**Requisition Number:** 68954 **Employment Type:** University Staff **Schedule:** Full Time Student Health and Wellbeing at CU Boulder encourages applications for a Healthcare Quality and Safety Program Manager! This role provides a critical leadership role within CU Boulder's Health and Well-being (HWB) team, managing the development and implementation of comprehensive quality and safety programs across the continuum of care and services. This position ensures the development, implementation, and evaluation of quality-related policies, practices, and programs and is accountable for the management of these programs, including reporting of quality and patient safety metrics, reporting of clinical and outcome data, regulatory and accreditation compliance, and education and training on standard processes. This position is responsible for integrating quality improvement into all aspects of Health & Well-being by incorporating peer review, improvement methodology, infection prevention and safety, and risk management. CU is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing nondiscrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply, including protected veterans and individuals with disabilities.
**Who We Are**
Medical Operations & Compliance staff in Student Health and Wellbeing understand and are committed to the unique health concerns of our student population, making us an unparalleled source of advocacy for student wellness at CU Boulder! The Wardenburg Medical Clinic provides a wide range of health care services for students including: primary care for illnesses and injuries, as well as chronic conditions, physicals, sexually transmitted infection testing and treatment, allergy shots, vaccinations, travel health care, and concussion care.
**What Your Key Responsibilities Will Be**
Quality and Safety Program Design & Implementation
+ Ensure implementation, maintenance and evaluation of efficient, integrated, department-wide quality improvement, regulatory readiness, and patient safety programs, engaging collaborators to improve organizational performance using evidence-based practice based on available data.
+ Be a resource for leadership, medical, and other HWB staff for improving performance related to quality, safety, processes, and operations. Provide leadership and reporting for design, implementation, and maintenance of improvement systems enabling HWB to meet AAAHC accreditation standards and improve clinical and operational outcomes.
+ Coordinate and monitor efforts of various departments related to safety and quality. Develop and maintain corresponding dashboards for ongoing quality and healthcare safety monitoring.
+ Lead 3-5 active improvement activities including design, team member identification and communication, data collection, analysis, reporting, system testing, and follow-up related to quality improvement, assurance, and healthcare safety. Collaborate as an improvement coach and liaison for other Unit-led improvement activities. Lead Quality Improvement Committee meetings, including HWB leadership and partners. Prepare and disseminate reports regarding improvement findings including reports required for accreditation and annual program summary reports for the HWB Governing Body.
+ Review and use information from external and internal benchmarking programs. Participate in developing performance metrics internally and as requested by external agencies. Develop and maintain mechanisms for communication of quality and patient safety related information.
+ Report to the Governing Body on key quality indicators, including patient and staff safety, clinical excellence, customer satisfaction, regulatory readiness, etc.
+ Review safety incident reports and participate in/facilitate root cause analysis as needed.
+ Develop, supervise and facilitate Quality Improvement education and trainings for staff regarding QI concepts and methodologies, and ongoing programs. Embed a spirit of continuous improvement in all levels of HWB.
Scholarly Dissemination & Professional Engagement
+ Prepare abstracts, posters, and oral presentations to highlight program initiatives and outcomes at local, regional, and national conferences.
+ Assist with drafting and submitting manuscripts for peer-reviewed journals relating to quality improvement and healthcare delivery.
+ Collaborate with interdisciplinary team members and collaborators to co-author scholarly products.
+ Maintain awareness of emerging literature and standard processes in quality improvement and patient safety, incorporating relevant findings into program dissemination.
+ Support the development of educational materials, case studies, and reports to share program outcomes.
**What You Should Know**
+ This is a hybrid position, with 3-4 days a week required to be in person. The role has an anticipated work schedule of Monday - Friday during regular business hours, and is not expected to work University recognized holidays, weekends, or evenings, and will not be on call at any time.
+ The position has regular interaction throughout clinical and administrative areas.
**What We Can Offer**
The salary range for this role is $70,900 - $88,600 annually.
**Benefits**
At the University of Colorado Boulder (************************** , we are committed to supporting the holistic health and well-being of our employees. Our comprehensive benefits package (*************************************** includes medical, dental, and retirement plans; generous paid time off; tuition assistance for you and your dependents; and an ECO Pass for local transit. As one of Boulder County's largest employers, CU Boulder offers an inspiring academic community and access to world-class outdoor recreation. Explore additional perks and programs through the CU Advantage (******************************************* program.
**Be Statements**
Be collaborative. Be strategic. Be Boulder.
**What We Require**
+ Bachelor's degree.
+ 5 years relevant experience in the Quality Improvement/Quality Assurance or healthcare field.
+ Project management experience (leading cross-functional teams, managing timelines/results).
+ Experience using data analysis and visualization tools (Tableau, Power BI, Excel, etc.).
**What You Will Need**
+ Excellent interpersonal communication and facilitation skills (able to engage clinical staff, leadership, and committees).
+ Understanding of patient safety and quality frameworks (IHI Model for Improvement, Baldrige, Donabedian model).
+ Able to work with sensitive patient data in compliance with HIPAA and/or FERPA.
+ Ability to take responsibility for actions and contributions; demonstrate honesty and integrity; address issues promptly; commit to organizational success and cultivate commitment in others.
+ Adaptability: Maintain effectiveness during significant changes; remain flexible with evolving structures, processes, and cultures.
+ Leverage data (EHR and other sources) to enhance outcomes and workflows; apply knowledge of HWB functions, AAAHC standards, and relevant laws/regulations (HIPAA, FERPA) to guide program and policy improvement.
+ Ability to work across teams to achieve shared goals; treat others with respect; value contributions; and communicate effectively with diverse audiences (clinical, lay, executive).
+ Prioritize and manage time, resources, and budgets effectively; develop and implement project timelines; evaluate and adjust approaches as needed.
+ Able to build respectful, positive relationships and support colleagues in achieving goals and completing work.
**Special Instructions**
To apply, please submit the following materials:
1. A current resume.
2. A cover letter that specifically tells us how your background and experience align with the requirements, qualifications, and responsibilities of the position.
We may request references at a later time.
Please apply by **January 5, 2026** for consideration.
Note: Application materials will not be accepted via email. For consideration, please apply through CU Boulder Jobs (************************* .
In compliance with the Colorado Job Application Fairness Act, in any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.
**To apply, visit ******************************************************************************************** (******************************
Copyright 2025 Jobelephant.com Inc. All rights reserved.
Posted by the FREE value-added recruitment advertising agency (*****************************
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The University of Colorado does not discriminate on the basis of race, color, national origin, sex, age, pregnancy, disability, creed, religion, sexual orientation, gender identity, gender expression, veteran status, political affiliation, or political philosophy. All qualified individuals are encouraged to apply.
$70.9k-88.6k yearly 16d ago
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Quality Manager
Swinerton 4.7
Quality engineer job in Arvada, CO
Compensation Range:
$85,000.00 - $115,000.00 Annual Salary Take lead in implementing quality control processes, program(s), and activities on assigned project(s). Collaborate with teams to resolve quality issues and ensure project quality plans adhere to company standards, industry regulations, and customer requirements.
Job Description:
Position Responsibilities and Duties:
Able to perform essential Assistant Quality Manager responsibilities.
Serve as general Quality resource to project and operations teams to ensure high quality project delivery and customer satisfaction. Serve as subject matter expert on complex projects and quality matters.
Support with mentoring, coaching, and developing Quality team members.
Ensure company quality control program(s), processes, and procedures are implemented effectively.
Review and approve project specific quality control plans for trade partners/subcontractors; ensure compliance with company, client, and industry requirements.
Evaluate quality management plans for compliance with owner contracts and company requirements, monitor implementation and team accountability.
Partner with project teams to identify high risk definable features of work scopes and oversee implementation.
Review submittal documents to ensure compliance with contract documents.
Partner with project team to prepare for and document pre-installation meetings, first-work inspections, and material verifications.
Perform inspections and witness tests applicable to discipline to determine acceptance of work.
Conduct internal/external quality control assessments and coach teams on quality best practices.
Conduct root cause analysis of quality issues, defects, or non-conformance, and partner with project teams to develop and implement corrective and preventive actions plans.
Assist and document commissioning processes; escalate quality concerns.
Oversee quality document management including inspection records, performance records, and findings to create reports for leadership and regulatory agencies.
