Quality control technician jobs in Eagan, MN - 440 jobs

The position is for a local contract Cath Lab Technologist in Minneapolis requiring an active US license, BLS, ACLS, RCI or CCI certifications, and at least two years of relevant experience. The role involves working 40 hours per week for 13 weeks in a specialized allied health setting. The employer provides medical benefits, paid leave, and direct contract opportunities focused on federal healthcare facilities. Ghost RX Inc is seeking a local contract Cath Lab Technologist for a local contract job in Minneapolis, Minnesota. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 8 hours Employment Type: Local Contract Qualifications Active, unrestricted license from any US state or territory. Any state license is accepted. Proof of eligibility to work in the United States BLS, ACLS, RCI or CCI At least 2 years of recent experience in specialty and a like setting. Ghost RX Benefits Medical, dental, vision insurance Paid time off Paid sick leave Paid holiday and federal holiday Exclusive/direct contracts with no outside competition. Qualified candidates will be approved for the job they are submitted for in a timely manner. Ghost RX Inc Job ID #511. About Ghost RX Inc Ghost RX provides Healthcare personnel to federal hospitals and healthcare facilities the country. Our exclusive contracts cut out the outside competition and the VMS black hole. Your profile is delivered directly to the hiring manager, allowing for immediate approvals and offers. Contracts vary in length from 6 months to 5 years. Ghost RX is a Service Disabled Veteran Owned Small Business. Keywords: Cath Lab Technologist, Cardiovascular technology, contract healthcare jobs, BLS certification, ACLS certification, RCI certification, healthcare staffing, Minnesota healthcare jobs, allied health professional, medical technologist

Job Title: Lab Technician- 2nd shift Type: 12 Months Contract Pay range: $40.00-$50.00 per hour on W2 Schedule: 12:00 PM -10:00 PM We are seeking a highly skilled technician with at least 5 years of hands-on experience in circuit board rework and electronic hardware support. The ideal candidate will be comfortable in an engineering lab setting, where they will be responsible for reworking extremely complicated PCBs that utilize state-of-the-art components. You will work closely with engineering teams to repair, modify, and validate advanced electronic assemblies. In this role, you will also be at ease running and maintaining basic lab equipment, such as multimeters, oscilloscopes, function generators, and solder/desolder stations. Additionally, you will exercise various software commands and scripts to perform diagnostic tests on our products, supporting the engineering team in troubleshooting and validation tasks. Success in this position requires careful attention to detail, the ability to follow precise procedures, and clear communication of findings. You will play a key role in ensuring the performance and reliability of our cutting-edge hardware solutions while maintaining an organized and efficient lab environment. Key Responsibilities and Requirements: Work independently in a fast-paced engineering lab environment, demonstrating strong self-motivation and time management skills. Rework and repair extremely complicated PCBs utilizing state-of-the-art components, ensuring high quality and reliability. Operate and maintain basic lab equipment (such as oscilloscopes, multimeters, and soldering stations) and execute software commands to perform product tests. Collaborate effectively with remote engineering teams, communicating findings and progress clearly through digital platforms. Support the engineering team in troubleshooting, validation, and documentation of hardware issues and solutions. Maintain an organized and efficient lab environment, adhering to safety and procedural standards. Job is 100% in-person; candidates must be available to work onsite at our engineering facility, 40 hours per week, between the hours of 12-10PM. Must Have: 5 years of hands-on experience in circuit board rework and electronic hardware support Experienced engineering lab setting Operate and maintain basic lab equipment (such as oscilloscopes, multimeters, and soldering stations)

This position is for a travel Cath Lab Technologist on a 13-week assignment in Minneapolis, working 4 days a week with 10-hour day shifts. The role involves assisting in cardiac catheterization procedures, monitoring equipment, and recognizing arrhythmias in a short-term acute care hospital. Candidates must have 1-2 years of experience in cath lab settings and relevant certifications such as ACLS and BLS. Malone Healthcare - Nursing is seeking a travel Cath Lab Technologist for a travel job in Minneapolis, Minnesota. & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type: Travel Day 4x10-Hour (07::30)is the shift for this role. The Job Description: Position / Specialty- Cath Lab Tech Shift:7AM-5:30 PM 4-days per week. Years of experience REQ: 1-2 First-timers accepted: Yes - with minimum of 2 years cath lab experience scrubbing and monitoring Weekend REQ: On-call approximately every 4th - 5th weekend. Occasional Sunday Certs REQ:ACLS BLS Is on-call REQ? Yes - Approximately one day per week and every 4th - 5th weekend Will clinician float within scope to meet facility needs? Will float as needed Open to accommodating block schedule? No Locals accepted: Yes Pending License accepted: Yes RTO Restrictions: Ideally no more than 5 days. Guaranteed Hours: Client may cancel up to 3 shifts at any time for any assigned Aya Candidate without any penalty or obligation to pay Aya for such cancelled time. On-call hours do not count towards the guaranteed minimum hours. Special Requirements: Work Setting Experience Required: Diagnostic Cardiac Cath Lab Interventional Cardiac Cath Lab Cardiac Cath Lab Procedure Experience Required: Cardiac Stent Placement Diagnostic Catheterizations Adult Hemodynamic monitoring IABP Placement/Removal Interpretation of dysrhythmias Left heart catheterization Percutaneous Coronary Interventions PCI Percutaneous Transluminal coronary Angioplasty PTCAPulmonary Artery PA Line insertion Right heart catheterization Scrub procedures Temporary Pacemaker Procedural Responsibilities Experience Required: Accurate Monitoring Equipment set up Perform EKG lead placement Prep access site Recognition of life-threatening arrhythmias Room circulator Scrub-maintain sterile field Vascular Closure Systems Hospital Highlights Type of Facility: Short Term Acute Care Magnet / Teaching / Level Trauma if applicable: Magnet / Teaching / Level III Trauma Total Staffed Beds: 672 Scrub Color: provided by unit Charting: Excellian/Epic Parking Cost: Parking is a flat rate of .55/hour. This rate applies to all shifts. Shift Info: Day 4x10-Hour 07::30 About Malone Healthcare - Nursing With a commitment to providing a higher standard of service and experience in patient care, Malone Healthcare places expert nurses and allied health professionals in rewarding careers throughout the United States. As a leading healthcare staffing agency, Malone's focus on compliance and integrity translates to a seamless experience for our team members and partner facilities. When you work with Malone Healthcare, you can rely on over 50 years of proven experience placing exceptional professionals in quality healthcare settings. Benefits Weekly pay Holiday Pay Guaranteed Hours Continuing Education 401k retirement plan Pet insurance Referral bonus Medical benefits Dental benefits Vision benefits License and certification reimbursement Life insurance Keywords: Cath Lab Technologist, Cardiac Catheterization, Cardiovascular Technician, Interventional Cardiology, ECG Monitoring, Travel Healthcare Jobs, Allied Health Professional, ACLS Certification, Cardiac Stent Placement, Percutaneous Coronary Intervention

