Quality Manager
Quality engineer job in Plymouth, MN
Trelleborg Medical Solutions is seeking a NPD Quality Manager to join their team. The NPD Quality Manager develops and achieves New Product Development (NPD) Quality initiatives to support Trelleborg Goals and Objectives. Oversees the Validation and verification requirements of new products/programs as well as ensuring that all related quality activities are carried out in accordance with industry standards and regulations. Manages overall NPD Quality resources and ensures that capacity and capability meet the customer demand. Optimizes both human and capital resources through continuous improvement activities.
Tasks and Responsibilities
Provides leadership for NPD Quality Team within the Innovation Center or remotely located at an H & M Manufacturing site, with varying degrees of expertise and experience
Manages & oversees all aspects of the H&M NPD Quality Team (multiple sites) involved in quality related product/program development projects from conceptualization & validation phase through release to manufacturing
Must be knowledgeable and adhere to H&M Trelleborg Quality Management System and its requirements
Drives and supports QMS initiatives and continuous improvement activities.
Ensures direct reports are successfully performing their duties as assigned. Provides coaching on an ongoing basis.
Assigns projects and responsibilities to the direct reports. Ensures skill-sets of staff are in alignment with expected duties.
Establishes and develops site-specific processes as required/requested
Reviews and approves processes, Quality Plans, protocols/reports, as necessary.
Ensures proper resource allocation to support needs to ensure delivery expectations of customers
Provides recommendations for goals and objectives for the Quality Department
Works closely with internal resources to establish processes and resolve issues
Drives best practices through the application of effective quality engineering principals and procedures across functions
Ensures proper controls are being systematically applied to both new and legacy products
Supports internal and external audits
Provides recommendations based on data for improvements that are measurable.
Education and Experience
Required:
4-year degree in Engineering or Science-related field
6 years of increasing experience providing technical support and leadership in medical device manufacturing environment
2 years Leadership/Supervisory-level experience, with decision-making authority/responsibility
Quality certifications (ASQ CQE, CQA, CQM, etc.)
Class I, II, III Medical Device Manufacturing experience
Knowledge and experience with ISO/FDA: ISO 9000/9001; ISO 13485, and 21CFR Part 11/820 (and 4/210/211 as applicable)
Desired
Experience in coaching and utilizing performance management tools and disciplines
Experience in a CMO producing Medical Devices
Experience with ERP, Document Control, MES, and other types of software
Experience auditing (internal and external) for all elements of ISO 9001 and/or ISO 13485
Experience with the successful completion of multiple projects for new product development or improvement initiatives
Extensive experience with statistical analysis, Minitab software (or equivalent), GD&T and CAPA investigation and resolution
Competencies
Ability to read, write, speak and understand the English language
Ability to communicate clearly by conveying and receiving ideas, information and direction effectively
Ability to demonstrate adequate job knowledge to deliver a world class performance
Ability to challenge oneself to consistently meet all goals and deadlines
Willingness to strive for excellence by producing work that is free of errors and mistakes
Demonstrated active leadership skills
Strong statistical background and understanding
Ability to lead cross functional groups for continuous improvement projects
Ability to apply Six Sigma Methodologies to manufacturing processes and experience teaching others these techniques
Strong verbal, written, organizational and interpersonal skills. Ability to communicate clearly and effectively to customers either in person or via video or telephone conference
Ability to work flexible schedule as required by workload/project
As a valued team member with Trelleborg, you will enjoy:
Competitive compensation: Plus, bonus opportunities!
Generous benefits package: Includes health, dental, vision, STD, LTD, life, 401k, paid time off, tuition reimbursement, and more!
Clean work environment: Enjoy working in a very clean and climate-controlled environment every day!
Greater opportunity for impact: You will impact the production of life-saving devices.
Growth and advancement: Join a global company that loves to promote from within and allows for advancement.
Salary range: $109,000-125,000/year
NOTE: This job description is not intended to be all-inclusive. Employees may perform other related duties as required to meet the ongoing needs of the organization.
EEO Statement
Quality Assurance Manager
Quality engineer job in Plymouth, MN
PRIMARY FUNCTION
Responsible for implementing and performing quality system processes that ensure Endogenex meets requirements of internal procedures and applicable external standards/ regulations (including but not limited to ISO 13485, 21 CFR 820,806 and 803, EU MDR, MDSAP).
PREFERRED QUALIFICATIONS
Bachelor's degree with 7+ years of quality experience in medical device and/or comparable regulated environment
Familiarity with applicable external standards/ regulations (ISO 13485, USA, EU MDR, MDSAP, UK and Australian)
Strong interpersonal, organizational, and technical writing skills
Strong communication and leadership skills, with the ability to work effectively in a fast-paced, collaborative environment.
Ability to manage multiple priorities with commitment and performance to deadlines
Experience with implementing and completing activities that maintain compliance with document control requirementsand quality system management software systems (experience with Grand Avenue preferred)
Experience implementing and completing activities related to Post Market Surveillance, Complaints, CAPAs, and Nonconformances along with corresponding risk management determinations
Strong computer skills and statistical trending techniques
RESPONSIBILITIES:
Implement and maintain document control and assigned portions of the quality system in compliance with applicable regulations and standards.
Processing document change requests, including reviewing for completeness, managing approvals, releasing documents, and managing document control assigned tasks following document release.
Responsible for all manufacturing and quality system trending and post-market surveillance activities.
Responsible for generating and managing all NCM and Servicing files .
Performs all quality system metric recording and report records.
Tracking and trending CAPAs, nonconformances, complaints and other quality system monitoring.
Implements complaint investigation process, including but not limited to complaint file documentation, departmental coordination, proper escalation, and initial reporting assessments.
Appropriately identifies outputs from work processes which drive additional efforts within the product lifecycle including but not limited to risk management updates, management review recommendations and quality system alert/alarm levels.
Manage calibrated equipment, including tracking when calibration is due, coordinating completion of calibration, and reviewing calibration certificates for accuracy without impacting production or R&D programs.
Manage employee training files and training program, ensuring employees stay up to date with required training. Lead efforts in streamlining and incorporating training material updates as required.
Manage creation, implementation, and ongoing monitoring of supplier and part approvals
Manage return material authorization (RMA) process.
Assist in preparation of management review presentations.
Tracking release of and coordination with affected department for implementation of new standards. Provide gap analysis assessment reports to affected departments.
Performs product dispositioning documentation on behalf of quality and execute quality assurance in return/service/rework programs - This includes responsibility for certificates of conformance approvals and finished goods inspection and lot release.
Performs all device related inspection procedures requiring quality oversight and approval
Supports production quality documentation retention for finished goods
Perform other duties and responsibilities as assigned.
Special Physical Demands and Working Conditions
1)
Physical demands
: While performing the duties of this job, the employee is occasionally required to walk; sit; use hands to finger, handle or feel objects, tools, or controls; reach with hands and arms; balance; stoop; talk and hear. Specific vision abilities required by the job include close vision and distance vision. Ability to occasionally lift and/or move up to 35 pounds.
2)
Work environment
: Fast paced work environment. While performing the duties of this job, the employee will experience in/out of the office noise at a minimal level. Must be capable of transporting self to various business locations. If using your own motor vehicle, must have a current, valid state driver's license and proof of insurance coverage that at least meets current residence's state minimum requirements. US and OUS travel may be required.
Job Type: Full-time
Benefits:
401(k)
Dental insurance
Health insurance
Paid time off
Application Question(s):
Do you live within driving distance of Plymouth, MN, zipcode 55441?
Education:
Bachelor's (Required)
Experience:
Quality systems: 5 years (Required)
Work Location: In person
Manager of Quality Assurance
Quality engineer job in Bloomington, MN
Notice: MCRA's Talent Solutions division works to unite top talent with opportunities on our clients' teams. This posting is not for a position directly at MCRA, but rather for a position with an MCRA client that our team is helping to recruit and fill.
MCRA Talent Solutions is proud to partner with an emerging MedTech startup advancing AI-driven neurotechnology to support individuals with neurological conditions. Their wearable therapeutic has recently received FDA clearance. Additionally, their implantable technology has been recognized with multiple FDA breakthrough designations for its potential in intuitive device interaction and pain management. We are looking to identify a Manager of Quality Assurance to join this growing team who will be responsible for leading and evolving the company's quality systems across both pre-market and post-market phases.
Key Responsibilities
Develop, implement, and maintain design controls, risk management (ISO 14971), and product development documentation in accordance with 21 CFR 820 and ISO 13485.
Ensure effective design transfer to manufacturing and supplier quality oversight.
Support clinical and regulatory teams with quality documentation for FDA, CE, and other submissions.
Manage quality inputs during product development, including verification/validation protocols, usability studies, and labeling reviews.
Oversee complaint handling, investigation, and Medical Device Reporting (MDR).
Manage CAPA processes, including root cause analysis and effectiveness checks.
Lead post-market surveillance activities, including trend analysis and risk re-evaluation.
Support audits and regulatory inspections by FDA, Notified Bodies, or other agencies.
Maintain and improve the company's Quality Management System (QMS).
