Quality manager jobs in Fort Collins, 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 ****************************** .

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.

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 (**************************************** .

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.

Full-time Description Pilatus is hiring a Director Quality & Safety to join our team in Broomfield, CO. In this role, you will be responsible for overseeing all quality assurance and regulatory compliance activities for U.S.-based operations, including FAA Repair Stations (Part 145), Production (PMA/Part 21), EASA Part 145/21, and Safety Management Systems. This leadership role ensures alignment with global quality standards and drives continuous improvement across product quality, supplier performance, and internal compliance systems. Take your career to the next level with Pilatus Business Aircraft Ltd! Essential Duties/Responsibilities Ensures full compliance with requirements of FAA (14 CFR Part 145, Part 21, Part 43) and EASA Part 145/21 Maintains and develops the Quality Management System (QMS) and Safety Management System (SMS), ensuring integration across repair station, completions, and production operations Leads Quality strategy for North American supplier base Implements and oversees a risk-based supplier evaluation and audit program, including source inspections, supplier scorecards, and corrective action follow-ups Collaborates with Procurement and Engineering to resolve supplier non-conformances and drives root cause and CAPA initiatives Directs a multi-disciplinary Quality team including Production Inspection, Final Inspection, Seat & Paint Inspection, and Special Projects Provides mentorship, training, and performance management for Quality team personnel Coordinates cross-functional quality initiatives with Swiss headquarters (Pilatus Aircraft Ltd.) to align with global standards and system upgrades Drives continuous improvement through data analysis, trend monitoring, and cross-functional collaboration with Production, Engineering, and Flight Operations Oversees internal regulatory authority audits including preparation, identification, and investigation of non-conformance issues, and the application of corrective or preventive actions Requirements Skills/Qualifications Bachelor's degree in Engineering, Aviation Maintenance, or related technical field (Master's preferred) Knowledge of EASA Part-21 and 14 CFR Part 145 and Part 21 regulations is required Experience with Safety Management Systems within Aviation Minimum 7 years general aviation industry experience Previous supervisory experience required Demonstrated experience with project management and implementation of companywide processes Proficiency in MS Office software including Outlook, Word, PowerPoint, and Excel Excellent problem-solving, organization, communication, writing, and presentation skills Willingness and ability to travel both domestically and internationally, at times on short notice What We Offer 11 paid holidays a year, plus 15 days of paid vacation time, and 6 days of paid sick/personal time to start with an increase to 20 days of paid vacation time after 5 years with Pilatus 90% of medical, dental, and vision premiums paid for single coverage and 80% for family coverage, averaging $9,600 annually Monthly health savings account (HSA) contributions totaling $2,250 for single coverage and $3,000 for family coverage annually 401(k) retirement plan matching up to 6% Life and long-term disability insurance premiums paid in full Tuition assistance available annually after the first year The salary range for this position is $105,975 - 150,418 per year depending on experience. Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data. Pilatus Business Aircraft Ltd was founded in Broomfield, Colorado in 1996. Pilatus' new 118,000 square foot facility is custom-designed to conduct aircraft interior and exterior completions for all PC-12 PRO and PC-24 aircraft delivering to North and South America. This new completions center consolidates the operations Pilatus has performed at the Rocky Mountain Metropolitan Airport for over 20 years. With over 3,000 employees and about 200 apprentices at its headquarters in Stans, Switzerland and completion center in Broomfield, Colorado, the Pilatus family unites people from over 40 countries. We offer a secure, innovative, international, and sustainable work environment. Courage, vision, and outstanding performance have made us a strong company. Our culture is shaped by a high level of quality awareness, close customer relationships, and a high degree of employee commitment. Pilatus Business Aircraft Ltd provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. To submit a paper application, please mail your resume to 12300 Pilatus Way, Broomfield, CO 80021 Attention: Human Resources. No walk-ins please. If personalized assistance is needed to complete an online application for this position, please email ********************************** with your request. Salary Description $105,975 - 150,418 / Year