Pay Rate Low: 18 | Pay Rate High: 20 Our client is a global Bio-Industrial organization with operations all over the country. They are seeking a Laboratory Technician to be r esponsible for the daily management of laboratory samples and document retention systems and Support the processing team in sample preparation for both chemical and physical analysis. Located in North Minneapolis, MN 6 month contract with extension Pay: $18-20/hour First shift Key Responsibilities: Daily retention management of laboratory samples. Tasks include but are not limited to storing, disposing, and relocating samples to maintain an accurate retention period for all samples Support processing teams with sample processing and testing. Tasks include but are not limited to sample grinding, NIR scanning, labeling, and weighing Data entry and inventory management within laboratory LIMS database system. Maintain laboratory supplies by monitoring inventory, placing orders, and verifying receipt. Handle complex clerical, administrative, technical, or customer support tasks with minimal supervision, escalating only the most complex issues. Perform other duties as assigned. Preferred Qualifications: Bachelor's or Associate's degree in a scientific field or equivalent experience. **This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!** #INDBH #LI-DNP

Join VitalPath in Maplewood as a Quality Technician! VitalPath is a trusted contract manufacturing partner that delivers high-quality complex catheter solutions around the world that save lives and restore patient health and vital function. We strive to treat every product we design and manufacture to the highest level of quality and awareness that these products are going to be used inside of a patient, possibly even our own family members. Our employees impassioned hard work and dedication are at the core of our success. Every function within our organization plays a crucial role in our mission and is deeply valued for its contribution to achieving our shared goals of quality, innovation, continuous improvement, and operational excellence. As a fast-growing organization, we bring harmony and standardization across VitalPath with a strong vision in mind - We are one VitalPath. We embrace our diversity, celebrate each others success, support one another through change, and continue to grow as a high-performing organization. We aim to shape our corporate culture to enhance team member engagement, skills, and productivity so that VitalPath is an employer of choice. If you're ready to contribute to groundbreaking medical advancements in a collaborative, fast paced environment, we invite you to apply and be part of our growth! About the Position Perform product or raw material inspection using inspection tools and methodologies. Initiate nonconforming material reports when nonconforming product or material is found. Perform packaging, labeling, and shipping of finished product or raw material. May apply accept or reject labels on product or raw material. Work Location/Schedule This position requires the employee to be onsite at our VitalPath Maplewood, MN location. Shift/Schedule: First Shift (4x10 hour days) Monday-Thursday 5am-3:30pm VitalPath does not offer relocation assistance for this position. Responsibilities Review Documentation (travelers) to ensure good documentation practices are performed by operator/technician. Perform product or raw material inspection suing microscope, pin gage, caliper, ruler, laser micrometer, and other tools or methods. Initiate nonconforming material reports for product or raw material found to be out of specification or as part of a customer return. Perform line audits to ensure that good manufacturing practices are being followed. Ensure product or raw material are properly segregated from defective product or raw material. Work with production supervisors, technicians, and operators to communicate the importance of quality and following procedures. Support good manufacturing practices and good documentation practices throughout all phases of productions. Support calibration program for measurement equipment. Provide support to inspection team. Additional responsibilities as determined by the supervisor. Required Qualifications High School diploma or GED or related work experience and/or training 2-5 years of experience in a quality role Ability to interpret dimensional requirements on drawings Proficient in reading, writing, and speaking English Highly focused and detail oriented Excellent attention to detail, including spotting product or material nonconformity Must exhibit a willingness to work on teams and promote teamwork among other employees General computer skills with Microsoft Office Suite Must be able to work with a microscope, rulers, micrometer Must be able to sit and/or stand for extended period of time Compensation Package The hourly range for this position is $25.74 - $33.57 . The posted hourly range complies with federal and local regulations and may vary based on factors such as market conditions, level of experience and training, education, certifications, as well as internal and external equity. This position is eligible to earn an annual performance bonus based on meeting VitalPath's bonus performance plan. Benefits Comprehensive, Low Cost Health and Dental Insurance Plans Available Vision Insurance Health Savings Account with company contribution Short and Long Term Disability Supplemental insurances (short term disability, AD&D, life insurance, and more) Parental Leave Paid Time Off Minnesota Earned Sick & Safe Time Paid Holidays 401K with company match Opportunities for career growth and advancement