Track key quality metrics and key performance indicators (KPIs) to measure and report on quality performance.
Facilitate Quality Control trainings and educate teams on quality tools, best practices, and procedures.
Attend necessary meetings, share lessons learned, quality updates, and case studies.
Participate in conferences and industry-related events to remain up to date with industry regulations and standards. Ensure construction operations adhere to all relevant quality guidelines.
Identify and document safety issues and concerns, stop work and elevate as needed.
Complete other responsibilities as assigned.
Minimum Requirements or Experience Requirements:
Technical degree or certification in relevant field a plus.
Minimum of 4-6 years' experience in quality control inspection, construction, operations, or relevant field; or equivalent combination of education/training and experience.
Experience with managing and/or supervising others.
Require NAVFAC/USACE Contractor Quality Control (CQC) certification, or equivalent; able to obtain within one year.
Obtain ICC certifications in Building and/or Trade specific inspection within (1 per year)
Enhanced knowledge and experience with quality control inspection standards, procedures, and codes.
Enhanced knowledge and extensive experience with developing and implementing effective quality management plans onsite.
Understanding and knowledge of commercial construction means and methods.
Able to determine acceptance or rejection of work based on assigned criteria. Can educate teams on best practices.
Understands specifications and can differentiate between product requirements, submittal criteria, and execution of work identified in each individual specification section.
Experience with BIM 360 (and/or other similar software) utilized for quality document management.
Attention to detail and a commitment to maintaining high-quality standards.
Strong and effective English written and verbal communication skills.
Critical thinking ability with strong analytical skills; able to assess and mitigate risk.
Relationship driven individual with effective problem-solving and conflict resolutions skills.
Able to partner with teams and trade partners to deliver high quality on project delivery and ensure customer satisfaction.
Summary of Benefits:
This role is eligible for the following benefits: medical, dental, vision, 401(k) with company matching, Employee Stock Ownership Program (ESOP), individual stock ownership, paid vacation, paid sick leave, paid holidays, bereavement leave, employee assistance program, pre-tax flexible spending accounts, basic term life insurance and AD&D, business travel accident insurance, short and long term disability, financial wellness coaching, educational assistance, Care.com membership, ClassPass fitness membership, and DashPass delivery membership. Voluntary benefits include additional term life insurance, long term care insurance, critical illness and accidental injury insurance, pet insurance, legal plan, identity theft protection, and other voluntary benefit options.
Anticipated Job Application Deadline:
01/05/2026
$85k-115k yearly Auto-Apply 30d ago
Quality of Life Program Manager- Hemophilia- Paragon Healthcare
Carebridge 3.8
Quality engineer job in Denver, CO
Be Part of an Extraordinary Team A proud member of the Elevance Health family of companies, Paragon Healthcare brings over 20 years in providing life-saving and life-giving infusible and injectable drug therapies through our specialty pharmacies, our infusion centers, and the home setting.
Title: Quality of Life Program Manager- Paragon
Ideal candidates will be comfortable traveling 60-70% of the time to local Hemophilia chapters across the U.S.
The ability to attend Programs scheduled on nights and weekends will be required.
Field: This field-based role enables associates to primarily operate in the field, traveling to client sites or designated locations as their role requires, with occasional office attendance for meetings or training. This approach ensures flexibility, responsiveness to client needs, and direct, hands-on engagement.
Please note that per our policy on hybrid/virtual work, candidates not within a reasonable commuting distance from the posting location(s) will not be considered for employment, unless an accommodation is granted as required by law.
Build the Possibilities. Make an Extraordinary Impact.
The Quality of Life Program Manager- Paragon is responsible for developing and implementing innovative ""Quality of Life"" (QOL) programs for individuals with bleeding disorders to drive health outcomes and improve therapy adherence.
How you will make an impact:
Primary duties may include, but are not limited to:
* Collaborate with territory representatives to leading the increased business generation and customer retention.
* Develops and maintain business relationships with local chapters, clinics, and healthcare providers to enhance the business unit presence and impact in respective territories.
* Utilize lifestyle tools and resources within the QOL program to empower patients in managing their health, thus fostering a sense of control over their condition.
* Strategically integrate QOL initiatives into sales efforts to shorten the sales cycle and promote seamless health management solutions for patients.
* Leverage the QOL program as a significant referral source, contributing to business growth while maintaining cost-effectiveness compared to traditional event sponsorships.
* Monitor and evaluate the effectiveness of QOL programs regularly, making data-driven adjustments to ensure optimal patient engagement and satisfaction.
* Collaborate with cross-functional teams to align QOL initiatives with overall company objectives and marketing strategies.
Minimum Requirements:
* Requires a BA/BS degree and a minimum of 10 years of related experience in Specialty Pharmacy; and experience in marketing software (Aperture and Photoshop); or any combination of education and experience which would provide an equivalent background.
* Joint Health, Health and Nutrition and CPR certification are required.
Preferred Skills, Capabilities and Experiences:
* Prior experience as a professional Public Speaker is strongly preferred.
For candidates working in person or virtually in the below location(s), the salary* range for this specific position is $71,544 to $112,194
Locations: Colorado, Washington State
In addition to your salary, Elevance Health offers benefits such as, a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements). The salary offered for this specific position is based on a number of legitimate, non-discriminatory factors set by the Company. The Company is fully committed to ensuring equal pay opportunities for equal work regardless of gender, race, or any other category protected by federal, state, and local pay equity laws.
* The salary range is the range Elevance Health in good faith believes is the range of possible compensation for this role at the time of this posting. This range may be modified in the future and actual compensation may vary from posting based on geographic location, work experience, education and/or skill level. Even within the range, the actual compensation will vary depending on the above factors as well as market/business considerations. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law
Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health.
Who We Are
Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve.
How We Work
At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business.
We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few.
Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process.
The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws.
Elevance Health is an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance.
Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.
$71.5k-112.2k yearly Auto-Apply 60d+ ago
Quality of Life Program Manager- Hemophilia- Paragon Healthcare
Elevance Health
Quality engineer job in Denver, CO
Title: Quality of Life Program Manager- Paragon Ideal candidates will be comfortable traveling 60-70% of the time to local Hemophilia chapters across the U.S. The ability to attend Programs scheduled on nights and weekends will be required. Field: This field-based role enables associates to primarily operate in the field, traveling to client sites or designated locations as their role requires, with occasional office attendance for meetings or training. This approach ensures flexibility, responsiveness to client needs, and direct, hands-on engagement.
Please note that per our policy on hybrid/virtual work, candidates not within a reasonable commuting distance from the posting location(s) will not be considered for employment, unless an accommodation is granted as required by law.
Be Part of an Extraordinary Team
A proud member of the Elevance Health family of companies, Paragon Healthcare brings over 20 years in providing life-saving and life-giving infusible and injectable drug therapies through our specialty pharmacies, our infusion centers, and the home setting.
Build the Possibilities. Make an Extraordinary Impact.
The Quality of Life Program Manager- Paragon is responsible for developing and implementing innovative ""Quality of Life"" (QOL) programs for individuals with bleeding disorders to drive health outcomes and improve therapy adherence.
How you will make an impact:
Primary duties may include, but are not limited to:
* Collaborate with territory representatives to leading the increased business generation and customer retention.
* Develops and maintain business relationships with local chapters, clinics, and healthcare providers to enhance the business unit presence and impact in respective territories.
* Utilize lifestyle tools and resources within the QOL program to empower patients in managing their health, thus fostering a sense of control over their condition.
* Strategically integrate QOL initiatives into sales efforts to shorten the sales cycle and promote seamless health management solutions for patients.
* Leverage the QOL program as a significant referral source, contributing to business growth while maintaining cost-effectiveness compared to traditional event sponsorships.
* Monitor and evaluate the effectiveness of QOL programs regularly, making data-driven adjustments to ensure optimal patient engagement and satisfaction.
* Collaborate with cross-functional teams to align QOL initiatives with overall company objectives and marketing strategies.
* Travels to worksite and other locations as necessary.
Minimum Requirements:
* Requires a BA/BS and a minimum of 5 years of healthcare; or any combination of education and experience which would provide an equivalent background.
Preferred Skills, Capabilities and Experiences:
* Prior experience as a professional Public Speaker is strongly preferred.