Vitesse Systems is looking for a Quality Manager to join the team in Longmont, Colorado! The Quality Manager is the independent owner of the Mission of QA, which is to verify compliance of all product and processes, and facilitate company-wide process improvement. About Vitesse Systems Vitesse Systems is a leading provider of highly engineered antenna, thermal management, and mission critical solutions used in radar, electronic warfare and C5ISR applications. No challenge is too difficult for the Vitesse Team. From complex specification driven requirements to precision manufactured components, Vitesse Systems has the experience and expertise needed to execute. Our Core Values Our core values of Integrity, Initiative, Impact, and Integration translate to an environment where every team member is valued and rewarded. The mission-critical solutions we design and manufacture at Vitesse make our country and our world safer. Our Benefits 3 Weeks of Paid Time Off 10 Paid Company Observed Holidays Birthday & Anniversary Incentives 401K Employer Match Medical, Dental and Vision Insurance Company-paid Life Insurance Company-paid Short & Long-term Disability Continuing Education Reimbursement Program Generous Referral Program The Role This leader is responsible for measuring and reporting successful realization of the QA mission to on-site and platform-level management. Successful leadership of this business unit involves effective management of People, Processes, and Performance in QA and across the company. The compliance and regulatory environment includes AS9100 compliance, Nadcap compliance, and wide-ranging customer-specific requirements. Customer-specific requirements include DoD requirements, aerospace prime manufacturer requirements, and various R&D and commercial manufacturer requirements. Key Responsibilities Safety and 5S measures 5S of QA rating as world class Safety culture and environment in QA world class Quality measures: Company warranty returns below goal QA escapes below goal No Major customer and external audit findings Delivery measures: Internal audit completion on time Nonconformance process cycle time below goal Management QMS review completion on time Cost control measures: Inspection budget vs actual hours below goal QA direct time vs indirect time below goal QA direct time vs manufacturing direct time below goal Cost of Poor-Quality reported company-wide to facilitate department-specific improvements Other duties as assigned Qualifications & Experience B.S. Degree in an Engineering or related discipline 3-5 years of Quality, Engineering, or related experience including MRB authority/participation. Knowledge of International Standard ISO 9001 and AS9100 Quality Management Systems AS9100 Lead Auditor certified highly desired Experience in Aerospace Industry Certification by the American Society for Quality (ASQ) as a Certified Quality Engineer (CQE), Certified Six Sigma Black Belt (CSSBB), or Certified Quality Manager (CQMgr) preferred Knowledge of manufacturing and quality practices Experience with quality improvement tools and techniques (i.e., Lean, Six Sigma, Statistical Process Control, and Failure Mode & Effects Analysis) Detailed familiarity with ISO 17025 and ANSI Z540 Detailed familiarity with CMM programming Detailed familiarity with drawing review with specific GD&T experience Ability to obtain a DoD Secret clearance Demonstrated leadership, project management, facilitation, and problem-solving skills Excellent communication skills (oral and written) for liaising and communicating with customers, and internal departments Standard development and implementation Process Improvement Ability to multi-task, make decisions, and maintain accountability Ability to interface directly with cross-functional teams and to build and maintain lasting relationships with other departments and key business partners Ability to motivate, lead, and manage employees Must provide proof of eligibility to work in the United States. Ability to pass a drug screen per Vitesse's drug testing policy. Ability to pass a criminal background check per Vitesse's policy. Vitesse Systems, LLC performs work controlled by the International Traffic in Arms Regulations (ITAR) and Export Administration Regulations (EAR). These statutes require the protection of technical data and products. The regulations require that such data not be disclosed in written, oral, or visual form to any foreign national without prior export authorization from the Department of State. A foreign national is defined by the U.S. Government under EAR 734.2(b)(2)(ii) and 8 USC 110 (a)(20) as one who: Is not a United States citizen Is not lawfully admitted for permanent residence in the U.S. Does not have politically protected status (embassy, refugee, or asylum) Vitesse Systems, LLC is an Equal Employment Opportunity / Affirmative Action (EEO/AA) Veterans / Disabled Employer.

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.

The Blackhawk Group is an Equal Opportunity Employer. Compensation Range: 140-180 k (Depending on Experience)