Lead internal audits and train teams on quality procedures and compliance culture.
Evaluate and implement eQMS tools for scalable documentation control and traceability.
Collaborate cross-functionally with R&D, clinical, operations, and regulatory teams.
Qualifications
Bachelor's degree in engineering, life sciences, or a related field (Master's preferred)
5+ years in medical device quality assurance (experience in similar devices a plus)
In-depth knowledge of 21 CFR 820, ISO 13485, ISO 14971
Strong understanding of both design controls and post-market quality systems
Experience preparing for or participating in FDA inspections or ISO audits
Familiarity with eQMS platforms (e.g., Greenlight Guru, MasterControl, Veeva)
Excellent project management and communication skills
Passion for innovation, compliance, and patient impact
Compensation and Benefits:
Competitive salary and benefits package
Gain hands-on experience in a fast-growing, cutting-edge industry.
Collaborative work environment with the opportunity to make a significant impact on patient's lives.
Opportunities for career advancement and personal development within the company.
Quality Manager (Supply Quality)
Quality engineer job in Anoka, MN
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.
Supplier Quality Management
Be the primary liaison between the assigned supply base, program team, production and nVent customers with a key responsibility to resolve supplier quality issues.
Implement daily supplier management actions to improve supplier quality performance and flag, if necessary.
Establish supplier engagement & cadence.
Visit supplier locations. Travel up to 30%.
Participate in supplier assessments and internal/external audits as needed.
Coach, mentor and conduct trainings for suppliers as needed.
Problem Solving & Corrective Actions
Lead RCCA activities for supplier quality problems:
Issue supplier-corrective actions.
Evaluate whether corrective actions are thorough and effective
Evaluate what impact this may have on our overall relationship with the supplier.
Communicate urgency/severity of concern with suppliers/customer.
Validate the effectiveness of the actions taken by suppliers.
Process & Product Quality
Establish strong relationships with the customer, the program team, engineering, supplier partnerships, sourcing and quality department to understand requirements and production risks and develop plans with each supplier to ensure the highest quality without disruption.
Support APQP and PPAP activities for new product introductions and engineering changes.
Support suppliers' process capability studies, FMEA reviews, and control plan validations.
Continuous Improvement
Lead supplier-quality focused improvement activities to drive zero-defect environment.
Support a collaborative environment with suppliers, operations, quality, program and sourcing teams, and other key functions to cultivate a zero-defect mentality.
Drive supplier development initiatives, including Lean and Six Sigma projects.
Identify opportunities for cost reduction and quality improvement across the supply base.
Compliance & Documentation
Maintain supplier quality documentation, audit reports, and performance records.
Ensure compliance with environmental, health, and safety standards where applicable.
YOU HAVE
Bachelor's degree in Metallurgical Engineering, Industrial Engineering, Mechanical Engineering, Manufacturing/Automation Engineering, Chemical Engineering, Materials Engineering
Strong knowledge of APQP, PPAP, SPC, Process Capability Studies, FMEA, Control Plans, and GD&T.
Proficient in root cause analysis investigation, (such as RCCA, 8D, and 3L5Y).
4+ years in Supplier Quality related functions
Quality Certifications (CQE, CMQ, CQA) and ISO 9001:2015 Internal Auditor trained a plus.
Effective communication at all levels of the organization
Ability to coach, mentor and conduct trainings for suppliers
Good process management, planning and change management skills.
Some knowledge and experience in reliability.
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:
$105,000.00 - $195,000.00
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.
#LI-MB1
#LI-Onsite
Manufacturing Engineer II - Advanced Manufacturing (Onsite)
Quality engineer job in Burnsville, MN
Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: This job requires a U.S. Person. A U.S. Person is a lawful permanent resident as defined in 8 U.S.C. 1101(a)(20) or who is a protected individual as defined by 8 U.S.C. 1324b(a)(3). U.S. citizens, U.S. nationals, U.S. permanent residents, or individuals granted refugee or asylee status in the U.S. are considered U.S. persons. For a complete definition of "U.S. Person" go here:
Security Clearance:
None/Not Required
This position is for an emerging professional engineer with experience in manufacturing processes and systems to deploy state of the art manufacturing technology into production. These systems will be used to improve processes and enable digital connectivity throughout operations. You will be a key contributor in defining and scoping projects, project planning, developing manufacturing technology in a lab environment, and proliferating technology deployments in support of our industry 4.0 transformation.
Our ideal candidate will have a strong background in manufacturing support and process development in a mechanical assembly factory. You will also have exposure to metal joining processes such as welding and brazing. Experience with process automation and machine connectivity, along with strong project management and communication skills is preferred.
WHAT YOU WILL DO:
Apply engineering knowledge and collaborate with other organizations to improve manufacturing operations.
Own all phases of project execution from concept development through deployment.
Plan, prioritize, and manage multiple engineering projects.
Participate in cross functional teams to ensure effective deployment to live production.
Prioritize tasks to ensure that the team's overall resources are used effectively and that deadlines are met.
Maintain current knowledge of Industry 4.0 technologies and develop related project proposals.
Effectively communicates with operations and technical leadership on proposals and active projects.
QUALIFICATIONS YOU MUST HAVE:
Typically requires a University Degree and minimum 2 years of prior relevant experience oran Advanced Degree in a related field or in absence of a degree, 6 years of relevant experience.
2+ years of experience as an industrial or manufacturing engineer.
QUALIFICATIONS WE PREFER:
University Degree in manufacturing or industrial engineering.
Background in Manufacturing Support in a high-mix factory.
Experience with metal joining processes such as welding and brazing.
IIOT deployment experience.
Effective communication and interpersonal skills, with the ability to collaborate with cross-functional teams to achieve operational goals.
Detail-oriented and capable of managing multiple priorities in a fast-paced environment.
Experience using analytical and problem-solving skills to effectively identify and resolve issues and mitigate risks.
Ability to remain focused under pressure to assess and resolve challenges.
Collins Enterprise Values including Safety | Trust | Accountability | Respect | Collaboration | Innovation.
WHAT WE OFFER
BENEFITS
Some of our competitive benefits package includes:
Medical, dental, and vision insurance
Three weeks of vacation for newly hired employees
Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option
Tuition reimbursement program
Student Loan Repayment Program
Life insurance and disability coverage
Optional coverages you can buy pet insurance, home and auto insurance, additional life and accident insurance, critical illness insurance, group legal, ID theft protection
Birth, adoption, parental leave benefits
Ovia Health, fertility, and family planning
Adoption Assistance
Autism Benefit
Employee Assistance Plan, including up to 10 free counseling sessions
Healthy You Incentives, wellness rewards program
Doctor on Demand, virtual doctor visits
Bright Horizons, child and elder care services
Teladoc Medical Experts, second opinion program
And more!
This position may be eligible for relocation.
Learn More & Apply Now!
Collins Aerospace, an RTX company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio, and expertise to solve customers' toughest challenges and to meet the demands of a rapidly evolving global market.
Avionics delivers advanced cockpit displays, vision systems, and comprehensive digital solutions for global government, commercial and business aviation customers. We provide connectivity and managed data services to ensure safety and seamless communication for passengers, crews, and militaries, from aircraft and airports to air traffic management. Join us in creating solutions that connect the world, one flight at a time. Start your application today.
Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. Regardless of your role type, collaboration and innovation are critical to our business and all employees will have access to digital tools so they can work with colleagues around the world - and access to Collins sites when their work requires in-person meetings.
At Collins, the paths we pave together lead to limitless possibility. And the bonds we form - with our customers and with each other -- propel us all higher, again and again.
Apply now and be part of the team that's redefining aerospace, every day.
The salary range for this role is 66,000 USD - 130,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills.
Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.
Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.
This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.
RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window.
RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act.
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Senior Quality Technician
Quality engineer job in Eden Prairie, MN
A medical device client is looking to hire a full time, Senior Quality Technician onsite in Eden Prairie, Minnesota. This Monday-Friday, onsite quality professional will need to perform material and product assessment testing in support of medical device development and manufacturing in compliance with GMP. This person will be assigned complaint, RMA tasks and perform engineering related requests as assigned. The individual is also responsible for, receiving and in-process inspections, material release in support of medical device manufacturing. Our client is looking for someone who will be responsible for reviewing and approving DHRs prior to product release and should feel comfortable supporting the administration of quality systems within the electronic quality management system. This position works cross functionally with process stakeholders to ensure quality system processes are documented appropriately and are completed within the expected timeframes.
Must Haves:
HS diploma and minimum 2 years relevant medical device/ISO 13485 experience or 2 yr degree.
Knowledge and experience with electronics manufacturing preferred.
Knowledge of quality systems including use of electronic quality management systems software preferred.
Knowledge of electrical and mechanical testing techniques.
Good math and technical skills.
Excellent computer skills including MS Office.
Maintains positive attitude when working with peers, customers or suppliers.
Comfortable working in a self-directed team environment and giving or asking for instructions.
Demonstrate an understanding of the medical industry.
Provide training to peers on technician level skills.
Works effectively on cross functional teams to establish appropriate processes pertaining to quality
Ability to review, analyze, summarize and interpret data; draw conclusions and make appropriate recommendations and decisions.
