Quality assurance specialist jobs in Colorado - 272 jobs

RELOCATION ASSISTANCE: No relocation assistance available CLEARANCE TYPE: SecretTRAVEL: NoDescriptionAt Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the world today, and for generations to come. Our pioneering and inventive spirit has enabled us to be at the forefront of many technological advancements in our nation's history - from the first flight across the Atlantic Ocean, to stealth bombers, to landing on the moon. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work - and we have an insatiable drive to do what others think is impossible. Our employees are not only part of history, they're making history. Northrop Grumman Space Sector has an exciting career opportunity for a Documentation Specialist - 3. The Threat Modeling Center is responsible for the development and delivery of high fidelity threat modeling products in support of MDA and MDA's Missile Defense System. This position is on-site at Schriever Space Force Base. The Threat Documentation Specialist 3 requires a detailed-oriented person responsible for the development of technical documents containing graphs, charts, maps, large tables and technical details of threat scenarios used in the Missile Defense Agency's (MDA) Missile Defense System (BMDS) ground tests and other events. Must have excellent written, verbal, and interpersonal communication skills, and the ability to follow established processes and procedures. Must be a motivated team player with a can-do attitude and a willingness to ask questions and learn. Must be able to adapt to rapid changing project requirements and meet firm product schedule delivery dates. Must be able to understand and translate technical intelligence and engineering parameters into layman's terms. Will also serve as the final quality control checkpoint for documents for delivery including technical content and proper classification markings. Basic Requirements: Bachelor's degree and 5 years of related experience, or a Master's degree and 3 years of related experience, or a PhD and 1 years of related experience. Must be familiar with template-based document production tools such as Adobe Framemaker Experience with Linux and LaTeX Must be familiar in Microsoft Office products, including Word, PowerPoint and Excel Must have basic understanding of the DoD Guide for Marking Classified Documents and of proper procedures for tracking, storing and cataloging classified documents Must be self-motivated, able to work in a dynamic team environment Must be detailed oriented and able to analyze documents for erroneous or technical anomalies Applicants must have a current active in-scope U.S. Government DoD issued Secret security clearance at the time of application and is required to start. Preferred Requirements: Previous experience with technical writing in a Modeling and Simulation area is preferred Understanding of basic ballistic missile and air breather system characteristics a plus Background in intelligence or a related career field or area of study a plus Ability to obtain DoD Top Secret Clearance #NGSpace #COSpace #NGFeaturedJobs Primary Level Salary Range: $77,800.00 - $116,800.00The above salary range represents a general guideline; however, Northrop Grumman considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions.Depending on the position, employees may be eligible for overtime, shift differential, and a discretionary bonus in addition to base pay. Annual bonuses are designed to reward individual contributions as well as allow employees to share in company results. Employees in Vice President or Director positions may be eligible for Long Term Incentives. In addition, Northrop Grumman provides a variety of benefits including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business.The application period for the job is estimated to be 20 days from the job posting date. However, this timeline may be shortened or extended depending on business needs and the availability of qualified candidates.Northrop Grumman is an Equal Opportunity Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO and pay transparency statement, please visit *********************************** U.S. Citizenship is required for all positions with a government clearance and certain other restricted positions.