We are seeking a dedicated Quality Control Manager to support a significant underground utilities project in Longmont. This project involves the replacement of 4-5 miles of underground utilities, including gas, storm, and sanitary systems. **Responsibilities** + Ensure full on-site presence during construction to oversee quality procedures and ensure compliance with project specifications. + Oversee a utility subcontractor team of 10-20 people. + Provide client-facing updates to the FAA on the project schedule. + Perform daily inspections and maintain a detailed log of inspections. + Create and manage quality control reports. **Essential Skills** + Experience in 3-phase quality control procedures. + Knowledge of construction and construction inspection. + Familiarity with USACE standards and civil construction. + Experience with utility superintendent roles. + Holds QCM or CQM-C certification. **Additional Skills & Qualifications** + Minimum of 5 years of experience as a superintendent or QCM on federal projects. + Experience overseeing civil scopes of work or underground utility projects. + Proficiency in Microsoft Office software, including Outlook, Word, Excel, and MS Projects. **Why Work Here?** Join a tribally owned business based in Golden, CO, known for consistent federal projects and a supportive work environment that values its employees. **Work Environment** This position requires 100% on-site presence during construction. When not on-site, you will work out of the Golden, CO office. Relocation and per diem benefits may be available for the right candidate. **Job Type & Location** This is a Contract to Hire position based out of Longmont, CO. **Pay and Benefits** The pay range for this position is $48.00 - $70.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) **Workplace Type** This is a fully onsite position in Longmont,CO. **Application Deadline** This position is anticipated to close on Dec 16, 2025. **About Aerotek:** We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry - from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies' construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow. Aerotek offers weekly pay, employee benefits including medical, dental & vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts. The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Job Description Umoja Biopharma is a game-changing biotech start-up with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington, and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting edge drug development. We are committed to the principles of Diversity Equity and Inclusion and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja as a leader in this front. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families. Umoja Biopharma - Your Body. Your Hope. Your Cure. POSITION SUMMARY Umoja Biopharma is seeking a highly motivated individual to join our growing Quality Assurance team. This individual will play a key role in Umoja's state-of-the-art lentiviral vector development and internal GMP manufacturing facility, The CLIMB in Louisville, CO. In collaboration with Quality management and multiple functions, this individual will execute, mature, and drive continuous improvement of key quality systems and associated records (e.g., deviations, CAPA, change controls, product complaints, etc.) utilizing a phase appropriate, risk-based approach as the Quality Assurance Subject Matter Expert (SME). Additionally, this role will collaborate with cross-functional teams to ensure quality requirements are defined, clearly communicated and understood, and met as part of routine and advancing GMP operations. This is a full-time onsite role based out of our Louisville, CO GMP manufacturing facility. CORE ACCOUNTABILITIES Specific responsibilities include: Effectively contributing within a high-performing GMP QA team, fostering a culture of quality, accountability, collaboration, and organizational flexibility & adaptability in alignment with Umoja's values & principles and Umoja's quality culture Independently provides Quality Assurance oversight and direction in support of Quality Record execution (Deviations, CAPAs (Corrective and Preventive Actions), Change Controls, and product complaints) in support of internal GMP manufacturing operations Reviewing and approving Deviations, CAPAs, and Change Controls and other Quality Records Performing assessments and investigations related to product complaints in close coordination with Quality management Collaborating closely with key stakeholders and Quality management to define key performance indicators and metrics for quality systems performance, identifying and driving continual improvement Developing visual management tools and other business processes to increase effectiveness and efficiency of quality record management and execution in compliance with approved procedures and standards Developing and delivering training materials to key stakeholders on core quality systems Identifying and driving updates to electronic quality systems, where necessary, to increase effectiveness and efficiency of system usage and align with quality system continual improvement Compiling and arranging applicable metrics and data in support of Quality Management Review Providing support during preparation and execution of audits and inspections Supporting continuous improvement and maturation of core Quality Systems Interfacing and effectively collaborating and communicating with other departments (e.g., Supply Chain, Process Sciences, Facilities, Validation, Manufacturing, and Quality Control) to ensure compliance with all applicable procedures, policies, and standards Owning, reviewing and approving SOPs, work instructions, and other controlled documents related to operations and other cGMP activities May assist with material and product disposition, as needed. Other duties as assigned The successful candidate will have: Bachelor's degree in Engineering, Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or other life science with minimum of 7 years of work experience in GMP biotech or pharma setting. Equivalent combination of education and experience will be considered. Knowledge and understanding of regulatory governing bodies, phase-specific cGMP requirements, guidance documents, laws, and regulations, and how to practically apply these in GMP manufacturing environment to ensure quality and compliance Phase-appropriate cGMP knowledge, experience, and effective and consistent risk-based approach to quality system establishment, execution, and maturation Extensive experience with quality oversight, review, and approval of investigations/deviations, CAPA, and change control using a phase-appropriate approach Experience with, and proficiency in, product complaints processes and performing associated investigations Experience using and maturing electronic quality systems in support of internal GMP manufacturing operations (e.g., Veeva. Trackwise) Strong understanding of unit operations and processes supporting GMP manufacturing operations in an aseptic environment Strong history of successfully leading and implementing operational excellence initiatives and process simplification related to Quality Systems Proficiency in developing effective, concise training materials and delivering Instructor-Led training to audiences varying in size Independent and risk-based decision-making capability with clear understanding of decision-making impact in dynamic environment. Ability to work and communicate effectively and efficiently in a collaborative manner across multiple functional areas Previous experience participating in partner audits and health authority inspections Experience with material and product disposition to drive at material disposition impact assessment and support disposition-related activities Preferred Qualifications: Experience in cGMP cell and gene therapy manufacturing across all phases of development (i.e., Phase 1 through commercial) Experience with Lean and/or Six Sigma quality system methodologies Physical Requirements: Ability to gown aseptically and work in a Clean Room environment Ability to work while gowned for extended periods of time, including standing for extended periods of time. Ability to sit in office setting for extended periods of time Ability to work weekends or evenings as needed Salary: $105,060 - $129,780 Benefits Offerings Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.

