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<h3>Job Description</h3>
Job Title: Manufacturing Quality Engineer - Medical Device
Duration: 9+ Months (Possible extension)
Location: Arden Hills, MN 55112
Hybrid Role

Responsibilities:
<ul>
<li>The Supplier QA Engineer will play a key part in leading performance improvement of suppliers and increasing the suppliers’ capabilities to consistently meet client's requirements.</li>
<li>Will support Global Sourcing, supplier manufacturing operations, and global quality systems by participating in global communities of practice and value improvement projects</li>
<li>Drives improvement and corrective actions in the quality of components sourced from outside suppliers.</li>
<li>Assess &amp; drive reactive as well as proactive supplier project(s)/investigations partnering with Supplier Engineering, Manufacturing/Test operations, Commercial Sourcing, Design Assurance, R&amp;D</li>
<li>Develops solutions to a variety of complex problems of diverse scope and complexity where analysis of data requires evaluation of identifiable factors.</li>
<li>Plans and organizes non-routine tasks with approval.</li>
<li>Initiates or maintains work schedule and priorities. Plans and organizes project assignments and maintains project schedules</li>
<li>Establishes and cultivates a wide range of business relationships to facilitate completion of assignments. Interacts with suppliers.</li>
<li>Demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.</li>
<li>Assures that appropriate resources (personnel, tools, etc.) are maintained in order to assure Quality System compliance and adherence to the Quality Policy.</li>
</ul>
 
Education/Experience:
<ul>
<li>BS degree in an Engineering related field, such as: Mechanical Engineering, Materials Engineering, Chemical Engineering, Electrical Engineering, or similar technical degree with 2-3 years related experience.</li>
<li>Experience in Quality Management Systems, regulatory compliance, and risk management.</li>
<li>People with Med device QMS preferred or experience working with Manufacturing.</li>
<li>Experience with problem solving quality tools, Corrective/Preventive Actions (CAPA), Technical Documentation</li>
<li>Preferred Qualifications:</li>
<li>Experience with or lead auditor certification to ISO 13485, 9001, TS 16949 standards</li>
</ul>

Manufacturing Quality Engineer

<h3>Job Description</h3>
Job Description: Quality Engineer II
 
 
About Our Client
Our client is a pioneering medical device company focused on developing the world’s first fully implantable, Class III cardiovascular implantable product. Their team is driven by a powerful purpose: to transform the lives of patients with end-stage heart failure by delivering innovative, reliable, and life-saving cardiac technology. Join them as they continue advancing toward clinical use and commercialization.
 
Position Summary
Our client is seeking a Quality Engineer II to join their team, with a primary focus on working with external suppliers to investigate and resolve Non-Conformance Reports (NCRs). This role is pivotal in ensuring that incoming materials and supplier processes meet stringent quality standards for their Class III cardiovascular implantable product.
The ideal candidate thrives in fast-paced, regulated environments and is adept at supplier collaboration, root cause analysis, and detailed technical writing. Frequent travel (35% or more) is expected to visit suppliers for audits, investigations, and quality improvement initiatives.
 
Key Responsibilities
<ul>
<li>Lead supplier NCR investigations, from initial issue identification to root cause determination and corrective action verification.</li>
<li>Develop, author, review, and maintain comprehensive NCR documentation in compliance with ISO 13485, 21 CFR 820, and other applicable regulations.</li>
<li>Participate in document control, training, and change control activities.</li>
<li>Support CAPA investigations and root cause analysis.</li>
<li>Assist with internal and external audits and inspection readiness.</li>
<li>Collaborate closely with suppliers to ensure timely closure of quality issues and effective corrective/preventive actions (CAPA).</li>
<li>Conduct on-site supplier audits and process inspections; provide technical guidance to address non-conformances.</li>
<li>Partner with internal teams (R&amp;D, Manufacturing, Regulatory Affairs) to ensure supplier-provided materials meet design and manufacturing requirements.</li>
<li>Develop and maintain supplier quality agreements, inspection criteria, and control plans.</li>
<li>Support quality system compliance activities and contribute to continuous improvement projects.</li>
<li>Help ensure compliance with FDA QSR, ISO 13485, ISO 14971, and other applicable standards.</li>
<li>Support the receiving and inspection of materials and components for quality conformance.</li>
<li>Assist with identifying and documenting nonconforming product and supporting investigations.</li>
<li>Contribute to supplier evaluations and support follow-up on quality-related issues.</li>
<li>Assist in managing quality records, design history files, and change control documentation.</li>
<li>Support process validation activities, facility controls, and ensure adherence to good documentation practices.</li>
</ul>
 