Duties & Responsibilities Refine and maintain the company written QA/QC Plan. Conduct new hire training on the key aspects of the QA/QC plan, as well as periodic recurrent training for existing employees. Meet with every project team to ensure they have a project specific QA/QC plan in place at the beginning of the project. Provide assistance as needed. At a minimum the plan should include / require: Preconstruction meetings with each subcontractor Subcontractor QA/QC plans Mock ups of key components First day inspections of each trade's work Pre-planned phase inspections Waterproofing and roofing inspection/testing Deficiency tracking and notification Punch-list process Owner turnover procedures Warranty hand-off Periodically audit the program for each project to ensure compliance and effectiveness. Provide a written summary of the results of the audit to the General Superintendent. Facilitate a handoff meeting from operations to warranty, ensuring the punchlist is complete and accepted prior to initiating the warranty reporting and tracking system Periodically solicit feedback from the Warranty Department for the purposed of evaluating the effectiveness of the QAQC program. At the end of the warranty period, facilitate a post job review with operations and warranty. Document performance of both, and share any lessons learned. Provide similar services to the companies Self Perform Services group. Skills Required Thorough knowledge and understanding of the general construction practices and techniques, construction document reading, and construction means, methods and materials. Knowledge and experience with residential construction, particularly the punch-list, turnover and customer service process. Familiarity with Microsoft Office and database management tracking tools such as Latista. Strong management, leadership and interpersonal skills combined with strong written and verbal communication skills. Capable of working independently. What's in it for you? Competitive Benefits and Salary Rewarding Challenges Professional Environment Legendary Quality Dynamic Team Environment Opportunities for advancement Let's Talk Blue Ridge Executive Search P.O. Box 1237 Etowah, NC 28729 Phone ************ Fax ************ *********************** For more information for this position please forward your resume or email us at ************************** We work hard for our candidates. You want a company that understands your industry and is willing to go the extra mile. Blue Ridge Executive Search is that company. We have successfully recruited and placed hundreds of candidates within the construction industry.

Our Vision: To ignite the imagination of every generation by being the most trusted source for model rocketry. Our Mission: To create safe, successful rocketry experiences for customers everywhere, from their backyards and schoolyards to worlds beyond. These statements are at the core of the Quality Assurance Specialist's role at Estes Industries. Located in Penrose, CO, Estes Industries has been the world leader in model rocketry for over 65 years. Our model rockets have played an influential role in the development of today's astronauts, aerospace engineers, and space enthusiasts; and we are dedicated to continuing the inspiration for the next generation's ever-growing aerospace endeavors. We staff a growing Quality Department in our efforts to meet the highest expectations of our customers. We monitor supplier quality and measure the outputs of our own production. This position is involved with the manufacturer of model rocket kits, accessories, and the engines which propel them into the sky. There is a balance of hands-on material tests, with the interpretation of the results as they relate to specifications. We welcome anyone who has the internal motivation for promoting excellence, is interested in the technical study of manufacturing output, and has the penchant for detailed evaluations of a complex interaction of raw materials as a finished product. Essential Functions Ability to pass a background check to obtain various permits is mandatory Maintain accurate and thorough record of all inspections performed. Closely interface with personnel in assembly and engine manufacturing. Follow rules and procedures relative to hazardous materials. Inspect all incoming finished goods and raw materials following established protocols. Conduct visual inspections for cosmetic defects (scratches, dents, misalignments) within the assembly department. Perform functional tests to ensure the product operates correctly (e.g., electrical components, moving parts, pressure tests). Check for loose, missing, or incorrect parts and ensure all components are properly assembled. Verify labeling and packaging meet specifications. Conduct routine inspections of work in process in assembly and engine manufacturing to ensure production meets established quality criteria. Sample and test model rocket engines. Complete required inspections in accordance with Estes Industries Quality Procedures. Work cross-functionally with Operations, Safety, and Product Development departments to assist in the development of new products and processes. Communicate results of