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

Established in 1991, Collabera has been a leader in IT staffing for over 22 years and is one of the largest diversity IT staffing firms in the industry. As a half a billion dollar IT company, with more than 9,000 professionals across 30+ offices, Collabera offers comprehensive, cost-effective IT staffing & IT Services. We provide services to Fortune 500 and mid-size companies to meet their talent needs with high quality IT resources through Staff Augmentation, Global Talent Management, Value Added Services through CLASS (Competency Leveraged Advanced Staffing & Solutions) Permanent Placement Services and Vendor Management Programs. Collabera recognizes true potential of human capital and provides people the right opportunities for growth and professional excellence. Collabera offers a full range of benefits to its employees including paid vacations, holidays, personal days, Medical, Dental and Vision insurance, 401K retirement savings plan, Life Insurance, Disability Insurance. Job Description Design and deliver the medical device and supplies breakthroughs that make a difference in the lives of millions of patients. Responsible for ensuring that software used in the development, manufacturing and as part of medical devices is developed according to good design practices and follows the corresponding requirements set forth by local procedures, regulatory authorities and notified bodies. Provide leadership, oversight and training to division manufacturing plants for computerized system validation. Mentor design teams on quality systems and requirements. Qualifications • Working knowledge of the FDA Quality System Regulation, ISO 13485, and the Medical Device Directive • Skilled in product risk assessment (ISO 14971), requirements management and tracing, defect tracking, configuration management techniques, and knowledge of how these are applied in the software development lifecycle • Experience in Agile software development techniques and IEC 62304 requirements, versed in guidance documents such as TIR-45, IEC TR 80002-1 and Cyber security guidance from FDA • Understanding of current Software Quality techniques, software industry standards (e.g. ISO, IEEE, CMMI), and FDA Quality System Regulations and their impact on internal procedures, software quality, safety and efficacy of products • Experience in risk evaluation techniques, such as Product Risk Assessment and FMEA including software risk assessment and software FMEA • Familiar with reliability analysis and test methods, including software reliability modeling • Working knowledge of C and C++ • Good verbal (including presentation) and written communication skills • Ability to effectively work on project teams. Additional Information To get further details or to schedule an interview please contact: Shristi Kshmata ************ ********************************

