Quality Control Manager
Quality manager job in Denver, CO
STAQ is currently hiring for a Quality Control Manager in the Denver area
Monday to Friday, 8 AM to 5 PM
Salary: $105K-$110K/year
STAQ Pharma is a 503B Outsourcing Facility located in Denver. STAQ Pharma produces sterile injectable medications for adults and pediatric patients, compounded under cGMP standards. STAQ's ownership and board are composed of large hospital systems ensuring the priority focus remains on delivering needed medications in a safe and timely manner. We are looking for exception people to join the STAQ team.
This role is responsible for leading all Quality Control (QC) activities at the site. The QC Manager will encourage and motivate associates to be successful and focused on Safety, Transparency, Availability, and Quality (STAQ) objectives.
Roles and Responsibilities
Establish an environmental monitoring program for the facility utilizing a risk-based approach to new and existing procedures.
Develop, manage, and improve QC processes and procedures to ensure compliance with all applicable laws, regulations, and STAQ Quality standards in support of cGMP standards for pharmaceutical manufacturing (503B).
Prepare, review, manage, and approve controlled documents (SOPs, protocols, logbooks, reports, etc.) relevant to STAQ QC operations.
Lead and draft investigations/deviations/change controls/OOS/CAPAs as they relate to environmental monitoring or Quality Control deviations.
Provide expertise and support to the Operations, Regulatory, and Quality teams.
Subject matter expert during audits or inspections as it relates to microbiology/environmental monitoring.
Recruit, retain, and mentor direct reports to comprise the QC team. Promote personal and professional growth of team members.
Support the batch disposition process including management of reserve samples and QC samples for batch release testing.
Manage the budget for the QC Lab department to meet financial objectives.
Lead the Stability Program including study management, protocol development & evaluation, timely completion of stability tests, data trending, etc.
Collect, submit, ship, and manage appropriate raw material, microbiological and finished goods samples to third party testing laboratories.
Coordinate and facilitate operations within the internal laboratory to ensure Environmental Monitoring samples are performed, tested, reviewed, and trended appropriately.
Conduct routine and non-routine viable, non-viable and surface environmental monitoring in all classified areas of the facility. Analyze and interpret trends and identify opportunities to improve processes and achieve state of control.
Focus on responsiveness, ability to multi-task, attention to detail, effective problem-solving skills, consistent follow-up, and ability to make timely and sound decisions.
Implement methods of continuous improvement in daily work and in evaluation of company processes and performance.
Other duties as assigned.
Preferred Qualifications and Education
B.S. or B.A. in Microbiology or a closely related field / or equivalent experience.
Minimum five (5) years' experience in a quality control environment.
Experience in a cGMP pharmaceutical/aseptic manufacturing environment.
Must demonstrate understanding and/or working knowledge of regulations/guidelines such as FDA, USP, ICH, etc.
Proficiency/experience with environmental monitoring program for aseptic manufacturing facility, including personnel monitoring, and qualification program.
Preferred Experience and Skills
Working knowledge of aseptic/sterile manufacturing techniques.
Ability to coordinate multiple priorities in a fast-paced environment.
Strong communication skills with the ability to interact with all levels across the organization.
Demonstrated excellent interpersonal skills and flexibility.
Familiarity with 21 CFR Part 11/210/211.
Additional Notes
Join a dynamic team at the leading edge as we build out a new 137K sq. ft. manufacturing facility.
This position will work closely with cross functional teams and report quality data to the department heads for each team, as needed
Timeline: We will be accepting applications on an ongoing basis until position is filled.
Director of Quality, Aerospace
Quality manager job in Denver, CO
PLEASE NOTE: This postion is onsite and direct hire. It is NOT C2C/ 3rd party eligible.
Our company is growing rapidly and is hiring for a Manufacturing Quality Engineer. Thank you in advance for taking a look at the list of responsibilities and qualifications. We look forward to reviewing your resume.
Responsibilities
Oversees an organization's manufacturing and engineering processes by ensuring the proper use of tools, materials and procedures.
Work with the quality team to create and maintain standards for manufactured products.
Work with suppliers to make sure all the components and raw materials meet the organization's quality standards
Analyze customer feedback to identify potential flaws in the manufactured products and implement changes when necessary
Monitor the quality of employee training and the safety standards required in the manufacturing process
Document any issues in the production process and develop ways to fix them
Stay up to date with legal standards the manufactured products meet and ensure all products are within those standards
Create and present quality reports that analyze internal and external quality standards
Qualifications
Previous experience as a Quality Engineer
5+ years of leadership
Senior Quality Assurance Manager
Quality manager job in Longmont, CO
Coherent Aerospace & Defense Inc, Emerging Products & Technologies (EP&T) Business Unit is seeking a Sr. Quality Assurance Manager to lead quality and product assurance across the portfolio of EP&T programs and site operations. Our Quality Assurance Manager will have the responsibility to ensure product, process, and supplier requirements are met with high levels of quality, customer satisfaction, and program execution to support cost, schedule and on-time delivery. The Senior Quality Manager will also have responsibility for facility upkeep, maintenance and monitoring.
This role involves the collaboration with engineering and manufacturing teams on exciting and challenging product developments and program tasking in the areas of High Energy Lasers, gimballed assemblies, space-based optical telescopes, and active sensing.
Primary Duties & Responsibilities
The Sr. Quality Assurance Manager responsibilities include:
Responsible for site QMS i.e., Mgt. Review, Calibration, CAPA, NCR, Calibration etc.
Material Review Board
Corrective Action Board and provide metrics.
Quality representation in program baseline management activities (e.g., Milestone Reviews (SRR, PDR, CDRs), CCB, peer reviews, code reviews, release planning, configuration management, CCB, test witnessing)
Partner with suppliers to assure high quality of incoming product.
Perform internal and supplier AS9100D audits.
Continually improve quality program, including policies, objectives, plans, organization, procedures, and appraisals.
Generates regular progress, summary, and management review reports including Quality Metrics
Through knowledge of quality improvement tools, including: 5 Why, 8D, Fishbone, Poke-yoke, NPI, FMEA's Manage the Inspection and Quality Engineering team and as required perform hands-on Inspection to include receiving inspection & test, in-process inspections, final inspection & test. Quality inspection and maintenance tasks include:
Verification and data archival of critical dimensions on ALL incoming custom fabricated parts (This may involve the use of an articulating arm CMM, calipers, and gauge blocks)
Verification and archival of passing certs for all COTS parts
Electronics/soldering inspection (must be able to achieve IPC certification)
Qualified space electronics inspection desired
Calibration oversight for all shop floor and facility equipment
Maintenance, monitoring and calibration for ESD equipment
Particle count
Customer quality requirements have been adequately defined to permit appropriate quality planning and implementation and that these quality requirements are met or exceeded.
Maintains relationships with Operations to assure adequate process capability, control, improvement, and quality information feedback.
Works with Customers and Sales to ensure that customer quality requirements have been adequately defined to permit appropriate quality planning and implementation and that these requirements are met or exceeded.
Interfaces with major customers to ensure Customer Satisfaction and clarify quality requirements through personal visits, verbal, and written communication.
Facility oversight responsibility to include:
Maintenance & Repairs. Coordination of facility cleaning, preventative and repair maintenance activities including electrical, HVAC, plumbing, communications, security, and safety systems with appropriate contractors and vendors.
Safety & Compliance. Ensure facility and shop floor layout meet all OSHA and Coherent EH&S requirements. This includes documentation and monitoring of safety events and corrective actions.
Space planning & layout. Coordinate layout of both office and shop floor areas, including workstation allocation, for optimal workflow and efficiency
Hazardous Materials. Manage handling, storage and removal of hazardous materials and waste
Facility upgrade. Develop budgets and proposals for facility upgrades as appropriate to complete execution of funded programs
Quality manager will also be a key leader for future facility expansion, upgrade and oversight.
Education & Experience
Bachelor's Degree in a Business Management, Quality Technology or STEM discipline and Minimum of 8+ years of relevant experience, master's degree and 3+ years of relevant managerial/leadership experience.
Prior experience in plant management, industrial engineering, and manufacturing operations is highly desirable.
Skills
Preferred skills and experience:
Experience in Optical Quality Inspection, testing and process improvements for optics, fibers, and optical system quality for the Aerospace and Defense Industry
Experience in Optical and fiber component handling, cleaning of optical and fiber components.
Experience with calipers, micrometers, torque wrenches, test plates, electronic gauges, light sources, interferometers, autocollimators and working with automation of test equipment.
Previous Supply Chain and/or Supply Chain Quality operations
ASQ Certified Quality Auditor or Certified AS9100 Lead Auditor
Experience in creating and maintaining useable, actionable metrics to drive department decisions and processes
Analytical, decision making, and problem-solving skills
Working Conditions
Job operates in a professional office environment, manufacturing floor, and in clean room facilities
Routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines
Work in a cubicle area - must be able to work in environment where employees are on the phone / speaking causing potential distractions throughout the day.