What You'll Do:
Conduct functional testing as required by component drawings, manufacturing instructions, and/or test instructions.
Responsible for receiving inspection activities including, but not limited to inspection and gathering all defined requirements and documentation to release parts/components.
Responsible for performing in-process and final component, sub-assembly and product inspection.
Document non-conformance reports once parts fail specification or requirements.
Performs and/or supports troubleshooting, investigations and problem solving of issues and non-conformances.
Complaint related tasks.
RMA tasks.
Assures quality systems documentation and record keeping activities are carried out and completed in compliance with established procedures and work instructions.
Demonstrates safe work habits, maintains clean and safe work area.
Completes all other duties as assigned by supervisor.
Develop and write quality systems procedures as requested by supervisor.
Provides support during customer audits.
Supports supervisor in preparation of Management Review.
Pay of $32 - 36 an hour, direct hire, full time + benefits
Process Engineer
Quality engineer job in Brooklyn Park, MN
The Process Engineer will take ownership of manufacturing and packaging process leadership-evaluating current systems, identifying areas for improvement, and driving initiatives that enhance efficiency, quality, and compliance. This role requires a self-starter with strong process validation experience, a continuous improvement mindset, and the confidence to lead cross-functional initiatives in a regulated medical device environment.
Key Responsibilities:
Lead process improvement efforts across manufacturing and packaging operations to optimize quality, performance, and throughput.
Assess current processes, identify root causes of inefficiencies, and implement data-driven solutions.
Plan, execute, and document IQ/OQ/PQ validations in compliance with FDA and ISO 13485 requirements.
Partner with Regulatory and Quality teams to evaluate process changes and ensure full regulatory compliance.
Provide engineering support for process changes related to new product introductions, packaging redesign, and manufacturing transfers.
Use CAD tools to support packaging redesigns, equipment layouts, and process documentation.
Lead cross-functional teams in implementing continuous improvement and lean manufacturing initiatives.
Prepare and maintain technical documentation, including protocols, reports, and risk analyses.
Qualifications:
Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related field.
5+ years of experience in process engineering within a medical device (Class III preferred) or similarly regulated manufacturing environment.
Proven experience with IQ/OQ/PQ validations and process documentation.
Strong understanding of FDA regulations, ISO 13485, and GMP principles.
Demonstrated success leading continuous improvement or lean manufacturing projects.
Excellent analytical, communication, and project management skills.
CAD proficiency (SolidWorks or equivalent) preferred.
Must be self-motivated, proactive, and capable of driving initiatives independently.
Manufacturing Engineer
Quality engineer job in Shakopee, MN
Passionate people create exceptional things Did you know that the solutions we develop are a key part of most industries? Electronics, medical research, renewable energy, food production, infrastructure and many more. We're everywhere! Working with us means working with the latest technologies and groundbreaking, sustainable innovations. With our inclusive and caring environment, you get the support and inspiration you need to grow.
Here, your ideas are embraced, and you never stop learning. Interested in being part of our team?
Join us on our journey for a better tomorrow.
The Manufacturing Engineer is responsible for developing/improving processes, manufacturing capabilities and reducing the product cost through operational efficiency.
As Manufacturing Engineer, you will report into the Lead Mechanical Engineer.
Your job responsibilities will include:
Provides manufacturing engineering support to the operational team where needed.
Drives continuous improvement activities in quality, cycle times, cost reduction and process improvement through lean techniques and value engineering.
Eliminates routing and material variances impacting financial results of Product Company.
Performs time studies for the assembly processes to create the correct routings and to optimize the balancing of the assembly process.
Accounts for the definition, setup, preparation, and optimization of manufacturing tooling. This includes but is not limited to all automated manufacturing equipment.
Ensures value stream mapping, specification and implementation of logistical flows for the manufacturing cells.
Creates and maintains documented work procedures and technical specifications for manufacturing equipment and test specifications.
Performs active training processes, procedures, documentation, and traceability to create and sustain the workforce competences within the manufacturing zones.
Works with other departments and suppliers to support all the quality issues on components and products in the manufacturing zones.
Collaborate with cross-functional engineers and technicians to support successful new product introductions, ensuring smooth transition from design to production.
Create, manage and complete manufacturing related Engineering Change Orders through the use of Gamma Vacuums ERP system's and CAD systems.
Motivated and self starting contributor that is willing to learn.
Maintains punctual, regular and predictable attendance; works collaboratively in a team environment with a spirit of cooperation.
Respectfully takes direction from [supervisor/ manager] and other duties as assigned.
Provides routine comunication to team members and leadership team.
Ability to perform essential job duties with or without reasonable accommodation and without posing a direct threat to safety or health of employee or others. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties.
Education level
Bachelor degree in mechanical or manufacturing engineering preferred. Degree in sciences is sufficent with supporting manfucturing or operations experience.
Relevant Previous experience
Minimum 4 years of experience in manufacturing, assembly or operations environment.
Knowledge areas/Skills
Experience/knowledge of 6S and basic Lean Manufacturing principles.
Strong analytical and problem-solving skills with the ability to prioritize work and manage multiple tasks.
Experience with CREO CAD systems or equivalant 3D CAD software.
Working knowledge of ERP systems.
Programming skills (LabView and PLC) preferred.
Interaction between manufacturing equipment and I.T. systems.
Advanced Excel, Word, PowerPoint, Publisher, Autocad skills.
Other requirements
Strong verbal and written communication skills.
Experience in project management and leading improvement projects.
Demonstrated skill and achievement in implementing Lean practices in an operations environment. This includes driving 6S opportunities, streamlining processes, improving process flow, fixturing, etc.
While performing the duties of this job, the employee is regularly exposed to work near moving mechanical parts. The employee is occasionally exposed to work in high, precarious places, toxic or caustic chemicals and risk of electrical shock. The noise level in the work environment is usually moderate.
While performing the duties of this job, the employee is regularly required to sit, stand, walk, use stairways to climb to floors within office building, and talk or hear. The employee is occasionally required to use hands and fingers to type or dial, climb or balance, stoop, kneel, crouch or crawl, and reach with hands and arms.
The employee must occasionally lift and/or move up to 40 pounds. This position requires frequent computer use. Specific vision abilities required by this job include close vision, color vision, distance vision, depth perception, and ability to adjust focus.
Even if you don't meet all the points, but are ready for a challenge, click on "Apply" anyway. We love your spirit!
In return, we offer
Part of the Atlas Copco Group with a wide-reaching internal job market
Work in a globally diverse environment
You can grow with us: we always look for internal candidates before checking the market and have training programs
We have a family-like atmosphere - and that is not just a claim on the wall, it's a true fact
You can be creative and promote your own ideas
We believe and foster a learning culture where global mobility is an important enabler for growth.
Our learning culture supports you on your journey: benefit from our individual learning opportunities, our feedback culture, the internal job portal, global project assignments, or on site training from our academy
We support you and your well-being with different programs like fitness groups, family parties, team events, and more
We offer health insurance, paid leave and retirement benefits.
Job location
This is an onsite position located in Shakopee, MN.
Diverse by nature and inclusive by choice
Bright ideas come from all of us. The more unique perspectives we embrace, the more innovative we are. Together we build a culture where difference is valued and we share a deep sense of purpose and belonging.
Manufacturing Engineer II (Onsite)
Quality engineer job in Burnsville, MN
Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract.
Security Clearance:
None/Not Required
We are adding a Manufacturing Engineer II to the Engine Sensing Manufacturing Support Team at the Collins Aerospace Burnsville facility.
In this role, you will make an impact by evaluating and solving everyday manufacturing problems related to design, process, and supplier issues for the manufacture of high-quality sensing assemblies in a collaborative team environment. You will provide technical support to operations in the form of enabling and improving the flow of manufacturing utilizing the principles of quality and industrial engineering.
Our ideal candidate will be a curious self-starter with excellent teaming, communication, and relationship building abilities. The candidate will also have a passion for LEAN principles and processes and be eager to contribute to improved efficiency and productivity using their LEAN toolkit.
Joining Collins Aerospace isn't just about finding a job; it's about embarking on a journey to redefine the future of aerospace.
WHAT YOU WILL DO:
Drive manufacturing process improvements across multiple assembly process steps
Support production build operators with immediate needs on tooling and processes to meet production schedule.
Implement procedure and process improvements based on safety, quality, and productivity.
Identify and address safety concerns.
Analyze and understand factory needs and requirements.
Improve production facilities and equipment layouts.
Provide information to management as the status of equipment, manpower, space, and other elements affecting manufacturing.
Identify and manage risk in process development (primarily utilizing and driving Production Part Approval Process (PAPP) core elements e.g. PFMEA, MSA, Process Flow and Control Plans, etc.).
Perform evaluations and conducts special process assessments or audits. Types of special process specifications include but are not limited to Welding, Brazing, NDT, heat treat, soldering, and chemical processing.
QUALIFICATIONS YOU MUST HAVE:
Typically requires a University Degree and minimum 2 years of prior relevant experience oran Advanced Degree in a related field or in absence of a degree, 6 years of relevant experience.