Key Qualifications
Required
<ul>
<li>Bachelor’s degree in Biomedical, Mechanical, Electrical Engineering, or a related field.</li>
<li>5+ years of experience in medical device quality or manufacturing, including at least 2 years in Class II (or higher) regulated medical devices.</li>
<li>Proven experience with supplier quality management, NCR investigation, and CAPA implementation.</li>
<li>Strong knowledge of ISO 13485, 21 CFR 820, ISO 14971, and related standards.</li>
<li>Excellent root cause analysis, problem-solving, and technical writing skills.</li>
<li>Experience reviewing technical documentation for medical or safety-critical software.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to travel frequently (35%+), including domestic and international trips to supplier sites.</li>
</ul>
 
Preferred
<ul>
<li>Experience in Class III medical devices or implantable systems.</li>
<li>ASQ certification (CQE, CRE, or similar) preferred.</li>
<li>ISO 13485 auditor experience or training.</li>
</ul>
 
What Our Client Offers
<ul>
<li>The opportunity to contribute to a life-saving technology at the forefront of medical innovation.</li>
<li>A collaborative, mission-driven team in a fast-paced startup environment.</li>
<li>Hybrid work flexibility with the expectation of regular in-office collaboration.</li>
<li>Competitive salary package and development opportunities.</li>
</ul>

Quality Engineer

<h3>Job Description</h3>
Job Description
Now Hiring Inspectors – 1st &amp; 2nd Shift | $24+/HR | Rochester &amp; Portsmouth, NH
Join a Premier Manufacturer and take your career to the next level!
Why You’ll Love Working Here:
•Full-Time, Monday–Friday Schedule
•Competitive Pay + Overtime Opportunities
•Paid, Onsite Training Provided
•Career Growth &amp; Advancement Opportunities
•Long-Term Job Stability
Your Role:
As an Inspector, you’ll play a key role in ensuring product quality and precision. You’ll inspect components, verify accuracy, and help maintain the high manufacturing standards our client is known for.
Key Responsibilities:
•Review inspection data to confirm part integrity and resolve any discrepancies
•Operate inspection equipment and run basic programs to measure parts
•Interpret blueprints and assign correct dimensional values and tolerances
•Work cross-functionally as needed to support business goals
•Perform other related duties as assigned
Qualifications:
•High school diploma or GED
•Basic proficiency in blueprint reading and GD&amp;T symbology
•Experience with precision measuring tools such as calipers, micrometers, height gauges, surface plates, comparators, and gauge blocks
 Pay Details: $24.00 to $32.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://uat.adecco.com/en-us/candidate-privacy" target="_blank">https://uat.adecco.com/en-us/candidate-privacy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 
Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Now Hiring - 1st & 2nd Shift Inspectors

<h3>Job Description</h3>
Our Sandy Springs, Georgia office is seeking a Senior Process Engineer – Water/Wastewater to join our dynamic and growing team.
 
 In this role, you will lead technical efforts on water and wastewater treatment and conveyance projects, helping shape critical infrastructure that impacts public health and the environment. With a strong emphasis on collaboration, quality, and innovation, you’ll mentor junior engineers, manage project execution, and deliver sustainable, cost-effective process designs.
 