Noise level - Usually moderate for the manufacturing floor and clean room facilities
Physical Requirements
Standing. Particularly for sustained periods of time. 25% of the time.
Walk. Occasionally move about inside the office to access file cabinets, office machinery, etc.
Talking. Expressing or exchanging ideas by means of the spoken word. Those activities in which they must convey detailed or important spoken instructions to other employees accurately, loudly, or quickly.
Hearing. Perceiving the nature of sounds at normal speaking levels with or without correction. Ability to receive detailed information through oral communication, and to make the discriminations in sound.
Lifting. Raising objects from a lower to a higher position or moving objects horizontally from position-to-position. This factor is important if it occurs to a considerable degree and requires substantial use of upper extremities and back muscles. No more than 10 to 15 pounds.
Sedentary Work. Sedentary work involves sitting most of the time. Jobs are sedentary if walking and standing are required only occasionally and all other sedentary criteria are met.
Visual acuity. Specific vision abilities required by this job include close vision and ability to adjust focus.
Safety Requirements
All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards.
Quality and Environmental Responsibilities
Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System.
Culture Commitment
Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.:
Integrity - Create an Environment of Trust
Collaboration - Innovate Through the Sharing of Ideas
Accountability - Own the Process and the Outcome
Respect - Recognize the Value in Everyone
Enthusiasm - Find a Sense of Purpose in Work
Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
This role involves access to technology, materials, software, or hardware subject to U.S. export control laws. Therefore, to be considered, candidates must be classified as a “U.S. Person” under applicable regulations or be eligible for authorization under a U.S. government export license.
Must be eligible for and able to obtain and maintain a U.S. Government Security Secret Clearance, (or higher if required).
If you need assistance or an accommodation due to a disability, you may contact us at
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Auto-ApplyDirector, Quality Assurance
Quality manager job in Boulder, CO
This position in Quality Assurance provides strategic and technical support of the Quality Management System (QMS) and is responsible for ensuring GxP and QMS compliance. This position is responsible for ensuring Quality Programs are developed, implemented, and effectively administered in a manner that is fit for purpose, maximizes efficiency, complies with development-stage biotech industry standards, and achieves desired compliance with regulatory, clinical, and business operations goals. The ideal Quality Assurance candidate will have small-molecule, development-phase GMP experience, and also have a strong desire and proven ability to implement quality initiatives across GxP functions. The candidate should have previous experience managing and mentoring others in Quality Assurance and be passionate about instilling a practical, efficient, and risk-based quality approach within the Quality Assurance group and throughout the company.
Essential Duties and Responsibilities:
Lead and manage the OnKure Quality Assurance team
Own the OnKure QMS and oversee the implementation of fit-for-purpose quality initiatives, processes, tools and trackers
Partner with other members of the Quality Assurance team to provide enhancements to Quality Systems to improve efficiency, regulatory compliance, and reduce manual processes
Author and manage to resolution quality events including deviations, CAPAs, investigations, and change controls
Perform or oversee GxP and vendor audits
Implement and perform periodic quality management reviews, develop phase-appropriate Quality metrics/KPIs
Continually assess compliance status of clinical and CMC development programs
Perform quality review and approval of IMP manufacturing documentation and provides disposition of drug substance, drug product and clinical trial material
Liaise between external QP and internal teams to ensure prompt IMP distribution
Manage supplier activities, including support of supplier qualification assessments and verification of approval requirements, approved supplier listing and supplier file maintenance, and any ongoing monitoring of supplier relationships and deliverable expectations
Business system owner for the electronic QMS and support the Quality Systems Associate with:
Drafting and periodic review of controlled documentation, including SOPs, WIs, and Corporate Policies
Document archiving
Partnering with cross functional teams to evaluate training assignments, develop and maintain training matrices, and drive training completion timelines
This position requires the incumbent to perform daily hands-on Quality administrative activities as required.
Preferred Experience and Qualifications:
Bachelor's degree or equivalent
10+ years (Director) of quality experience, in pharmaceutical industry; including experience in development phase GMP QA
Strong knowledge of GxP regulations, Quality Systems (including Document Control, Training, Change Control, computer system validation, 21 CFR Part 11) and relevant regulatory guidance documents
Strong leadership skills with ability to provide strategic input into quality programs as well as contributing to tactical and administrative tasks
Excellent interpersonal skills and regarded as trustworthy and collaborative by peers
Ability to work with cross functional teams to assess complex issues and to recommend pragmatic, relevant, and realistic solutions, and when appropriate leading implementation of solutions
Proficiency and experience with electronic Quality Management Systems including management and maintenance
Experience with FDA and/or other regulatory agency inspections and inspection readiness activities
About OnKure:
OnKure, Inc. is a clinical-stage biopharmaceutical company focused on the discovery and development of precision medicines that target biologically validated drivers of cancers that are underserved by available therapies. Using a structure- and computational chemistry-driven drug design platform, OnKure is committed to improving clinical outcomes for patients by building a robust pipeline of small molecule drugs designed to selectively target specific mutations thought to be key drivers of cancer.
To attract the very best talent, OnKure offers a generous compensation and benefits package that includes competitive pay, performance-based bonus opportunities, stock options, insurance coverage (health, dental, life, and disability) for full-time employees, self-managed paid time off, and a 401(k) plan with company match. Candidates who live in or are willing to relocate to the Boulder, CO area are preferred.
The expected annual compensation range for this role, based on experience, is $200,000-225,000.
OnKure is an equal opportunity employer and welcomes all job applicants. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, protected veteran status, disability, or any other protected factors.
Director, Quality - Life Sciences
Quality manager job in Denver, CO
Datavant is a data platform company and the world's leader in health data exchange. Our vision is that every healthcare decision is powered by the right data, at the right time, in the right format. Our platform is powered by the largest, most diverse health data network in the U.S., enabling data to be secure, accessible and usable to inform better health decisions. Datavant is trusted by the world's leading life sciences companies, government agencies, and those who deliver and pay for care.
By joining Datavant today, you're stepping onto a high-performing, values-driven team. Together, we're rising to the challenge of tackling some of healthcare's most complex problems with technology-forward solutions. Datavanters bring a diversity of professional, educational and life experiences to realize our bold vision for healthcare.
Datavant is seeking a strategic and hands-on **Director of Quality** to lead product and supplier quality assurance efforts within our **Life Sciences business unit** , which includes the **Datavant Connect** and **Aetion Evidence Platform** . These platforms deliver regulatory-grade real-world data (RWD) solutions through tokenization, data linkage, and privacy-preserving analytics.
As Director of Quality, you will own the implementation and evolution of GxP-aligned quality practices that support regulated data services and software. This includes oversight of software validation, privacy compliance, supplier qualification, and audit readiness. You will also lead a team of quality specialists and partner cross-functionally with Product, Engineering, Security, Privacy, and Customer Assurance to ensure that we meet or exceed regulatory expectations and customer trust standards.
This role is essential to operationalizing Datavant's **Quality Management System (QMS)** across internal and external stakeholders and enabling continued growth in regulated RWD and evidence generation environments.
**What You Will Do**
+ Lead the development and continuous improvement of Datavant's QMS across Life Sciences products and supplier relationships, ensuring GxP and privacy compliance.
+ Manage and mentor a team of quality specialists responsible for core functions such as CAPA, internal audits, validation, and supplier monitoring.
+ Serve as the primary quality liaison to product development teams (Connect and Aetion), providing guidance on SDLC quality controls, validation strategies (GAMP 5, Part 11), and regulatory risk mitigation.
+ Oversee supplier qualification and re-evaluation processes, including risk-based assessments, audit coordination, and performance monitoring.
+ Establish and maintain quality metrics (e.g., CAPA closure, audit readiness scores, supplier performance) and drive continuous improvement initiatives.
+ Support readiness for and participation in customer audits and external assessments (e.g., pharma clients, CROs, regulatory partners).
+ Partner with Security and Privacy teams to align product and supplier practices with frameworks like HIPAA, GDPR, and FedRAMP.
+ Lead or support periodic management reviews of the QMS and contribute to strategic quality planning and resource allocation.
+ Ensure clear documentation and traceability across all quality activities, systems, and changes in compliance with FDA 21 CFR Part 11 and ICH E6(R3).
+ Represent Datavant's quality program in external communications, including client onboarding, RFIs, and quality-related escalations.
**What You Need to Succeed**
+ 8+ years of experience in quality, compliance, or regulatory roles within life sciences, digital health, or regulated software organizations.
+ Strong working knowledge of relevant regulations and frameworks, including **FDA 21 CFR Part 11, GAMP 5, ISO 9001, ICH E6(R3), HIPAA** , and **GDPR** .
+ Proven leadership in scaling and operationalizing a **QMS in a SaaS, RWD, or GxP context** .
+ Experience managing and mentoring cross-functional teams.
+ Demonstrated success overseeing **validation, supplier oversight, internal audits, and CAPA management** .
+ Deep understanding of **data governance, privacy, and security** best practices.