2+ years of experience as a manufacturing engineer supporting production.
QUALIFICATIONS WE PREFER:
Problem-solving skills with ability to proactively identify alternate solutions to overcome difficult technical challenges.
Effective communication and interpersonal skills, with the ability to collaborate with cross-functional teams to achieve operational goals.
Detail-oriented and capable of managing multiple priorities in a fast-paced environment.
Experience using analytical and problem-solving skills to effectively identify and resolve issues and mitigate risks.
Proven ability to facilitate difficult conversations and communicate early and concisely with individuals at all organizational levels.
Collins Enterprise Values including Safety |Trust | Accountability | Respect | Collaboration | Innovation.
WHAT WE OFFER
BENEFITS
Some of our competitive benefits package includes:
Medical, dental, and vision insurance
Three weeks of vacation for newly hired employees
Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option
Tuition reimbursement program
Student Loan Repayment Program
Life insurance and disability coverage
Optional coverages you can buy pet insurance, home and auto insurance, additional life and accident insurance, critical illness insurance, group legal, ID theft protection
Birth, adoption, parental leave benefits
Ovia Health, fertility, and family planning
Adoption Assistance
Autism Benefit
Employee Assistance Plan, including up to 10 free counseling sessions
Healthy You Incentives, wellness rewards program
Doctor on Demand, virtual doctor visits
Bright Horizons, child and elder care services
Teladoc Medical Experts, second opinion program
And more!
This position may be eligible for relocation.
Learn More & Apply Now!
Collins Aerospace, an RTX company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio, and expertise to solve customers' toughest challenges and to meet the demands of a rapidly evolving global market.
Avionics delivers advanced cockpit displays, vision systems, and comprehensive digital solutions for global government, commercial and business aviation customers. We provide connectivity and managed data services to ensure safety and seamless communication for passengers, crews, and militaries, from aircraft and airports to air traffic management. Join us in creating solutions that connect the world, one flight at a time. Start your application today.
Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. Regardless of your role type, collaboration and innovation are critical to our business and all employees will have access to digital tools so they can work with colleagues around the world - and access to Collins sites when their work requires in-person meetings.
At Collins, the paths we pave together lead to limitless possibility. And the bonds we form - with our customers and with each other -- propel us all higher, again and again.
Apply now and be part of the team that's redefining aerospace, every day.
As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote.
The salary range for this role is 66,000 USD - 130,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills.
Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.
Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.
This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.
RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window.
RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act.
Privacy Policy and Terms:
Click on this link to read the Policy and Terms
Senior Process Manufacturing Engineer
Quality engineer job in Minneapolis, MN
At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe. Responsible for conceptual development, management, and final results of complex engineering projects designed to improve operational performance, reduce cost, enhance safety, or establish compliance. Provides guidance and direction to other Project Engineers and serves as technical expert for multiple projects. Must be able to manage multiple complex projects across multiple sites concurrently.
This is a remote role with the expectation of frequent travel up to 70%
What You'll do as a Sr Process Manufacturing Engineer
Develops project objectives, scope, schedules, and fees by analyzing project requirements and collaborating with Engineering, Sales, and Operations management. Establishes detailed project plan from pre-design to completion by determining budgets, staffing and schedules including contractor and construction budgets.
Organizes project team by selecting and orienting team members, and delegating responsibilities and tasks including determining and monitoring the scope and priority of assignments of all internal disciplines and outside contractors. Determines additional service requirements and initiates contract adjustments.
Plans, organizes, and conducts complex technical projects and/or serves as technical expert or oversees the development of engineering projects.
Conceives, plans, and oversees or conducts process equipment evaluations and upgrades.
Evaluates, tests, and prepares technical analysis and implementation plans for equipment improvements; makes recommendations for equipment purchases by researching and testing products and participating in negotiations with management and outside vendors.
Develops and implements process controls which ensure consistent equipment and process performance.
Keeps abreast of, and is well informed on, new developments and technology through contact with educational institutions and professional organizations, trade shows, and technical publications.
Assists with the coordination or directs engineering/facility projects through resolution of operational problems implementing and overseeing testing, reviewing design and safety issues, and overseeing contracted resources.
Obtains information for the design/development of components, assemblies and other operating equipment through manufacturer's information, technology, databases, consultants, and contractors.
Performs professional engineering assignments of varying and significant complexity under general direction with considerable discretion as to work detail and provides guidance and direction to other Engineering staff in completing complex assignments.
Assists in maintaining a safe, clean, secure, and efficient working environment by implementing and enforcing procedures, rules, and regulations, supports plant safety meetings that evaluate plant machinery, equipment and/or working conditions.
Ensures that all federal, state, and local regulations as well as building codes pertaining to, but not limited to, radioactive materials, licensing compliance, safety, EPA, OSHA, NFPA, FDA rules and regulations are adhered to. Maintains a working knowledge of regulations.
The Experience, Skills, and Abilities Needed
Required:
Bachelor's Degree in a technical discipline with minimum of 10 years' experience or minimum of 20 years' experience in lieu of degree
Minimum of 5 years of related experience in complex project management, process improvement, and/or project engineering
Ability to read, interpret and practically apply electrical ladder diagrams and mechanical blueprints
Working knowledge of PLC (Programmable Logic Controllers) or other types of process control equipment
Ability to effectively read, write and verbally communicate
Ability to work independently under general guidelines and supervision
Computer skills and word processing, spreadsheet, and software capabilities
Effective interpersonal skills as demonstrated through prior management experience
Above average organizing, analyzing and Level 4 math skills (practical application of fractions, percentages, ratios, proportions, measurements, and basic algebra) to determine organizational Customer and regulatory problems and formulate corrective action plans
Attention to detail
Other:
Able to adapt to changing duties and responsibilities
Able to influence people in the opinions, attitude or judgments and to generalize, evaluate and decide and to adapt to situations under stress
Requires normal hearing range sufficient to hear alarms, bells, horns, and normal visual acuity
What STERIS Offers
We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future.
Here is a brief overview of what we offer:
Market competitive pay
Extensive paid time off and (9) added holidays
Excellent healthcare, dental, and vision benefits
Long/short term disability coverage
401(K) with company match
Maternity and parental leave
Additional add on benefits/discounts for programs such as pet insurance
Tuition reimbursement and continued educational programs
Excellent opportunities for advancement in a stable long-term career
#LI-HT
#LI-REMOTE
Pay range for this opportunity is $90,737.50 - $117,425.00. This position is eligible for bonus participation.
Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.
STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits
Open until position is filled.
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare and life sciences products and services around the globe. For more information, visit ***************
If you need assistance completing the application process, please call 1 (440) ###.####. This contact information is for accommodation inquiries only and cannot be used to check application status.
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location's HR Office during normal business hours.
Req ID: 51718
Job Category: Engineering
Location:
Manufacturing Engineer II
Quality engineer job in Saint Paul, MN
Who Are We? Do you want to help to make the world a better place? Join our team! At TSI our vision is to create a better world by helping to protect people, products and the environment. We are proud of the wide range of solutions we provide that solve our customer's problems around the world. From helping to ensure worker safety and understanding air quality to supporting complex highly technical industries such as pharmaceuticals manufacturing, semiconductor, and research customers, TSI employees are part of something special with a purpose.
Manufacturing Engineer II at TSI
Under general supervision, the Manufacturing Engineer II provides higher level floor support for assigned value streams to meet internal and external customer needs. They will identify, analyze, create, and implement effective manufacturing and business processes and procedures. Work is varied in nature. Also plans and performs engineering duties for parts of a major project. Duties and responsibilities are moderate in complexity.
What Will You Do?
In order to grow and build a successful career with TSI, you will be responsible for:
Interface with ERP System (SAP) to prepare new and revise existing manufacturing documents, drawings, and Bills of Materials (BOM) used to manufacture and test instruments.
Solve day to day manufacturing problems, implement Engineering Change Orders (ECO), and work proactively to find and eliminate waste and increase productivity.
Investigate and resolve supplier quality problems and customer complaints.
Respond to corrective actions and feedback that relates to the production floor to solve customer needs.
Lead structured problem solving (8-D) teams and Kaizen events in assigned area.
With limited guidance, perform complex analysis on data sets.
Train manufacturing staff, team leaders, and peers on changes to manufacturing or business processes in assigned area.
Participate on cross-functional teams that require coordinating with staff from continuation engineering, quality, production control, inventory, and purchasing.
May be assigned to lead small projects or parts of a larger project.
Maintain best practices on the manufacturing floor including Lean Manufacturing, 5S, and Point of Use inventory.
Use established policies and procedures to complete work assignments.
Develop technical understanding of assigned products and associated calibration systems.
Follow all safety guidelines and report unsafe conditions to supervisor or safety committee member.
Complete other assignments as requested.
What Do You Need?