What You Will Do:
<ul>
<li>Interpersonal Skills:</li>
<li> As a senior technical expert, you’ll collaborate with multidisciplinary teams—civil, mechanical, electrical, and structural engineers—to develop integrated solutions. You’ll build strong relationships with clients, junior staff, and regulators, using excellent communication to foster teamwork and project success.</li>
<li>Innovation and Expertise:</li>
<li> Design and optimize water and wastewater treatment systems including activated sludge, membrane filtration, disinfection, nutrient removal, and biosolids handling. You'll use process modeling and simulation tools to troubleshoot challenges and propose data-driven improvements.</li>
<li>Technical Mastery:</li>
<li> Prepare and review technical reports, process flow diagrams (PFDs), Process and Instrumentation Diagrams (P&amp;IDs), and hydraulic profiles. You’ll lead or support permitting activities, pilot studies, and on-site assessments while ensuring engineering excellence and regulatory compliance.</li>
<li>Leadership and Mentorship:</li>
<li> Manage the execution of projects from concept to construction. Mentor junior engineers, promote internal standards development, and ensure technical quality and innovation in every deliverable.</li>
</ul>
 
What You Bring:
<ul>
<li>Experience:</li>
<li> Minimum of 5 years in water/wastewater treatment and conveyance project design and implementation within a consulting environment.</li>
<li>Education:</li>
<li> Bachelor’s degree in Environmental, Civil, Chemical Engineering, or related discipline.</li>
<li>Licensing:</li>
<li> Registered Professional Engineer (PE) in Georgia, or the ability to obtain within 6 months.</li>
<li>Technical Skills:</li>
<li> Proficiency in process modeling software, AutoCAD, and Microsoft Office. Strong understanding of state and federal environmental regulations and permitting requirements.</li>
<li>Problem Solving:</li>
<li> Demonstrated ability to analyze system performance, identify opportunities for improvement, and deliver innovative solutions that balance cost, performance, and sustainability.</li>
</ul>
 
The Things About Us You Will Appreciate!
Our comprehensive benefit package includes the following:
<ul>
<li>Three medical plan options</li>
<li>Dental &amp; vision plans</li>
<li>Company-paid group life, short- and long-term disability insurance</li>
<li>Voluntary life insurance</li>
<li>Flexible and dependent care spending accounts</li>
<li>Additional supplemental plans (Critical Illness, Hospital Indemnity, Accident)</li>
<li>401(k) with company match</li>
<li>Paid Time Off (PTO) which starts accruing upon hire</li>
</ul>
 
About Rochester | DCCM
Since 1966, the Rochester | DCCM name has been synonymous with quality, reliability and expertise. As Georgia’s premier infrastructure solution provider, our team of engineers, land surveyors, and GIS professionals—along with our exceptional support staff—deliver seasoned guidance and technical knowledge with a responsiveness our clients trust.
We provide civil engineering, land surveying, and program management services to both public and private sectors. Over 75% of our business is from repeat clients, many of whom have partnered with us for decades.
 
Equal Opportunity Employer
 Rochester | DCCM is an equal opportunity employer and is committed to fostering a diverse and inclusive workplace.

Process Engineer- Wastewater

<h3>Job Description</h3>
Job Description
Develops and implements the Quality Control Plan (QCP) and ensures all services meet contract standards at FLETC Glynco, GA.
Key Responsibilities:
<ul>
<li>
Develop and execute the QCP.
</li>
<li>
Monitor performance of staff, scheduling, and logistics.
</li>
<li>
Conduct inspections, audits, and performance assessments.
</li>
<li>
Track deficiencies, implement corrective actions, and report outcomes.
</li>
<li>
Provide written QC reports to leadership and the Government.
</li>
</ul>
Minimum Qualifications:
<ul>
<li>
Bachelor’s degree or equivalent experience.
</li>
<li>
5+ years of quality control or quality assurance experience.
</li>
<li>
Familiarity with ISO 9001 or other recognized standards.
</li>
<li>
Strong analytical and documentation skills.
</li>
</ul>
Location &amp; Travel: Based at FLETC Glynco, GA, with required travel to other FLETC facilities as needed.
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QFIvp22zk2