+ Experience interacting with external auditors, customer compliance teams, or regulatory agencies.
+ Strong communication skills-capable of explaining complex quality topics to product, legal, technical, and customer-facing stakeholders.
**What Helps You Stand Out**
+ Prior experience supporting real-world data (RWD) platforms or evidence generation technologies used in regulatory submissions.
+ Background working in or with tokenization, health data linkage, or privacy-enhancing technologies.
+ Experience interfacing directly with pharmaceutical, biotech, or CRO quality teams.
+ Training or certification in Six Sigma, ISO Auditing, or software validation methodologies.
+ Familiarity with supplier portals, quality dashboards, or eQMS platforms (e.g., Veeva, MasterControl).
+ Experience contributing to industry working groups on quality, data integrity, or health data compliance.
\#LI-BC1
We are committed to building a diverse team of Datavanters who are all responsible for stewarding a high-performance culture in which all Datavanters belong and thrive. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status.
At Datavant our total rewards strategy powers a high-growth, high-performance, health technology company that rewards our employees for transforming health care through creating industry-defining data logistics products and services.
The range posted is for a given job title, which can include multiple levels. Individual rates for the same job title may differ based on their level, responsibilities, skills, and experience for a specific job. This role is eligible for additional variable compensation.
The estimated base salary range (not including variable pay) for this role is:
$165,000-$230,000 USD
To ensure the safety of patients and staff, many of our clients require post-offer health screenings and proof and/or completion of various vaccinations such as the flu shot, Tdap, COVID-19, etc. Any requests to be exempted from these requirements will be reviewed by Datavant Human Resources and determined on a case-by-case basis. Depending on the state in which you will be working, exemptions may be available on the basis of disability, medical contraindications to the vaccine or any of its components, pregnancy or pregnancy-related medical conditions, and/or religion.
This job is not eligible for employment sponsorship.
Datavant is committed to a work environment free from job discrimination. We are proud to be an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, or other legally protected status. To learn more about our commitment, please review our EEO Commitment Statement here (************************************************** . Know Your Rights (*********************************************************************** , explore the resources available through the EEOC for more information regarding your legal rights and protections. In addition, Datavant does not and will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay.
At the end of this application, you will find a set of voluntary demographic questions. If you choose to respond, your answers will be anonymous and will help us identify areas for improvement in our recruitment process. (We can only see aggregate responses, not individual ones. In fact, we aren't even able to see whether you've responded.) Responding is entirely optional and will not affect your application or hiring process in any way.
Datavant is committed to working with and providing reasonable accommodations to individuals with physical and mental disabilities. If you need an accommodation while seeking employment, please request it here, (************************************************************** Id=**********48790029&layout Id=**********48795462) by selecting the 'Interview Accommodation Request' category. You will need your requisition ID when submitting your request, you can find instructions for locating it here (******************************************************************************************************* . Requests for reasonable accommodations will be reviewed on a case-by-case basis.
For more information about how we collect and use your data, please review our Privacy Policy (**************************************** .
Assurance Director
Quality manager job in Denver, CO
Our Firm Sorren is a top 50 national advisory firm that blends deep expertise with a human-first approach. We don't just work with numbers-we work with people, building lasting relationships and delivering strategic solutions in accounting, assurance, tax, advisory, and private client services.
At Sorren, we believe that success is a shared journey. Our culture fosters collaboration, innovation, and professional growth, ensuring that every team member has the support and opportunities they need to thrive. We offer a high-performing yet balanced work environment where career development and personal well-being go hand in hand.
We're committed to helping you grow, whether that means advancing your career, expanding your expertise, or achieving a fulfilling work-life balance. Because at Sorren, your success is our success.
Your Journey
Our team members support the firm by delivering timely, accurate work and maintaining clear communication. They take ownership of their development, seek feedback, and build strong relationships. By managing responsibilities effectively and aligning their efforts with firm values, they establish a foundation for long-term success and growth. All team members are expected to excel in Relationships, Communication, Quality Service, Operational Excellence, and Innovation & Growth, contributing to the firm's success through collaboration, exceptional service, and continuous growth.
Position Summary:
As a firm experiencing significant continued growth and the advancement of our existing leaders, we are seeking Directors who are ready to take the next step in their career and help shape the future of our firm. This role is designed for entrepreneurial leaders who are energized by building teams, expanding client relationships, and driving strategic growth. Our Directors play a pivotal role in guiding the firm's direction - and for those who demonstrate strong leadership, business development, and client impact, this position serves as a defined path to Partnership.
Your Impact (Essential Duties):
Provide strategic oversight and leadership for the planning, execution, and delivery of the firm's most complex and high-risk assurance engagements, including audits, reviews, and agreed-upon procedures
Serve as the firm's lead technical authority on GAAP, GAAS, PCAOB standards, and SEC reporting, providing critical guidance on complex accounting issues such as revenue recognition, lease accounting, consolidations, and internal controls
Direct and review the preparation and distribution of all periodic financial statements for external reporting, ensuring compliance with professional standards, firm policies, and regulatory requirements
Advise senior leadership and clients on trends and changes in accounting standards and regulatory reporting requirements; recommend and implement best-practice responses
Oversee all engagement strategies and ensure alignment with client goals, risk management protocols, and evolving industry and regulatory expectations
Act as a liaison with external auditors and regulators where applicable, and coordinate preparation of materials for boards, audit committees, or shareholders as needed
Approve engagement budgets and resource planning, ensuring profitability while maintaining quality standards and effective use of staff
Drive innovation and process improvement by enhancing audit methodology, adopting emerging technologies, and evaluating new tools and workflows to increase efficiency and quality
Mentor, coach, and develop senior managers and managers, overseeing their progression and succession planning while fostering a culture of accountability, technical growth, and collaborative leadership
Review and approve all major deliverables, including financial statements, audit reports, and internal control communications, ensuring clarity, compliance, and strategic insight
Serve as a trusted advisor to clients, helping them interpret audit outcomes, understand business implications, and strengthen internal financial reporting functions
Lead firm-wide business development efforts by contributing to proposals, pricing strategies, client pitches, and relationship expansion initiatives
Champion firm values and culture, contributing to key initiatives, promoting inclusion and collaboration, and representing Sorren at professional associations, conferences, and community forums
Maintain technical and leadership excellence through continuous learning, thought leadership, and participation in standard-setting and industry advocacy groups Perform other duties and display flexibility to take on a variety of responsibilities assigned by firm leadership
Meet annual billable hour and other targets to fulfill individual and team performance and overall firm productivity
Your Background:
10+ years of experience in assurance-related work
CPA license
Bachelor's degree in accounting or a related field
Authoritative expertise in U.S. GAAP, GAAS, PCAOB, and SEC regulations, with the ability to interpret complex and evolving accounting standards and advise on their practical application across a wide range of industries and client structures
Extensive experience leading high-profile and high-risk assurance engagements, including group audits, public company audits, and engagements involving significant estimates, judgments, or internal control considerations
Mastery of assurance technologies and analytics platforms, with a proven ability to assess, implement, and optimize tools to enhance engagement efficiency, data accuracy, and business insights for clients
Demonstrated success in managing and developing senior leaders, including mentoring Senior Managers and Managers through succession planning, performance coaching, and technical development
Exceptional executive communication skills with the ability to build trusted relationships at the C-suite and board levels, lead critical conversations with clients, and represent the firm in regulatory or oversight contexts
Strategic advisory mindset, capable of aligning assurance services with clients' business goals, risk profiles, and growth strategies, while contributing to the firm's long-term vision and innovation efforts
Strong financial and operational acumen, including the ability to evaluate engagement profitability, oversee budget planning, and drive continuous improvement in resource utilization and service delivery
Advanced problem-solving and risk management capabilities, with the judgment to resolve complex technical and client service challenges, and the foresight to mitigate engagement and firm-level risk
Proven contributor to firm-wide initiatives, including methodology enhancement, quality control, talent development, and business development strategies
Recognized thought leader, actively engaged in professional development, technical training, and knowledge-sharing through firm channels, industry events, or professional associations
Commitment to ethical leadership and quality-first culture, modeling integrity, accountability, and technical excellence in every aspect of client service and team leadership
Full-time commitment and flexibility to work beyond regular hours to meet team deadlines
Pay range for CO applicants-$170,000-$195,000
Why Choose Us?
At Sorren, we're invested in your growth-both personally and professionally. We'll support you as you advance in your career while also giving you the flexibility to enjoy life outside of work. We believe balance fuels success, and we've designed our culture and benefits to reflect that.
What We Offer*:
Generous paid time off
Comprehensive medical, dental, and vision coverage, plus life and disability insurance
401(k) retirement savings plan
Paid holidays, including a firmwide winter break (December 24 - January 1)
Paid parental leave (available after one year of service)
Mentorship and career development programs
CPA exam support to help you succeed on the path to licensure
Firm-sponsored events and spontaneous team activities
Celebrations to mark milestones like the end of busy season and the holidays
*Benefits are available to full-time employees regularly scheduled to work at least 30 hours per week.