For candidates working in person or virtually in the below location(s), the salary* range for this specific position is $71,544 to $112,194
Locations: Colorado, Washington State
In addition to your salary, Elevance Health offers benefits such as, a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements). The salary offered for this specific position is based on a number of legitimate, non-discriminatory factors set by the Company. The Company is fully committed to ensuring equal pay opportunities for equal work regardless of gender, race, or any other category protected by federal, state, and local pay equity laws.
* The salary range is the range Elevance Health in good faith believes is the range of possible compensation for this role at the time of this posting. This range may be modified in the future and actual compensation may vary from posting based on geographic location, work experience, education and/or skill level. Even within the range, the actual compensation will vary depending on the above factors as well as market/business considerations. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law
Job Level:
Non-Management Exempt
Workshift:
Job Family:
SLS > Sales Operations
Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health.
Who We Are
Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve.
How We Work
At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business.
We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few.
Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process.
The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws.
Elevance Health is an Equal Employment Opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.
$71.5k-112.2k yearly 2d ago
Quality Technician - Night shift
Aurora Dairy Corp 4.7
Quality engineer job in Platteville, CO
Join our dynamic Quality Assurance team at our Organic Dairy Processing facility in Platteville, CO. Be a part of a 2025 Top Workplace USA!
Purpose:
The Quality Assurance Lab Technician is responsible for in-process and finished product quality testing, maintaining accurate and complete records, and alerting management to any potential quality issues.
S hift
Nights
6pm - 6am
Thurs - Sat and alternating Wednesdays
Essential Responsibilities:
All plant personnel have the responsibility to monitor and report any deviations from our Food Safety and Food Quality (HACCP & SQF) programs to your immediate supervisor.
Assist in all in-bound and finished product milk processing including but not limited to: Customer Service, working with our Laboratory and Product Information Management System, Tanker/Silo Inventory Control, administrative assistant duties.
Competency in Microsoft Windows and Office products.
Responsible for performing process control testing in a manufacturing environment.
Maintain accurate and complete laboratory testing result records.
Maintain Good Manufacturing Practices, Good Laboratory Practices and Safety Procedures.
Communicate any potential quality issues to QA Management.
Professional communication and customer service skills in working with multiple departments and external partners.
Other Required Responsibilities:
Laboratory testing result data entry.
Member of HACCP team.
Other quality department responsibilities as deemed necessary.
Knowledge & Experience:
High School Diploma or equivalent.
Bachelor's degree in Dairy Manufacturing, Food Science, Microbiology, or related field preferred.
Experience in dairy laboratory testing procedures preferred.
Knowledge of laboratory testing methods.
Detail oriented and team member.
Strong, honest work ethic with ability to handle multiple tasks daily.
Good communication skills.
Physical Requirements:
Must be able to sit for extended periods of time; Must be able to stand or walk for more than 50% of the shift. Must be able to bend, stoop, kneel or crawl; reach grasp and lift, push, pull up to 50 lbs. regularly and up to 80 lbs. occasionally.
$45k-64k yearly est. Auto-Apply 12d ago
Drinking Water Process Engineer
Kennedy/Jenks Consultants 4.1
Quality engineer job in Denver, CO
Kennedy Jenks is seeking a Drinking Water Process Engineer to provide technical expertise and support for drinking water treatment projects. The ideal candidate will have experience in drinking water treatment technologies and regulations, with a strong interest in continuing to develop their skills in water treatment. This role offers opportunities to work alongside experienced engineers and support clients on a variety of water quality and treatment projects.
Key Responsibilities:
Provide technical support for drinking water treatment projects, including treatment process evaluation, process selection, and operations optimization.
Assist in preliminary engineering studies and feasibility assessments for municipal drinking water treatment systems.
Support project teams with design and technical contributions, including developing process flow diagrams and design criteria for water treatment facilities.
Collaborate with client service managers by contributing technical insights during project meetings and presentations.
Participate in research and process improvements related to water quality and treatment technologies.
Provide input on water treatment facility performance evaluations and assist in operations optimization.
Stay engaged in water-focused professional organizations and present technical material at conferences.
Qualifications:
Bachelor's or Master's degree in civil / environmental engineering, or related scientific discipline required.
7+ years of experience in drinking water treatment engineering
Practical professional engineer (PE) license or ability to obtain licensure within one year of hire. License in one or multiple states (CA, CO, FL, HI, OR, TX, VA, WA) preferred.
Strong familiarity with drinking water treatment regulations and technologies.
Ability to work as part of a project team, supporting senior staff and contributing to technical deliverables.
Strong communication skills and ability to convey technical information clearly to colleagues and clients.
Kennedy Jenks supports a healthy work-life balance and utilizes a hybrid model of home and office work, with a minimum of two days per week in the office. This approach empowers our people to thrive, collaborate, and achieve their full potential.
The salary range for this position is anticipated to be $110,000 to $140,000, and may vary based upon education, experience, qualifications, licensure/certifications and geographic location.
This position is eligible for performance and incentive compensation.
#LI-Hybrid
$110k-140k yearly 42d ago
Process Engineer
Agilent Technologies 4.8
Quality engineer job in Boulder, CO
"What's it like to work at Agilent in Manufacturing? Watch the video"
Agilent inspires and supports discoveries that advance the quality of life. We provide life science, diagnostic and applied market laboratories worldwide with instruments, services, consumables, applications and expertise. Agilent enables customers to gain the answers and insights they seek -- so they can do what they do best: improve the world around us. Information about Agilent is available at ****************
Want to take your knowledge and experience further? Ready to provide technical leadership and make key decisions? This is your opportunity - not only to join a committed, professional, and forward-thinking team but also to lead in the design and implementation of complex manufacturing processes and transform broad concepts into structured results-focused projects.
Join a growing team with this exciting new opportunity for an Process Engineer at our Boulder, Colorado GMP facility. Work in our dynamic, fast-paced, API-Biopharma manufacturing environment with the ability to contribute to the growing industry of oligonucleotide (DNA-RNA) based therapeutics.
Responsibilities may include but are not limited to:
Provide project/process engineering support of a GMP manufacturing process (Upstream, Midstream, Downstream, Utilities).
Responsible for any area of focus with the existing manufacturing process. Area of focus will also be supported during projects.
Supporting small to large sized capital projects throughout all phases of the project lifecycle, including the development of user requirement specifications, process design integration, equipment and instrumentation specification/selection, equipment procurement, installation, commissioning, qualification, and turn-over to manufacturing.
Participate with project management through coordination of multi-disciplinary teams.
Collaborate with Chemical Development and Manufacturing Services groups with activities such as technical transfer and scale-up of processes into manufacturing.
Collaborate and facilitate project EHS activities including Process Hazard Analysis, Safety Checklist, and PSM compliance to meet OSHA standards.
Ensure for all projects a high level of cGMP compliance to meet the ICH requirements for pharmaceutical buildouts.
Support Validation activities including review of Factory Acceptance Test and Site Acceptance Test (FAT/SAT) protocols and participating in FAT/SAT execution, review of installation, operational, and performance qualification (IQ/OQ/PQ) protocols, participating in IOPQ execution, and review of final reports.
Support regulatory activities including writing, review, and/or resolution of Change Controls (CC/CSC), Corrective and Preventive Actions (CAPAs), and audit responses.
Integrate with Manufacturing and Quality Assurance groups with day-to-day troubleshooting and maintenance activities for projects/process, through identification of process improvement and optimization opportunities, including review of SOPs and MBRs.
Perform job functions and responsibilities independently and with limited direction.
Leads the development, design of new product/ process technology advancements; is the key technical contributor.
Solves complex, high impact design/ development problems.
Qualifications
Bachelor's or Master's Degree in Mechanical, Electrical, or Chemical Engineering or equivalent education/experience.
4+ years of combined experience in pharma/biopharma and fine chemicals industry to include 3+ years of experience with process and instrumentation diagrams, facility layouts, equipment sizing calculations, user requirement specifications (URSs), standard operating procedures (SOPs) and process troubleshooting.
Preferred Skills:
2+ years of experience supporting small to large-sized projects through all phases, including architectural and engineering design, design review, process safety management, process hazard analysis, equipment procurement, installation, commissioning, and qualification, is desirable.
Self-motivated, hands-on problem solver with the ability to work within multi-disciplinary teams, including process development, manufacturing, validation, quality, safety, and project management personnel.
