Location: Schuyler, NE
Quality Assurance (QA) jobs involve ensuring that products and services meet certain standards of quality before they reach the consumer. Those in QA roles are responsible for developing and implementing testing processes, inspecting products for defects and non-compliance, and analyzing quality data to drive improvements. A key characteristic of QA positions is the focus on preventing errors rather than just correcting them, which necessitates a proactive approach and attention to detail. Additionally, QA professionals often collaborate closely with production teams to foster a culture of quality throughout an organization.
Quality and Productivity to help the company consistently move forward. Provides front line support with internal quality issues and supports the Quality Manager with determining root cause and corrective actions. Develops supporting fixtures and devices as requested by production to improve safety, quality and/or productivity.
Our Culture and Our Beliefs Kinney Manufacturing strives to keep things simple. Some parts we produce have critical tolerance and very precise applications, but they are still a metal part. Based on this, we always need to keep our activities in perspective. We expect our team members to come to work each day with the expectation of working safely, making good
quality parts and being productive. We then want our team members to go home and enjoy their time away from Kinney Manufacturing with their family and friends.
Kinney Manufacturing's commitment is to provide our customers, suppliers and team members with the information and/or materials to accomplish their activities efficiently and without drama. We want to communicate information clearly and only once, and then we all can have the expectation that the work will be completed. We want to treat everyone that interacts with Kinney Manufacturing fairly and how we would want to be treated in return. Living by this simple concept should make it obvious how to solve problems and help others.
We believe that the key to maintaining and growing a successful business is to answer the phone when people call and deliver product on-time.
Quality parts and a competitive price have become a requirement to be in business these days, and it is only with great customer service that our business will thrive. Apply online at: http: //kinneymfg.
than 90 countries. Lindsay Corporation’s infrastructure division offers a wide range of products that aid in roadway maintenance and transportation safety. Since 1955, Lindsay Corporation has been at the forefront of research and development of products and services designed to meet the needs of a constantly evolving world.
Position Description Lindsay Corporation is hiring a Summer Quality Assurance Intern at Lindsay, Nebraska location. This is a temporary role for 2024 summer (from end of May or early June) for 3 to 4 months duration (or until school starts back in the fall). This position will report to Lindsay Plant Quality Manager and will work with the Quality Assurance Team. Position
Details This position is full-time (40 hours/week) and will be working on first shift (7:00 am to 4:00 pm) at Lindsay, Nebraska location. There is no travel requirement for this role.
Duties & Responsibilities Learn about Lindsay’s products, Quality Assurance and Production procedures, personnel, philosophies, and strategies. Learn, perform and assist with various Quality Control functions throughout the Lindsay, NE site including variable gauge inspection, attribute gage inspection, CMM and Vision System inspections, Incoming, In-Process and Outbound inspections. Work directly with the Quality Engineer Team and Manager to: Initiate corrective and preventative action Root cause analysis
Containment activities Research and analysis Quality improvement initiatives.
Take ownership of your own corrective action/quality improvement project from initiation to closure. You will present your project to the Leadership Team at Lindsay upon completion. Preferred Qualifications Experience and proficiency in MS Office, more specifically MS Word, MS Excel and Visio English language proficiency Technical writing skill and proficiency Understanding of ISO requirements related to controlled Ddcuments is preferred. Physical Requirements Ability to work safely in a manufacturing environment.
insights and solutions to the needs of our customers, stakeholders, and society. At SEE, we are creating a community of inventors, problem solvers, and future makers that are passionate about fulfilling our purpose. SEE generated $6 billion in revenue in 2022 and has approximately 17,700 employees who serve customers in 129 countries/territories.
To learn more, visit . Job Summary A Field Quality Analyst job is currently available at SEE. You will work with SEE Supply Chain, Sales and customers to quantify and improve the quality and performance of SEE’s products. Investigate and analyze quality issues and lead resolution efforts. Provide training to customer personnel in the proper use
of SEE packaging materials and equipment. Recommend, assist with, and/ or initiate programs designed to improve performance of SEE products and equipment, as well as customer packaging processes.
Job Description Determine the fitness of the total customer packaging process through the use of statistical audits, process observation, and customer interaction. Identify problems and opportunities in the Customer’s process (potentially including shipping and destination testing) and recommend product / process quality improvements that provide value to SEE and our customers. Serve as the SEE quality representative in the field and provide guidance, advice, and training to customers about quality
improvement techniques. Act as advisor/liaison between internal and external customers and Supply Chain, identify areas of potential improvement and communicate those findings to customers and SEE plants.
Pro-actively address quality issues within assigned territory/area of responsibility. Initiate the appropriate communications and drive the root cause investigation and corrective actions to resolve the issues. Work with Supply Chain, Sales, Technical Sales, Applications/R&D, and PESC on special projects to address customer needs such as line layout, equipment recommendations, and new product development (team member or team leader as needed). Required Qualifications Education: BS/BA required, preferably in a technical field, or a minimum of 5 years of technical experience in SEE operations.