© 2025 “Sorren” is the brand name under which Sorren CPAs, P.C. and Sorren, Inc. and its subsidiary entities provide professional services. Sorren CPAs P.C. and Sorren, Inc. and its subsidiary entities practice as an alternative practice structure in accordance with the AICPA Code of Professional Conduct and applicable laws, regulations, and professional standards. Sorren CPAs P.C. is a licensed independent CPA firm that provides attest services to its clients, and Sorren, Inc. and its subsidiary entities provide tax and business consulting services to their clients. Sorren, Inc. and its subsidiary entities are not licensed CPA firms.
Auto-ApplyQuality Manager
Quality manager job in Denver, CO
About the Positions
We're seeking Quality Managers at various levels to support large, heavy-civil infrastructure programs-including highways, roads, bridges, transit (including rail and bus), and airport projects delivered through both traditional and alternative methods. These positions will oversee program or project level quality practices including:
quality management (overarching framework and approach to quality),
quality assurance (oversight of design and delivery processes and procedures),
quality control (verification of compliance), and/or
other activities to ensure adequacy, implementation, and effectiveness).
This posting is for future roles and not for a specific opportunity that is available right now. We accept applications and conduct interviews in advance of upcoming hiring needs. When a candidate is selected, their profile is activated in our talent pool for this specialty area. We notify our talent pool candidates first whenever we have a project need. This posting targets Denver, CO.
Responsibilities
may include, but are not limited to, the following:
Develop, implement, and/or maintain Quality Management Systems in alignment with ISO 9001:2015 standards and our client requirements.
Establish and manage project-specific QA/QC plans and inspection test plans for design and delivery disciplines.
Oversee quality inspections, audits, and nonconformance reporting; ensure timely closure of nonconformances and implementation of corrective/preventive actions.
Coordinate with design teams, contractors, and consultants to resolve quality issues and ensure consistency throughout design, procurement, construction, and commissioning phases.
Conduct root cause analyses and lead continuous improvement initiatives using Lean Six Sigma, or similar methodologies.
Provide quality training and mentorship to project teams, subcontractors, and field personnel.
Lead quality meetings, compile reports, and deliver project quality performance metrics to internal and external stakeholders.
Attributes
Excellent written and verbal communication and interpersonal skills.
Excellent multitasking, organizational, and time management skills.
Collaborative mindset that fosters teamwork, trust, and positive relationships.
Detail-oriented, observant, logical, tenacious, and investigative.
Natural curiosity, problem-solving abilities, and a passion for continuous improvement both personally and in work.
Ability to analyze complex data and/or situations and resolve them using sound professional judgment.
Confidence in speaking up to address issues and resolve problems.
Minimum Qualifications
Bachelor's degree in civil engineering, quality, construction management, or a related field, or an equivalent combination of education and experience.
10+ years of professional experience in quality management for large (>$500M), complex, heavy-civil infrastructure projects.
Experience leading quality assurance audits.
Expertise with ISO 9001:2015 and industry standard QA/QC practices.
Experience with construction drawings and codes (e.g., IBC, ASTM, ACI, ASME).
Proven experience coordinating with a project management team and providing appropriate levels of support, coaching, and influence.
Proficiency with Microsoft Office Suite/Office 365 (e.g., Outlook, Teams, Word, Excel, PowerPoint, etc.).
Preferred Qualifications
Bachelor's degree in civil engineering, quality, or construction management.
Active ASQ CQE or CQA certification.
Active ISO 9001:2015 Lead Auditor certification.
Active Six Sigma Black or Green Belt certification.
Experience with large (>$500M), complex, heavy-civil infrastructure projects that include highways, roads, bridges, transit (including rail and bus), and/or airport projects.
Experience delivering projects through both traditional and alternative methods (e.g., DB, CM/GC, P3).
Experience in quality roles supporting owners.
Experience managing, coaching, guiding, and assisting technical and administrative staff.
Experience with Microsoft Power BI, Oracle Cloud Analytics, or other dashboard KPI reporting software.
Compensation Details
The salary range listed for this role is $120k-$160k/year ($57-$76/hour). The final salary offered will be based on multiple factors and thoughtfully aligned with each candidate's level of experience, breadth of skills, total education achieved, certifications/licenses that have been obtained, geographic location, etc.
Just LOOK at the Benefits We Offer!
Unlimited flexible time off
Paid holidays
Paid parental leave
Health, dental, and vision insurance
Flexible spending accounts (healthcare and dependent or elder care)
Long-term disability insurance
Short-term disability insurance
Life insurance and accidental death and dismemberment policy
401(k) plan with guaranteed employer contribution
Formal career planning and development program
$2,500 annually toward professional development
Wellness program with monthly wellness stipend
Company cell phone or cell phone plan reimbursement
Free personalized meal planning and nutrition support with a registered dietitian
Free personal financial planning services
Employee assistance program
Employee discounts
Employee referral bonus
Specific plan details and coverage for each benefit noted above will be provided upon offer.
Luster is committed to creating an inclusive work environment with a diverse workforce. All qualified applicants will receive consideration for employment without regard to criminal history, race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. This employer participates in E-Verify. The employer will provide the Social Security Administration (SSA) and, if necessary, the Department of Homeland Security (DHS) with information from each new employee's I-9 to confirm work authorization.
All positions may be subject to a background check and drug test once a conditional offer of employment is made for any convictions directly related to its duties and responsibilities, in accordance with all applicable local, state, and/or federal regulations.
This job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties and skills for the position.
Luster does not accept unsolicited resumes. In the absence of a signed agreement, Luster will not consider or agree to payment of any kind. Any unsolicited resumes presented to Luster personnel, including those submitted to Luster hiring managers, are deemed to be the property of Luster.
Please email ***************** for accommodations necessary to complete the application process.
Auto-ApplyQuality Manager
Quality manager job in Louisville, CO
Job Description
JOB PURPOSE:
At H3X, we are building the most advanced electric propulsion systems in the world to enable sustainable aviation. At >10 kW/kg power density, the HPDM family of integrated motor drives is a step change in electric propulsion technology and removes one of the main barriers blocking widespread proliferation of electric aircraft. We have several power classes of motors ranging from 30kW to 3MW and are selling to markets of aviation, aerospace and defense, marine, and specialized ground vehicles.
We are seeking an experienced Quality Manager to join our rapidly growing team here in Louisville, Colorado. The Quality Manager will be responsible for building our Quality Management System (QMS) and promoting continuous process improvement.
RESPONSIBILITIES:
Develop and maintain a Quality Management System (QMS) that complies with the required industry standards (AS9100 / ISO 9001), accreditation requirements, and business requirements across the organization through existing and new procedures
Train staff on QMS processes and procedures
Monitor and audit product quality and production processes to ensure adherence to quality standards
Identify and conduct root cause analysis on quality issues and implement corrective action plans
Conduct risk assessments to identify potential quality issues
Work closely with the team to improve QMS, while ensuring compliance with customer standards and staying agile in a fast-paced environment
Contribute to new business opportunities and communicate the impact on the QMS
Develop and execute quality roadmap to determine the level of quality system required
Be flexible with the quality system based on the specific requirements for different projects
Manage all external registration requirements to ensure they are met. Liaise with external bodies on all matters relating to registration
Ensure that all quality records and documents are maintained, updated, and stored securely
Develop and manage quality budgets and timelines
REQUIRED QUALIFICATIONS:
Associate's or Bachelor's degree in engineering, quality assurance, or a related field
5+ years of experience working in an AS9100 (or similar standard) manufacturing and inspection environment
5+ years of experience in developing and implementing quality procedures and work instructions in aerospace or aviation
High intelligence, high energy, and high integrity
Excellent understanding of the aerospace industry standards and regulations
Highly organized with the ability to prioritize tasks and manage time efficiently
Very high attention to detail
Ability to work independently with little to no supervision
Excellent written and verbal communication to effectively share knowledge and build the collective mindshare of the company
Proficient in Microsoft Office and quality assurance software
A high degree of emotional intelligence: ability to collaborate closely with coworkers in a respectful and empathetic manner
U.S. Person status is required as this position needs to access export-controlled data
COMPANY BENEFITS:
Employee equity incentive plan
Health insurance: Medical, Vision, Dental, ST & LT Disability, and Life
Gym membership stipend (up to $60/month)
Epic or IKON Ski/Snowboard Pass (up to $869 provided)
Flexible hours (deliverable-based goals)
Flexible time off (just need manager approval)
Continuing professional education benefit
Relocation package
Monthly company events
401k program
SALARY: $70,000-130,000 USD
THE COMPANY:
H3X Technologies is a U.S.-based manufacturer of electric motors for sustainable aviation, marine, industrial, and defense applications. They have developed a family of integrated motor drives that can scale in power from 30kW to 30MW with power densities as high as 12 kW/kg and best-in-class efficiency. This high performance is enabled by novel scalable core technology and proprietary manufacturing processes for motor stacking, winding, and assembly. The design, manufacturing, and testing of their products is done in-house at their headquarters in Louisville, Colorado.