Familiarity with current ASME BPE sanitary piping and equipment design standards, electrical standards such as National Fire Protection Association / National Electrical Code (NFPA 70 / NEC) and International Fire and Building Codes.
Project Management experience in biopharma.
Experience with design and programming of industrial control systems, including SCADA, PLCs, and BAS and validation documentation, including installation, operational and performance qualification (IQ/OQ/PQ) protocols.
Engineering, communication, and organizational skills to support the safe, efficient, and compliant production of API within a fast-paced, dynamic, contract manufacturing facility.
#LI-DT1
Additional Details
This job has a full time weekly schedule. Applications for this job will be accepted until at least November 10, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $103,200.00 - $161,250.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: 10% of the TimeShift: DayDuration: No End DateJob Function: Manufacturing
$103.2k-161.3k yearly Auto-Apply 60d+ ago
Lead Supplier Quality Engineer - Non-Destructive Testing
GE Aerospace 4.8
Quality engineer job in Denver, CO
Our Supplier Quality Engineer (SQE) for Non-Destructive Evaluation (NDE) & Testing Processes, will apply their demonstrated knowledge of NDE to lead improvement and sustain quality practices within our Composites supply chain.
SQE Deliverables Include:
- Support supplier process quality strategy for GE Aerospace.
- Drive quality for assigned suppliers, including quality plan implementation.
- Lead suppliers through root cause and corrective actions to address any quality findings.
- Select suppliers through qualification processes.
- Own supplier quality system requirements, drive improvements utilizing supplier scorecards.
- Own supplier audits, ensuring compliance, and driving improvement plans where needed.
- Mentor team members within the Composites supplier quality team.
- Demonstrate an in-depth understanding of key business drivers; uses this understanding to accomplish own work.
- Demonstrate an in-depth understanding of how work within our own team integrates with other teams and contributes to the area.
**Job Description**
**Roles and Responsibilities**
+ Role is responsible for supplier processes, from initial qualification, maintenance, and necessary improvement driven by business quality needs.
+ Position includes regular supplier audits, in conjunction with our GE Aerospace process experts and system assessments for quality preparedness and process controls to remain adherent to GE Aerospace process specifications and agency regulations.
+ Requires specialized knowledge within the field of NDE, including but not limited to: CT Scanning & Ultrasonic evaluation processes. Influence the development of strategy for the area of responsibility, including control of resources and influences policy formulation.
+ Interprets simple internal and external business challenges and recommends best practices to improve products, processes, or services. Stays informed of industry trends that may inform work. Coordinating with the GE Aerospace Inspection Solutions (AIS) experts and operations teams and their approved supplier technical plans, to ensure product meets the approved process requirements and specifications.
+ Uses high level of judgment to make decisions and handle complex tasks or problems in areas of operational, product management, manufacturing, technology, or engineering. Has ability to assess quality of information given and ask pertinent questions to stakeholders. Able to offer new solutions to problems outside of set parameters and can construct and provide recommendations. Uses multiple internal and some external sources outside of own function to help arrive at a decision.
+ May lead functional teams or projects with minimal resource requirements, risk, and/or complexity. Communicates difficult concepts and may influence others' options on specific topics. May guide others to consider a different point of view.
**Required Qualifications**
+ Bachelor's Degree from an accredited college or university (or a high school diploma/GED with a minimum of 4 years (Materials Science, Physics, Chemistry, Mathematics, or Engineering) experience + minimum of 3 years (Materials Science, Engineering, or Quality) related roles experience
**Desired Characteristics**
+ demonstrating proficiency of their time within Non-Destructive Evaluation operations, team leadership, and aerospace supply chain familiarity.
+ Demonstrated expertise and experience with Non-Destructive Evaluation and Testing
+ Proficiency in reading and applying engineering drawings and specifications.
+ Demonstrated organizational leadership in quality systems foundations and adherence, via industry requirements and audit experience.
+ Demonstrated experience in manufacturing or supplier quality, statistical analysis
+ Certified or willingness to achieve a Level 2 NAS410 qualification for certification in CT, and UT
+ Strong oral and written communication skills. Demonstrated ability to analyze and resolve problems. Ability to document, plan, market, and execute programs. Established project management skills.
+ Demonstrated history of problem solving, root cause and corrective action methodology, data analysis and quality experience
+ Humble: respectful, receptive, agile, eager to learn
+ Transparent: shares critical information, speaks with candor, contributes constructively
+ Focused: quick learner, strategically prioritizes work, committed
+ Leadership ability: strong communicator, decision-maker, collaborative
+ Problem solver: analytical-minded, challenges existing processes, critical thinker
The base pay range for this position is 110-130k. The specific pay offered may be influenced by a variety of factors, including the candidate's experience, education, and skill set. This position is also eligible for an annual discretionary bonus based on a percentage of your base salary/ commission based on the plan. This posting is expected to close on [include anticipated date expected to close December 1. 2025.
GE Aerospace offers comprehensive benefits and programs to support your health and, along with programs like HealthAhead, your physical, emotional, financial and social wellbeing. Healthcare benefits include medical, dental, vision, and prescription drug coverage; access to a Health Coach from GE Aerospace; and the Employee Assistance Program, which provides 24/7 confidential assessment, counseling and referral services. Retirement benefits include the GE Aerospace Retirement Savings Plan, a 401(k) savings plan with company matching contributions and company retirement contributions, as well as access to Fidelity resources and planning consultants. Other benefits include tuition assistance, adoption assistance, paid parental leave, disability insurance, life insurance, and paid time-off for vacation or illness.
GE Aerospace (General Electric Company or the Company) and its affiliates each sponsor certain employee benefit plans or programs (i.e., is a "Sponsor"). Each Sponsor reserves the right to terminate, amend, suspend, replace or modify its benefit plans and programs at any time and for any reason, in its sole discretion. No individual has a vested right to any benefit under a Sponsor's welfare benefit plan or program. This document does not create a contract of employment with any individual.
_This role requires access to U.S. export-controlled information. Therefore, employment will be contingent upon the ability to prove that you meet the status of a U.S. Person as one of the following: U.S. lawful permanent resident, U.S. Citizen, have been granted asylee or refugee status (i.e., a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3))._
**Additional Information**
GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer (****************************************************************************************** . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).
**Relocation Assistance Provided:** No
\#LI-Remote - This is a remote position
GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
$79k-101k yearly est. 60d+ ago
Quality Technician
Cornerstone Building Brands
Quality engineer job in Denver, CO
JOB DETAILS Base Pay: $24 per hour Benefits Start Day 1 80 Hours Paid Time Off On Demand Pay - easy access to your pay when you need it DUTIES AND RESPONSIBILITIES We are currently seeking a Quality Technician to help us ensure that non-conforming products do not continue through the production process and are not distributed to customers. In this role, you will conduct routine quality inspections of raw materials and finished goods throughout production, including in-process and final inspections. During these inspections, Quick Problem-Solving, and Root Cause Analysis methods will be performed to support the manufacturing process and ensure delivery of quality material.
Drive quality at the source by providing work areas with the quality at the source necessities
Outline critical to quality process steps and understand capabilities, controls, and necessary equipment and tools to adequately perform job functions
Create work instructions and visual aids to support lines
Embody a no defect forward culture
Supports supervisor and operations with line calls
Maintain quality at the source through general quality controls and inspections
Audit the quality of in-coming materials, work in progress materials, and finished product in accordance with standards
Perform all required ASTM quality control testing on aggregate and concrete products including, but not limited to, field-testing (slump, air content, unit weight, yield, cylinders, etc.), gradations on production aggregates, and lab work (compression testing and scheduling)
Ensure test equipment is calibrated and working correctly and lab area is organized
Maintain accurate and up-to-date documentation of testing completed with results
Report quality nonconformances to the supervisor immediately
Participate with internal and external team members, vendors, and Regional Quality Manager in resolving quality problems by investigating complaints, collecting necessary data, and solving complaint utilizing established Cornerstone Building Brands Quality Problem-Solving methodology
Analyze and interpret technical information and effectively present information to sales, project managers, operations, and other employees within the organization
Support existing product specifications and new product request by documenting customer expectations and trialed product through detailed process steps, mix designs, and recipes
Qualifications
English/Spanish Bilingual
High school diploma or GED, Associate's degree preferred
Experience as an Inspection or quality technician
Experience in manufacturing environments that are fast-paced
The employee must occasionally lift and/or move anywhere up to 75 lbs
Skills & Competencies
Working computer knowledge; including applicable Microsoft software
Understanding of mathematical concepts such as ability to add, subtract, multiple and divide in all units of measure, using whole numbers, common fractions, and decimals
Working with a sense of urgency
Ability to work alone with minimal supervision
Teamwork - Contributes to building a positive team spirit
Judgment - Exhibits sound and accurate judgment
Planning/Organizing - Uses time efficiently and has advanced organizational skills
Professionalism - Approaches others in a tactful manner; Reacts well under pressure; Accepts responsibility for own actions
Safety and Security - Observes safety and security procedures; Determines appropriate action beyond guidelines; Reports potentially unsafe conditions; Uses equipment and materials properly
Adaptability - Adapts to changes in the work environment; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events
Attendance/Punctuality - Is consistently at work and on time
Dependability - Follows instructions, responds to management direction; Commits to long hours of work when necessary to reach goals
Initiative - Asks for and offers help when needed
Innovation - Generates suggestions for improving work
Other
The employee is frequently required to sit, climb, and use hands to signal and handle equipment
The employee is occasionally required to stand, walk, crawl, kneel, bend, and reach with hands and arms above their shoulders
Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision and depth perception
Additional Information
Site Address: 6300 E 44th Ave, Denver, CO 80216
Why work for Cornerstone Building Brands?