Sierra Space Careers: At Sierra Space, we build the missions and systems that keep our world secure in the domain above Earth. Sierra Space team members share a spirit of innovation and collaboration and a belief that we can deliver on the boldest missions in space today. Together with our customers, we aim to safeguard our nation, sustain human presence in space, and secure the freedom of operations in low Earth orbit and beyond. Our success is measured by the trust of those who rely on what we build and deliver, and our technologies keep the United States and its allies mission-ready throughout space. We are mission-driven, and together, we are an extraordinary team. About the RoleThe Quality Engineer II is responsible for designing, implementing, and maintaining quality assurance protocols and methods for processing materials into partially finished or finished products. This role involves planning, implementing, and managing compliance of manufacturing and production processes with internal and external safety, quality, and regulatory standards requirements for worldwide distribution. The engineer will design methods and procedures for inspecting, testing, and evaluating the precision and accuracy of production processes, production equipment, and finished products. This role involves designing, implementing, and maintaining quality assurance protocols and methods for processing materials into partially finished or finished products. It requires planning, implementing, and managing compliance of manufacturing and production processes with internal and external safety, quality, and regulatory standards to meet requirements for worldwide distribution. The role also includes designing methods and procedures for inspecting, testing, and evaluating the precision and accuracy of production processes, equipment, and finished products. Responsibilities include conducting inspections and tests to ensure products meet quality standards and specifications, analyzing data to identify trends, and recommending improvements in production processes and quality assurance protocols. Collaboration with cross-functional teams is essential to address quality issues and implement corrective actions. Additional duties include documenting quality assurance activities, maintaining accurate records, and utilizing knowledge of electrical and mechanical drawings along with familiarity with Geometric Dimensioning and Tolerancing (GD&T). The position also ensures compliance with IPC and NASA requirements, applies understanding of Root Cause and Corrective Action (RCCA) and Corrective and Preventive Action (CAPA), and actively participates in Corrective Action Reports (CAR). Finally, the role involves participating in internal audits and applying basic internal audit training.About You Our mission is driven by an unyielding commitment to advancing space-based technology in service of our customers and safeguarding national security. We seek individuals who are passionate about innovating beyond boundaries and relentlessly pursuing solutions that protect, preserve and empower - to join us in this critical mission. We're looking for team members who align with our values, mission and goals - while also meeting the minimum qualifications below. The preferred qualifications are a bonus, not a requirement. Minimum Qualifications: Requires Bachelor's degree in a related field (or equivalent work experience in lieu of degree). Typically 2+ years of related experience. Basic understanding of Root Cause and Corrective Action (RCCA) and Corrective and Preventive Action (CAPA). Basic Internal Audit Training. Preferred Qualifications: Certifications in quality assurance or inspection (e.g., ASQ Certified Quality Engineer). Experience in a manufacturing or quality assurance environment. Proficiency with quality management systems and standards (e.g., ISO 9001). Experience with advanced quality assurance tools and techniques, such as Failure Mode and Effects Analysis (FMEA) and Statistical Process Control (SPC). Familiarity with quality management software and databases. Strong analytical and problem-solving skills. Excellent communication and interpersonal skills. Ability to work independently and as part of a team. Experience conducting internal audits and implementing corrective actions. Compensation: Pay Range: $78,925.00 - $108,542.50 Your actual base compensation will be determined on a case-by-case basis and may vary based on job-related knowledge and skills, education, experience, internal equity and market competitiveness. Elevate Your Career At Sierra Space, we are committed to your personal and professional development. We empower you to make profound and meaningful contributions and foster a vibrant culture of collaboration, where teamwork ignites breakthrough innovations. We also offer a generous benefit package, including medical, dental, and vision plans, 401(k) with 150% match up to 6%, life insurance, 3 weeks paid time off, and more. Sierra Space is an industry-leading space and defense technology company providing satellites, spacecraft, and enabling mission systems and components. We deliver mission-proven technologies to our customers that safeguard our nation, protect space-based assets and enable space exploration. Application Deadline: This role will remain posted until a qualified pool of candidates is identified. Please note: Sierra Space does not accept unsolicited resumes from contract agencies or search firms. Any unsolicited resumes submitted to our website or to Sierra Space team members not through our approved vendor list or Talent Acquisition will be considered property of Sierra Space, and we will not be obligated to pay any referral fees. Sierra Space Corporation is an equal opportunity employer and is committed to working with and providing reasonable accommodations to applicants with disabilities. If you need special assistance or a reasonable accommodation related to applying for employment with Sierra Space or at any stage of the recruitment process, please contact us.