inspection observations with Operations teams. Follow all safety rules and notify management of any unsafe condition. Perform other duties as assigned. Competencies Attention to detail Time management in a fast-paced environment Problem-solving Critical thinking Written and verbal communication Ability to work as part of a team. Strong Computer skills with the ability to learn complex systems Physical Demands Must be able to lift and carry up to 50 lbs. Must be able to push or pull up to 150 lbs. on a cart Must be able to push or pull up to 500 lbs. on a pallet jack Must be able to stand or walk 95% - 100% of shift Must be able to reach, bend, twist, stoop, kneel, and crouch with no difficulty Ability to adequately see and read written and digital documents Work in an environment subject to temperature changes Required Education and Experience High school diploma/GED Previous experience in quality assurance or similar field Working knowledge of measurement tools, methods, and concepts of quality assurance Good communication skills Excellent data collection and analysis skills Strong attention to detail Preferred Education and Experience Bachelor's Degree in technical field Certificate in quality assurance Forklift experience is a plus Additional Eligibility Qualifications Ability to pass a background check and obtain various permits is mandatory Salary: $17.00 - $17.50 per hour

Division Automation Function Other USA, Denver Making complexity accessible At Mikron we are committed to delivering the best assembly systems and all needed services throughout your product's entire life cycle. With our extensive engineering know-how, complex process expertise, scalable platforms and lifelong support we are driving lasting success for your business. With more than 4,000 assembly and test systems in use worldwide, our team of over 800 qualified employees have unique process expertise and the rigor for complex project management in a wide range of industries. Mikron experts will work closely with you to design an automated assembly system that meets your unique, industry-specific processes, whether for high-volume, medium-volume or lab-scale production. Mikron's standard systems are scalable and customizable to meet your current needs and adapt to future production requirements, without the need for costly and extensive future upgrades. Your main tasks The Quality Assurance Specialist is responsible for assure products, processes, facilities, documentation, and systems conform to quality standards, internal procedures, systems, and governmental regulations. Essential Duties & Responsibilities * Perform internal audits and author internal audit reports * Lead CAPA investigations * Verify effectiveness of CAPA actions * Close Non-Conforming Reports and Engineering Change Control Reports * Participate in customer audits and ISO audits * Perform supplier audits and author supplier audit reports * Provide ISO 9001 orientation training for new hires * Gather and analyze quality metrics and key performance indicators to identify trends and risks * Train employees to processes and procedures * Author customer Quality Agreements * Maintain and develop standard operating procedures to support the Quality Management System * Support and/or Lead Continuous Improvement initiatives * Assist other departments with the creation and revision of controlled procedures * Perform ad hoc duties as needed Company Responsibilities * Keeps a Customer focus when performing work and communicating both with internal and external customers * Is always striving to better themselves by taking personal responsibility to learn and grow while helping the department adapt and grow while maintaining a positive and professional attitude. * Maintains Customer Confidentiality * Values Teamwork and Collaboration * Leadership * Strengthens Accountability * Builds Effective Teams * Motivates and Develops others * Manages Conflict * Leads with Ethics * Strong attention to detail * Flexible with the ability to remain highly organized while addressing diverse responsibilities and maintaining workload Required Education, Experience, Knowledge, & Skills * Bachelor of Arts or Bachelor of Science degree * Or 3 to 5 years relevant experience * Thorough understanding of the ISO 9001 * Knowledge of ISO 13485 and IS0 45001 regulations * Familiar with Microsoft Office tools * Ability to adapt to priority changes * Ability to communicate in an open, clear, precise, and effective manner with customers, peers, and management * Must have initiative to learn and demonstrate positive behavior toward teamwork * Strong problem solving, analytical, and organizational skills * Strong written and oral communication skills * Certified Quality Auditor * Six Sigma or Green Belt certifications Additional Requirements * Must be eligible to work in the United States, have a valid state driver license and be eligible to obtain a passport for international travel * Ability to fluently speak, read and write in English. * Must be able to travel or work flexible hours as required for project deliverables. * Mikron Corporation Denver is a drug free working environment. * Must be able to work on-site at least three days per