Location: Salt Lake City, UT
Company: Becton Dickinson
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. As directed by the Quality Manager, the Senior Quality Engineer will be a member of the Advanced Access Devices (AAD) platform and is accountable for product maintenance and new product development through the application of Quality engineering skills for medical devices. This person will handle projects
and tasks, from product inception through product launch and maintenance and play an active role in the processes to ensure products meet quality standards consistent with both Corporate and unit policies, while meeting all design control and other regulatory requirements.
Responsibilities: Provide guidance and Quality oversight to ensure establishment and execution of robust design control programs aligned with regulatory requirements and industry standards. Support new product development and existing product sustaining activities to ensure work follows proper designcontrol. Ensure controls meet BD and FDA regulatory requirements by actively participating on product developmentteams
and identifying Quality needs, product improvements and customer requirements.
Ensures adequate design control documentation and records are maintained to support life cycle of design history. Support new product development execution of design control and ensure tasks are completed adequately to include projectplanning, design inputs, critical to quality characteristics, risk analysis, design reviews, validations, verifications, anddesign history files and other activities as needed. Provide guidance and training to cross-functional associates to help increase knowledge of regulations andstandards for Devices and Combination Products. Responsible to evaluate design verification results and data utilizing statistical analysis to ensure design delivers anacceptable quality level during manufacturing with properly established product specifications.
Ensures the design is appropriately specified and established before transferring into manufacturing to avoid increased risk. Review and authorize Quality approval for new product and/or device design specifications including productperformance specifications, test methods, acceptance criteria, and release. Review and backss work performed by R&D and other BD business units to help ensure Quality issues with device(s) or component(s) are adequately addressed and when needed corrective actions are taken to prevent recurring quality issues.
Work with Validation team providing Quality Engineering support for Product and/or Device transfer, Scale-Up, and Process Validation. Lead or participate in ISO 14971Risk Management activitiesappropriate to the initiative or situation. Monitor quality data from Product Incident Report process, Manufacturing reports, Service reports and customerinput. Identifies, investigates, troubleshoots and resolves identified quality issues independently or by working with Field Assurance, Manufacturing, Engineering, Regulatory and Biostatics.
Initiate Corrective and Preventative Action plans and perform efficacy follow up. Conduct as needed supplier evaluations and meet with suppliers to establish required controls to meet BD andregulatory requirements. Participate as assigned with supplier capability and internal audits as a means of evaluating effectiveness of GMPsand established Quality Systems. Support Regulatory Affairs, as appropriate, by providing input for submissions or response to agency queries. Support regulatory inspections as needed. Lead investigation and Field activities relating to Field Corrective Actions, when needed.
Qualifications: Bachelor's degree in STEM and six (6) years of engineering experience, OR Master's degree in STEM and four (4) years of engineering experience required. Design Controls, Risk Management and Change Controls is required. Experience in medical device industry is required. American Society of Quality (ASQ) certification (CQE, CQA, etc)preferred. Experience with drug-device combination products is strongly preferred. 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 Primary Work Location USA UT - Salt Lake City Additional Locations Work Shift Apply Save Job Responsibilities Job Description Summary 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. As directed by the Quality Manager, the Senior Quality Engineer will be a member of the Advanced Access Devices (AAD) platform and is accountable for product maintenance and new product development through the application of Quality engineering skills for medical devices.
This person will handle projects and tasks, from product inception through product launch and maintenance and play an active role in the processes to ensure products meet quality standards consistent with both Corporate and unit policies, while meeting all design control and other regulatory requirements. Responsibilities: Provide guidance and Quality oversight to ensure establishment and execution of robust design control programs aligned with regulatory requirements and industry standards.
Support new product development and existing product sustaining activities to ensure work follows proper designcontrol. Ensure controls meet BD and FDA regulatory requirements by actively participating on product developmentteams and identifying Quality needs, product improvements and customer requirements. Ensures adequate design control documentation and records are maintained to support life cycle of design history. Support new product development execution of design control and ensure tasks are completed adequately to include projectplanning, design inputs, critical to quality characteristics, risk analysis, design reviews, validations, verifications, anddesign history files and other activities as needed.
Provide guidance and training to cross-functional associates to help increase knowledge of regulations andstandards for Devices and Combination Products. Responsible to evaluate design verification results and data utilizing statistical analysis to ensure design delivers anacceptable quality level during manufacturing with properly established product specifications. Ensures the design is appropriately specified and established before transferring into manufacturing to avoid increased risk.