Quality Control Manager

<h3>Job Description</h3>
Job Description
Posting – Stamping Press Punch Press Set-up Operator
Are you ready to step into a new role that offers opportunities for impact and growth? We offer a 4-day work week in a climate-controlled environment. With 50-years of success, this family-owned company is on a trajectory of aggressive expansion, and we're seeking a talented Punch Press Set-up/Operator to propel our Metal Stamping Production team to new heights!
As the Punch Press Set-up/Operator, you'll have the exciting responsibility of setting up multiple punches ranging from 45 to 400 tons. While you'll have the support from experienced shift supervisors, your hands-on expertise with the equipment will be the cornerstone of your success.
Do you fit the bill for our ideal candidate? We're looking for someone who has a solid background in running Punch Presses in a metal stamping environment, has progressed from being an Operator to a Set-up role, and continually seeks opportunities to learn and grow.
Here are the qualifications we're seeking: &nbsp;1st, 2nd shift and Weekend Shifts positions available.
<ul>
<li>Two years of Stamping Punch Press Set-up experience is required.</li>
<li>Experience operating Minster, Blow, Komatsu and Stamp Tech equipment is ideal!</li>
<li>3 years of monitoring quality of output while working on equipment</li>
<li>A strong focus on safety while producing</li>
</ul>
Job Duties and Responsibilities
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Setting up and operating a variety of punch presses to safely produce metal stampings that meet internal and external quality requirements utilizing complex progressive tools, compound blanks, transfer tools and short run temporary tooling in punch presses ranging in capacity from 45 ton to 400 tons.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Properly set safety equipment in and around the press.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Set-up and troubleshoot tooling that includes progressive dies, stage tooling, and short run temporary tooling.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Set-up and use coil handling equipment, such as servo feeds, automatic straighteners and cradle or reel unloaders.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Perform first and last piece inspection.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Start production operators on jobs, checking that all safeties are in place and properly adjusted.
Additional Job Duties and Responsibilities
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Observe machine operation to detect product defects or machine malfunctions.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Perform minor machine maintenance such as cleaning and oiling of machines.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Perform preventative maintenance as specified, and document as required.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Set-up secondary manufacturing machines or assembly equipment to make parts or products to specification – (tapping, countersinking, riveting, etc.).
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Accurately complete production documentation in a timely manner.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Measure and visually inspect products for surface and dimensional defects to ensure conformance to specifications, using precision measuring instruments including micrometers, calipers, protractors, indicators, and height gauges.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Train new employees in proper procedures and techniques.
Benefits:
<ul>
<li>401(k)</li>
<li>Dental insurance</li>
<li>Employee assistance program</li>
<li>Flexible spending account</li>
<li>Health insurance</li>
<li>Health savings account</li>
<li>Life insurance</li>
<li>Paid time off</li>
<li>Retirement plan</li>
<li>Tuition reimbursement</li>
<li>Vision insurance</li>
</ul>
Schedule:&nbsp; Three options are available