week at Mikron Automation's facility. Remote work may be permitted for up to two days per week, subject to project requirements and team alignment. Company Offered Benefits * PTO * 10 paid holidays (1-2 floating holidays depending on start date) * Pet Insurance * Excellent Medical, Dental, and Vision insurance * Short Term Disability, Long Term Disability, Life Insurance & ADD * FSA, HSA * Eligible for Over Time * Employee Assistance Program * 401k with matching up to 5%, immediately vested * Tuition and Continuing Education Reimbursement * Professional Growth Opportunities Work Environment * Noise level in the work environment is usually moderate as in a typical office setting. * Ability to work flexible hours. * Mikron Corporation Denver is a drug free working environment. * This job will close on 02/06/2026 all applications will be accepted through 02/06/2026* Pay Range * $32 to $36 an hour If you are interested what you have read and want to join our team, we would be keen to hear from you! Apply

**University of Colorado Anschutz Medical Campus** **School of Medicine | Department of Medicine | Division of Allergy and Clinical Immunology | ClinImmune | The Center for Clinical Immunology** **Job Title: Quality Assurance Coordinator (Entry - Senior Level)** **Position: #00838151 - Requisition: #37493** **Job Summary:** **Key Responsibilities:** + Participates in regulatory submissions for Biological License Applications (BLA), filings, and communications with regulatory and accreditation agencies including audits including but not limited to the FDA, AABB, CAP, ASHI, FACT, and AATB and leads internal audits to ensure compliance. + Oversees quality assurance in compliance with strict regulatory standards to make sure ClinImmune is delivering pure, and potent products for patient treatment and following proper laboratory protocols for patient sample testing and resulting. This requires laboratory oversight, and meeting regulatory agency requirements to ensure no harm can come to a patient. + Reviews and assists with the preparation of occurrence (deviation) reports, complaints, and corrective and preventative actions (CAPA). + Recognizes and reports trends and opportunities for improvement (OFI) through audits and occurrence reports to the Director of Regulatory Affairs and/or Quality Manager, which are then shared with ClinImmune management and staff. + Reviews supplier qualifications, inventory quality control functions, change control functions, as well as developing and implementing risk mitigation strategies for regulatory and accreditation compliance. + Reviews and assists with validation and verification proposals and summaries for equipment, software, and/or processes to ensure that all contain appropriate testing to show the subject of the validation is fit for use. + Performs review of cell and gene therapy product files and sponsor protocols, ensuring accurate documentation, donor eligibility review for correct labeling of products and product safety, and that regulatory, accreditation, and quality processes are being followed for all cellular therapy products administered to University of Colorado Hospital patients, whether standard of care cellular therapy products or sponsored cellular therapy clinical trials **Work Location:** Hybrid **Why Join Us:** **Why work for the University?** + Medical: Multiple plan options + Dental: Multiple plan options + Additional Insurance: Disability, Life, Vision + Retirement 401(a) Plan: Employer contributes 10% of your gross pay + Paid Time Off: Accruals over the year + Vacation Days: 22/year (maximum accrual 352 hours) + Sick Days: 15/year (unlimited maximum accrual) + Holiday Days: 10/year + Tuition Benefit: Employees have access to this benefit on all CU campuses + ECO Pass: Reduced rate RTD Bus and light rail service **Qualifications:** **Minimum Qualifications:** **Entry Level:** + Bachelor's degree in biological sciences, chemistry, or clinical laboratory science. Other degree holders need not apply. **Intermediate Level:** + Bachelor's degree in biological sciences, chemistry, or clinical laboratory science. Other degree holders need not apply. + One (1) year of professional health care or clinical quality assurance experience. **Senior Level:** + Bachelor's degree in biological sciences, chemistry, or clinical laboratory science. Other degree holders need not apply. + Two (2) years of professional health care or clinical quality assurance experience. **Preferred Qualifications:** + Experience with cell and gene therapies and HLA. + Relevant, patient- focused biomedical experience (*equipment not included). + Certification in quality management (e.g. ASQ or Six Sigma). + Experience working with an electronic document control system. + Direct healthcare-related experience. + Two (2) - four (4) years of related quality assurance and regulatory affairs experience in a clinical laboratory. + MT(ASCP) or MLS certification. **Knowledge, Skills, and Abilities:** + Ability to communicate effectively, both in writing and orally. + Ability to establish and maintain effective working relationships with employees at all levels throughout the institution. + Outstanding customer service and