Required
Bachelor's degree in engineering or related discipline
Minimum of 3 years manufacturing engineering experience or related intern or technician experience
Design, testing and troubleshooting techniques experience
Knowledge of principles of statistical process control or other quality system tools
Knowledge of lean manufacturing principals, 5S, Demand Flow, Quality Systems or related
Knowledge of manufacturing systems, manufacturing engineering concepts and procedures
Desired
Bachelor's degree in mechanical, electrical, manufacturing, or industrial discipline
Knowledge of an engineering design software (CREO desired)
What Can We Give You?At TSI, our employees are our most valuable assets, and we care about their health and happiness. We offer a competitive benefits program to keep our employees and their family members protected and foster a healthy work-life balance. Additionally, we are committed to employee development and growth, and encourage and foster an environment of collaboration, and innovation. Our work has meaning and the products we design and build help protect people and the environment.
Dress for your day: We want our employees to be comfortable at work and we know they are more productive when they're comfortable. The dress for your day policy allows employees' discretion to select appropriate dress for the business of each workday.
Free Beverages/On-site Cafeterias: Enjoy complimentary coffee, tea and hot chocolate each day at work. We also have two large cafeterias employees can eat lunch in, as well as an outside patio area that employees can enjoy during the summer months.
Pay & Benefits:
Competitive market salary from $90,000 - $97,000 per year* depending on qualifications and experience. For eligible Leadership and individual contributor roles, additional bonus opportunities may be available and awarded at the discretion of the Company.
Benefits:
Health Insurance: Comprehensive medical, dental, and vision coverage.
Retirement Plan: 401(k) with company match.
Paid Time Off Program: Paid time off, paid holidays, and paid floating holidays.
Other Benefits: Life insurance, employee assistance program (EAP), and professional development opportunities.
*Pay amount does not guarantee employment for any particular period of time.
Legal authorization to work in the United States without the need for sponsorship. We require proof of eligibility to work in the United States.
EOE/Vet/Disability
TSI provides trusted measurement, application guidance, and data analytics solutions that enable our global customers to make informed decisions. We are creating a better world by helping protect people, products and the environment, as well as by optimizing research and industrial processes.
Senior Manufacturing Engineer
Quality engineer job in Minneapolis, MN
Workplace Flexibility: Onsite For more than 100 years, Olympus has focused on making people's lives healthier, safer and more fulfilling. Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill their desires, dreams, and lives.
Our five Core Values empower us to achieve Our Purpose:
Patient Focus, Integrity, Innovation, Impact and Empathy.
Learn more about Life at Olympus.
Job Description
Provide technical leadership and mentorship within the Manufacturing Engineering function, with a primary focus on the development, implementation, and continuous improvement of automated production equipment and systems. This role requires a strong background in mechanical, pneumatic, electrical, PLC, and vision systems, and the ability to lead complex automation initiatives from concept through deployment. Act as a representative of Manufacturing Engineering to support new product introduction and manufacturing automation strategies, ensuring alignment with business objectives. May have direct technician reporting structure. May influentially lead engineers.
Job Duties
Drive operations and new product/process development activities
Lead the design, development, and implementation of automated production equipment and manufacturing systems, ensuring solutions meet operational performance, quality, and safety requirements.
Provide technical expertise in mechanical design, pneumatics, electrical systems, PLC programming, and machine vision technologies to support automation initiatives.
Drive system changes (GWIs, GSOP forms) and business systems (Line Balance, work content tools)
Mentor/Lead the validation of equipment and processes as required (IQ, OQ, PQ)
Mentor and implement capacity planning, cost improvement and
facilities layout for equipment moves and additions
Perform operator training for new and existing processes
Lead discussions with resources such as suppliers and Olympus sites to resolve technical issues or improve processes or products
Assess process capabilities, prioritize process improvement opportunities. Innovate and implement process improvement activities
Leadership of cross functional project teams
Review prints for new and existing products
Follows GWI's, GSOP and owns MP's to ensure control of
product/process design
Other duties as assigned
Job Qualifications
Required:
A minimum of a Bachelor's degree (B.S.) in science or engineering discipline.
Minimum of 5 years' experience.
Applied experience using LEAN and Six Sigma tools.
Leadership and mentoring capabilities with statistical analysis.
Ability to work well/Lead multiple cross functional teams.
Proficient technical writing skills.
Experience with leading risk management documentation.
Proficient time management skills.
Demonstrated fixture and tooling experience.
CAD experience.
Supervision of technical resources.
Why join Olympus?
We offer a holistic employee experience supporting personal and professional well-being through meaningful work, equitable offerings, and a connected culture.
Equitable Offerings you can count on:
Competitive salaries, annual bonus and 401(k)* with company match
Comprehensive medical, dental, vision coverage effective on start date
24/7 Employee Assistance Program
Free live and on-demand Wellbeing Programs
Generous Paid Vacation and Sick Time
Paid Parental Leave and Adoption Assistance*
12 Paid Holidays
On-Site Child Daycare, Café, Fitness Center**
Connected Culture you can embrace:
Work-life integrated culture that supports an employee centric mindset
Offers onsite, hybrid and field work environments
Paid volunteering and charitable donation/match programs
Employee Resource Groups
Dedicated Training Resources and Learning & Development Programs
Paid Educational Assistance
*US Only
**Center Valley, PA and Westborough, MA
Are you ready to be a part of our team?
Learn more about our benefit and incentives.
The anticipated base pay range for this full-time position working at this location is $93,793.00 - $126,621.00 / year, plus potential for annual bonus (subject to plan eligibility and other requirements). Olympus considers a variety of factors when determining actual compensation for this position including: level of experience, working location, and relevant education and certifications.
At Olympus, we are committed to Our Purpose of making people's lives healthier, safer and more fulfilling. As a global medical technology company, we partner with healthcare professionals to provide best-in-class solutions and services for early detection, diagnosis and minimally invasive treatment, aiming to improve patient outcomes by elevating the standard of care in targeted disease states.
For more than 100 years, Olympus has pursued a goal of contributing to society by producing products designed with the purpose of delivering optimal outcomes for its customers around the world.
Headquartered in Tokyo, Japan, Olympus employs more than 31,000 employees worldwide in nearly 40 countries and regions. Olympus Corporation of the Americas, a wholly owned subsidiary of Olympus Corporation, is headquartered in Center Valley, Pennsylvania, USA, and employs more than 5,200 employees throughout locations in North and South America. For more information, visit ***********************
You Belong at Olympus
We value a workforce that reflects a wide range of perspectives, backgrounds, and experiences. We foster an environment where all employees feel valued, respected, and supported. And we provide employees with equal access to opportunities for growth and development.
Applicants Requesting Accommodations: Olympus is committed to the full inclusion of all qualified individuals. As part of this commitment, Olympus will ensure that persons with disabilities are provided reasonable accommodations for the hiring process. If reasonable accommodation is needed, please contact [email protected]. If your disability impairs your ability to email, you may call our HR Compliance Manager at 1-888-Olympus (1-888-###-####).
Let's realize your potential, together.
It is the policy of Olympus to extend equal employment and advancement opportunity to all applicants and employees without regard to race, color, national origin (including language use restrictions), citizenship status, religious creed (including dress and grooming practices), age, sex (including pregnancy, childbirth, breastfeeding, medical conditions related to pregnancy, childbirth and/or breastfeeding), gender, gender identity and expression, sexual orientation, marital status, disability (physical or mental) and/or a medical condition, genetic information, ancestry, veteran status or service in the uniformed services, and any other characteristic protected by applicable federal, state or local law.
Posting Notes: || United States (US) || Minnesota (US-MN) || Brooklyn Park || Manufacturing & Repair
Sr Advanced Quality Engineer
Quality engineer job in Plymouth, MN
The Development/Design/Program Quality Engineer is responsible for ensuring that all program and project designs meet internal and external quality standards, including Quality Management System (QMS), and Statement of Work (SOW) requirements. This role reviews, verifies, and approves design documentation such as Engineering Change Orders (ECOs), drawings (DWGs), Bills of Materials (BOMs), requirements, test methods, manufacturing methods, and project plans. The engineer leads collaboration between design, development, manufacturing, and stakeholder teams to ensure the final product meets all requirements and expectations.
WHATS IN IT FOR YOU?
In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Honeywell employees are eligible for a comprehensive benefits package. This package includes employer subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays. For more information visit: Benefits at Honeywell
US CITIZENSHIP REQUIREMENTS
Due to compliance with U.S. export control laws and regulations, candidate must be a U.S. citizen, U.S. permanent resident, or have asylum or refugee status in the U.S.
The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates.
Must Have:
8 + years of experience with QMS, and quality assurance in a design, development, or manufacturing environment.
WE VALUE:
10+ years of experience with QMS, and quality assurance in a design, development, or manufacturing environment.
Bachelors degree in engineering/or related field
Strong analytical, problem-solving, and communication skills.
Experience leading cross-functional teams and driving corrective actions.
Knowledge of quality tools and methodologies (e.g., FMEA, RCA, CAPA).
Certification in quality engineering (CQE) or Six Sigma is preferred.
The annual base salary for this position is $106,000.00-$132,000.00. Please note that this salary information serves as a general guideline. Honeywell considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as market and business considerations.