H3X's world-class team is composed of experts from Tesla, SpaceX, GE Aviation, and Siemens with deep knowledge in electric machines, power electronics, material science, control systems, and advanced manufacturing. H3X takes pride in their multidisciplinary approach, relentless dedication, high capital efficiency, and Skunkworks-style execution.
H3X has raised over $30M with backing from top VC firms and strategic firms, including Lockheed Martin, Hanwha, Y Combinator, Cubit Capital, Metaplanet, TechNexus, and Liquid 2 Ventures.
H3X is poised to become the world's leading supplier of advanced electric motors by 2030 to drive deep decarbonization in aviation, marine, and heavy industrial applications and unlock next-generation electrified defense technology to strengthen national security.
H3X is an equal opportunity-affirmative action employer and considers all qualified applicants for employment based on business needs, job requirements and individual qualifications, without regard to race, color, religion, sex, age, disability, sexual orientation, gender identity or expression, marital status, past or present military service or any other status protected by the laws or regulations in the locations where we operate.
Quality Control Manager
Quality manager job in Denver, CO
What We Do We empower our defense and law enforcement customers to focus on their primary mission by removing friction points and setting them up for long-term success. VWI provides facilities and infrastructure management; our specific services include housing management, custodial services, facilities management, operations & maintenance, and various professional services. By providing strategic, responsive, and mission-driven solutions, we forge long-term partnerships with our customers, vendors, and team members. We invite you to join our team, providing essential services for those who serve our country.
What You'll Do
Manage and implement the contractor's Quality Control Plan (QCP).
Ensure compliance of both contractor and subcontractor personnel with QC standards.
Monitor QC activities across all work centers and provide remedial training when necessary.
Maintain inspection and testing documentation and coordinate with the COR for oversight.
Ensure deficiencies are identified and corrected before performance becomes unacceptable.
What You'll Have
At least two years of experience in QC evaluation and reporting for construction or facility management.
Ability to oversee inspections, testing, and reporting of facility systems.
Must be present on-site during normal duty hours or have a qualified alternate.
What We Offer
At VWI, our people are our greatest strength. Our respect for the skills and expertise of our employees drives every decision we make. We strive to uphold our values of respect, dignity, teamwork, and transparency in the benefits and compensation we offer to our employees.
Medical, dental, and vision insurance, covered by employer-funded Health & Welfare contributions, as per SCA regulations.
Paid Time Off and Vacation Days
Opportunities for bonuses and compensation increase over and above guaranteed SCA wages.
Opportunities for promotion to supervisor and management positions
Leadership and development opportunities
VWI is an Equal Opportunity Employer
Head of Safety, Quality, and Mission Assurance
Quality manager job in Denver, CO
Job Description
Urban Sky is a venture-backed aerospace startup that pioneers utilization of the stratosphere and reimagines the way humans view and analyze the earth. We design, build, operate, and sell stratospheric balloon systems, and the data we collect supports a wide range of applications, from real-time wildfire monitoring to urban mapping. Our technology is also employed by government customers including the Department of Defense (DoD), NASA, and others. Urban Sky sends flight vehicles to the stratosphere on a weekly basis.
Our team consists of engineers, makers, developers, and doers who believe in the power of human potential when passion meets utility within a small, supportive team. At Urban Sky we strive to create a team culture grounded in candor, inclusion, respect and empowerment.
We aim to build the next chapter of stratospheric history in Denver and are seeking self-starting, open-minded, and hard-working team members.
About The Role:
Urban Sky is currently seeking a leader in safety, quality, and mission assurance to join our team in Denver, CO. This position will be responsible for fostering a collaborative culture of safety and quality, aimed at enhancing the overall safety, quality, reliability, and mission success of Urban Sky's stratospheric systems across the organization. The successful candidate will collaborate with various teams including product management, manufacturing, design, and operations to lead the development of processes, systems, and strategies that improve the safety and reliability of our balloons, payloads, avionics, firmware, and software. We believe that safety and quality are shared responsibilities, and the person who fills this role will have the vitally important job of ensuring our systems are safe, reliable and performant while empowering passionate engineers and technicians to own the safety and reliability of the systems they build while following your guidance.
Key Responsibilities:
Develop and Implement Quality Management Systems: Design, implement, and maintain quality management systems aligning with industry standards to ensure product quality and compliance. Ideally the candidate would have exposure to and an understanding of ISO 9001, AS9100, etc., though not a requirement. Utilizing and leading the implementation of tools such as DFMEAs, PFMEAs, and Control Plans to ensure system safety, quality, and reliability of Urban Sky's products from ideation through manufacturing and mission execution.
Safety and Quality Metrics: Monitor safety compliance and quality performance and implement systems necessary to track these metrics.
Problem-Solving and Root Cause Analysis: Identify quality issues, investigate their technical and systemic root causes, and lead the implementation of corrective and preventive actions (CAPA) to resolve them.
Management of Training Protocols: Develop training for staff on quality standards, best practices, and quality tools to ensure a culture of quality across all departments.
Supplier Quality Management: Collaborate with suppliers to ensure that raw materials, components, and services meet the required quality standards.
Continuous Improvement: Drive initiatives for continuous improvement in product quality, processes, and operational efficiencies, often using methodologies like Lean, Six Sigma, or Kaizen.
Compliance and Regulatory Requirements: Ensure that the organization complies with safety regulations, quality standards, and document compliance through reports and certifications.
Reporting and Documentation: Maintain records of safety critical decisions, risk management, quality inspections, audit results, corrective actions, and other documentation related to mission safety and quality control and report this information to upper management.
Safety & Mission Assurance: Lead safety reviews prior to stratospheric flights, lead the evaluation of mission successes and failures, and ensure lessons learned from ground and flight tests are incorporated into future missions.
Develop and Lead Mission Assurance Strategy: Define and implement a mission assurance program aligned with both internal performance requirements and external regulatory/contractual obligations (e.g., DoD, FAA, NASA).
Flight Readiness Reviews (FRRs): Coordinate and lead mission readiness evaluations.
Safety Program Development: Develop and maintain a flight safety management system, including ground operations, airspace integration, and recovery procedures.
Hazard Analysis: Perform and maintain System Safety Hazard Analyses (SSHA), Preliminary Hazard Analyses (PHA), and Operating Hazard Analyses (OHA) specific to balloon launch and recovery operations.
Qualifications:
Bachelor's or Master's degree in Electrical, Mechanical, Aerospace Engineering, Manufacturing, Quality Management, or equivalent experience.
Industry experience: 5-10+ years of experience in safety, quality, quality control, or quality assurance roles, with increasing responsibilities including management.
Communication skills: Ability to lead communication regarding safety and quality cross-functionally, including coordination between company leadership, product management, engineering, flight operations, and manufacturing. Maintain the authority and confidence to push back diplomatically yet firmly when safety or quality standards are at risk, ensuring alignment with Urban Sky standards and customer requirements.
Project management: Ability to lead quality and safety-related projects, coordinate cross-functional resources, track progress, and meet deadlines in a fast-paced environment.
Analytical skills: Ability to analyze data and generate reports on quality performance.
Nice-to-Haves/Preferred Skills:
Experience leading Safety & Mission Assurance activities for high-consequence systems or missions (e.g., flight readiness reviews, test/mishap evaluation).
Demonstrated ability to apply lessons learned from flight tests and operational feedback into engineering and procedural improvements.
Statistical tools: Proficiency with tools such as Minitab for statistical analysis of quality data.
Industry Standard Familiarity: Experience with quality management systems following standards outlined in ISO 9001, AS9100, or similar.
Capable of maintaining meticulous documentation of inspections, test results, risk assessments, safety reviews, and quality system records.
Requirements:
Must be US Citizen or Permanent Resident
Must be located near Denver, CO and must work at the company's Denver office.
Willing to consider relocation.
Benefits:
Salary $100,000 - $155,000 per year
We are required to post this salary range per Colorado law. Your salary will be determined based on your abilities and experience.
Stock Options
Medical, Vision and Dental
Unlimited Vacation Days
Cell Phone Bill Stipend
Maternity/Paternity Leave
Urban Sky is required to post this salary range per Colorado law. Your salary will be determined based on your abilities and experience.
Colorado Pay Transparency$100,000-$155,000 USD
We expect all team members to actively leverage and continuously adapt to emerging AI tools as a core part of their daily workflow. Proficiency with job-relevant modern AI tools (e.g., ChatGPT, Claude, GitHub Copilot) is expected and integral to success in this role.
NOTE: Research suggests that women and BIPOC individuals may self-select out of opportunities if they don't meet 100% of the job requirements. We encourage anyone who believes that they have the skills and the passion necessary to succeed here to apply for this role.