Our teams are at the heart of our purpose to positively contribute to the communities where we
live, work and play.
Full-time* team members receive** medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development. You can also join one of our Employee Resource Groups which help support our commitment to providing a diverse and inclusive work environment.
*Full-time is defined as regularly working 30+ hours per week. **Union programs may vary depending on the collective bargaining agreement
All your information will be kept confidential according to EEO guidelines.
The US pay for this full-time position is $23.81 per hour + medical, dental, vision benefits starting day 1 + 401k and PTO. (Full-time is defined as regularly working 30+ hours per week. Union programs may vary depending on the collective bargaining agreement.)
Why work for Cornerstone Building Brands?
Our teams are at the heart of our purpose to positively contribute to the communities where we
live, work and play
. Full-time* team members receive** medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development.
*Full-time is defined as regularly working 30+ hours per week. **Union programs may vary depending on the collective bargaining agreement.
Cornerstone Building Brands 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, pregnancy, genetic information, disability, or status as a protected veteran. You can find the Equal Employment Opportunity Poster
here
. You can also view Your Right to Work Poster
here
along with This Organizations Participation in E-Verify Poster
here
. If you'd like to view a copy of the company's affirmative action plan for protected veterans or individuals with disabilities or policy statement, please contact Human Resources at ************ or
[email protected]
. If you have a disability and you believe that you need a reasonable accommodation in order to search for a job opening or to submit an online application, please contact Human Resources at ************ or
[email protected]
. This email is used exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only emails received for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.
All your information will be kept confidential according to EEO guidelines.
California Consumer Privacy Act (CCPA) of 2018
Must be at least 18 years of age to apply.
Notice of Recruitment Fraud
We have been made aware of multiple scams whereby unauthorized individuals are using Cornerstone Building Brand's name and logo to solicit potential job-seekers for employment. In some cases, job-seekers are being contacted directly, both by phone and e-mail. In other instances, these unauthorized individuals are placing advertisements for fake positions with both legitimate websites and fabricated ones. These individuals are typically promising high-paying jobs with the requirement that the job-seeker send money to pay for things such as visa applications or processing fees. Please be advised that Cornerstone Building Brands will never ask potential job-seekers for any sort of advance payment or bank account information as part of the recruiting or hiring process.
$24 hourly 21h ago
Quality Technician
Belmar Pharma Solutions
Quality engineer job in Golden, CO
Role and Responsibilities
This position is responsible for working cross functionally to support Quality Assurance & Quality Control tasks, with focus on visual inspection of drug products. The Quality Technician will support Belmar Pharma Solutions in carrying out the mission of the company. This position reports to the Quality Manager.
Responsibilities include:
Primary responsibility to perform visual inspection of parenteral pharmaceutical products in accordance with regulatory guidelines
Create & review all labels (in-process and finished goods) and Batch Production Records for accuracy and adherence to Good Documentation Practices (GDPs)
Incoming materials receipt: inspect, document, unpack, label, shelve, and organize materials
Obtain samples of raw, in-process, and finished goods materials and send to third party labs for testing. Results to be entered into applicable spreadsheets.
Review Logs of Use and Maintenance (LUMs) for accuracy and GDP
Finished drug product batch release checks
Perform Quality checks on in-process product and facility controls as needed
Sterilization: Prepare, receive, and organize product for sterilization
Environmental Monitoring (EM): Collect routing EM samples. Enter, report and trend sample data.
Identify nonconformances and escalate to leadership
Attend all required meetings and provide clear, professional verbal and email communications.
Special projects as assigned by Management
Other duties as assigned
$33k-46k yearly est. 15d ago
Quality Technician: Inspection and Testing
Trisalus Life Sciences, Inc. 3.8
Quality engineer job in Westminster, CO
Duties and Responsibilities:
Work effectively with the Quality, Operations, and R&D departments to perform all work accurately, with a sense of urgency and a positive attitude. Activities include the following:
In-Process and Final Device Inspection and Test : Support Manufacturing as the QC inspector for clean-room & packaging inspection activities. Perform and document in-process and final inspection/test of devices and sub-assemblies. Provide inspection/test assistance to R&D, Operations and Quality Engineering in support of design and process verification/validation activities.
Receiving Inspection and Test : Perform and document receiving inspection/test of device components & raw materials in accordance with drawings/specifications. Maintain accurate & timely records of inspection activities and recording such activities in the QC Receiving Log.
Non-Conforming Materials : Identify, segregate and quarantine non-conforming materials resulting from inspection activities. Initiate NCRs and notify the workstream owner in a timely manner. Execute and record disposition activities in accordance with approved NCRs.
Microbiological Monitoring : Participates in periodic microbiological and particulate testing of the cleanroom and products as required.
Returned Goods Authorization : Perform timely inspections and maintain accurate records of all returned TriSalus products through the RGA process. Correctly dispositions returned product as defined in approved procedures.
Quality Record maintenance : Receive, verify, scan and physically file Quality Records in an organized manner as needed.
Shipping QC : Verify TriSalus products and associated paperwork are accurate and complete prior to shipment.
Audit Assistance : Help retrieve, review, organize and re-file documentation during all TriSalus site audit activities (internal, FDA, ISO registrar).
GP Dynamics : Transfer released materials in the ERP software for material management as needed.
Training Record support : Enter complete training/certification records into the eQMS as needed.
General : Perform other quality inspection, test or administration activities as assigned.
Qualifications
Education & Certifications:
High School diploma. Advanced education or certifications a plus.
Work Experience:
2+ years of Quality Control / Inspection experience in a medical device or similar technical product manufacturing company.
Experience working with sterile disposable products in a cleanroom environment a plus.
Knowledge, Skills & Abilities:
Able to read and interpret engineering drawings, specifications and detailed technical documents.
Able to read and follow quality procedures and detailed work instructions (QLPs/OPs).
Able to perform component and product inspection/testing using tools such as microscopes, calipers, micrometers, pin gauges, depth gauges, pull force test systems and vision measuring systems. (Sufficient knowledge to select and use the correct measurement tool for the required inspection accuracy.
Able to accurately document results of inspections using good documentation practices.
Able to understand and apply inspection sampling plans, such as C=0 or ANSI Z1.4.
Able to utilize basic math skills.
Able to use MS Word and MS Excel.
Must possess strong attention to detail.
Possess good communication skills and able to interact with peers in a professional manner.
Possess knowledge and application of US and international standards for quality management (FDA 21 CFR 820, ISO 13485).
Demonstrates excellent critical thinking skills.
Ability to adapt to and rapidly learn new processes.
Strong verbal and written communication skills and confidence in making inspection related decisions.
Participates as a member of cross functional technical teams to support process improvements, special projects and investigations as needed.
Approaches work tasks with a positive attitude and seeks feedback on performance to continually improve.
Physical Requirements:
Ability to safely and successfully perform the essential job functions consistent with the ADA, FMLA and other federal, state and local standards, including meeting qualitative and/or quantitative productivity standards.
Must be able to lift and carry up to 30 lbs.