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $24.40 - $33.55 Advanced Quality Technician, Hematology QC Lab Description Position Summary: This position will require setup, maintenance, troubleshooting, and operation of Hematology analyzers. This position will require monitoring instrument performance throughout the QC process and troubleshooting the instrument when necessary. This position will test and approve hematology products for homogeneity during the bottling process by following established methods. You will assist the QC Laboratory Manager/Supervisor with releasing products to bottle and ship, writing procedures, and validating instruments. Proof reading labels, assay sheets and bottling documents. This position will adhere to safety regulations. Consistently demonstrate the ability to meet and understand ISO protocols and other applicable standards. Perform additional duties as assigned. Key Responsibilities · Perform, interpret, and approve laboratory homogeneity testing on control product. · Proofread documents, labels, and assay sheets. · Troubleshoot the bottling and QC instruments when necessary. · Perform manual testing on controls. · Perform sign out of bulk tested and bottled product. · Perform and write instrument validations and procedures. · Participate in training new employees. · Propose and implement process improvements. · Work with other departments at all stages of the manufacturing process. · Follow company policies and practices as outlined in the Handbook and follow guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance with the job. Qualifications Education and Experience: · Position requires an MLT/MLS degree, bachelor's degree in biology, or related field of study with a minimum of 3 years of laboratory experience. Knowledge, Skills, and Abilities: · Knowledge of laboratory equipment and clinical test methods. · Knowledge of laboratory safety standards and practices. · Knowledge of quality control and quality assurance. · Skills in moderate problem solving; ability to identify problems and appropriately suggest a course of action. · Ability to act independently on routine assignments or projects. · Ability to plan, organize, and multitask to complete assignments in an efficient manner. · Ability to maintain a clean and organized laboratory environment. · Ability to communicate professionally, both oral and written. · Ability to perform at a high-level accuracy. · Ability to consistently demonstrate quality requirements in daily work. · Established knowledge of multiple processes and/or products. · Ability to work hours that conform to standard business operations (9:30a-6p, No Holidays). · Attention to detail, organization, and data analysis skills are required. · Collaborate on projects of moderate complexity. · Data entry skills. Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

Minco is a global provider of thermal solutions, temperature sensing and control solutions, and flex circuit solutions for medical, aerospace, defense, oil and gas, power generation, and other high-reliability applications. Our experienced team couples advanced product technologies, expert design and engineering services, and a deep understanding of our customers' applications to provide comprehensive solutions that meet exacting requirements for quality, reliability, and performance. Job Summary As a Quality Technician in First Article Inspection, you will help Minco succeed by working with CMM machines, partnering with Process and Design Engineers, and embodying Minco's icare values: Integrity, Communication, Accountability, Respect, & Energy. Responsibilities Key Responsibilities: Read and interpret customer PO, clauses, drawings, and specifications to identify appropriate inspection and verification methods Interpret Geometric Dimensioning and Tolerancing specifications Program a Micro-Vu CMM for all inspections as required Perform first article inspections on new and existing products by AS9102B Proficient in the use of measurement tools (calipers, micrometers, microscopes, etc.) Communicate quality issues and concerns with production and engineering staff Perform in-process inspections Participate in problem-solving teams to support Corrective Action/Preventive Action (CAPA) activities Collect, analyze, and report on inspection data and maintain data files Participate in continuous improvement activities (i.e., waste reduction activities, reducing lead-time, and maintaining 5S standards) Assist with calibration and receiving inspection as needed Performs other duties as identified. Qualifications Skills: Good verbal and written communication skills Ability to work well with other departments or groups Demonstrated ability to communicate well with co-workers Strong problem-solving skills Performance Driven Qualifications: Two or more years of experience as a Quality Technician in a manufacturing environment Two or more years of experience operating CMM Associate's Degree in a technical field or equivalent education and experience Preferred Qualifications (Not Required): Two or more years of experience with Geometric Dimensioning and Tolerancing (ASME Y14.5-2009), or the ability/interest to learn CMM Programming experience, or the ability/interest to learn Excellent computer skills, including typing and the use of Microsoft Office applications (Outlook, Word, and Excel) Experience as a first article inspector Experience using a Micro Vu CMM machine, or the ability/interest to learn Knowledge of Discuss and InSpec software, or the ability/interest to learn Experience navigating within an ERP system (IFS) Understanding of technical engineering processes and equipment Understanding of mathematical calculations involving basic statistics and operational data Experience with basic measurement equipment for part and product inspection Familiar with ANSI Z1.4-2003, ANSI Z1.9-2003, or the ability/interest to learn Familiar with ISO9001:2008 and AS9100C standards, or the ability/interest to learn Able to collect, analyze and report data Demonstrated continuous improvement skills (Lean, 6σ), or the ability/interest to learn Why Minco? At Minco, we offer benefits and services that help balance work life and personal life, a competitive wage and benefits package, opportunities for continuous improvement and personal growth, and company celebrations - some of the many reasons that make Minco a great place to work! Find out why you would love working at Minco by learning more about our company culture and the rewards of working with us at ********************* - then apply! Current Minco Employees: Please apply via your employee page. If you need assistance, please contact ************************ Reports To: Quality Inspection Manager Location: Fridley, Minnesota Benefits: Healthcare benefits are eligible on the first of the month following the hire date, 401K with an employer match after 61 days of full-time employment, Short Term Disability Insurance, Long Term Disability Insurance, HAS, and FSA available, Tuition Reimbursement, Employee Managed Time-Off We are proud to be an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, national origin, veteran, marital, or disability status. We maintain a drug-free workplace and perform pre-employment substance abuse testing and background checks. Minco Products, Inc. is an E-Verify employer. This position requires the use of information or access to hardware and software that is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons, as defined by ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee)