ABOUT HONEYWELL
Honeywell International Inc. (NYSE: HON) invents and commercializes technologies that address some of the world's most critical challenges around energy, safety, security, air travel, productivity, and global urbanization. We are a leading software-industrial company committed to introducing state of the art technology solutions to improve efficiency, productivity, sustainability, and safety in high growth businesses in broad-based, attractive industrial end markets. Our products and solutions enable a safer, more comfortable, and more productive world, enhancing the quality of life of people around the globe.
THE BUSINESS UNIT
At Honeywell Advanced Connected Sustainability Technologies (ACST), our outstanding team of thinkers, innovators, and doers help make the future. We build environments and technologies that meet our customers' needs. The groundbreaking scientists, engineers, and professionals that make up our nimble group have the agility of a start-up backed with the power and investment of Honeywell.
Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.
#ACST
Key Responsibilities:
Review, verify, and approve design documents, ECOs, drawings, BOMs, requirements, test methods, manufacturing methods, and project plans.
Lead collaboration among design, development, manufacturing, and stakeholder teams to ensure all requirements and expectations are met.
Conduct audits of program plans and processes to ensure compliance with QMS, and SOW requirements.
Provide quality cost estimates and develop Quality Management Plans (QMP) for projects.
Participate in risk management activities, including maintaining the risk register.
Lead root cause analyses (RCAs) and corrective and preventive actions (CAPAs) as required.
Document lessons learned and ensure tracking and allocation of QA resources.
Support continuous improvement initiatives and drive quality culture within the organization.
Develop and maintain quality management systems and procedures.
Conduct internal audits to ensure adherence to company quality standards.
Train and mentor staff on quality processes and best practices.
Analyze quality data to identify trends and implement strategies for enhanced performance.
Communicate quality status and progress to customers and stakeholders, providing regular reports and updates.
Ensure supplier capability and compliance with Honeywell and customer requirements.
Foster a proactive, customer-focused quality culture within the organization.
Coordinate with Supplier Quality Engineering (SQE) and Manufacturing/Pre-Production Quality Engineering (MFGQE).
Manage process and service non-conformances (NCs).
Participate in Failure Review Boards (FRB), Change Control Boards (CCB), and risk reviews.
Oversee the delivery of quality related objectives for the company development process. .
Provide quality metrics from manufacturing, pre-production, field, service, process, and software reports to drive continuous improvement and maintain compliance.
Auto-ApplyAdvanced Quality Engineer*
Quality engineer job in Maplewood, MN
Job Title Advanced Quality Engineer Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your professional and personal life, so it's equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a wide variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers.
This position provides an opportunity to transition from other private, public, government or military experience to a 3M career.
The Impact You'll Make in this Role
As an Advanced Quality Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact by:
* Partnering with/providing oversight to global manufacturing sites to drive Operational Quality Excellence: Working to identify, address sources of risk and variability, standardize work, and error proof operations.
* Leading and providing support to global teams on the resolution of quality issues including product recalls, complaints, nonconforming materials, while monitoring and addressing root causes.
* Quality support for New Product Introductions and Change Management Requests for source of supply and/or manufacturing operational changes to ensure robust Quality Function Deployment, test method development/implementation, qualifications, design reviews, and risk mitigation.
* Driving Supplier Quality improvement through the execution of governance plans based on risk.
* Championing a culture of continuous improvement to drive customer satisfaction and achieve business and plant objectives.
Your Skills and Expertise
To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:
* Bachelor's degree or higher (completed and verified prior to start)
* Two (2) years combined quality engineering and/or manufacturing experience in a private, public, government or military environment
Additional qualifications that could help you succeed even further in this role include:
* Experience in a regulated industry (e.g. NIOSH, FDA)
* Demonstrated strong communication and interpersonal skills
* Demonstrated leadership skills
* Experience with championing and/or deploying quality continuous improvement methodologies (e.g. DMAIC, Six Sigma, PPU, Qualifications)
Work location: This role has on-site working model, with the employee working at least 4 days a week in the office at 3M Center, located in Maplewood, MN
Travel: May include up to 15% domestic/international
Relocation Assistance: May be authorized
Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).
Responsibilities of this position may include direct and/or indirect physical or logical access to information, systems, technologies subjected to the regulations/compliance with U.S. Export Control Laws.
U.S. Export Control laws and U.S. Government Department of Defense contracts and sub-contracts impose certain restrictions on companies and their ability to share export-controlled and other technology and services with certain "non-U.S. persons" (persons who are not U.S. citizens or nationals, lawful permanent residents of the U.S., refugees, "Temporary Residents" (granted Amnesty or Special Agricultural Worker provisions), or persons granted asylum.
To comply with these laws, 3M must help assess candidates' U.S. person status.
The questions asked in this application are intended to assess this and will be used for evaluation purposes only. Failure to provide the necessary information in this regard will result in our inability to consider you further for this particular position.
Supporting Your Well-being
3M offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope.
Chat with Max
For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting assistant on 3M.com/careers.
Applicable to US Applicants Only:The expected compensation range for this position is $98,413 - $120,282, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: ***************************************************************
Good Faith Posting Date Range 10/13/2025 To 11/12/2025 Or until filled
All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M.
Learn more about 3M's creative solutions to the world's problems at ********** or on Instagram, Facebook, and LinkedIn @3M.
Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.
Safety is a core value at 3M. All employees are expected to contribute to a strong Environmental Health and Safety (EHS) culture by following safety policies, identifying hazards, and engaging in continuous improvement.
Pay & Benefits Overview: https://**********/3M/en_US/careers-us/working-at-3m/benefits/
3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law.
Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.
3M Global Terms of Use and Privacy Statement
Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms.
Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.
Auto-ApplyStandards Engineer
Quality engineer job in Dayton, MN
Ramsey,MN
Exp 2-5 yrs
Degree Bach
Job Description
We are the largest electrical distribution cooperative in Minnesota and is a progressive organization that provides electric service to customers in a 7-county area north of the Twin Cities. Our organization received the highest ranking in reliability and the ability to restore power of all electric utilities nationwide in the 2014 American Customer Satisfaction Index.
We are currently seeking an experienced Engineer with excellent analytical skills to guide the Engineering department in developing and applying standards that result in the most cost effective, reliable distribution system. The individual in this position will develop and maintain construction standards and specifications for the distribution system that includes new technologies, materials, methods and products. Key areas of responsibilities include:
• Create standards and identify new materials to design, construct, and maintain a quality system while continuously analyzing and striving to make improvements
• Develop and maintain construction specifications
• Research and prepare major material purchase specifications for equipment
• Research and evaluate new products
• Review equipment and material failures and implement necessary corrective measures
• Provide technical guidance to distribution system design and construction departments
• Develop, publish, and distribute construction specification books to ensure all system construction will meet strength and clearance requirements and to minimize construction costs, while meeting standards and codes
Required Talents, Skills, Expertise, Education
• BS degree in Electrical, Civil, Mechanical or Industrial Engineering
• Five years' experience in electric distribution, transmission or substation engineering in a utility focused environment
• Engineer-in-training with ability to obtain Professional Engineer license in Minnesota
• Knowledge and ability to apply standards and codes
• Excellent oral and written communication skills
Preferred Talents, Skills, Expertise, Education
• Knowledge and ability to apply National Electrical Safety Code
• Power emphasis in Electrical Engineering
• Professional Engineer license in Minnesota
• Drafting software skills
SKILLS AND CERTIFICATIONS
Engineer-in-training with ability to obtain Professional Engineer license in Minnesota
Excellent oral and written communication skills
SCREENING QUESTIONS
Please seriously evaluate where Ramsey, MN is located and the climate in this area. Based on your evaluation and if necessary, would you be willing to relocate to MN?
Do you have a BS degree in Electrical, Civil, Mechanical or Industrial Engineering?
Do you have five or more years experience in electric distribution, transmission or substation engineering in a utility focused environment?
IDEAL CANDIDATE
The ideal candidate has 5+ years' experience in electric distribution system applications. A Power emphasis in Electrical Engineering, Professional Engineer license in Minnesota, familiarity with National Electric Code and drafting software skills would be ideal.
IDEAL CANDIDATE SHOULD HAVE WORKED FOR THE FOLLOWING COMPANY(IES):
Xcel Energy, other electric co-operatives or municipalities, engineering consulting firms that specialize in power
Additional Information
All your information will be kept confidential according to EEO guidelines.
Direct Staffing Inc
Quality System Specialist
Quality engineer job in Delano, MN
About the Company
Trelleborg Medical Solutions partners with the world's leading medical device and biopharmaceutical companies, collaborating from concept to commercialization to bring to market impactful solutions that improve patient quality of life. It leverages decades of design and manufacturing experience, in-depth knowledge of polymer materials and a deep understanding of customer applications and end-use environments to deliver pioneering, engineered solutions for transformative health technologies. Utilizing its global quality system and engineering and manufacturing network, the company is a production partner of choice for medical device and biopharmaceutical companies.
About the Role
The Quality Systems Specialist is focused on the maintenance of the Quality Management System (QMS) to ensure compliance with regulatory, quality, company policies and manufacturing requirements. Supports all aspects of the internal audit program, ISO notified body audits, customer audits and FDA inspections.
Responsibilities
Serve as an auditor for internal audits.