Ability to maintain regular, punctual attendance consistent with the ADA, FMLA and other federal, state and local standards.
$30k-37k yearly est. Auto-Apply 26d ago
Quality Technician II
Trelleborg Sealing Solutions 4.6
Quality engineer job in Louisville, CO
The Quality Technician II is responsible for maintaining the Quality Management System by following the required procedures and ensuring customer requirements are identified and met.
Essential Duties & Responsibilities
Reads part drawings and assesses dimensions.
Supports inspection equipment operation within the production cell as required, including Coordinate Measurement Machine.
Initiates Management Review Board and performs actions as assigned.
Performs Final Inspection - Ensures required documentation from all inspections are complete and all functions of the manufacturing process have been verified as complete.
Ensures correct product identification and traceability of materials is maintained throughout the operations process.
Initiates Quality-related turnbacks and communicates with production.
Creates basic and intermediate certifications as required by the Work Order, including FAIRs.
Performs specialised inspection, including visual and dimensional checks.
Assists with Internal Auditing as required.
Assists with measurement tool calibration as required.
Creates basic CMM programs in the production cell to aid in inspection.
Participates in small projects or other tasks as required.
Education and Experience
This position requires a High School Diploma or GED equivalent. This position should have 2-3 years of experience in a quality role in a manufacturing environment. Experience with QMS compliance software (e.g., Qualtrax) and enterprise resource planning system (e.g., JD Edwards or SAP) is required.
Knowledge, Skills, and Abilities
Must have the ability to multitask in a fast-paced environment.
Excellent interpersonal skills and ability to effectively communicate with all levels of the organization both written and verbal in English.
Ability to work in a team environment.
Must have a high level of attention to detail and excellent problem-solving skills.
Must be proficient with Microsoft Office, specifically Excel and Outlook, and general computer skills.
High knowledge of materials and material requirements as they relate to customer orders.
High knowledge of purchase order requirements.
Ability to read blueprints and product drawings and interpret requirements as needed.
Must be able to operate various inspection tools such as dial calipers, micrometers, optical comparator, height gages, pin & plug gages, pi tape and microscopes.
Must have excellent math aptitude.
Work Environment/Physical Demands/Equipment Used
This position is located in a manufacturing facility which requires prolonged sitting, standing, walking, squatting, twisting, and bending. This position will spend about 90% of their time on the production floor where heavy machinery is present and loud sounds exist. Requires manual dexterity for typing and considerable time at a computer.
Health and Safety - PPE Requirements
Safety Glasses to be worn at all times when on the production floor
Safety Shoes to be worn at all times when on the production floor
Must wear appropriate PPE for all work activities performed; varies based work
$33k-41k yearly est. 60d+ ago
Engineer-Process Validation
Us Tech Solutions 4.4
Quality engineer job in Boulder, CO
US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ************************ We are constantly on the lookout for professionals to fulfill the staffing needs of our clients, sets the correct expectation and thus becomes an accelerator in the mutual growth of the individual and the organization as well.
Keeping the same intent in mind, we would like you to consider the job opening with US Tech Solutions that fits your expertise and skillset.
Job Description
Job Details:
The Process Validation Engineer will ensure consistent implementation of corporate and regulatory compliance of validation activities within a pharmaceutical manufacturing facility.
Primary functions of the role include
:
Oversees trial runs of a production or production- related process to substantiate the validity of the equipment/process and completion of all associated documentation.
Works with project engineers and other support groups to have an in-depth understanding of new and existing equipment capabilities.
Tests critical and key process parameters to assure reliability, quality and proper documentation to support the associated process and results.
Develops a working knowledge within assigned area of responsibility of equipment function, design, and utilization.
Presents updates, reports and presentations as necessary to the department, plant staff and regulatory agencies.
Provides a key role in assuring the integrity of the manufacturing process.
Qualifications
Requirements
:
BS/BA degree required in engineering or an engineering related field
Minimum of three years of experience, preferably in the pharmaceutical industry.
Proven ability to understand equipment design and functions to assure appropriate utilization and validation of the process.
Excellent multi-tasking skills and the ability to document details of the work performed are required.
Advanced computer skills
Additional Information
Regards,
Sneha Shrivastava
************
$73k-92k yearly est. 21h ago
Quality Technician
Kratos Industries
Quality engineer job in Arvada, CO
Full-time Description
ROLE AND RESPONSIBILITIES
• Inspect mechanical parts fabricated internally using industry standard inspection tools
• Inspect mechanical parts and components provided externally by suppliers at inspection stations.
• Inspect and monitor incoming raw materials/packaging and finished goods, including paint, for specification compliance
• Inspect electrical wire routing, torquing and continuity as required
• Conduct electrical testing of product as required
• Assist in troubleshooting non-compliant inspected parts and components
• Responsible for inspection related document control and records storage
• Document and record inspection results in electronic and hardcopy format
• Interpret mechanical drawing dimensional features and acceptable tolerances
• Maintain a “floor presence” as an “auditor of quality” throughout the manufacturing facility and process
• Regularly review work instructions, travelers, and production records for continuous compliance to manufacturing requirements
• Works closely with production managers and manufacturing personnel conducting quality assurance checks
• Participates in regular procedure training activities in production
• Provides support for quality related projects, objectives and deadlines beyond the normal job scope as required
• Makes key decisions concerning product quality on their own, including pausing the line when processes do not conform to specification
• Facilitates GEMBA Walks, Quality Stand-up meetings, and other public speaking activities as needed
• Compiles and distributes weekly quality metrics data at the direction of the Dir of Quality
QUALIFICATIONS AND EDUCATION REQUIREMENTS
• A minimum of 3 years' experience as a Quality Inspector in an ISO 9001 environment is required for this position
• A minimum of 3 years' electrical/electronic manufacturing experience is required
• ASQ CQT certification or current pursuit of certification is highly desired
• A 2-year technical or vocational certificate is highly desired
• Advanced working knowledge of ISO 9001:2015 is highly desired
• Knowledge of AQL acceptance sampling plans using ANSI Z1.4 is strongly desired
• Knowledge of 5S +1 principles highly desired
PREFERRED SKILLS
• Advanced hands-on experience using common inspection tools and instruments
• Highly proficiency in MS Office Suite (e.g., Excel)
• Highschool math skills required
• Experience inspecting SS and CRS weld joints is highly desirable
• Ability to manage multiple concurrent tasks is required
• Deliver results accurately and on time while utilizing a strong learning mindset
• Must be capable of working independently to achieve production schedules and quality goals
• Effective interpersonal skills involving the ability to work effectively, cross-functionally and cross-culturally
• Excellent communication skills adaptable to all levels of the organization
• Ability to communicate clearly in a proactive positive sense
BENEFITS
• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance
PERFORMANCE BONUS - Eligible
A written and / or practical skills assessment will be required of the successful applicant.
Salary Description $26.00 - $32.00
$33k-46k yearly est. 60d+ ago
Process Engineer(10 yrs project management)_ITIL preferred
360 It Professionals 3.6
Quality engineer job in Denver, CO
360 IT Professionals is a Software Development Company based in Fremont, California that offers complete technology services in Mobile development, Web development, Cloud computing and IT staffing. Merging Information Technology skills in all its services and operations, the company caters to its globally positioned clients by providing dynamic feasible IT solutions. 360 IT Professionals work along with its clients to deliver high-performance results, based exclusively on the one of a kind requirement.
Job Description
We are looking to fill a position for Sr. process Engineer with at least 10 yrs. of relevant experience in [Project Management Practices.
The key areas of focus and deliverables are:
Cradle-to-grave process artifacts for Application Lifecycle Management, Knowledge Management, Asset Management, Change Management, Problem Management, and Incident Management
Evaluation and gap analysis for Application Lifecycle Management, Knowledge Management, Asset Management, Change Management, Problem Management, and Incident Management effectiveness review and continuous improvement recommendations of the Off-boarding process available to supervisors in the Customer Service Portal
To accomplish this, the Senior Process Engineer will:
· Assess current in-scope processes and make additional recommendations for improvements related to efficiency
· Make heavy use of available materials in the above mentioned areas as fodder for process engineering activities
· Develop process maps
· Identify associated process goals, and metrics for measurement of each goal, to ensure that process performance can be measured and quantitatively managed
· Meet with any applicable stakeholders to capture data and information as necessary and with Chief Customer Officer approval
· Draft, or facilitate preparation of, process flows and instructional materials in coordination with Communications team
· Ensure process interface with dependent, or related, processes across the enterprise
· Apply industry process engineering best practices to legacy and new processes
Qualifications
Three or more years' experience with Process Engineering techniques and models
· Expert knowledge in designing and implementing processes and process assets and/or frameworks
· Successful completed the Intermediate Concepts of CMMI course
· Active Project Management Professional (PMP) An understanding of IT Service Management framework
· 10+ years' experience with Project Management practices
· ITIL certification a plus
· Knowledge of large-scale process methodologies and frameworks in State government environments is a plus
Additional Information
Webcam interview is acceptable.