Who we are: We're transforming one of the world's oldest industries with cutting-edge technology and an innovative approach. Backed by top-tier investors and recognized by Time as one of the "best Inventions of 2024" and Fast Company as one of 2024's "Next Big Things in Tech", Electra is scaling rapidly and we're looking for bold, driven individuals to help us reshape the future of iron production. If you're ready to make a real impact in a company that's redefining heavy industry for a cleaner, smarter world, we want to hear from you. What you will do: The Quality Engineer II is responsible for assisting the Quality Manager in planning, implementation, and management of various aspects of the quality management system. This role will collaborate cross-functionally with engineering, design, and other stakeholders to uphold quality standards, drive process improvements, and maintain compliance throughout project lifecycles. Responsibilities include: Collaborate with project teams to develop and maintain project quality documentation, including quality control plans, inspection checklists, and inspection test procedures (ITP). Coordinate with suppliers and contractors to ensure timely resolution of quality issues and adherence to project schedules. Visit suppliers, as appropriate, to understand capabilities. Operate effectively and safely in a fast-paced startup environment, balancing structured quality systems with flexibility to support rapid prototyping, scale-up, and evolving production needs. Review quality-related documentation, such as quality control plans, procedures, and test protocols. Ensure proper documentation and traceability of quality records, including non-conformance reports, inspection reports, and corrective action reports with vendors and contractors. Support Electra's transition from pilot to Beta Plant operations by documenting, standardizing, and scaling inspection methods and quality processes to handle increased throughput. Maintain accurate records of all quality activities, ensuring traceability and readiness for audits or client reviews. Review and provide feedback for drawings with design engineers to ensure parts are inspectable. Partner with engineers to design measurement fixtures for inspections. Consolidate measurement data to collaborate with engineers for design improvements Partner with manufacturing engineers and technicians to validate processes, ensure inspection methods are practical for production use, and resolve quality issues at the point of manufacture. Train and mentor technicians on inspection methods, defect identification, and proper documentation practices to ensure consistent quality execution on the shop floor. Develop and maintain controlled inspection plans, checklists, and process sheets for technician use, ensuring consistency and traceability across production. Expand use of quality dashboards to include defect tracking, Pareto analysis, and real-time visibility tools that provide manufacturing and engineering teams with actionable insights. Conduct internal and external audits to ensure ongoing compliance. Other Quality support, as necessary, to support the Quality team and Electra team members. Operate safety around hazardous materials. What we need you to bring to the team: Bachelor's degree in Engineering (Mechanical or Design preferred) or a related technical field 2+ years of experience in quality assurance or quality control within a regulated environment Proven experience working with Quality Management Systems such as ISO 9001 or IATF Strong knowledge of quality management principles and methodologies Demonstrated ability to develop and execute quality plans, perform data analysis, conduct inspections, and manage non-conformance processes Excellent analytical and problem-solving skills with strong communication abilities Collaborative mindset with experience working across multidisciplinary teams Familiarity with document control systems, inspection techniques, and testing methodologies Certification in quality engineering (e.g., ASQ CQE) is considered an asset Develops professional expertise and applies company policies and procedures to resolve a variety of issues Determines course of action based on guidelines and modifies processes and methods as required Works on problems of moderate scope that are varied and routine, requiring analysis of multiple factors Exercises judgment within defined procedures and practices to determine appropriate action Applies learned techniques and contributes to analysis and investigation to solve problems Receives minimal instruction on day-to-day work and general guidance on new assignments Builds productive internal and external working relationships to resolve mutual problems Focuses on providing standard professional advice and creating initial reports and analyses for review by senior team members Compensation: The anticipated starting pay range for this position is $80,000-$90,000 and may be more or less depending upon skills, experience, and education. Benefits For You: 100% paid premiums across all medical, dental, vision, telemedicine, short-term disability, long-term disability, and basic life insurance plans Reasonable use PTO $1,800 in annual employer HSA contributions (health savings account) Benefits For Your Family: 100% paid premiums across all medical, dental, vision, and telemedicine plans 12 weeks of paid parental leave Benefits For Your Future: 401k with up to 5% matching contributions which vest 100% on day one Eligibility for incentive stock options If you need an accommodation during the application or interview process, reach out to us at careers@electra.earth We're here to help.

360 IT Professionals is a Software Development Company based in Fremont, California that offers complete technology services in Mobile development, Web development, Cloud computing and IT staffing. Merging Information Technology skills in all its services and operations, the company caters to its globally positioned clients by providing dynamic feasible IT solutions. 360 IT Professionals work along with its clients to deliver high-performance results, based exclusively on the one of a kind requirement. Our services are vast and we produce software and web products. We specialize in Mobile development, i.e. iPhone and Android apps. We use Objective C and Swift programming languages to create native applications for iPhone, whereas we use Android Code to develop native applications for Android devices. To create applications that work on cross-platforms, we use a number of frameworks such as Titanium, PhoneGap and JQuery mobile. Furthermore, we build web products and offer services such as web designing, layouts, responsive designing, graphic designing, web application development using frameworks based on model view controller architecture and content management system. Our services also extend to the domain of Cloud Computing, where we provide Salesforce CRM to effectively manage one's business and ease out all the operations by giving an easy platform. Apart from this, we also provide IT Staffing services that can help your organization to a great extent as you can hire highly skilled personnel's through us. We make sure that we deliver performance driven products that are optimally developed as per your organization's needs. Take a shot at us for your IT requirements and experience a radical change. Job Description Medical Device sytems testimg Experience. Systems V&V experience in white & black box Testing.embedded systems is must Navigation experience is advantage. Additional Information Unfeigned Regards, Preeti Nahar | Sr. Technical Recruiter - TAG US | 360 IT Professionals Inc. O: 510-254-3300 EXT 140