We're looking for people who put their innovation to work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. Experience the opportunity to excel in a role that sets you on a path to becoming a quality engineering expert. At nVent Management Company, we are committed to nurturing your ambition, ensuring you can develop your skills in an environment dedicated to flawless execution and world-class standards. As a Quality Technician, you will gain invaluable experience and contribute to our mission of achieving exceptional quality. You will: Lead root cause problem-solving activities aimed at enhancing internal and external quality levels. Perform process validations, in-process inspections, and quality monitoring of manufacturing processes and products. Support design, manufacturing, and quality engineering functions through data collection, analysis, product reviews, and process capability assessments. Develop and adhere to Quality Management Systems (QMS) objectives, and train personnel to align with QMS standards. Conduct internal ISO standard audits and provide necessary audit support. Prepare formal documented First Article Inspection (FAI) reports for both customer and internal use. Identify and apply suitable measuring tools and equipment to confirm dimensional and functional requirements. Communicate effectively across various departments such as Operations, Supply, Manufacturing Engineering, Design, Quality, Customer Service, Production Planning, and Logistics. Lead or assist in maintaining the calibration status of inspection, test, and measurement equipment. Perform other related duties as assigned. No corrective actions or performance improvement plans within six (6) months of the job posting opening date. No decision making leaves within 12 months of the job posting opening date. Most recent performance rating achieves or higher. Successfully completed six (6) months in current job bid classification OR current career advancement classification. Requirements: High school diploma or equivalent experience. American Welding Society (AWS) Certification as Certified Welding Inspector preferred. Proficiency in reading blueprints; knowledge of Geometric Dimensioning and Tolerancing (GD&T) is a plus. Interest in academic and career development preferred. Minimum of 2 years of experience in quality. Preferable experience with precision metal fabrication measurement tools and techniques. Strong knowledge of charting and process control methods. Familiarity with Quality Management Systems (QMS) is preferred. WE HAVE: A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day nVent is a leading global provider of electrical connection and protection solutions. We believe our inventive electrical solutions enable safer systems and ensure a more secure world. We design, manufacture, market, install and service high performance products and solutions that connect and protect some of the world's most sensitive equipment, buildings and critical processes. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation. Our principal office is in London and our management office in the United States is in Minneapolis. Our robust portfolio of leading electrical product brands dates back more than 100 years and includes nVent CADDY, ERICO, HOFFMAN, ILSCO, SCHROFF and TRACHTE. Learn more at ************** Commitment to strengthen communities where our employees live and work We encourage and support the philanthropic activities of our employees worldwide Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: Innovative & adaptable Dedicated to absolute integrity Focused on the customer first Respectful and team oriented Optimistic and energizing Accountable for performance Benefits to support the lives of our employees Pay Transparency nVent's pay scale is based on the expected range of base pay for this job and the employee's work location. Employee pay within this range will be based on a combination of factors including knowledge, skills, abilities, experience, education, and performance. Where federal, state, or local minimum wage requirements exist, employee pay will comply. Compensation Range: $20.40 - $37.80 Per Hour Depending on the position offered, employee may be eligible for other forms of compensation, such as annual incentives. Benefit Overview At nVent, we value our people and their health and well-being. We provide a broad benefits package with meaningful programs for eligible full-time employees that includes: Medical, dental, and vision plans along with flexible spending accounts, short-term and long-term disability benefits, critical illness, accident insurance and life insurance. A 401(k) retirement plan and an employee stock purchase plan - both include a company match. Other supplemental benefits such as tuition reimbursement, caregiver, personal and parental leave, back-up care services, paid time off including volunteer time, a well-being program, and legal & identity theft protection. At nVent, we connect and protect our customers with inventive electrical solutions. People are our most valuable asset. Inclusion and diversity means that we celebrate and encourage each other's authenticity because we understand that uniqueness sparks growth. Billing Identifier: DS / EQP - Anoka, MN

Permanent About Heraeus Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead. About Heraeus Medevio Together we improve lives. At Heraeus Medevio, we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group, we are committed to the growth of our teams and organization by providing an open space for open minds. To reach our vision of improving 100 million lives every year, we foster a culture of curiosity that thrives on challenge, continuous learning, growth, and the opportunity to try new things. With sites in the United States, European Union, and Asia, and over 2,200 employees worldwide, together, we will meet tomorrow's challenges today. Position Summary The primary responsibility of the Quality Technician II will be to support Quality Systems including calibration and document control to assure that equipment and documents are maintained in compliance with Heraeus procedures and applicable regulations and standards. What You'll Do Every Day: * Maintains calibrated equipment in calibration system with accuracy and completeness. * Tracks calibration status of equipment and notifies departments/owners when equipment is due for calibration. * Reviews calibration records to ensure compliance to ISO standard and calibration procedure requirements. * Identifies, reports and documents all discrepancies, and potential problems. Participates in root cause analysis. Assists QE in nonconforming out of tolerance report transactions, management and tracking of nonconformances to completion. * Performs complex visual and dimensional inspection of various calibrated tools and equipment to ensure compliance with drawings and specifications. * Assures document control and record keeping activities are carried out and completed in compliance with established procedures and work instructions. * Processes document change requests within the document control system through document approvals and release. Compile calibration and document control data for internal review and trending. * Occasional travel for cross site support between White Bear Lake and Fridley, Minnesota. * Other duties may be assigned as required. What We're Looking For: * High school diploma required; trade school, associate/technical degree or CQT/CMI certification a plus. * Minimum 3 years of relevant experience in inspection or quality systems. * Proficient with use of precision tools such as calipers, gauges, microscopes, comparator, laser micrometer and video inspection equipment. * Proficient in Geometric Dimensioning and Tolerancing and Statistical techniques. * Proficient using Microsoft Office and calculators. * Experience with ISO 17025, ISO 10012, ISO 13485 and NIST standards a plus. * Fluent in English, both written and verbal. * Train the Trainer experience a plus. Medevio is committed to providing competitive total compensation and benefits packages. The expected hiring range for this position is between $24.00/hr and $31.25/hr based upon a full-time schedule. This is a good faith estimate on the applicable range. Base salaries are determined by taking a variety of factors in account, including, but not limited to, candidate qualifications, geographic locations, market conditions and internal equity. This position is bonus eligible. Our total compensation package includes eligibility for comprehensive medical, dental, and vision coverage, a 401(k) plan with company match, education reimbursement, paid parental leave and paid time off. Curious? Apply now! Heraeus is proud to be an employer that provides equal access to opportunities for all its employees. We provide fair and equal consideration to all qualified applicants, regardless of sex, gender identity, sexual orientation, race, color, religion, national origin, physical or mental disability, protected veteran status, age, or any other legally protected characteristic. A diverse and inclusive culture is at the heart of our Vision, Mission, and Values. We are dedicated to cultivating a workforce that reflects a broad spectrum of cultures, backgrounds, and perspectives. We participate in E-Verify to confirm employment eligibility after hire. Learn more at **************** Any further questions? If you need any assistance or have questions, please contact ***************************** or visit our website at jobs.heraeus.com. ReqID: 58699

