Location: Salt Lake City, UT
Company: Betterbutter
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
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
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
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
Quality Assurance (QA) jobs involve ensuring that products or services meet specific standards and satisfy customer expectations. Professionals in this field focus on systematic processes and preventative measures during production or development to prevent mistakes and defects. QA roles typically require keen attention to detail, problem-solving skills, and knowledge of industry standards. They may encompass various tasks, such as developing quality assurance plans, conducting tests, and analyzing data to improve quality and reliability. QA jobs contribute significantly to a company's reputation by guaranteeing product consistency and safety.