Review and authorize Quality approval for new product and/or device design specifications including productperformance specifications, test methods, acceptance criteria, and release. Review and backss work performed by R&D and other BD business units to help ensure Quality issues with device(s) or component(s) are adequately addressed and when needed corrective actions are taken to prevent recurring quality issues. Work with Validation team providing Quality Engineering support for Product and/or Device transfer, Scale-Up, and Process Validation.
Lead or participate in ISO 14971Risk Management activitiesappropriate to the initiative or situation. Monitor quality data from Product Incident Report process, Manufacturing reports, Service reports and customerinput. Identifies, investigates, troubleshoots and resolves identified quality issues independently or by working with Field Assurance, Manufacturing, Engineering, Regulatory and Biostatics. Initiate Corrective and Preventative Action plans and perform efficacy follow up. Conduct as needed supplier evaluations and meet with suppliers to establish required controls to meet BD andregulatory requirements.
Participate as assigned with supplier capability and internal audits as a means of evaluating effectiveness of GMPsand established Quality Systems. Support Regulatory Affairs, as appropriate, by providing input for submissions or response to agency queries. Support regulatory inspections as needed. Lead investigation and Field activities relating to Field Corrective Actions, when needed. Qualifications: Bachelor's degree in STEM and six (6) years of engineering experience, OR Master's degree in STEM and four (4) years of engineering experience required. Design Controls, Risk Management and Change Controls is required.
Experience in medical device industry is required. American Society of Quality (ASQ) certification (CQE, CQA, etc)preferred. Experience with drug-device combination products is strongly preferred. 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 Primary Work Location USA UT - Salt Lake City Additional Locations Work Shift Apply Save Job PDN-9ae5d82b-c622-4bdb-a92e-2963cdbb7aa9
machine repair leaders and believe that hard work can also be fun. In addition to great pay and our exceptional culture , we offer the following benefits and perks: Medical, dental, and vision insurance Life and critical illness insurance Accident coverage A 401(k) plan with a company match An employee assistance program (EAP) Short-term disability (STD) and long-term disability (LTD) Education tuition assistance A health savings account (HSA) Paid time off (PTO) and holiday pay Responsibilities: Develop and maintain ASME " S" and " U" stamps as well as the National Boiler Inspection Code " R" stamp.
Develop, implement, and maintain welding and NDT procedures
as well as welder qualification program. Manage and participate in NDT qualification programs as required. Maintain welding records for weld certifications, PQR, WPQ and WPS development.
Maintain current knowledge of industry standards and practices and act as company representative with agencies such as ASME, AWS, NBI and others. Perform welding qualifications and training to support the welding programs. Perform in-process and final inspections of welding and dimensions of parts. Ensure that all quality documentation is accurate and complete and submitted in a timely manner. Support Sales with technical bid review to mitigate quality risks. Attend project kick-off meetings to support
contract review mitigating quality risks by implementing project specific quality plans.
Review contract documents and design documents for quality considerations. Act as liaison for customers regarding all quality issues. Train area managers and craftsmen regarding ASME/NBI quality policies and procedures. NCR investigation and root cause analysis to identify recommendations for corrective actions and prevent reoccurrences. Evaluate and/or qualify quality programs/procedures of suppliers and subcontractors. Identify and develop third-party inspection subcontractors to support quality efforts. Serve on the Material Review Board (MRB) to correct nonconformance on ASME/AWS projects.
Provide technical direction for craftsman as required regarding code requirements. Other duties as assigned. Qualifications: Current SCWI or CWI level II certification. College degree in engineering discipline or related field preferred, or equivalent commensurate experience. Experience with performing PT, MT, and UT inspections. Advanced knowledge with interpreting assembly and manufacturing drawings, GD&T and standard symbols. Basic machining experience and advanced knowledge of manufacturing and welding processes. Proficient with Microsoft office suite, scheduling programs and ability to use company programs as required.
Excellent communication both written and verbal. Well organized and detail oriented. Ability to work in the United States without sponsorship. Valid Driver's license with acceptable MVR. Other: Must be capable working in heavy industrial environments. May be required to; climb on and around equipment, lift tools and components, bend, or crawl to obtain correct positions, and reach for tools, equipment or machine components. Must be a mature individual not easily upset - remaining calm during adverse situations. Must be able to create internal systems and processes.