OverviewLightship is the first American all-electric recreational vehicle manufacturer currently developing an aerodynamic, battery-powered trailer for the electric age. As the macro transition to an all-electric transportation ecosystem accelerates, Lightship is bringing the increased convenience and superior performance that electrification offers to a pastime enjoyed by over 11 million American families. Honoring Diverse PerspectivesLightship is committed to hiring and developing top talent from diverse backgrounds. We believe representing and supporting diverse groups is key to the success of our team members, customers, shareholders and the achievement of our mission and vision. We operate in a collaborative environment with a flat organizational structure and expect a high degree of integrity, autonomy and creativity from all members of the team. About the RoleAs an experienced Senior Quality Engineer, you will help support the production of a high-quality luxury recreational vehicle. You will develop and maintain quality standards, lead investigations, drive continuous improvement, and manage supplier quality.The daily team briefing begins promptly at 8:00 am, and you are expected to be present and ready to work at that time.Responsibilities Development of manufacturing requirements, quality standards and product quality plans to assure products will meet expectations of our target customers Identification of critical requirements to assure proper supplier and production focus on features and necessities Support development of manufacturing equipment, controls and test plans to address risks identified in FMEA Support process capability analyses to investigate the ability of suppliers and production processes to meet defined specifications and quality standards Manage and facilitate the root cause & corrective actions system through tracking and validation of issues and support in root cause analysis through facilitating brainstorming, use of lean methodologies, hypothesis testing, design of experiments, etc Communicating well with internal and external teams, traveling to suppliers in different regions, and on-the-spot critical decision making Lead the MRB process to ensure parts are dispositioned in a timely and efficient manner to minimize inventory and production impact. Assist with implementation and execution of change control. Support line side with sorting / rework instruction development and execution, training operators or technician to carry those instructions in a proper manner Engage supply chain, engineering and design team members for driving resolution to quality issues related to suppliers This can require travel up to 20% of the time Minimum Qualifications Bachelor of Science in Electric, Mechanical, Materials, Industrial Engineering, or evidence of exceptional experience in related fields or equivalent practical experience 5+ years of experience with broad technical background and the ability to work with engineering, manufacturing, service and suppliers across a wide variety of issues Strong interpersonal and communication skills to establish effective working relationships within Lightship and outside Excellent oral, written and presentation communication skills PPAP/APQP processes, an advanced working knowledge of Statistical Process Control (SPC), Geometric Dimensioning and Tolerancing (GD&T) and Lean Manufacturing, and how to apply these skills to improve quality, capacity, and reduce cost Able to work under pressure while managing competing demands and tight deadlines Well organized with meticulous attention to detail Preferred Qualifications Experience creating technical specifications for manufacturing equipment, and introducing new products and new processes from a prototype environment to a production environment Specific training and demonstrated success in applying design for quality and problem-solving methodologies, FMEA, process capability analysis, hypothesis testing, DoE, SPC, etc Previous experience with CMM and/or scanning equipment Excellent team building skills in dealing with suppliers, peers and other functional areas Equity Lightship compensation consists of the yearly salary above plus equity, which gives you a stake in the company. Employee Benefits & Philosophy - Applies to Full Time Employees only- Healthcare, Dental, Vision- 401k - Flexible Paid Time Off - that we actually want you to use!- 8 Company Holidays + the company observes a period of scheduled downtime during the end of the year for a week, allowing all employees to enjoy a break- 12 weeks paid parental leave- $2,000 per year towards an RV trip of your own &/or professional development opportunities - we call this a LightTrip Lightship offers all of its full time employees and their dependents full benefits including health, dental and vision insurance and covers 100% of the insurance premium. We are on a mission to create a more healthful all-electric experience for a pastime that millions of families enjoy and believe strongly that our team should not have to worry about quality healthcare for themselves or their loved ones along the way.

Join our team in Boulder, CO, where the stunning landscapes meet technological innovation. Play a key role in our company's quality and compliance by maintaining and updating the Approved Supplier List, supporting supplier-related compliance projects, and ensuring our suppliers meet rigorous quality standards. You'll qualify new suppliers, lead audits to uphold GMP and regulatory requirements, and work closely with engineering teams to resolve issues and implement effective quality strategies for new products. This position offers the opportunity to directly influence product reliability, patient safety, and continuous improvement across our supply chain. Responsibilities Drive and manage supplier quality activities related to projects (approved supplier list updates, PPAPs, and general project support). Ensure that suppliers deliver quality parts, materials, and services. Qualify suppliers according to company standards and may administer a Certified Supplier Program in receiving inspection to ensure cost effectiveness. Monitor parts from acquisition through the manufacturing cycle and communicate and resolve supplier-related problems as they occur. Develop and prioritize an auditing schedule to ensure that designated suppliers are audited on a regular basis to ensure good manufacturing practices (GMP) and quality standards are met. Evaluate suppliers'internal functions to assess their overall performance and provide feedback in assessment of their operation. Collaborate with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy, Approved Supplier List coordination, Supplier Owned Quality deployment, and Control Plans for new products. Define Receiving Inspection requirements as required and associated test method validation for all internal Test Methods. Provide technical guidance and quality compliance for Supplier Quality engagement throughout the NPD lifecycle on newly qualified parts from NPD and implementing strategies for driving product quality and continuous improvement. Must Have: Minimum Requirements Requires advanced knowledge of job area combining breadth and depth, typically obtained through advanced education combined with experience. Requires a University Degree and minimum of 2 years of relevant experience, or advanced degree with a minimum of 0 years relevant experience. Nice to Have Strong written and verbal communication skills Solid presentation and computer skills (Excel/Word/PowerPoint/Projects, etc.) Project management skills Self-starter, self-motivated attitude with the ability to multitask and thrive in a fast-paced environment Excellent interpersonal communication skills