Quality Technician II Permanent About Heraeus Making displays foldable? Helping hearts beat with medical innovations? Or breathing new life into precious metals? As a family-owned global technology group we help our customers to always being one step ahead. About Heraeus Medevio Together we improve lives. At Heraeus Medevio, we bring lifesaving and life-changing medical devices to market through partnerships with medical device manufacturing companies. Backed by Heraeus Group, we are committed to the growth of our teams and organization by providing an open space for open minds. To reach our vision of improving 100 million lives every year, we foster a culture of curiosity that thrives on challenge, continuous learning, growth, and the opportunity to try new things. With sites in the United States, European Union, and Asia, and over 2,200 employees worldwide, together, we will meet tomorrow's challenges today. Position Summary The primary responsibility of the Quality Technician II will be to support Quality Systems including calibration and document control to assure that equipment and documents are maintained in compliance with Heraeus procedures and applicable regulations and standards. What You'll Do Every Day: Maintains calibrated equipment in calibration system with accuracy and completeness. Tracks calibration status of equipment and notifies departments/owners when equipment is due for calibration. Reviews calibration records to ensure compliance to ISO standard and calibration procedure requirements. Identifies, reports and documents all discrepancies, and potential problems. Participates in root cause analysis. Assists QE in nonconforming out of tolerance report transactions, management and tracking of nonconformances to completion. Performs complex visual and dimensional inspection of various calibrated tools and equipment to ensure compliance with drawings and specifications. Assures document control and record keeping activities are carried out and completed in compliance with established procedures and work instructions. Processes document change requests within the document control system through document approvals and release. Compile calibration and document control data for internal review and trending. Occasional travel for cross site support between White Bear Lake and Fridley, Minnesota. Other duties may be assigned as required. What We're Looking For: High school diploma required; trade school, associate/technical degree or CQT/CMI certification a plus. Minimum 3 years of relevant experience in inspection or quality systems. Proficient with use of precision tools such as calipers, gauges, microscopes, comparator, laser micrometer and video inspection equipment. Proficient in Geometric Dimensioning and Tolerancing and Statistical techniques. Proficient using Microsoft Office and calculators. Experience with ISO 17025, ISO 10012, ISO 13485 and NIST standards a plus. Fluent in English, both written and verbal. Train the Trainer experience a plus. Medevio is committed to providing competitive total compensation and benefits packages. The expected hiring range for this position is between $24.00/hr and $31.25/hr based upon a full-time schedule. This is a good faith estimate on the applicable range. Base salaries are determined by taking a variety of factors in account, including, but not limited to, candidate qualifications, geographic locations, market conditions and internal equity. This position is bonus eligible. Our total compensation package includes eligibility for comprehensive medical, dental, and vision coverage, a 401(k) plan with company match, education reimbursement, paid parental leave and paid time off. Curious? Apply now! Heraeus is proud to be an employer that provides equal access to opportunities for all its employees. We provide fair and equal consideration to all qualified applicants, regardless of sex, gender identity, sexual orientation, race, color, religion, national origin, physical or mental disability, protected veteran status, age, or any other legally protected characteristic. A diverse and inclusive culture is at the heart of our Vision, Mission, and Values. We are dedicated to cultivating a workforce that reflects a broad spectrum of cultures, backgrounds, and perspectives. We participate in E-Verify to confirm employment eligibility after hire. Learn more at **************** Any further questions? If you need any assistance or have questions, please contact ***************************** or visit our website at jobs.heraeus.com.

What We Want to Give You: We offer a competitive wage and wide array of benefits including: • health/dental/vision insurance • flexspending accounts • short & long-term disability • paid holidays and vacation • bonus opportunities (referral, production, etc.). Job Summary: The Quality Tech is responsible for ensuring that all elements of food safety within the Quality Monitoring Scheme are being met. Ensures that all regulatory, customer, and company quality initiatives are being met and maintained. Job Duties and Responsibilities: · Perform Quality checks on production lines in a timely and accurate fashion every hour per line. (Will frequently be responsible for 3 lines at any given time). · Brings discrepancies with the QMS to the attention of Supervisor or Quality Manager. These discrepancies are but not limited to HACCP programs, Allergen programs, Sanitation procedures, GMP findings, Foreign Material findings, and HOLD procedures. · Ensure that product being produced meets all legal and customer requirements as outlined in the Bluebook for each product. · Complete paperwork in a timely and accurate fashion each day. · Perform required tasks to maintain 5-S and keep work areas clean. · Keep all information pertaining to our operations (products, customers, production details, etc.) confidential. · Maintain instrumentation and equipment in good condition and store appropriately. · Label, store, and organize samples and product retentions. · Follow Hold Procedures for all non-conforming materials or product. · Perform HACCP and Preventive Controls checks/tasks as needed. · Assist in test runs and new product trials as needed. · Perform other audits or inspections as required. · Perform other duties as required by supervisor. Minimal Qualifications: · High School Diploma or GED required · Post High School education preferred · Required - 3 months of as a Quality Assurance Technician. · Preferred - 1 years of experience as a QA Technician or other Technical department. · Must have good attention to detail and be able to spot defects on fast-moving production lines. · Must be able to gain a basic understanding of how different machinery operates as it relates to the quality of the product and adjustments that need to be made to correct certain conditions. · Good verbal and written communication skills. Ability to speak, write, and comprehend Spanish is a plus. · Must be able to perform simple mathematic calculation, including working with fractions, ratios and percentages. · Must be able to maintain good interpersonal communications and work collaboratively with co-workers, employees from other departments, and superiors. · Experience with MS Office Suite is needed. · Follow all safety processes and procedures set forth by site leadership. Work Environment and Physical Requirements: · Manufacturing environment - exposure to a variety of machines, noise levels, and varying temperatures. · Depending on which location, our environments can be very warm or refrigerated. · Team environment - must be able to work well with others and communicate in a respectful and professional manner. · Must have ability to lift 40 pounds occasionally and stand or sit for lengthy durations. · Must be able to work necessary overtime based on staffing needs and customer demand, as well as across shifts. Starting Pay: $22.00/hr., a shift differential of $1.25 is offered for this 3rd shift opportunity. We offer a comprehensive benefits package for full-time employees including health, dental, 401k and wellness benefits beginning on the 90th day of employment. This information is provided per the relevant state and local pay transparency laws for the location in which this position will be performed. Base pay information is based on market location.