<ul>
<li>1st Shift Monday-Thursday, 6:0am to 4:30pm (10 hours/shift)</li>
<li>2nd Shift Monday-Thursday, 4:00pm to 2:30 am (10 hours/shift)</li>
<li>Weekend Shift Friday-Sunday 6:00am to 6:30 pm (12 hours/shift)</li>
</ul>
Experience:
<ul>
<li>Punch Press Setting up Tooling in Press: 2 years (Required)</li>
</ul>
Company DescriptionCompany History At Rotation Engineering, we have been satisfying your most critical metal stamping requirements since 1973. Our Beginnings Rotation Engineering was founded by James A. Lorence in 1973 as a tool and die company in Minnesota. In response to demand for single-source responsibility, Rotation Engineering added metal stamping operations in 1975. Continued Growth Business expanded rapidly and soon Rotation Engineering added manufacturing capabilities, including Electrical Discharge Machining (EDM) and laser equipment, press brakes and shears, welding, and machining centers. By the early 1990s, the company’s facility had grown from its initial 2,500 square feet to 20,000 square feet. Expansion to Brooklyn Park Facility In 1995, Rotation Engineering moved into a new, custom-designed 38,000 square-foot building in Brooklyn Park, its current location. Responding to increased business, Rotation Engineering also expanded the services offered to customers. This further differentiated the company and provided customers with lower costs and faster response times. These services, in conjunction with extensive manufacturing capabilities, have become the foundation of Rotation Engineering’s customer appeal. The Next Chapter In 2010, Craig Komschlies purchased Rotation Engineering. Komschlies has over 20 years of experience in the metal stamping business. Today, located in Brooklyn Park, Minnesota, Rotation Engineering is a progressive engineering, metal stamping and manufacturing company that has earned the respect and loyalty of its customers. Our Facility Rotation Engineering’s 38,000-square-foot office and production facility is located in the northern suburbs of Minneapolis/St. Paul, near major transportation infrastructure, manufacturing vendors and suppliers. 
<h3>Company Description</h3>
Company History\nAt Rotation Engineering, we have been satisfying your most critical metal stamping requirements since 1973.\n\nOur Beginnings\nRotation Engineering was founded by James A. Lorence in 1973 as a tool and die company in Minnesota. In response to demand for single-source responsibility, Rotation Engineering added metal stamping operations in 1975.\n\nContinued Growth\nBusiness expanded rapidly and soon Rotation Engineering added manufacturing capabilities, including Electrical Discharge Machining (EDM) and laser equipment, press brakes and shears, welding, and machining centers. By the early 1990s, the company’s facility had grown from its initial 2,500 square feet to 20,000 square feet.\n\nExpansion to Brooklyn Park Facility\nIn 1995, Rotation Engineering moved into a new, custom-designed 38,000 square-foot building in Brooklyn Park, its current location. Responding to increased business, Rotation Engineering also expanded the services offered to customers. This further differentiated the company and provided customers with lower costs and faster response times. These services, in conjunction with extensive manufacturing capabilities, have become the foundation of Rotation Engineering’s customer appeal.\n\nThe Next Chapter\nIn 2010, Craig Komschlies purchased Rotation Engineering. Komschlies has over 20 years of experience in the metal stamping business. Today, located in Brooklyn Park, Minnesota, Rotation Engineering is a progressive engineering, metal stamping and manufacturing company that has earned the respect and loyalty of its customers.\n\nOur Facility\nRotation Engineering’s 38,000-square-foot office and production facility is located in the northern suburbs of Minneapolis/St. Paul, near major transportation infrastructure, manufacturing vendors and suppliers.