Must be able to work with minimal supervision. Ability to provide presentations using MS Office or other software. Must be able to train, teach, instruct. ABOUT PRIME FIELD SERVICE. Established in 2004, we provide emergency industrial equipment repair and new component fabrication services to a wide range of customers statewide and beyond! From millwright field services to state-of-the-art laser inspection services, we do it all! As a world-class leader in part fabrication, we take pride in our operations because everything we do affects important fields of work such as the defense, aerospace, hydraulics, power, mining, oil, and gas industries.
We are a critical infrastructure industry, and our values are second to none. Every day we strive to give our best work so that the world around us can continue to properly function and advance! We are a rapidly expanding company with great opportunities for advancement , so we are always looking for great additions to our team. Our staff is the key to our success, so we take care of them. We offer our amazing employees an excellent benefits package, top wages, a positive working environment, and great technology!
We produce world class products and want our employees to be world class in all they do. Come see all the exciting projects we get to be a part of! ARE YOU READY? If you are excited to join our machine repair team and take on this welding and fabrication opportunity, don't delay. Apply today! We look forward to meeting you! Job Posted by Applicant Pro
a mobile app to assist participants worldwide in care management of medical conditions or creating a process to flow health insurance claims to individuals and teams across many disciplines, there is no shortage of business problems to be solved. As an Appian developer at DMBA, you will.
backss software quality through manual and automated testing Design, develop, and deploy Appian applications Find and report bugs and glitches Share your expertise as an Appian developer while building solutions from the bottom up Integrate your projects with various back-end APIs, services, and databases Collaborate with fellow team members to gather and refine project specifications Develop and deploy
test scripts Maintain and support existing applications Execute test cases (manual or automated) and analyze results Conduct end-to-end testing on software applications Participate in peer reviews of software design, coding, and testing Spend time honing and enhancing your skills through ongoing training We expect to see.
0-3 years of experience in IT (preference for experience in Appian BPM or other low-code solution such as Pega, Salesforce, K2, etc). Experience as a Quality Assurance Tester or similar role Ability to write and understand Appian SAIL code Understanding of basic development Knowledge and understanding in Agile methodologies and regression testing Understanding of relational
database management systems, database design, and SQL Experience with configuration, deployment, and testing of enterprise software applications Familiarity with RESTful APIs What We Offer: Competitive pay Rich medical, vision and dental benefits with low premiums (we are the #1 health plan in Utah!
) Rich retirement planning; including 401(k) company match, life insurance, and full-service Financial Planners onsite at no cost Generous paid leave plan that starts accruing your first day, your birthday off, additional sick leave and 11 paid holidays World class wellness program with health coaching, ability to earn 3 additional days off a year, fun activities, and onsite gym.
Tuition reimbursement. Employee assistance program. Career development through company sponsored programs and over 5000 on-demand online training courses through our learning management system. Job Posted by Applicant Pro
pathogens, and helping to conduct investigations whenever a potential food safety issue occurs. Additionally, the Senior QA Technician helps to improve food safety by assisting in verifying and validating our SQF (Safe Quality Foods) food safety program. We pay our Senior QA Technician $24.06 per hour.
Shift: Days Observe/monitor compliance of production staff with policies and procedures Conduct training in current Good Manufacturing Practices (GMPs) for new employees Administer quarantines and releases for raw materials Complete QA section of Post-Operation Checklist Conduct and record results of water activity testing for finished product Conduct and record results of cleaning validations
(ATP swab testing) Verify that finished product meets specifications and release product for sale. Conduct weekly environmental monitoring swabs. Manage the holds and release process.
Test ingredients and finished products for microorganisms. Update regulatory portals like Kosher, Genesis (labeling), and customer portals Be a member of the HACCP food safety team Other duties as assigned by Director Regulatory, Compliance, and Food Safety Job Requirements: Previous QA Tech experience in food manufacturing preferred. High School Diploma or equivalent (preference will be given for a college degree in a relevant field or prior QA experience working with food safety). Demonstrated excellent
teamwork Ability to demonstrate a high degree of initiative. High attention to detail.