Quality Technician Micro-Matics Inc. is a leader in providing high quality precision Swiss components and assemblies to some of the largest companies in the medical, aerospace, and commercial industries. We offer competitive wages, and a comprehensive benefits package with a safe and clean working environment. Responsibilities: Candidate must have experience in First Article (Set-Up), In-process, and Final inspections. Visually inspect machined parts for defects, (burrs, edge breaks, surface/tool blends etc.) to ensure they meet Customer specifications and quality standards. Maintain accurate records of Final & In-process inspections, First Article, PPAP and data collection. Assist in identifying and resolving quality issues, working with other team members and teams. Participate in continuous improvement projects and processes. Maintain compliance with the company's policies and procedures. Maintain clean and organized work environment. Maintain compliance with ISO 13485, ISO 9001-AS9100 certified procedures and practices Requirements Minimum 1 year experience Must be able to interpret blueprints with GD&T and have practical and/or formal training in Inspection documentation. Experience in the use of and programming OGP/CMM (vision system), statistical/data software, complaint & CAPA documentation and experience with supplier communication is a plus. Individual must have experience using inspection tools (micrometers, calipers, drop indicators, thread gauges, plug gauges, comparators, microscope, etc.) Candidate must know how to apply measurement techniques to dimensions. Skills: Needs to have solid communication skills and the ability to work under minimal supervision. Candidate must be on time for the start of your shift and be able to work overtime if needed. Candidate needs to be a self-motivated team player with a good work ethic and produce quality work in a timely fashion. Benefits: Competitive wage Paid PTO & holidays Medical, dental, vision, H.S.A 401k & match Monthly & annual incentive plan Shift Hours: Day Shift Monday - Thursday 9am-5:30pm, Fridays 7-1pm

Up North Plastics is currently seeking Quality Control Technicians to join our quality team on our Night Shift. Up North Plastics produces several lines of plastic products including high quality trash bags, construction films, and agricultural tubes. Pay Rate: $19.50 Qualifications Strong computer skills Strong attention to detail Previous manufacturing experience a plus Previous quality experience a plus Responsibilities Quality Control Technicians at Up North Plastics are responsible for conducting quality audits on finished product to ensure that they meet required specifications. This role is also responsible for analyzing data and forming solutions to any issues that may arise from completed audits. The role may involve additional responsibilities and opportunities as they become necessary and/or are assigned by management. Up North Plastics provides indepth on the job training with a lot of opportunity for growth. Also, Up North Plastics allows a great deal of overtime and paid breaks. Up North Plastics offers competitive compensation packages including Medical/Dental, paid vacations and holidays, ESST, and 401(K).

METAL CRAFT , located in Elk River, MN is a precision machining company, and our company mission is to provide custom precision manufacturing and innovative services to medical, aviation, space, defense, and emerging high-tech industries. We are seeking a QUALITY TECHNICIAN to join our team! An ideal candidate is an individual that is passionate about their work and committed to quality, service, excellence, and innovation. Our Culture is best in class! “BUILT RIGHT. EVERY TIME” is not just a slogan, we build things that make a difference in people's lives. A career at METAL CRAFT is rewarding for far more reasons than you might imagine. Your experience and expertise are highly valued, your contributions are recognized, and your professional goals are supported. We understand there are lots of choices out there, that is why for over 40 years we have been providing stability, a safe and clean environment, challenging work and are invested in the growth of our people to take them as far as they want to go. In this role, the QUALITY TECHNICIAN will ensure materials and finished goods conform to all company and customer standards. Perform inspections on incoming materials and in-process and final product to ensure quality levels are met. Perform first piece set-up and First Article Inspections in accordance with established inspection plans. Assist Quality Engineers in the execution of engineering studies. QUALITY TECHNICIAN DUTIES AND RESPONSIBILITIES include but not limited to: Conduct receiving, in-process, final inspections, and first piece set-up utilizing the appropriate measuring tools and equipment to verify dimensional and functional requirements. Conduct visual examination of product in accordance with customer specifications and company workmanship standards. Perform formal documented First Article Inspection (FAI) reports for internal and external customers. Prepare, maintain, and review inspection reports. Assist Quality Engineers in the creation of inspection plans. Perform containment activities preventing potential or additional quality defects. Develop in-process control charts for monitoring / improving performance as requested. Perform as auditee in respect to inspection processes for internal and external audit support as requested. Assist engineering in the execution of engineering studies such as measurement system analysis, capability analysis, etc. as requested. Perform problem solving activities for both product and manufacturing processes. Effectively communicate with cross-functional areas: supply chain, manufacturing, engineering, quality engineering, customer service, production planning. Train and Mentor Quality Technicians I and II. Participate in lean activities as required. Other miscellaneous duties as assigned. Responsible to conduct yourself and ensure your subordinates (if applicable) conduct themselves in a manner consistent with company mission, values, code of ethics, policies, and other standards of conduct. EDUCATION/EXPERIENCE Associates degree or equivalent combination of education and experience. Minimum 5+ years of quality assurance experience required. KNOWLEDGE/SKILLS/ABILITIES Skilled in use of standard inspection equipment and basic hand tools, such as: calipers, micrometers, steel rules, pin gages, go-no-go gages, CMM and Vision equipment. Understanding of Geometrical Dimensioning and Tolerancing (GD&T), engineering drawings and specifications, sampling techniques, and safety information. Working knowledge of ISO 13485, AS 9100, FDA Quality System Regulations, and Good Manufacturing Practices (GMP). Problem solving and decision-making skills and the ability to think independently. Ability to demonstrate a record of excellent performance in meeting high standards of quality, quantity and dependability (attendance and punctuality). Strong listening, verbal, and written communication skills. Ability to collaborate and work well with others. Advanced knowledge of Microsoft Office including Word, Excel and Outlook. Must be detail oriented to keep accurate records and files. Show initiative in work by being a self-starter, suggesting new ideas for completing a job, giving input as to how to improve the efficiency of a job, and organizing work time in order to complete jobs in a timely matter. CORE VALUES People - We can do it Innovation - We work together Service - We honor our word Quality - We do what's right Monday - Friday 7AM - 3:30PM plus overtime as needed Non-exempt (hourly) Benefits Eligible position (Health, Dental, Vision, 401K, profit sharing, holiday pay, PTO) Metal Craft and Riverside are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other federally protected class.