Experience: Minimum of 5 years of experience in packaging, food packaging, or flexible films manufacturing, quality or technical field. Ability to use hand tools, read calipers for measurements. Skills/Certifications/Special Training: Six-Sigma/Lean certification is desirable, or ability to be certified. Personal computer skills with standard software systems (WORD, EXCEL, POWERPOINT especially) are essential. Additional Qualifications Demonstrated ability to work and communicate effectively with all levels of a manufacturing team, from operators to quality managers to plant managers.
Demonstrated success in logical, data-driven problem solving. Ability to stay cool in stressful situations. Extensive regional travel, 80%, required. Requisition id: 44965 Relocation: Yes The Company is committed to providing equal employment opportunities to all applicants for employment and to all employees, without regard to race, color, religion, gender, interactionual orientation, gender identity or expression, national origin, age, protected disability, veteran status, or any other protected status in accordance with applicable federal, state or local laws.
Please be cautious of fraudulent recruiting efforts using the SEE name or logo. SEE will never request private information during the application process, such as a Driver's License or Social Security Number. If you have any concerns about information received from SEE during the application process, please reach out to us directly at xyz X@. LINK1 MON1
medical, or related manufacturing, is required. Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities.
We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best
self. Become a maker of possible with us. Job Description: Configures, validates, deploys, and administrates quality related software systems. Composes and implements validations for CSD&V and AME applications.
Functions as a domain expert in software validation, provides mentorship, and reviews software development/validation documents written by other individuals. Applies compliance and notification trends to identify areas of manufacturing improvement using product knowledge, existing specifications, and engineering principles. As needed, develops and employs technical understanding of product characteristics and functional end-use in order to optimally investigate complaint trends
or other targeted product functionality improvements. Applies problem solving processes to site quality issues and sources potential software related solutions.
Effectively manages project timelines and communicates updates to collaborators. Crafts and coordinates training and procedures related to compliance and quality software packages. Builds or modifies plant control plans with process remediation activities. Leads or participates on multi-functional process remediation and improvement teams as assigned by local quality management. Independently identifies process improvement opportunities and implements software solutions. Qualifications: Education/Experience Required: BS Degree in Computer Science, Engineering, or a related field Accomplished experience and knowledge may be considered in lieu of a degree.
Experience in medical device, medical, or related manufacturing is required. Preferred: Understanding of software/process validation and quality theories Six Sigma Certification Statistical Process Control Certification (SPC)Good Manufacturing Practices knowledge (GMP)For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required.
Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do.
We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
PDN#earlytalent#ET Primary Work Location USA NE - Broken Bow Additional Locations Work Shift Apply Save Job Responsibilities Job Description Summary Responsible for configuring, validating, deploying, and administrating quality-related software systems, as well as identifying areas for manufacturing improvement and implementing software solutions. A degree in computer science, engineering, or a related field, along with experience in medical device, medical, or related manufacturing, is required.
Job Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve.
Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Job Description: Configures, validates, deploys, and administrates quality related software systems. Composes and implements validations for CSD&V and AME applications. Functions as a domain expert in software validation, provides mentorship, and reviews software development/validation documents written by other individuals. Applies compliance and notification trends to identify areas of manufacturing improvement using product knowledge, existing specifications, and engineering principles.
As needed, develops and employs technical understanding of product characteristics and functional end-use in order to optimally investigate complaint trends or other targeted product functionality improvements. Applies problem solving processes to site quality issues and sources potential software related solutions. Effectively manages project timelines and communicates updates to collaborators. Crafts and coordinates training and procedures related to compliance and quality software packages. Builds or modifies plant control plans with process remediation activities.
Leads or participates on multi-functional process remediation and improvement teams as assigned by local quality management. Independently identifies process improvement opportunities and implements software solutions. Qualifications: Education/Experience Required: BS Degree in Computer Science, Engineering, or a related field Accomplished experience and knowledge may be considered in lieu of a degree. Experience in medical device, medical, or related manufacturing is required. Preferred: Understanding of software/process validation and quality theories Six Sigma Certification Statistical Process Control Certification (SPC)Good Manufacturing Practices knowledge (GMP)For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19.
In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work.
It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit /careers Becton, partinson and Company is an Equal Opportunity/Affirmative Action Employer.
We do not unlawfully discriminate on the basis of race, color, religion, age, interaction, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or interactionual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. PDN#earlytalent#ET Primary Work Location USA NE - Broken Bow Additional Locations Work Shift Apply Save Job PDN-9ac9ad92-e718-4ca8-9e4c-2196a4951381