This position may require the candidate to deal with commodities, software, technology, defense articles, and/or technical data which are subject to the Export Administration Regulations and/or the International Traffic in Arms Regulations. Additional information may be requested so as to determine whether export authorization is required from the Bureau of Industry and Security and/or the Directorate of Defense Trade Controls. If authorization is required, employment will be contingent upon the Company successfully obtaining such authorization from the relevant government agency.
Urban Sky is an equal opportunity employer, and we value diversity. All employment is decided on the basis of qualifications, merit, and business need.
Manager, Regional Quality Assurance
Quality manager job in Platteville, CO
The position of Quality Assurance manager is responsible for all facets of the operation of the Quality Assurance and Food Safety functions across two Colorado locations: Platteville and Sterling. The duties expected include: accurate analysis of samples, recording of results and distribution of results to appropriate individuals, routine shipment of samples to outside laboratories for analyses not performed in house, monitoring product specifications and making changes in product specifications as needed, establishing wheat blends to meet specifications of flour to be produced, overseeing functional operation of regulatory programs to assure plant compliance, (including HACCP, GMP's, Master Sanitation Schedules, BRC standards and FDA standards), championing Root Cause/Corrective Action activities. monitoring effectiveness of recalls. Communicating with customers is a vital function performed by the Quality Assurance Manager. Communications include timely submitting of C.O.A.'s to the customer and answering customer questions and complaints.
The Quality Assurance Manager will lead all facets of the Quality Assurance Department including Quality Programs, Food Safety, Sanitation Programs, Customer Programs, Data Management, Process Improvement and Laboratory Analyses and will have a staff of Lab Technicians and Food Safety Supervisor working under their direct supervision to help accomplish the above responsibilities.
ESSENTIAL DUTIES AND RESPONSIBILITIES
include the following. Other duties may be assigned.
Actively lead and champion Root Cause identification and Corrective Actions.
Maintain adherence to the BRC Global Standard for Food Safety with annual certification including processes, programs, documentation and records.
Guide and lead the teams in areas of plant sanitation, regulatory inspections and program administration.
Collaborate with customer to effectively resolve any quality or food safety related customer complaint.
Monitor and report on quality standards, deviations, and cost/value opportunities for all products manufactured at the Platteville or Sterling facility.
Ensure quality control lab maintenance.
Lead initiatives to support Corporate Quality Assurance business plan and site programs such as safety and recognition.
Provide clear communication with all the key stakeholders to ensure QA vision is understood and implemented correctly.
Provide technical leadership and expertise within the field of Quality Assurance and Testing.
Ensure that production and other teams adhere to the principles, guidelines and best practices of the QA strategy as defined.
Direct activities of each plant's quality assurance team including selection, training and leadership, work schedules, vacations and assigning daily tasks.
Lead interviews, onboarding, training and performance evaluation of QA teams.
Be an escalation point for all matters related to testing and quality assurance and operate as a primary point of contact for QA teams.
Possess the ability to handle conflict effectively.
QUALIFICATIONS
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Bachelor's Degree in Food Science, Cereal Science, Biology, Chemistry, Milling Science or equivalent.
5+ years of laboratory Management, Quality Control or Quality Assurance experience.
Technical expertise in all aspects of quality, food safety and sanitation for food manufacturing.
Strong working knowledge of food plant operations, production equipment, cleaning and sanitizing procedures, and food quality standards such as HACCP, USDA, FDA, AOAC, FSMA
Decisive leadership skills and strong desire to take initiative.
Employee management experience including setting clear expectations, defining schedules and milestones, conducting performance reviews, developing career advancement plans, etc.
Clear track record of driving continuous improvement; Lean, Six Sigma, Kaizen, or CQE. certification is a plus. Must be able to apply mathematical concepts to practical operational situations.
Prior grain milling manufacturing experience is highly preferred.
Problem-solver with the ability to define problems, collect data, establish facts and draw valid conclusions. Formal root cause analysis training is a plus.
Self-motivated and capable of working independently to meet performance expectations across both locations.
PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Be able to stand and/or walk for extended periods of time
Occasionally required to bend, stoop, kneel crouch or crawl.
Routinely sits for long periods of time at a workstation.
Finger and hand dexterity to type at a keyboard, and to use laboratory equipment.
Vision requirements are close vision, distance vision, color vision and depth perception.
WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, exposure to routine dust and fumes common to cereal grain processing laboratories is common. Noise level with in the laboratory is moderate most of the time. Noise levels of over 90 decibels may be expected when in the production environment.
FOOD SAFETY/SECURITY REQUIREMENTS
The company is committed to producing and delivering defect-free products. To ensure this, all employees are required to be trained on and adhere to the Good Manufacturing Policies set forth by the Company as they pertain to personnel practices, equipment, and facilities. It is also vital that all employees be aware of their work environment and prevents any accidental or intentional adulteration of products produced at this facility.
Field Quality Manager
Quality manager job in Denver, CO
We're seeking a Field Quality Manager who's ready to put your skills to work on projects that matter - and build a career with a company that's building North America. Job Title: Field Quality Manager | Req ID: 15050 | HR Contact: Fredric Victor THOMPSON | Location: Acoma Office CO
ABOUT THE ROLE
Ensure accurate sample collection and quality control testing are performed for each manufacturing facility.
Provides verbal findings and written test results to management and production staff in a timely manner.
Assists Sales Manager with customer service issues as directed. Certifies results of laboratory findings as
needed. Supervises the Technicians across all sites. Ensures timely reporting of results, communication with
Operations and entry of data into Quadrel.
WHAT YOU'LL BE DOING
* Promotes Amrize's US Safety guidelines and standards as well as MSHA and OSHA
regulations, ensuring that safety and compliance requirements are met and followed at all times.
* Promote and adhere to Amrize's compliance policies.
* Report any violation immediately to senior management or through your compliance officer..
* Plant Control - Ensure that plant settings produce the products within specification. Report any
discrepancies to the facilities management & work with Operations to resolve any QC issues.
* Product Control - Ensures that all testing is conducted efficiently and consistently to ensure accurate
results. Ensure prompt communication of all results with Operations and entry into Quadrel.
* Customer Service - Assist in responding to customer concerns and complaints
* Examines laboratory samples to determine their physical and chemical properties. Uses a variety of
instruments and calculations to determine conformity. Performs various tests to make certain that
samples meet required standards.
* Ensures timeous feedback to customers with regards to customer complaints, working closely with the
relevant department for resolution.
* Works closely with Dispatch, Operations and sales colleagues to promote an effective work environment.
* Demonstrate a commitment to communicating, improving and adhering to health, safety and environmental policies in all work environments and areas. Promote a culture of safety and exhibit these behaviors.
WHAT WE'RE LOOKING FOR
Education: Bachelor's degree or 5 -7 years of equivalent experience
Additional Education Preferred: Master's degree
Field of Study Preferred: Engineering or Science
Required Technical Skills:· Microsoft Suite (Excel, Office, Powerpoint). Google Suite (Gmail, Spreadsheets, Documents, Drive), Quadrel SAP experience a plus
Additional Requirements:
* Successful candidates must adhere to all safety protocols and proper use of Amrize approved Personal Protection Equipment (PPE), including but not limited to respirators. Employees that are required to wear respirators must be clean shaven where the respirator seal meets the face in order to pass the qualitative and quantitative fit test.
WHAT WE OFFER
* Competitive salary
* Retirement Savings: Choose from 401(k) pre-tax and/or Roth after-tax savings
* Medical, Dental, Disability and Life Insurance
* Holistic Health & Well-being programs
* Health Savings Accounts (HSAs), Flexible Spending Accounts (FSAs) for health and dependent care
* Vision and other Voluntary benefits and discounts
* Paid time off & paid holidays
* Paid Parental Leave (maternity & paternity)
* Educational Assistance Program
* Dress for your day
This positon will remain open until 12/4/2025
Amrize is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
We thank all applicants for their interest; however, only those selected for an interview will be contacted.
BUILDING INCLUSIVE WORKSPACES
At Amrize, there is endless opportunity for you to play your part. Whether you're in a technical, managerial, or frontline role, you can shape a career that works for you. We're seeking builders, creative thinkers and innovators. Come put your expertise to work while developing the knowledge and skills to drive your career forward. With us you'll have the chance to build your ambition!
Amrize North America Inc. takes pride in our hiring processes and our commitment that all qualified applicants will receive consideration for employment without regard to age, race, color, ethnicity, religion, creed, national origin, ancestry, gender, gender identity, gender expression, sex, sexual orientation, marital status, pregnancy, parental status, genetic information, citizenship, physical or mental disability, past, current, or prospective service in the uniformed services, or any other characteristic protected by applicable federal, state or local law. Amrize North America Inc, and its respective subsidiaries are Equal Opportunity Employers, deciding all employment on the basis of qualification, merit and business need. Amrize Canada Inc. is committed to the principles of employment equity and encourages the applications from women, visible minorities, and persons with disabilities.
In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request accommodation in order to apply for a position with us, please email recruiting-accommodations@amrize.com. This email address should only be used for accommodations and not general inquiries or resume submittals. In Ontario, our organization/business is committed to fulfilling our requirements under the Accessibility for Ontarians with Disabilities Act. Under the Act, accommodations are available on request for candidates taking part in all aspects of the selection process.