Support laboratory operations by independently performing standard testing procedures and preparing samples for analysis. Responsibilities + Execute established testing protocols and prepare materials for analysis with minimal oversight. + Assemble and operate experimental setups under direction from senior team members. + Perform routine maintenance and calibration of lab instruments to ensure optimal performance. + Accurately document test results and maintain comprehensive logs of experimental activities. + Assist in tracking and replenishing laboratory inventory and consumables. + Adhere to safety standards and contribute to maintaining a clean and organized lab environment. Essential Skills + Proficiency in laboratory sample preparation and analytical chemistry. + Experience in data entry and laboratory documentation. + Familiarity with lab testing procedures. Additional Skills & Qualifications + Non-degree candidate or associate's degree with 1-3 years of lab experience. + Strong verbal and written communication skills for interaction with internal and external customers. + Ability and willingness to work in a team environment, preferably multinational. + PC skills in Windows (Word, Excel, PowerPoint). Work Environment The position is based in an analytical and materials testing lab at the Maple Grove site. The work environment is team-oriented, focusing on development and long-term growth within a small team that is part of a larger organization. Job Type & Location This is a Contract to Hire position based out of Maple Grove, MN. Pay and Benefits The pay range for this position is $23.00 - $24.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Maple Grove,MN. Application Deadline This position is anticipated to close on Jan 22, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

This role is for a Travel Cath Lab Technologist providing specialized cardiovascular catheterization lab services for a 13-week assignment in Minneapolis. Candidates must hold an active, unrestricted US state license, have at least 2 years of relevant experience, and possess certifications such as BLS and ACLS. The position offers benefits including medical insurance, paid time off, and exclusive contracts through Ghost RX Inc, a healthcare staffing company serving federal hospitals. Ghost RX Inc is seeking a travel Cath Lab Technologist for a travel job in Minneapolis, Minnesota. Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Duration: 13 weeks 40 hours per week Shift: 8 hours Employment Type: Travel Qualifications Active, unrestricted license from any US state or territory. Any state license is accepted. Proof of eligibility to work in the United States BLS, ACLS, RCI or CCI At least 2 years of recent experience in specialty and a like setting. Ghost RX Benefits Medical, dental, vision insurance Paid time off Paid sick leave Paid holiday and federal holiday Exclusive/direct contracts with no outside competition. Qualified candidates will be approved for the job they are submitted for in a timely manner. Ghost RX Inc Job ID #510. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. About Ghost RX Inc Ghost RX provides Healthcare personnel to federal hospitals and healthcare facilities the country. Our exclusive contracts cut out the outside competition and the VMS black hole. Your profile is delivered directly to the hiring manager, allowing for immediate approvals and offers. Contracts vary in length from 6 months to 5 years. Ghost RX is a Service Disabled Veteran Owned Small Business. Keywords: Travel Cath Lab Technologist, Cardiovascular Technologist, Catheterization Lab, Healthcare Staffing, BLS Certification, ACLS Certification, Travel Healthcare Jobs, Allied Health Professional, Medical Technologist Travel, Cardiology Technician

By joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $24.40 - $33.55 POSITION SUMMARY The responsibilities of an Advanced Quality Technician are to perform tasks in the process of inspecting and testing science products. Duties may require interpreting results, inventory, and participation in complaint investigations. This position will participate in the continuous improvement of our products and customer-centered culture. ESSENTIAL FUNCTIONS Conduct inspections of raw materials and finished goods to ensure specifications and quality standards are met with minimal instruction and supervision. Conduct inspection of product literature and labels to ensure accuracy. Attention to detail. Ability to reconcile documents. Compile, analyze and report on data of moderate complexity. Consistently advocate for Quality Ideals by demonstrating commitment to meeting quality requirements in daily work Make decisions based on data or results of work. Draft and revise standard operating procedures (SOP's). Propose and Implement process improvements. Utilize relevant internal databases and job-applicable software programs effectively. Demonstrate a high level of problem-solving ability with the capacity to suggest future changes. Participate in training less experienced employees. Fill in for all Quality Technician duties as needed. Follow guidelines and comply with all company safety, quality, and training procedures and regulations. Perform additional duties as assigned. JOB SPECIFICATIONS Education and Experience: This position requires a high school diploma or equivalent with 2+ years related experience or an associate degree with 0+ years of experience. Must have proficient computer and data entry skills, organizational skills, and excellent proofreading skills. Must be detail oriented. A working knowledge of Microsoft Word and Excel is required. Must be able to work in a fast-paced environment, multitask, and have good communication skills, both verbally and in writing. Knowledge, Skills, and Abilities Knowledge of Quality Assurance principles. Knowledge of ISO13485, ISO9001, and MDSAP Compliance. Knowledge of safety and company procedures and practices. Skills in coordination with Manufacturing departments. Skills in problem solving; including the ability to identify and appropriately evaluate a course of action. Skills in critical thinking. Ability to be flexible. Ability to act independently and with teams on projects. Ability to plan, organize and multi-task to complete assignments in an efficient manner. Ability to communicate professionally, both oral and written. Ability to pay attention to details and perform at a high-level of accuracy. Ability to work independently and with a team. Ability to work hours that conform to standard business operations (8:00 A.M. to 5:00 P.M.) Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees' financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