Excellent verbal/written communication skills. Bi-Lingual Spanish/English a plus. Ability to adapt to changing organizational and operational needs. Ability to communicate professionally and effectively with others at all levels in the organization. Strong organizational skills and the ability to multi-task. Genesis & SQF experience preferred CONDITIONS & EXPOSURE: General manufacturing working conditions exists. Exposures include, but are not limited to temperature changes, noise, dust, and moving equipment and machinery. Must be able to stand for 8+ hours. Job Posted by Applicant Pro
Atlantic Ocean, to stealth bombers, to landing on the moon. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work - and we have an insatiable drive to do what others think is impossible.
Our employees are not only part of history, they're making history. At Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the world today, and for generations to come. Embark on a career putting innovative, reliable, and agile products and
ideas into orbit, and beyond. Northrop Grumman has opportunities waiting for you that play a vital role in human space exploration, national defense, and scientific discovery, supporting multiple programs across the universe.
With us, you'll discover a culture of curiosity and collaboration that will have you Defining Possible from the day you start. Our space systems connect and protect millions of people on earth every day, now and for the future. Explore your future and launch your career today. Northrop Grumman Space Systems is currently seeking a Tool Quality Engineer to provide support for our Tool Quality Teams in Clearfield, Utah and Iuka, Mississippi. Successful candidate for
this position will reside in Clearfield, UT. This position may be filled as either a Quality Engineer (level 2) or a Principal Quality Engineer (level 3).
Role description Duties and Responsibilities: Successful candidate will be responsible for performing Tool Quality Engineer functions to help assure the quality of tooling and to ensure the tooling meets the company's quality standards and support the efficiency and effectiveness of tools use in production. Job responsibilities will include: Evaluate tool designs for compliance to industry dimension and tolerancing standards. Evaluate design to determine manufacturability of tool design to produce an acceptable, functional tool.
Create and provide accurate Tool Inspection Records to various organizations to tools meet engineering requirements. Concur with tooling review board dispositions for tooling non-conformances. Coordinate, identify tooling non-conformance history, and communicate trends. Provide and support tooling nonconformance analysis and associated processes. Review Supplier data package for accuracy completeness. Maintain accurate tool history data packets. Effectively interact with Tool engineering, Tool Quality Inspection, Operations, Materials and Process experts, Quality engineering and Process engineering, and Design engineering.
Day-to-day, side-by-side participation with operations, engineering, and inspection personnel to ensure high quality tooling and product associated for critical hardware support. Inspect tool configuration for drawing compliance, including fit, form and function. Support tooling suppliers as needed during tool fabrication and inspection. Support continuous improvement. Support Operations and Process Engineering in the use of tooling Competencies for Success: Strong interpersonal skills with ability to interface with an organization at all levels.
Excellent problem-solving skills Able to deal effectively with stress and conflict. High energy, results oriented, self-reliant, team player. Ability to multitask and prioritize. Excellent organizational and multi-tasking skills Strong attention to detail Demonstrated work ethic. Basic Qualifications for a Tool Quality Engineer (level 2): 2 Years with Bachelors in Science; 0 Years with Masters, in science or a STEM discipline experience in manufacturing or quality assurance Knowledge of ISO 9001 and AS9100 Application of Geometric Dimensioning and Tolerancing (ANSI/AMSE Y14.5) Dimensional Inspection Techniques Ability to interpret Engineering Drawings Experience using product verification instruments including Laser tracker is a plus.
Experience and familiarity with machine shop and weld shop practices is a plus. Organization skills to maintain accurate history records. Must be able to obtain a Do D Secret Clearance. Knowledge in reviewing and understanding customer certifications, specifications, contracts and purchasing requirements. Physical demands include standing or moving about the plant more than half the time. Some travel to suppliers required and supplier on-site backssment experience a plus.
Basic Qualifications for a Tool Quality Engineer (level 3): 5 Years with Bachelors in Science; 3 Years with Masters; 0 Years with Ph D, in science or a STEM discipline experience in manufacturing or quality assurance Knowledge of ISO 9001 and AS9100 Application of Geometric Dimensioning and Tolerancing (ANSI/AMSE Y14.5) Dimensional Inspection Techniques Ability to interpret Engineering Drawings Experience using product verification instruments including Laser tracker is a plus. Experience and familiarity with machine shop and weld shop practices is a plus. Organization skills to maintain accurate history records.