Create and maintain internal audit schedule.
Audit controlled document files in preparation for regulatory inspections and provides support during regulatory inspections and client audits.
Initiate and execute audits, including developing and documenting the audit plan, leading the audit, generating the audit report, and tracking subsequent actions with the team.
Provide support during external audits including scheduling, hosting, preparing audit responses.
Work with subject matter experts to ensure audit record content is accurate, well documented, and meets the requirement of the process.
Develop metrics and performs trend analysis of key QS areas such internal and external audit findings, CAPAs, nonconforming material, training, deviations, etc. to identify areas for improvement. Escalates trends to an appropriate quality system such as CAPA or CI; presents analysis to management.
Supports maintenance of the CAPA program.
Serves as CAPA Owner as needed, driving necessary investigation, correction, and corrective/preventive actions.
Ensures all internal and external audit findings are entered into the CAPA system, assigned to the appropriate personnel, and are completed in accordance to the CAPA procedures, within specified time periods.
Approve corrective action plans and verify effective and timely implementation of corrective actions for audit nonconformities.
Oversees completion and control of customer questionnaires and other customer-required documents.
Initiates, facilitates and/or manages projects to expand, change, enhance and improve the quality system, as assigned.
Supports and coordinates activities related to nonconforming material, complaint/customer feedback, deviations, RMA, and CAPA processes.
Provides quality system training for the organization as needed.
Manages review of documents to ensure ISO/FDA compliance of controlled documents lifecycle including annual review management.
Ensures all work is performed and documented in accordance with GMP requirements and existing company policies and procedures.
Other duties as assigned.
Qualifications
Required:
Minimum of 2 year degree in Quality, Regulatory, Manufacturing or related field; OR certificate in Regulatory Science or Medical Product Development
1 year of regulated industry work experience.
Desired: 4 year degree in Quality, Regulatory, Manufacturing or related field.
ISO13485:2016 and/or ISO9001:2015 Auditor Certification.
Knowledge and experience with GMP/ISO Standards: ISO 9000/9001, ISO 13485, and FDA 21CFR 820/11 (4/210/211 as applicable).
3+ years of quality/regulatory experience in medical device or related industry.
1 year experience conducting investigations and root cause analysis for complex/advanced issues.
Required Skills
Ability to read, write, speak and understand the English language.
Ability to communicate clearly by conveying and receiving ideas, information and direction effectively.
Ability to demonstrate adequate job knowledge to deliver a world class performance.
Ability to challenge oneself to consistently meet all goals and deadlines.
Willingness to strive for excellence by producing work that is free of errors and mistakes.
Desire to delight both customers and coworkers by offering encouragement, fostering teamwork and addressing conflict appropriately.
Commitment to making improvements company wide.
Demonstrated competence using Microsoft Office.
Comprehensive understanding of applicable cGMP requirements, including ISO standards, and FDA and other QS regulations.
Comprehensive understanding of internal documentation (e.g., QS Manual, SOPs, etc.) and records and how they relate to cGMP requirements.
Knowledge of effective root cause investigation, corrective and preventive action planning and execution and verification of effectiveness techniques.
Experience with metrics development and data analysis.
Able to provide compliance guidance based on knowledge of regulations, available relevant information, alternatives, and risk.
Effective trainer and project leader.
Ability to maintain a professional and respectful relationship with coworkers and company representatives.
As a valued team member with Trelleborg, you will enjoy:
Competitive compensation: Plus, bonus opportunities!
Generous benefits package: Includes health, dental, vision, STD, LTD, life, 401k, paid time off, tuition reimbursement, and more!
Clean work environment: Enjoy working in a very clean and climate-controlled environment every day!
Greater opportunity for impact: You will impact the production of life-saving devices.
Pay range and compensation package
$68-76,000/yearly
Manufacturing Engineer II (Onsite)
Quality engineer job in Burnsville, MN
Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract.
Security Clearance:
None/Not Required
We are adding a Manufacturing Engineer II to the Engine Sensing Manufacturing Support Team at the Collins Aerospace Burnsville facility.
In this role, you will make an impact by evaluating and solving everyday manufacturing problems related to design, process, and supplier issues for the manufacture of high-quality sensing assemblies in a collaborative team environment. You will provide technical support to operations in the form of enabling and improving the flow of manufacturing utilizing the principles of quality and industrial engineering.
Our ideal candidate will be a curious self-starter with excellent teaming, communication, and relationship building abilities. The candidate will also have a passion for LEAN principles and processes and be eager to contribute to improved efficiency and productivity using their LEAN toolkit.
Joining Collins Aerospace isn't just about finding a job; it's about embarking on a journey to redefine the future of aerospace.
WHAT YOU WILL DO:
Drive manufacturing process improvements across multiple assembly process steps
Support production build operators with immediate needs on tooling and processes to meet production schedule.
Implement procedure and process improvements based on safety, quality, and productivity.
Identify and address safety concerns.
Analyze and understand factory needs and requirements.
Improve production facilities and equipment layouts.
Provide information to management as the status of equipment, manpower, space, and other elements affecting manufacturing.
Identify and manage risk in process development (primarily utilizing and driving Production Part Approval Process (PAPP) core elements e.g. PFMEA, MSA, Process Flow and Control Plans, etc.).
Perform evaluations and conducts special process assessments or audits. Types of special process specifications include but are not limited to Welding, Brazing, NDT, heat treat, soldering, and chemical processing.
QUALIFICATIONS YOU MUST HAVE:
Typically requires a University Degree and minimum 2 years of prior relevant experience oran Advanced Degree in a related field or in absence of a degree, 6 years of relevant experience.
2+ years of experience as a manufacturing engineer supporting production.
QUALIFICATIONS WE PREFER:
Problem-solving skills with ability to proactively identify alternate solutions to overcome difficult technical challenges.
Effective communication and interpersonal skills, with the ability to collaborate with cross-functional teams to achieve operational goals.
Detail-oriented and capable of managing multiple priorities in a fast-paced environment.
Experience using analytical and problem-solving skills to effectively identify and resolve issues and mitigate risks.
Proven ability to facilitate difficult conversations and communicate early and concisely with individuals at all organizational levels.
Collins Enterprise Values including Safety |Trust | Accountability | Respect | Collaboration | Innovation.
WHAT WE OFFER
BENEFITS
Some of our competitive benefits package includes:
Medical, dental, and vision insurance
Three weeks of vacation for newly hired employees
Generous 401(k) plan that includes employer matching funds and separate employer retirement contribution, including a Lifetime Income Strategy option
Tuition reimbursement program
Student Loan Repayment Program
Life insurance and disability coverage
Optional coverages you can buy pet insurance, home and auto insurance, additional life and accident insurance, critical illness insurance, group legal, ID theft protection
Birth, adoption, parental leave benefits
Ovia Health, fertility, and family planning
Adoption Assistance
Autism Benefit
Employee Assistance Plan, including up to 10 free counseling sessions
Healthy You Incentives, wellness rewards program
Doctor on Demand, virtual doctor visits
Bright Horizons, child and elder care services
Teladoc Medical Experts, second opinion program
And more!
This position may be eligible for relocation.
Learn More & Apply Now!
Collins Aerospace, an RTX company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio, and expertise to solve customers' toughest challenges and to meet the demands of a rapidly evolving global market.
Avionics delivers advanced cockpit displays, vision systems, and comprehensive digital solutions for global government, commercial and business aviation customers. We provide connectivity and managed data services to ensure safety and seamless communication for passengers, crews, and militaries, from aircraft and airports to air traffic management. Join us in creating solutions that connect the world, one flight at a time. Start your application today.
Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance employees, as they are essential to the development of our products. Regardless of your role type, collaboration and innovation are critical to our business and all employees will have access to digital tools so they can work with colleagues around the world - and access to Collins sites when their work requires in-person meetings.
At Collins, the paths we pave together lead to limitless possibility. And the bonds we form - with our customers and with each other -- propel us all higher, again and again.
Apply now and be part of the team that's redefining aerospace, every day.
As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote.
The salary range for this role is 66,000 USD - 130,000 USD. The salary range provided is a good faith estimate representative of all experience levels. RTX considers several factors when extending an offer, including but not limited to, the role, function and associated responsibilities, a candidate's work experience, location, education/training, and key skills.
Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.
Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.
This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.
RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window.
RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act.
Privacy Policy and Terms:
Click on this link to read the Policy and Terms
NPI Manufacturing Engineer
Quality engineer job in Anoka, MN
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. Join nVent as a New Product Introduction (NPI) Manufacturing Engineer and play a key role in bringing innovative products to life. You'll lead NPI processes from program kickoff through Production Part Approval Process (PPAP), Safe Launch Containment, and Engineering Change Notices (ECNs). Using your engineering expertise, you'll apply lessons learned and anticipate new challenges to ensure products are safe, scalable, and built for success. Collaborate with multi-functional teams-Design, Operations, Program Management, Supply Chain-to drive launch excellence and deliver exceptional customer satisfaction.