The Quality Engineer plays an active role in maintaining the Quality Management System (QMS) and standardization of inspection methods, processes and procedures. Essential Duties & Responsibilities Communicate, report, and coordinate with the Quality Manager to establish and determine required actions, set priorities, development of project, standardization opportunities. Develops and initiates standards and methods for inspection, testing, and evaluation. Applies statistical process control (SPC) methods real time for analyzing data to evaluate the current process and process changes. Oversees the programming for various machines and applications in Quality, such as the Seebrez, CMM, Keyence, and QC Calc/QC Gage. Defines and interprets geometric dimensioning requirements from drawings. Completes Gage R&R and Capability studies as dirested by the Quality Manager. Reviews data as appropriate during quality control and quality assurance activities to ensure consistency with company policies and procedures. Maintains a working knowledge of government and industry quality codes and standards. Act as quality representative for customer source delegated inspection processes (SDR, DSQR). Implements quality training programs to key personnel in conjunction with manager. Plays active role in maintaining and improving the Quality Management System within organization. Review customer complaints, analyze returns and make recommendations for corrective action. Assist in conducting internal and external plant audits. Analyzes data of production runs to ensure parts are produced to meet customer requirements. Perform PPAP studies as necessary. Maintain and schedule Calibration of measuring & test equipment and inspection tools. Prepares and presents technical and program information to the management team. Comply with all safety policies, procedures, and practices. Instill an awareness and knowledge of accuracy and safety among the employees to minimize accidents and provide a safe work environment. Identifies and investigates quality problems by working with Manufacturing Engineering and other departments in implementing and verifying effectiveness of corrective actions. Train operators on new systems, quality updates and other areas as needed. Other duties as assigned. Education and Experience This position requires a minimum of 3 years previous quality supervision experience in an ISO 9001 certified manufacturing environment. Previous experience with Qualtrax, QC Gage/QC Calc, Keyence Programming, and/or JD Edwards is preferred. Experience with the following standards preferred: ISO 9001 AS 9100 ISO 14001 OHSAS 18001 FAA TSO C150 Knowledge, Skills, and Abilities Have the ability to read and evaluate drawings, specifications and procedures to identify requirements. This also includes knowledge of and use of Geometric Dimensioning and Tolerancing (GD&T). Have experience using precision inspection instruments (e.g. micrometers, calipers, optical comparator, CMM, etc.) and know when and where they are used (resolution), including accuracy and efficiency. Good interpersonal and communication skills. This person needs to have excellent analytical skills to communicate the standards and documents effectively. Must have high level of attention to detail and advanced problem solving skills (root cause analysis). Need good to intermediate computer skills to be proficient with Qualtrax, JDE, Microsoft Office as well as writing programs for SPC software (ie. QC Calc/QC Gage) and automated inspection measuring equipment (Seebrez, Keyence, CMM). Knowledge of materials and material requirements as they relate to customer orders. (ASTM, AMS, Customer Specifications.) Ability to program and operate the Seebrez, Keyence, QC Calc, and Coordinate Measurement Machine. Must have the ability to train other personnel. Work Environment/Physical Demands/Equipment Used This position is located in a manufacturing facility which requires prolonged sitting, standing, walking, squatting, twisting, and bending. This position will spend about 90% of their time on the production floor where heavy machinery is present and loud sounds exist. Requires lifting up to 50 lbs. Requires manual dexterity for typing. Health and Safety - PPE Requirements Safety Glasses to be worn at all times when on the production floor Safety Toe Shoes to be worn at all times when on the production floor

Job Description 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.