Stamping Press Punch Press Set-up Operator

<h3>Job Description</h3>
Supplier Quality Manager - Extrusion*
 
As the Manager, Supplier Quality Commodity Manager for Extrusion, you will lead the quality initiatives for our extrusion commodity, ensuring the reliability and compliance of externally sourced components and materials. This pivotal role bridges procurement, engineering, and quality assurance, driving supplier development, risk mitigation, and continuous improvement. As the quality lead for extrusion, you’ll manage supplier performance, conduct audits, and ensure adherence to regulatory standards while supporting new product introductions and strategic sourcing decisions. If you're passionate about quality, collaboration, and innovation in a global medical device environment, we invite you to make a lasting impact with us.
ESSENTIAL DUTIES
<ul>
<li>Develop and implement supplier quality strategies for assigned commodities working closely with supply chain and the quality assurance team.</li>
<li>Drives proactive solutions and development that improve overall supplier performance. Supports supplier performance and risk processes to create predictive measures to help prevent issues that might impact our facilities or customers.</li>
<li>Assume overall responsibility for the commodities quality performance within Company and in accordance with assigned KPI’s.</li>
<li>Conduct supplier audits and assessments to ensure compliance with quality standards.</li>
<li>Monitor, measure and action supplier performance using KPIs such as PPM, on-time delivery, and corrective action responsiveness.</li>
<li>Serve as a quality expert for the specific commodity and collaborate with engineering and sourcing to define quality requirements and specifications.</li>
<li>Acts as a lead for supplier quality in supplier selection. Drives the process to standard procedures, coordinates with supply chain, and holds the supplier quality team accountable to deliver quality suppliers that meet or exceed our expectations.</li>
<li>Drives supplier escalations and resolution, solving problems through problem solving methodology (8D, A3, DMAIC). Monitors solutions to prevent repeat issues.</li>
<li>Support supplier transfers, new product introductions, and projects that impact their commodity suppliers.</li>
<li>Provides guidance and mentorship to junior members of the team on the principles of supplier management, new product design, and component qualifications.</li>
<li>Instills quality processes and best practices within Client facilities and at suppliers. Assists in the development of new processes that improve supplier quality.</li>
<li>Leads and manages continuous improvement activities for the supplier quality team as assigned.</li>
</ul>
MINIMUM QUALIFICATION REQUIREMENTS
Education
<ul>
<li>Bachelor’s degree in business, supply chain, supplier quality, or operations field.</li>
<li>MBA preferred.</li>
</ul>
Experience
<ul>
<li>Minimum 7 years in similar role or related experience at a global manufacturing company.</li>
<li>Experience with Extrusion. </li>
<li>Preferred – Experience in Medical Device industry.</li>
</ul>
Skills
<ul>
<li>Supplier relationship management &amp; negotiation.</li>
<li>Executive-level communication and stakeholder management in a global company.</li>
<li>Excellent verbal and written communication, analytical, leadership, problem-solving and organizational skills.</li>
<li>Demonstrated ability to consistently work through multiple issues by capitalizing on available resources and prioritizing accordingly.</li>
<li>Demonstrated use of comprehensive analytical skills to determine alternatives and present recommendations.</li>
<li>Demonstrated ability to manage multiple projects simultaneously and ability to thrive in a continuous improvement environment.</li>
<li>Knowledge and use of relevant PC software applications and skills to use them effectively.</li>
</ul>
Certificates, Licenses, Registrations
Preferred, but not required: Supplier Quality Engineer, Quality Engineer, or Six Sigma.

Supplier Quality Manager

<h3>Job Description</h3>
Job Description
Overview:
&amp;#x14C;nin Staffing is looking for an experienced Millwright to join a trusted machine shop in Fairfield, AL. This role is ideal for someone with strong mechanical aptitude, problem-solving skills, and the ability to maintain, repair, and install industrial machinery with precision. Position Details:
<ul></ul>
Company DescriptionDon't miss this chance to enhance your experience in a production environment while enjoying competitive pay and a comprehensive benefits package. Plus, every &amp;#x14C;nin job comes with our amazing Teammate Benefits program, designed to give you the tools you need to protect your health, your money and the people and things you care about. Tools like: Weekly Pay $5 Prescription Drugs $5 Doctor's Visit Copays Free Teledoctor Service Free Counseling Services Life Insurance Included Vision Insurance Included Dental Insurance Included Vacation and Holiday Pay Scholarship Opportunities NEW! 401(k) Retirement Plan Free Legal Services Our unbeatable employee discount program If this sounds like something you would be interested in, Apply Now so we can hold a spot for you until we can schedule an interview. We can’t wait to talk to you! –Your &amp;#x14C;nin team