$77k-98k yearly est. 60d+ ago
Drinking Water Process Engineer
Kennedy/Jenks Consultants 4.1
Quality engineer job in Lakewood, CO
Kennedy Jenks is seeking a Drinking Water Process Engineer to provide technical expertise and support for drinking water treatment projects. The ideal candidate will have experience in drinking water treatment technologies and regulations, with a strong interest in continuing to develop their skills in water treatment. This role offers opportunities to work alongside experienced engineers and support clients on a variety of water quality and treatment projects.
Key Responsibilities:
Provide technical support for drinking water treatment projects, including treatment process evaluation, process selection, and operations optimization.
Assist in preliminary engineering studies and feasibility assessments for municipal drinking water treatment systems.
Support project teams with design and technical contributions, including developing process flow diagrams and design criteria for water treatment facilities.
Collaborate with client service managers by contributing technical insights during project meetings and presentations.
Participate in research and process improvements related to water quality and treatment technologies.
Provide input on water treatment facility performance evaluations and assist in operations optimization.
Stay engaged in water-focused professional organizations and present technical material at conferences.
Qualifications:
Bachelor's or Master's degree in civil / environmental engineering, or related scientific discipline required.
7+ years of experience in drinking water treatment engineering
Practical professional engineer (PE) license or ability to obtain licensure within one year of hire. License in one or multiple states (CA, CO, FL, HI, OR, TX, VA, WA) preferred.
Strong familiarity with drinking water treatment regulations and technologies.
Ability to work as part of a project team, supporting senior staff and contributing to technical deliverables.
Strong communication skills and ability to convey technical information clearly to colleagues and clients.
Kennedy Jenks supports a healthy work-life balance and utilizes a hybrid model of home and office work, with a minimum of two days per week in the office. This approach empowers our people to thrive, collaborate, and achieve their full potential.
The salary range for this position is anticipated to be $110,000 to $140,000, and may vary based upon education, experience, qualifications, licensure/certifications and geographic location.
This position is eligible for performance and incentive compensation.
#LI-Hybrid
$110k-140k yearly 46d ago
Quality Technician
Cornerstone Building Brands
Quality engineer job in Denver, CO
JOB DETAILS Base Pay: $24 per hour Benefits Start Day 1 80 Hours Paid Time Off On Demand Pay - easy access to your pay when you need it DUTIES AND RESPONSIBILITIES We are currently seeking a Quality Technician to help us ensure that non-conforming products do not continue through the production process and are not distributed to customers. In this role, you will conduct routine quality inspections of raw materials and finished goods throughout production, including in-process and final inspections. During these inspections, Quick Problem-Solving, and Root Cause Analysis methods will be performed to support the manufacturing process and ensure delivery of quality material.
* Drive quality at the source by providing work areas with the quality at the source necessities
* Outline critical to quality process steps and understand capabilities, controls, and necessary equipment and tools to adequately perform job functions
* Create work instructions and visual aids to support lines
* Embody a no defect forward culture
* Supports supervisor and operations with line calls
* Maintain quality at the source through general quality controls and inspections
* Audit the quality of in-coming materials, work in progress materials, and finished product in accordance with standards
* Perform all required ASTM quality control testing on aggregate and concrete products including, but not limited to, field-testing (slump, air content, unit weight, yield, cylinders, etc.), gradations on production aggregates, and lab work (compression testing and scheduling)
* Ensure test equipment is calibrated and working correctly and lab area is organized
* Maintain accurate and up-to-date documentation of testing completed with results
* Report quality nonconformances to the supervisor immediately
* Participate with internal and external team members, vendors, and Regional Quality Manager in resolving quality problems by investigating complaints, collecting necessary data, and solving complaint utilizing established Cornerstone Building Brands Quality Problem-Solving methodology
* Analyze and interpret technical information and effectively present information to sales, project managers, operations, and other employees within the organization
* Support existing product specifications and new product request by documenting customer expectations and trialed product through detailed process steps, mix designs, and recipes
Qualifications
* English/Spanish Bilingual
* High school diploma or GED, Associate's degree preferred
* Experience as an Inspection or quality technician
* Experience in manufacturing environments that are fast-paced
* The employee must occasionally lift and/or move anywhere up to 75 lbs
Skills & Competencies
* Working computer knowledge; including applicable Microsoft software
* Understanding of mathematical concepts such as ability to add, subtract, multiple and divide in all units of measure, using whole numbers, common fractions, and decimals
* Working with a sense of urgency
* Ability to work alone with minimal supervision
* Teamwork - Contributes to building a positive team spirit
* Judgment - Exhibits sound and accurate judgment
* Planning/Organizing - Uses time efficiently and has advanced organizational skills
* Professionalism - Approaches others in a tactful manner; Reacts well under pressure; Accepts responsibility for own actions
* Safety and Security - Observes safety and security procedures; Determines appropriate action beyond guidelines; Reports potentially unsafe conditions; Uses equipment and materials properly
* Adaptability - Adapts to changes in the work environment; Changes approach or method to best fit the situation; Able to deal with frequent change, delays, or unexpected events
* Attendance/Punctuality - Is consistently at work and on time
* Dependability - Follows instructions, responds to management direction; Commits to long hours of work when necessary to reach goals
* Initiative - Asks for and offers help when needed
* Innovation - Generates suggestions for improving work
Other
* The employee is frequently required to sit, climb, and use hands to signal and handle equipment
* The employee is occasionally required to stand, walk, crawl, kneel, bend, and reach with hands and arms above their shoulders
* Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision and depth perception
Additional Information
Site Address: 6300 E 44th Ave, Denver, CO 80216
Why work for Cornerstone Building Brands?
Our teams are at the heart of our purpose to positively contribute to the communities where we live, work and play. Full-time* team members receive medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development. You can also join one of our Employee Resource Groups which help support our commitment to providing a diverse and inclusive work environment.
* Full-time is defined as regularly working 30+ hours per week. Union programs may vary depending on the collective bargaining agreement
All your information will be kept confidential according to EEO guidelines.
The US pay for this full-time position is $23.81 per hour + medical, dental, vision benefits starting day 1 + 401k and PTO. (Full-time is defined as regularly working 30+ hours per week. Union programs may vary depending on the collective bargaining agreement.)
Why work for Cornerstone Building Brands?
Our teams are at the heart of our purpose to positively contribute to the communities where we live, work and play. Full-time* team members receive medical, dental and vision benefits starting day 1. Other benefits include PTO, paid holidays, FSA, life insurance, LTD, STD, 401k, EAP, discount programs, tuition reimbursement, training, and professional development.
* Full-time is defined as regularly working 30+ hours per week. Union programs may vary depending on the collective bargaining agreement.
Cornerstone Building Brands 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, pregnancy, genetic information, disability, or status as a protected veteran. You can find the Equal Employment Opportunity Poster here. You can also view Your Right to Work Poster here along with This Organizations Participation in E-Verify Poster here. If you'd like to view a copy of the company's affirmative action plan for protected veterans or individuals with disabilities or policy statement, please contact Human Resources at ************ or *******************************. If you have a disability and you believe that you need a reasonable accommodation in order to search for a job opening or to submit an online application, please contact Human Resources at ************ or *******************************. This email is used exclusively to assist disabled job seekers whose disability prevents them from being able to apply online. Only emails received for this purpose will be returned. Messages left for other purposes, such as following up on an application or technical issues not related to a disability, will not receive a response.
All your information will be kept confidential according to EEO guidelines.
California Consumer Privacy Act (CCPA) of 2018
Must be at least 18 years of age to apply.