We're looking for people who put their innovation to work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. We're looking for people who put their innovation work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. What you will experience in this position: Provide quality assurance support and lead root cause problem solving activities that are aligned to improve internal and external quality levels, supporting overall customer satisfaction of our products. Lead problem solving activities for both product and manufacturing processes, with assistance from Quality Engineer Perform process validations, in-process inspections, and monitoring, analyzing the quality of manufacturing processes and products Provide support to design, manufacturing, and quality engineering functions for data collection, analysis, product review, and process capabilities Understand, adhere to, and develop processes compliant with the Quality Management Systems (QMS) objectives, as well as train other personnel to adhere to QMS standards Perform internal ISO standard audits and provide audit support in designated areas Provide formal documented FAI reports suitable for customer or internal use as required Determine and use appropriate measuring tools and equipment to verify dimensional and functional requirements Effectively communicate with appropriate areas as needed, (Operations, Supply, Manufacturing Engineering, Design, Quality, Customer Service, Production Planning, Logistics, etc.) Lead and/or assist in supporting the activities that maintain the calibration status of inspection, test, and measurement equipment Perform other related duties as assigned You have: High school diploma or GED Ability to read schematics, blueprints and process related documents. GD&T knowledge is a plus. Knowledge of how Air Conditioning equipment operates and functions is a plus 2+ years working in the quality/manufacturing field Ability to use measurement tools and techniques Experience with Quality Management Systems (QMS) preferred Skills: Strong written, verbal, and interpersonal communication skills Attention to detail and ability to prioritize tasks is key to being successful in this role Must be able to interpret order requirements, quotes, drawings, and draw conclusions Ability to use precision measuring equipment (e.g., calipers, micrometer, paint mill gauges, etc.) Skilled in identifying root causes of routine problems/issues and the ability to develop recommendations for resolution Ability to interpret and apply Quality Systems / ISO procedures and documentation Comfortable using computer systems and software including MS Office Applications and ERP System (JD Edwards is a plus) Abilities to meet the physical and environmental demands: Lift up to 50lbs Stand and walk frequently Operate hand tools Work primarily indoors where there is frequently noise of 85 dB and occasional exposure to chemical hazards (solvents) We have: A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day We are a $2.4 billion, high-performance electrical company with a dedicated team of 10,000 people, across more than 80 global locations We have a robust portfolio of product brands dating back more than 100 years and including: nVent CADDY, ERICO, HOFFMAN, RAYCHEM, SCHROFF and TRACER Commitment to strengthen communities where our employees live and work We encourage and support the philanthropic activities of our employees worldwide Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: Innovative & adaptable Dedicated to absolute integrity Focused on the customer first Respectful and team oriented Optimistic and energizing Accountable for performance Benefits to support the lives of our employees WE HAVE: A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day nVent is a leading global provider of electrical connection and protection solutions. We believe our inventive electrical solutions enable safer systems and ensure a more secure world. We design, manufacture, market, install and service high performance products and solutions that connect and protect some of the world's most sensitive equipment, buildings and critical processes. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation. Our principal office is in London and our management office in the United States is in Minneapolis. Our robust portfolio of leading electrical product brands dates back more than 100 years and includes nVent CADDY, ERICO, HOFFMAN, ILSCO, SCHROFF and TRACHTE. Learn more at ************** Commitment to strengthen communities where our employees live and work We encourage and support the philanthropic activities of our employees worldwide Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: Innovative & adaptable Dedicated to absolute integrity Focused on the customer first Respectful and team oriented Optimistic and energizing Accountable for performance Benefits to support the lives of our employees Pay Transparency nVent's pay scale is based on the expected range of base pay for this job and the employee's work location. Employee pay within this range will be based on a combination of factors including knowledge, skills, abilities, experience, education, and performance. Where federal, state, or local minimum wage requirements exist, employee pay will comply. Compensation Range: $20.40 - $37.80 Per Hour Depending on the position offered, employee may be eligible for other forms of compensation, such as annual incentives. Benefit Overview At nVent, we value our people and their health and well-being. We provide a broad benefits package with meaningful programs for eligible full-time employees that includes: Medical, dental, and vision plans along with flexible spending accounts, short-term and long-term disability benefits, critical illness, accident insurance and life insurance. A 401(k) retirement plan and an employee stock purchase plan - both include a company match. Other supplemental benefits such as tuition reimbursement, caregiver, personal and parental leave, back-up care services, paid time off including volunteer time, a well-being program, and legal & identity theft protection. At nVent, we connect and protect our customers with inventive electrical solutions. People are our most valuable asset. Inclusion and diversity means that we celebrate and encourage each other's authenticity because we understand that uniqueness sparks growth.

Support laboratory operations by independently performing standard testing procedures and preparing samples for analysis. Responsibilities Execute established testing protocols and prepare materials for analysis with minimal oversight. Assemble and operate experimental setups under direction from team members. Perform routine maintenance and calibration of lab instruments to ensure optimal performance. Accurately document test results and maintain comprehensive logs of experimental activities. Assist in tracking and replenishing laboratory inventory and consumables. Adhere to safety standards and contribute to maintaining a clean and organized lab environment. Essential Skills Proficiency in laboratory sample preparation and analytical chemistry. Experience in data entry and laboratory documentation. Familiarity with lab testing procedures. Additional Skills & Qualifications Non-degree candidate or associate's degree with 1-3 years of lab experience. Strong verbal and written communication skills for interaction with internal and external customers. Ability and willingness to work in a team environment, preferably multinational. PC skills in Windows (Word, Excel, PowerPoint). Work Environment The work environment is team-oriented, focusing on development and long-term growth within a small team that is part of a larger organization. Job Type & Location This is a Contract to Hire position based out of Minneapolis, MN. Pay and Benefits The pay range for this position is $23.00 - $24.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Minneapolis,MN. Application Deadline This position is anticipated to close on Jan 27, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.