** nVent is growing, and we are hiring for multiple NPI Manufacturing Engineer positions. This role will work onsite, 5 days/week, in Anoka, MN. **
WHAT YOU WILL EXPERIENCE IN THIS POSITION:
Lead and support project kick-offs, ensuring internal requirements, layout data, and customer-specific needs are met; analyze Statistical Process Control (SPC) data and reduce Risk Priority Numbers (RPN).
Align product design with manufacturing processes and customer requirements to scale production while meeting exacting quality standards.
Document program results and manage compliance with internal and external requirements, including deviations.
Create key Advanced Product Quality Planning (APQP) outputs: Control Plans, Capability Studies, Failure Mode and Effects Analyses (FMEA), inspection instructions, and gage design with Gage Repeatability and Reproducibility (R&R) validation.
Partner with Manufacturing Engineering to design fixtures and job aids for smooth production launches.
Contribute to innovative solutions for complex product and process challenges.
YOU HAVE:
Bachelor's (B.S.) degree in Engineering and 3+ years as a Manufacturing Engineer OR Bachelor's (B.A. or B.S.) degree and 5+ years of relevant manufacturing experience.
Solid understanding of APQP principles, including managing ECNs and integrating changes into quality planning.
Experience developing Control Plans, conducting FMEAs, and running process capability studies.
Proficiency in Geometric Dimensioning and Tolerancing (GD&T) and interpreting engineering drawings; skilled in CAD tools such as SolidWorks or AutoCAD.
Ability to collaborate with Quality teams to create inspection plans and ensure compliance.
Hands-on experience with PPAP submissions and first article inspections.
Familiarity with ISO 9001 and other regulatory requirements.
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:
$76,000.00 - $141,100.00
Depending on the position offered, employee may be eligible for other forms of compensation, such as annual incentives.
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
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.
#LI-JM2
#LI-Onsite
Advanced Quality Engineer
Quality engineer job in Maplewood, MN
**Job Title** _Advanced Quality Engineer_ **Collaborate with Innovative 3Mers Around the World** Choosing where to start and grow your career has a major impact on your professional and personal life, so it's equally important you know that the company that you choose to work at, and its leaders, will support and guide you. With a wide variety of people, global locations, technologies and products, 3M is a place where you can collaborate with other curious, creative 3Mers.
**This position provides an opportunity to transition from other private, public, government or military experience to a 3M career.**
**The Impact You'll Make in this Role**
The person hired for the position of **Advanced** **Quality Engineer** will be responsible for ensuring consistent product quality aligned with customer needs throughout the designed product life. This specific role will support optical films, adhesives, materials, and novel combinations in Display and Electronics Product Platform through New Product Introduction (NPI) projects and providing support on Change Managed (CMP) projects through appropriate risk analysis (FMEA) and addressing key risks.
As an Advanced Quality Engineer you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative people around the world. Here, you will make an impact by:
+ Respond to customers as needed (product development and customer specifications, complaints and CAPA, key account management including customer agreements, data analysis, etc.)
+ Lead continual quality improvement projects to improve quality and reduce Defective Parts per Million (DPPM)
+ Lead quality tool usage within project teams
+ Manage customer complaints in 3M Customer Issue Resolution (CIR) system within product responsibility area
+ Develop test methods: documentation, training, Measurement System Analysis (MSA), round robins
+ Develop visual reference standards, visual test methods, and align visual detection systems
+ Product qualification planning, testing, and analysis
+ Lead the development of Quality Functional Deployment (QFD), Failure Mode and Effect Analysis (FMEA), Control Plans
+ Document and improve the Quality Management System
**Your Skills and Expertise**
To set you up for success in this role from day one, 3M requires (at a minimum) the following qualifications:
+ Bachelor's degree or higher in Science, Technology, Engineering or Mathematics discipline (completed and verified prior to start)
+ One (1) year of experience working or interning in a Quality Engineering, Product Engineering and/or Manufacturing environment in a private, public, government or military environment
Additional qualifications that could help you succeed even further in this role include:
+ Experience working with automated inspection systems
+ Bachelor's degree or higher in Engineering, Physics, Chemistry, Mathematics/Statistics or related discipline from an accredited institution
+ Minimum 3-years of Quality Engineering and/or Product Engineering
+ Experience in Manufacturing
+ Experience leading cross-functional teams and/or projects
+ Lean Six Sigma training with proven ability to understand and apply Lean Six Sigma and other quality tools to product, systems and process problems
+ Working knowledge of International Organization for Standardization (ISO) 9001 standards
+ Test method development experience
**Work location:**
+ **Work location:** This role follows an on-site working model, requiring the employee to work **at least four days a week at the 3M Center in Maplewood, MN** .
+ **Travel:** **May include up to** **25% domestic/international**
+ **Relocation:** **May be authorized**
**Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).**
**Supporting Your Well-being**
3M offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, 3M regularly benchmarks with other companies that are comparable in size and scope.
**Chat with Max**
For assistance with searching through our current job openings or for more information about all things 3M, visit Max, our virtual recruiting assistant on 3M.com/careers.
Applicable to US Applicants Only:The expected compensation range for this position is $98,413 - $120,282, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: ****************************************************************
Good Faith Posting Date Range 10/01/2025 To 10/31/2025 Or until filled
All US-based 3M full time employees will need to sign an employee agreement as a condition of employment with 3M. This agreement lays out key terms on using 3M Confidential Information and Trade Secrets. It also has provisions discussing conflicts of interest and how inventions are assigned. Employees that are Job Grade 7 or equivalent and above may also have obligations to not compete against 3M or solicit its employees or customers, both during their employment, and for a period after they leave 3M.
Learn more about 3M's creative solutions to the world's problems at ********** or on Instagram, Facebook, and LinkedIn @3M.
Responsibilities of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.
Safety is a core value at 3M. All employees are expected to contribute to a strong Environmental Health and Safety (EHS) culture by following safety policies, identifying hazards, and engaging in continuous improvement.
Pay & Benefits Overview: https://**********/3M/en\_US/careers-us/working-at-3m/benefits/
3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law.
**Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.**
**3M Global Terms of Use and Privacy Statement**
Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms.
Please access the linked document by clicking here (************************************************************************************************* , select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.
At 3M we apply science in collaborative ways to improve lives daily as our employees connect with customers all around the world. Learn more about 3M's creative solutions to global challenges at ********** or on Twitter @3M or @3MNews.
3M does not discriminate in hiring or employment on the basis of race, color, sex, national origin, religion, age, disability, veteran status, or any other characteristic protected by applicable law.
STANDARDS ENGINEER
Quality engineer job in Dayton, MN
We are the largest electrical distribution cooperative in Minnesota and is a progressive organization that provides electric service to customers in a 7-county area north of the Twin Cities. Our organization received the highest ranking in reliability and the ability to restore power of all electric utilities nationwide in the 2014 American Customer Satisfaction Index.
We are currently seeking an experienced Engineer with excellent analytical skills to guide the Engineering department in developing and applying standards that result in the most cost effective, reliable distribution system. The individual in this position will develop and maintain construction standards and specifications for the distribution system that includes new technologies, materials, methods and products. Key areas of responsibilities include:
• Create standards and identify new materials to design, construct, and maintain a quality system while continuously analyzing and striving to make improvements
• Develop and maintain construction specifications
• Research and prepare major material purchase specifications for equipment
• Research and evaluate new products
• Review equipment and material failures and implement necessary corrective measures
• Provide technical guidance to distribution system design and construction departments
• Develop, publish, and distribute construction specification books to ensure all system construction will meet strength and clearance requirements and to minimize construction costs, while meeting standards and codes
Required Talents, Skills, Expertise, Education
• BS degree in Electrical, Civil, Mechanical or Industrial Engineering
• Five years' experience in electric distribution, transmission or substation engineering in a utility focused environment
• Engineer-in-training with ability to obtain Professional Engineer license in Minnesota
• Knowledge and ability to apply standards and codes
• Excellent oral and written communication skills
Preferred Talents, Skills, Expertise, Education
• Knowledge and ability to apply National Electrical Safety Code
• Power emphasis in Electrical Engineering
• Professional Engineer license in Minnesota
• Drafting software skills
SKILLS AND CERTIFICATIONS
Engineer-in-training with ability to obtain Professional Engineer license in Minnesota
Excellent oral and written communication skills
SCREENING QUESTIONS
Please seriously evaluate where Ramsey, MN is located and the climate in this area. Based on your evaluation and if necessary, would you be willing to relocate to MN?
Do you have a BS degree in Electrical, Civil, Mechanical or Industrial Engineering?
Do you have five or more years experience in electric distribution, transmission or substation engineering in a utility focused environment?
IDEAL CANDIDATE
The ideal candidate has 5+ years' experience in electric distribution system applications. A Power emphasis in Electrical Engineering, Professional Engineer license in Minnesota, familiarity with National Electric Code and drafting software skills would be ideal.
IDEAL CANDIDATE SHOULD HAVE WORKED FOR THE FOLLOWING COMPANY(IES):
Xcel Energy, other electric co-operatives or municipalities, engineering consulting firms that specialize in power
Additional Information
All your information will be kept confidential according to EEO guidelines.
Direct Staffing Inc