While we sincerely appreciate all applications, only candidates selected for an interview will be contacted.
Quality Control Manager
Quality manager job in Westminster, CO
Please Note: To conform with the United States Government Space Technology Export Regulations, the applicant must be a U.S. citizen, lawful permanent resident of the U.S., conditional resident, asylee or refugee (protected individuals as defined by 8 U.S.C. 1324b(a)(3)), or eligible to obtain the required authorizations from the U.S. Department of State.
At CesiumAstro, we are developers and pioneers of out-of-the-box communication systems for satellites, UAVs, launch vehicles, and other space and airborne platforms. We take pride in our dynamic and cross-functional work environment, which allows us to learn, develop, and engage across our organization. If you are looking for hands-on, interactive, and autonomous work, CesiumAstro is the place for you. We are actively seeking passionate, collaborative, energetic, and forward-thinking individuals to join our team.
We are looking to add a Quality Control Manager to our team. If you enjoy working in a startup environment and are passionate about developing leading-edge electronics for satellites, spacecraft, and aerospace systems, we would like to hear from you.
JOB DUTIES AND RESPONSIBILITIES
* Establish and implement core production quality processes for new and scaling operations for assembly, integration, and test
* Grow and lead a team of quality engineers and inspectors to ensure operational execution and excellence.
* Determine assignments, responsibilities, and priorities for quality control personnel and ensure personnel training, certification, and qualification.
* Manage all aspects of production quality control, ensuring adherence to industry standards, company procedures, customer requirements, and AS9100 Quality Management System (QMS) requirements.
* Author, implement, and maintain quality documentation including written processes, procedures, inspection criteria, work instructions, production routings, etc.
* Define the required quality infrastructure, including layout and qualification of inspection areas, labs, nonconformance quarantine areas, and tool control.
* Support implementation of operations infrastructure including equipment preventive maintenance, calibration, and environmental controls.
* Drive root cause analysis and failure review for nonconformances and implement effective corrective actions to eliminate recurrence.
* Develop, drive, and assess quality objectives, measurable metrics, and continuous improvement initiatives.
* Ensure business systems (PLM, ERP, and MES) and tools are effective and available to support quality and production needs.
* Perform and support internal and external audits.
* Establish and maintain a training and certification program.
* Support continued compliance with all QMS requirements.
JOB REQUIREMENTS AND MINIMUM QUALIFICATIONS
* Bachelor's degree in engineering, quality, or a related technical field.
* Minimum of 7 years of experience in quality control or quality assurance within a manufacturing environment, with a minimum of 3 years in a leadership or management role.
* Deep understanding and experience in establishing and maintaining AS9100 Quality Management Systems for production environments.
* Expertise in root cause analysis methodologies and corrective action implementation.
* Proficiency in reviewing and interpreting engineering documentation, including drawings and schematics.
* Experience with aerospace and defense manufacturing.
* Demonstrated leadership, communication, and interpersonal skills.
$127,000 - $160,000 a year
CesiumAstro considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate's work experience, education/training, and key skills. Full-time employment offers include company stock options and a generous benefits package including health, dental, vision, HSA, FSA, life, disability and retirement plans.
CesiumAstro is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.
Please note: CesiumAstro does not accept unsolicited resumes from contract agencies or search firms. Any unsolicited resumes submitted to our website or to CesiumAstro team members will be considered property of CesiumAstro, and we will not be obligated to pay any referral fees.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Quality Manager
Quality manager 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
Auto-ApplyQuality Control Manager
Quality manager job in Denver, CO
Job Description
Quality Control Manager
Salary: $80/hr-$95/hr
Exp Federal is an established full-service architectural and engineering firm that provides a full range of exceptional design solutions and construction support to the federal government. Our team of professionals operates in some of the most challenging environments to provide support services to a variety of governmental agencies globally.
The Challenge:
Exp Federal is looking to add a part-time casual Quality Control Manager to join our growing team.
Principle areas of responsibility are:
Assure overall quality of contract deliverables and general contract compliance
Analyze and oversee the in-field inspections and repair processes that are taking place and offer suggestions to identify causes of defects or failures that occur during the project.
Provide quality control activities to monitor and record the results of quality assurance, measure quality performance levels and recommend necessary changes (corrective actions) to the overall quality management plan.
Suggest procedures for fault elimination.
Enter and review the results of corrective actions and produce Quality Control reports.
Perform Quality Control assessments and audits.
The Skills, Knowledge and Abilities We Seek:
Bachelor's degree in engineering, Construction Management, or related degree. Equivalent relevant experience may be considered in lieu of a degree.
Five or more years of quality control experience -related experience preferable with a US Government client or an equivalent combination of related education and experience.
PMP certification is a plus.
Ability to obtain and maintain US Security Clearance.
Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk or hear and taste or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus.
More About Us:
Exp Federal delivers full-service Architectural & Engineering and Construction solutions. You will be part of an expanding team that works collaboratively across our wider exp Federal design studios. As part of a project team, you will have the opportunity to work on a variety of projects that keep you engaged and showcase your individual talents. We believe in identifying potential in people and then providing opportunities to achieve success.
Our employees work on complex projects that require innovative, efficient solutions, and collaboration across various disciplines. Joining our team is a commitment to meaningful work supporting federal government clients across multiple sectors. Employees and clients alike will look to you for results that exceed their expectations.
Our Values:
Respect: We respect people, honor diversity, and treat each other fairly. These are the cornerstones of our culture and the key to our culture and the key to our ability to work successfully as a global team.
Unquestioned Integrity: We operate with the highest standards of honesty and responsibility - as individuals and as a corporation. We're people who meet routine, everyday obligations with honesty.
Safety: We place the highest priority on the health and safety of our employees and protection of our assets and the environment. Our goal is zero work-related injuries.
Customer Service: We listen and respond to the changing needs of our customers, the industry, and the environment, and draw upon lessons learned from our experiences around the world.
Impeccable Quality: We recognize that quality is fundamental in all our operations - it is everyone's responsibility. We have established procedures, assessments, and continuous improvement processes in place to ensure the quality of our work.
Sustainability: We understand the impact of our work on the environment and that sustainability is a part of everything we do. We work with customers to provide responsible, efficient, healthy, and effective project solutions to reduce our overall environmental impact.
What We Offer:
⌚ Exponential full-time professional growth and development
⏩ Fast-paced and professional work culture
???? ️Wellness reimbursement on fitness memberships and other qualified programs
???? Learning & Development tuition reimbursement
????️ Flexible work schedules
What Happens Next?
Our Talent Engagement Team will contact you via email to let you know what next steps at exp Federal look like for you! Make sure to check your spam. Don't worry, if you are not selected to move forward in the interview process, we will keep your resume on file for future opportunities you may be a better fit for.
*Actual compensation packages are based on several factors that are unique to each candidate, including but not limited to skill set, depth of experience, certifications, and specific work location. This may be different in other locations due to differences in the cost of labor.
Exp Federal is proud to be an Equal Opportunity Employer who fully and actively supports equal access for all people regardless of Race, Color, Religion, Gender, Age, National Origin, Veteran Status, Disability, and Family and Medical Leave.
U.S. Citizenship is required for our positions in accordance with 8 U.S.C. 1324b.2c.
Should you need any special accommodations, please feel free to contact us at ****************************** and we will arrange for the most suitable accommodations based on your needs.
Beware of Fraudulent Job Postings
Please be aware of recruitment scams where people or entities are misusing the name of exp Federal/exp Federal Pacific to post fraudulent job postings. We will never charge a fee for joining our company or to vet the authenticity of an employee or applicant.
Exp Federal | LinkedIn | ClearanceJobs | ADP Career Center
Quality Control Manager
Quality manager job in Golden, CO
The QC Manager is responsible for maintaining the quality and integrity of the compounded medications through managing product testing. In addition, they assist in all aspects of SOPs, testing, and inspections. The QC Manager demonstrates a commitment to the mission and goals of Belmar Select Outsourcing. This position is responsible for the direct supervision of Quality Control Personnel and reports to the Director of Quality.
RESPONSIBILITIES
Direct supervision of a team of Quality Control personnel, including incoming materials technicians, quality control technicians, and quality control specialists.
Correspond with contract laboratories to ensure timely receipt of results and direct path forward for OOS investigations.
Manage sample submission and results review for tests performed at contract laboratories on incoming materials and finished products.
Ensure timely processing of sterile loads to support product throughput.
Define team objectives to ensure business deliverables are met.
Ensure deviations, investigations, CAPA related to QC are closed in a timely manner.
Ensure compliance to 21CFR 210 and 21CFR211 for all activities performed in QC.
Represent QC in regulatory and state board of pharmacy audits.
Monitor performance by gathering relevant data and producing statistical reports.
Identify relevant training needs and delivering training.
