
• Collect dimensional and visual inspection data under the direction of Quality Supervisor.
• Promote teamwork and effective communication within the department, as well as peers and management.
• Follow all safety procedures and regulations.
• Maintain a tidy and clean workstation, including floors.

Job Skills:

• Execute OGP Flash 500/ 302/ Quest 450 Measuremind and Zone 3 software programs.
• Analyze OGP Data output with the use of Smart Profile or Smart Fit software.
• Operate Keyence IM, VR, and LM Systems.
• Capable of data analysis using Minitab software.
• Operate micrometers, calipers, comparators, CMM, automated vision systems, indicators, height gauges, profilometer and force gauges.
• Proficiency in Microsoft Office, Plex.
• Educated in 21 CFR 820 regulatory requirements & TS13485.
• Statistical interpretation and educated reaction of Pro-Link / QC Calc software results.

Education and Experience:

Minimum educational requirements listed below may be substituted by relevant experience, learned competencies and/or certifications obtained throughout one’s career.

• High School Diploma or GED equivalent
• Previous experience in Quality Field in Medical Device Preferred

Work Environment / Physical Requirements:

• Office, some work in manufacturing setting with noise, grinding dust & residue. Light lifting, (30 lbs or less)

Protective Clothing Required:

• Must wear safety glasses, ear protection and safety shoes while in the manufacturing areas.

Please complete an application or submit your resume, including salary history.
Brunk Industries, Inc. Attn: Human Resources, 1225 Sage Street, Lake Geneva, WI 53147
Fax: [phone] EOE