Notice of Recruitment Fraud
We have been made aware of multiple scams whereby unauthorized individuals are using Cornerstone Building Brand's name and logo to solicit potential job-seekers for employment. In some cases, job-seekers are being contacted directly, both by phone and e-mail. In other instances, these unauthorized individuals are placing advertisements for fake positions with both legitimate websites and fabricated ones. These individuals are typically promising high-paying jobs with the requirement that the job-seeker send money to pay for things such as visa applications or processing fees. Please be advised that Cornerstone Building Brands will never ask potential job-seekers for any sort of advance payment or bank account information as part of the recruiting or hiring process.
$24 hourly 29d ago
Quality Technician (BSO-Golden)
Belmar Pharma Solutions
Quality engineer job in Golden, CO
Role and Responsibilities
This position is responsible for working cross functionally to support Quality Assurance & Quality Control tasks, with focus on visual inspection of drug products. The Quality Technician will support Belmar Pharma Solutions in carrying out the mission of the company. This position reports to the Quality Manager.
Responsibilities include:
Primary responsibility to perform visual inspection of parenteral pharmaceutical products in accordance with regulatory guidelines
Create & review all labels (in-process and finished goods) and Batch Production Records for accuracy and adherence to Good Documentation Practices (GDPs)
Incoming materials receipt: inspect, document, unpack, label, shelve, and organize materials
Obtain samples of raw, in-process, and finished goods materials and send to third party labs for testing. Results to be entered into applicable spreadsheets.
Review Logs of Use and Maintenance (LUMs) for accuracy and GDP
Finished drug product batch release checks
Perform Quality checks on in-process product and facility controls as needed
Sterilization: Prepare, receive, and organize product for sterilization
Environmental Monitoring (EM): Collect routing EM samples. Enter, report and trend sample data.
Identify nonconformances and escalate to leadership
Attend all required meetings and provide clear, professional verbal and email communications.
Special projects as assigned by Management
Other duties as assigned
$33k-46k yearly est. 36d ago
Quality Technician: Inspection and Testing
Trisalus Life Sciences, Inc. 3.8
Quality engineer job in Westminster, CO
Duties and Responsibilities: Work effectively with the Quality, Operations, and R&D departments to perform all work accurately, with a sense of urgency and a positive attitude. Activities include the following: * In-Process and Final Device Inspection and Test: Support Manufacturing as the QC inspector for clean-room & packaging inspection activities. Perform and document in-process and final inspection/test of devices and sub-assemblies. Provide inspection/test assistance to R&D, Operations and Quality Engineering in support of design and process verification/validation activities.
* Receiving Inspection and Test: Perform and document receiving inspection/test of device components & raw materials in accordance with drawings/specifications. Maintain accurate & timely records of inspection activities and recording such activities in the QC Receiving Log.
* Non-Conforming Materials: Identify, segregate and quarantine non-conforming materials resulting from inspection activities. Initiate NCRs and notify the workstream owner in a timely manner. Execute and record disposition activities in accordance with approved NCRs.
* Microbiological Monitoring: Participates in periodic microbiological and particulate testing of the cleanroom and products as required.
* Returned Goods Authorization: Perform timely inspections and maintain accurate records of all returned TriSalus products through the RGA process. Correctly dispositions returned product as defined in approved procedures.
* Quality Record maintenance: Receive, verify, scan and physically file Quality Records in an organized manner as needed.
* Shipping QC: Verify TriSalus products and associated paperwork are accurate and complete prior to shipment.
* Audit Assistance: Help retrieve, review, organize and re-file documentation during all TriSalus site audit activities (internal, FDA, ISO registrar).
* GP Dynamics: Transfer released materials in the ERP software for material management as needed.
* Training Record support: Enter complete training/certification records into the eQMS as needed.
* General: Perform other quality inspection, test or administration activities as assigned.
Qualifications
Education & Certifications:
* High School diploma. Advanced education or certifications a plus.
Work Experience:
* 2+ years of Quality Control / Inspection experience in a medical device or similar technical product manufacturing company.
* Experience working with sterile disposable products in a cleanroom environment a plus.
Knowledge, Skills & Abilities:
* Able to read and interpret engineering drawings, specifications and detailed technical documents.
* Able to read and follow quality procedures and detailed work instructions (QLPs/OPs).
* Able to perform component and product inspection/testing using tools such as microscopes, calipers, micrometers, pin gauges, depth gauges, pull force test systems and vision measuring systems. (Sufficient knowledge to select and use the correct measurement tool for the required inspection accuracy.
* Able to accurately document results of inspections using good documentation practices.
* Able to understand and apply inspection sampling plans, such as C=0 or ANSI Z1.4.
* Able to utilize basic math skills.
* Able to use MS Word and MS Excel.
* Must possess strong attention to detail.
* Possess good communication skills and able to interact with peers in a professional manner.
* Possess knowledge and application of US and international standards for quality management (FDA 21 CFR 820, ISO 13485).
* Demonstrates excellent critical thinking skills.
* Ability to adapt to and rapidly learn new processes.
* Strong verbal and written communication skills and confidence in making inspection related decisions.
* Participates as a member of cross functional technical teams to support process improvements, special projects and investigations as needed.
* Approaches work tasks with a positive attitude and seeks feedback on performance to continually improve.
Physical Requirements:
* Ability to safely and successfully perform the essential job functions consistent with the ADA, FMLA and other federal, state and local standards, including meeting qualitative and/or quantitative productivity standards.
* Must be able to lift and carry up to 30 lbs.
* Ability to maintain regular, punctual attendance consistent with the ADA, FMLA and other federal, state and local standards.
$30k-37k yearly est. 26d ago
Quality Technician
Kratos Industries LLC
Quality engineer job in Arvada, CO
Job DescriptionDescription:
ROLE AND RESPONSIBILITIES
• Inspect mechanical parts fabricated internally using industry standard inspection tools
• Inspect mechanical parts and components provided externally by suppliers at inspection stations.
• Inspect and monitor incoming raw materials/packaging and finished goods, including paint, for specification compliance
• Inspect electrical wire routing, torquing and continuity as required
• Conduct electrical testing of product as required
• Assist in troubleshooting non-compliant inspected parts and components
• Responsible for inspection related document control and records storage
• Document and record inspection results in electronic and hardcopy format
• Interpret mechanical drawing dimensional features and acceptable tolerances
• Maintain a “floor presence” as an “auditor of quality” throughout the manufacturing facility and process
• Regularly review work instructions, travelers, and production records for continuous compliance to manufacturing requirements
• Works closely with production managers and manufacturing personnel conducting quality assurance checks
• Participates in regular procedure training activities in production
• Provides support for quality related projects, objectives and deadlines beyond the normal job scope as required
• Makes key decisions concerning product quality on their own, including pausing the line when processes do not conform to specification
• Facilitates GEMBA Walks, Quality Stand-up meetings, and other public speaking activities as needed
• Compiles and distributes weekly quality metrics data at the direction of the Dir of Quality
QUALIFICATIONS AND EDUCATION REQUIREMENTS
• A minimum of 3 years' experience as a Quality Inspector in an ISO 9001 environment is required for this position
• A minimum of 3 years' electrical/electronic manufacturing experience is required
• ASQ CQT certification or current pursuit of certification is highly desired
• A 2-year technical or vocational certificate is highly desired
• Advanced working knowledge of ISO 9001:2015 is highly desired
• Knowledge of AQL acceptance sampling plans using ANSI Z1.4 is strongly desired
• Knowledge of 5S +1 principles highly desired
PREFERRED SKILLS
• Advanced hands-on experience using common inspection tools and instruments
• Highly proficiency in MS Office Suite (e.g., Excel)
• Highschool math skills required
• Experience inspecting SS and CRS weld joints is highly desirable
• Ability to manage multiple concurrent tasks is required
• Deliver results accurately and on time while utilizing a strong learning mindset
• Must be capable of working independently to achieve production schedules and quality goals
• Effective interpersonal skills involving the ability to work effectively, cross-functionally and cross-culturally
• Excellent communication skills adaptable to all levels of the organization
• Ability to communicate clearly in a proactive positive sense
BENEFITS
• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance
PERFORMANCE BONUS - Eligible
A written and / or practical skills assessment will be required of the successful applicant.
Requirements:
How much does a quality engineer earn in Loveland, CO?
The average quality engineer in Loveland, CO earns between $58,000 and $94,000 annually. This compares to the national average quality engineer range of $61,000 to $103,000.