Formulate and manage the development and implementation of goals, objectives, policies, procedures and systems pertaining to the QC.
Maintaining awareness of the business context and company profitability, including budgetary control issues.
Performs other duties as assigned.
PHYSICAL REQUIREMENTS
Additional Notes?
Must be able to work in a variety of positions and locations such as sitting, standing, squatting, kneeling, reaching, and walking, for prolonged periods of time
Must be able to wear required PPE for long periods of time when required.
Position requires handling of laboratory chemicals or hazardous materials.
Must be able to use necessary equipment such as computers, scanners, or other technology devices as assigned.
Quality Assurance Manager
Quality manager job in Denver, CO
Job Description
Job Title: Quality Assurance Manager
FLSA Status: Full Time - exempt Reports to: Divisional Social Services Secretary
Schedule: Full Time
Rate of Pay: $95,000
Benefits: Standard; Full-Time, Exempt employees are eligible for but not limited to the following:
Health, vision, dental, life as well as voluntary life and disability insurance
Sick leave benefit - 1 day per month, 12 sick days per year (accrual and availability begins at hire)
Vacation benefit - 20 vacation days per year, accrued at the rate of .0769 hours for each hour worked (accrual begins at hire but may not be used until the completion of six months of employment)
One floating day off for use (accrued immediately, and again annually, but may not be used until the completion of the initial three-month introductory period of employment)
Pension Plan (after one year of continuous service)
Voluntary Tax-Deferred Annuity Plan (403(b)plan)
Position Summary
Quality Assurance Manager provides leadership in evaluation, compliance, and continuous improvement for social service programs across the Intermountain Division. This role oversees divisional systems to measure program quality, effectiveness, and compliance while driving innovative solutions to improve outcomes. The Manager also provides supervisory oversight of the divisional training function, ensuring staff receive appropriate onboarding, professional development, and compliance training. Direct supervisory responsibility includes the Divisional Database Compliance Administrator and the Financial Management, Mission Integration specialist, and Grant Compliance Specialist. In collaboration with the Director of Programs, this position will jointly provide leadership to the Divisional Social Services team.
Key Responsibilities
Quality Assurance
• Create and implement objective performance measurement systems across all program sites to assess program quality and effectiveness.
• Monitor compliance with divisional, territorial, and national standards as well as contract and regulatory requirements.
• Collaborate with program managers to review and evaluate compliance with National Social Services Standards (NSSS).
• Oversee the review and updating of policies and procedures to ensure alignment with TSA standards and divisional guidance.
Mission Impact Evaluation
• Develop and oversee a divisional evaluation framework to assess program health and effectiveness including guest experience, financial stability, policy compliance, and missional relevancy.
• Conduct onsite visits with local units, produce action plans, and track follow-up progress with Corps Officers and staff.
• Compile annual reports of program evaluations and consultation outcomes for Divisional Commander and leadership teams.
Innovation & Continuous Improvement
• Lead program evaluations and needs assessments to identify opportunities for service innovation and improved outcomes.
• Analyze client feedback, survey data, and divisional performance metrics to recommend system-wide improvements.
• Promote innovation by identifying and implementing best practices and evidence-based approaches across divisional programs.
• Build feedback loops to connect frontline insights with divisional strategic planning
• Support concept development, new program prototyping, and scaling of effective models
Supervision of Training & Compliance Functions
• Directly supervise the Divisional Database Compliance Administrator and the Financial Management and Grant Compliance Specialist.
• Oversee the divisional training function to ensure staff receive required onboarding, compliance training, and professional development aligned with divisional priorities.
• Support the integration of training and compliance outcomes into broader evaluation and quality assurance processes.
• Ensure supervisory staff adhere to TSA policies and contribute to a culture of continuous improvement.
Qualifications
Education & Experience
• Bachelor's degree in Social Work, Nonprofit Management, Public Administration, or related field required;
• Master's preferred.
• 7 - 10 years of experience in program evaluation, compliance, quality assurance, or related roles in nonprofit or social services.
• Supervisory experience required, with ability to oversee data compliance, financial/grant management, and training functions.
• Experience fostering innovation and implementing data-driven solutions.
Skills & Competencies
• Expertise in compliance monitoring, program evaluation, and outcome measurement.
• Strong analytical and problem-solving skills with the ability to develop innovative solutions.
• Excellent written and verbal communication skills, with ability to present findings to leadership and external stakeholders.
• Ability to foster collaboration across departments and promote continuous improvement.
Other Requirements
• Minimally 21 years of age and possessing a valid, in-state driver's license
• Commitment to The Salvation Army's mission and values.
• Willingness and ability to travel extensively (50-60%).
Quality Manager CNC Machine Shop
Quality manager job in Longmont, CO
Job DescriptionBenefits:
401(k)
401(k) matching
Competitive salary
Dental insurance
Health insurance
Paid time off
Training & development
Quality, On-time Delivery and Customer Satisfaction are of the upmost importance to MBK Machine. The duties of this job are to maintain & continuously improve these metrics where possible. The duties of the quality manager are to oversee quality operations, ensure excellent quality control of product and maintain and uphold the quality management system.
Responsibilities of the position:
Performing quality inspection, applying quality inspection techniques, and identifying nonconforming hardware.
Measure parts using most applicable method and ensure other inspectors are up to date on best measurement practices.
Perform first article inspections, in-process inspections, and final inspections.
4. Perform quality planning along with creation of bubble prints and required QC documentation to customer specifications.
5. Review outside processing certs and material certs for conformance.
6. Program and operate Coordinate Measuring Machines (CMM) to ensure the quality of our products meets customer and industry standards.
7. Record and log measurements for parts on AS9102 Form.
8. Oversee and coordinate quality operations and activities pertaining to our QMS system (Nonconformance logging, corrective actions, maintain calibration list, etc.) and serve as the QMS lead.
9. Act as the main point of contact in the quality lab for other inspectors as well as a liaison between the quality department & shop operations.
10. On board and train new quality employees to current MBK Machine quality practices.
11. Offer solutions to advance the progress and modernization of the quality department.
12. Safely working within a manufacturing environment.
13. Troubleshoot and resolve issues in a timely fashion.
Authorities: Instruct all levels of Operators, Setup and Programmers as needed to assure product quality as well as Quality Inspector Levels 1 & 2.
Required Education: High school diploma or GED. Bachelors degree preferred.
Experience: 3-5 years minimum.
Compensation for the position:
MBK Machine would like to offer the quality manager position at a compensation rate of $30-40/hr (depending on technical knowledge, capability and experience) with a pay evaluation after 60 days of employment. This would be a full-time position Monday-Friday. After 30 days of employment, we would start the following benefits:
6% dollar for dollar 401K company match
80 hours paid vacation
20 hours sick pay in case of emergency
Cover half of medical insurance premium
Cover half of Dental premium
QA Manager
Quality manager job in Denver, CO
The QA Manager has responsibility for setting the direction for our quality approach across the delivery teams. Specifically, these responsibilities include: •Provides the technical leadership in the definition, development and maintenance of the testing environments
•Provide Innovative test strategies and solutions to support successful product delivery
•Mentor and guide members of the QA teams
•Provides technical product and process guidance to other QA team members
•Partners with Product Management and Delivery teams throughout the software lifecycle
•Demonstrates agility, ability to foster and engage in healthy conflict, mentorship, ability to remove obstacles, and creates clarity from ambiguity
•Stays abreast of quality practices and techniques evangelizes such with the greater team
Qualifications
Key Skills
•Domain knowledge of the business in order to provide guidance to testers around what needs to be tested
•Strong analytical abilities
•Team building skills and coaching skills
•Ability to mine and analyze test results
•Automation scripting and framework skills
Additional Information
All your information will be kept confidential according to EEO guidelines
Manager, Supplier Quality (Medical Devices)
Quality manager job in Lakewood, CO
Play a key role ensuring the highest standards of quality and reliability for life-changing medical technologies. My client designs and manufactures advanced devices used in critical blood and cell therapies, and this position leads the supplier quality function for extrusion components that directly impact patient outcomes worldwide. This is your chance to shape supplier excellence, collaborate across global teams, and drive continuous improvement in a mission-driven organization advancing healthcare with heart.
Why You Should Apply
Lead supplier quality for a globally recognized medical technology manufacturer
Influence strategy across engineering, sourcing, and quality teams
Collaborate with top industry talent focused on innovation and patient safety
Comprehensive health, wellness, and retirement benefits with strong work-life balance
What You'll Be Doing
Develop and execute supplier quality strategies for extrusion commodities
Conduct supplier audits and assess compliance with quality and regulatory standards
Lead supplier performance monitoring, metrics, and corrective action initiatives
Partner with sourcing and engineering teams on supplier selection and development
Mentor team members and champion continuous improvement across the supply base
About You
Be able to do the job as described
Deep expertise in extrusion processes and supplier quality management
Skilled in cross-functional collaboration and executive communication
Experienced in medical device quality systems and global regulatory standards
Certified or trained in Six Sigma or Quality Engineering preferred