Millwright

<h3>Job Description</h3>
Job Description
CNC Machine Operator – 2nd &amp; 3rd Shift Location: Shelby Township, MI Pay Rate: $18.50 – $19.50 per hour
Contract to start with direct hire conversion possible
Schedule Options:
<ul>
<li>
2nd Shift: Monday–Friday, 3:00 PM – 11:00 PM
</li>
<li>
3rd Shift: Sunday–Thursday, 11:00 PM – 7:00 AM
</li>
</ul>
Position Summary: We are seeking dedicated CNC Operators to support production in a high-volume manufacturing environment. Operators will run machines, perform inspections, maintain equipment, and ensure consistent quality and efficient operations.
Key Responsibilities:
<ul>
<li>
Load raw parts into the manufacturing cell.
</li>
<li>
Maintain scrap bins, chip hoppers, and machine fluids (coolants, lubes).
</li>
<li>
Perform routine machine cleaning, including sweeping, mopping, and filter changes.
</li>
<li>
Run production parts and CMM programs as required.
</li>
<li>
Inspect parts at required intervals and respond to dimensional trends.
</li>
<li>
Record dimensional data and track process capability.
</li>
<li>
Complete production and downtime reporting.
</li>
<li>
Adjust machine settings or change tools based on part measurements or schedules.
</li>
<li>
Perform titrations and adjust concentrations for coolants and wash solutions.
</li>
<li>
Monitor machine operation to detect and address malfunctions.
</li>
<li>
Support continuous improvement initiatives.
</li>
<li>
Perform basic machine maintenance per instructions.
</li>
</ul>
Qualifications:
<ul>
<li>Previous experience as a CNC Machine Operator in a manufacturing environment</li>
<li>Familiarity with FANUC controls</li>
<li>Ability to read and interpret blueprints and technical drawings</li>
<li>Proficient with precision measuring instruments (calipers, micrometers, gauges, etc.)</li>
<li>Strong mechanical aptitude and troubleshooting skills</li>
<li>Knowledge of preventative maintenance practices</li>
<li>Experience with PLEX software a plus</li>
<li>Willingness to train on 1st shift before moving to assigned shift</li>
</ul>
Company DescriptionUsing the best business practices obtained from many years of experience in Business, Law, and Recruiting and Staffing, the Founders at CrossFire Group (“CrossFire”) started in downtown Royal Oak, MI more than a decade ago. With backgrounds in Information Technology (IT) and the Legal Industry, CrossFire began placing by IT and Legal Professionals in contract and direct-hire positions throughout the Midwest. Since our founding, CrossFire has grown into a full-service Human Capital Solutions Organization. We are proud of now providing full services beyond recruiting and staffing. Our portfolio of services includes HR supply chain management, human resources consulting, and many customized Human Resource related services. 
<h3>Company Description</h3>
Using the best business practices obtained from many years of experience in Business, Law, and Recruiting and Staffing, the Founders at CrossFire Group (“CrossFire”) started in downtown Royal Oak, MI more than a decade ago. With backgrounds in Information Technology (IT) and the Legal Industry, CrossFire began placing by IT and Legal Professionals in contract and direct-hire positions throughout the Midwest.\r\n\r\nSince our founding, CrossFire has grown into a full-service Human Capital Solutions Organization. We are proud of now providing full services beyond recruiting and staffing. Our portfolio of services includes HR supply chain management, human resources consulting, and many customized Human Resource related services.

CNC Machine Operator - $19/hr

<h3>Job Description</h3>
Job Description
West Side manufacturing company is currently seeking an experienced Operator for this Full-time position.
QUALIFICATIONS:
<ul>
<li>Experience in a manufacturing environment</li>
<li>Basic math in addition, subtraction, multiplication and division</li>
<li>Understanding of organization production quotas</li>
<li>Ergonomics</li>
<li>General shop and machine safety</li>
</ul>
DUTIES AND RESPONSIBILITIES
<ul>
<li>Operate metal stamping or metalworking machines</li>
<li>Manipulating or operating various objects</li>
<li>Indirect labor, cleaning, sweeping, organizing, stacking and packing parts, boxes and pallet assemblies</li>
<li>Lifting up to 40 lbs</li>
<li>Report IMMEDIATELY to direct supervisor any changes in the process operation</li>
<li>Observing and reporting defective or hazardous disruptions or disturbances regarding safety, machine operation or running of defective parts</li>
<li>Punctuality in arriving on time to report for assigned shift</li>
<li>Maintain work quotas and projects</li>
<li>Following instructions including, but not limited to, supervisor instructions; safety procedures and policies as outlined in all manuals</li>
</ul>
BENEFIT AND OPPORTUNITIES:
<ul>
<li>Competitive pay, shift differential, overtime</li>
<li>Company-paid employee medical and life insurance, 401(k), PTO, career growth potential</li>
<li>Attendance and Production bonus availability</li>
<li>Uniforms provided</li>
</ul>
Company DescriptionCleveland West Side Manufacturer 
<h3>Company Description</h3>
Cleveland West Side Manufacturer

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