Must be able to obtain a Do D Secret Clearance. Knowledge in reviewing and understanding customer certifications, specifications, contracts and purchasing requirements. Physical demands include standing or moving about the plant more than half the time. Some travel to suppliers required and supplier on-site backssment experience a plus. Preferred Qualifications: Geometric Dimensioning & Tolerancing knowledge Blueprint reading Machine Shop experience / knowledge Welding experience / knowledge Tool inspection experience / knowledge Active Do D Secret Clearance Salary Range: $68,500 - $102,700 Salary Range 2: $84,200 - $126,400The above salary range represents a general guideline; however, Northrop Grumman considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions.
Employees may be eligible for a discretionary bonus in addition to base pay. Annual bonuses are designed to reward individual contributions as well as allow employees to share in company results. Employees in Vice President or Director positions may be eligible for Long Term Incentives.
In addition, Northrop Grumman provides a variety of benefits including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business. Northrop Grumman is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer, making decisions without regard to race, color, religion, creed, interaction, interactionual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class.
For our complete EEO/AA and Pay Transparency statement, please visit http: ///EEO. U. S. Citizenship is required for most positions. PDN-9ae9da71-247d-4e52-bbbd-fced358ffeaf
the world’s leading supplier of solid rocket motors, a leading provider of launch vehicles, satellites and other space systems, and the nation’s largest manufacturer of ammunition. Orbital ATK is currently looking for a Quality Engineer to work in our Clearfield, UT location.
Job description: Support operations in high rate composite part production facility by executing essential Quality tasks and functions. Work closely with manufacturing personnel and engineering to solve production issues on highly automated processes using data based problem solving techniques. Learn and understand requirement to determine product impacts and execute disposition of the parts. Work in a cross functional
team to develop and implement process improvements. Requirements & Qualifications: • Bachelor’s degree in Manufacturing Engineering or related technical arena and 4 years of experience.
• Good organizational skills and ability to work with minimal direction in a changing environment. • Excellent computer skills. Skilled in working with Microsoft Office applications • Demonstrated exceptional problem solving skills • Excellent verbal and written communication skills • Adaptable and able to learn on the fly • Enjoys challenges and variety of work content day to day Preferred Skills and Experience: • Demonstrated Knowledge of root cause / corrective action processes and techniques • Experience
with Material Review Board activities (MRB) • Functional knowledge of Process Failure Modes and Effects Analysis (PFMEA) • Experience working with aerospace specifications and requirements preferred • Composite fabrication experience preferred • Understanding of Orbital ATK software toolbox including Solumina, e PIC, and Tiip QA • Experience using SPC to monitor and improve processes • High rate production experience preferred • Leadership experience a plus Competencies for Success: • Ability to multitask and prioritize • Strong attention to detail • Initiative, self-starter, adaptable, and high motivation for excellence • High energy, results oriented, self-motivated / self-reliant, team player • Strong interpersonal skills with ability to interface with an organization at all levels • Ability to work in a dynamic, fast paced environment • With annual revenues in of nearly $4.5 billion, over 12,000 employees, and operations in about 20 states, Orbital ATK is a company on the move.
Our mission is to ensure that our customers accomplish their mission — whether it’s a technological breakthrough, a satellite launch, or protecting our nation. The company is the world’s leading supplier of solid rocket motors, a leading provider of launch vehicles, satellites and other space systems, and the nation’s largest manufacturer of ammunition.
Role can be filled at one level lower 12S with a Bachelor’s degree in Manufacturing Engineering or related technical arena and 2 years of experience. If you are a dynamic, successful, driven professional, Orbital ATK is the company that will further your experience and career growth. We offer a highly competitive salary, comprehensive benefits including, medical, dental, 401k, tuition reimbursement, and much more. Orbital ATK Flight Systems Group provides products and services that span the launch, missile systems and aerospace markets.
We are a premier producer of solid rocket propulsion systems and specialty energetic products; a leading provider of small and medium class space launch vehicles for Civil, Do D and Commercial missions; a major supplier of interceptor boosters and target vehicles for missile defense; and a world class manufacturer of composite primary and secondary structures for commercial and military aircraft and launch vehicles. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, national origin, disability status, protected veteran status, or any other characteristic protected by law.
Equal Opportunity Employer M/F/V/D Are you a Veteran? Visit our Jobs for Veterans page to find jobs that match your military background.