active listening skills with the ability to recognize and take care of the patients' and clients' needs while following company procedures. + Proficiency with Microsoft functions. + Knowledge of human anatomy and medical terminology. + Possess essential knowledge of the principles of clinical laboratory testing and quality control as it relates to HLA testing and cellular therapy product processing, labeling, storage, and preparation for infusion. + Ability to be held accountable or answerable for one's work and conduct. + Organization skills with the ability to complete work within given deadlines. + Detail oriented with the ability to prioritize tasks accordingly and perform work accurately and thoroughly. + Ability to work effectively with a team to work toward a goal. + Ability to adapt to change in the workplace. + Ability to follow established guidelines, policies, standards, or legislation. **Conditions of Employment:** + To perform this job successfully, an individual must be able to perform each essential duty satisfactorily, with minimal supervision and critical thinking. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions. **How to Apply:** **Screening of Applications Begins:** **August 15** **th** **, 2025** **Anticipated Pay Range:** + **Entry Level:** $56,555 + **Intermediate Level:** $61,546 + **Senior Level:** $66,536 **Equal Employment Opportunity Statement:** **ADA Statement:** **Background Check Statement:** **Vaccination Statement:** **Job Category** **Primary Location** **Schedule** **Posting Date** **Unposting Date** **To apply, visit ******************************************************************** (****************************** Copyright 2025 Jobelephant.com Inc. All rights reserved. Posted by the FREE value-added recruitment advertising agency (***************************** Quality Assurance Coordinator (Entry - Senior Level) - 37493 University Staff The Quality Assurance Coordinator supports the mission, goals, and strategic plan of ClinImmune and the School of Medicine at the University of Colorado Anschutz Campus by performing monitoring, auditing, and overseeing the quality of clinical laboratory testing used to match organ donations with viable recipients. In addition, this position is responsible for the quality oversight of the stem cell processing services, transport, and cryopreservation of the product from the apheresis center, quality oversight of the performance of bedside thaw and infusion assistance in the hospital infusion center, and quality oversight of post-transplant surveillance of indicators of cell therapy product purity and potency.This role will be responsible for reviewing clinical laboratory testing performed in the cell therapy and HLA labs, providing quality oversight, teaching the principles and requirements of quality assurance, thereby performing indirect patient care in assuring that all testing and cellular therapy products released by ClinImmune for use in patient transplant are of the highest quality. The Quality Assurance Coordinator is responsible for supporting the quality assurance functions of the organization by performing essential regulatory and quality management functions in compliance with, but not limited to, FDA regulations, CLIA regulations, AATB standards, FACT standards, AABB standards, CAP standards, ASHI standards, and internal policies and procedures.At the Senior level, Quality Assurance Coordinators will operate independently and have a strong understanding of all relevant compliance, quality, and regulatory guidelines. These roles will act as key liaisons between ClinImmune, study sponsors and regulatory agencies in support of quality assurance, risk management, accreditation, and regulatory oversight. - this role is eligible for a hybrid schedule of 2 days per week onsite and as needed for in-person meetings once deemed trained and competent. As an academic based biotechnology company, ClinImmune is committed to providing the highest quality service and support to clinical customers and researchers locally and abroad. Our prime location at the University of Colorado Anschutz Medical Campus allows for collaboration with world-renowned clinicians and scientists. ClinImmune is an academic and clinical component of the University of Colorado Anschutz Medical Campus.We have AMAZING benefits and offerexceptional amounts of holiday, vacation, and sick leave! The University of Colorado offers an excellent benefits package including:There are many additional perks & programs with the CU Advantage (******************************************************* URL=************************** . Applicants must meet minimum qualifications at the time of hire. For full consideration, please submit the following document(s):1. Curriculum vitae / Resume2. Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address.Questions should be directed to: Timothy Lovato, ***************************** (******************************************************* URL=*****************************) Immediately and continues until position is filled. For best consideration, apply by . The starting salary range (or hiring range) for this position has been established as: The above salary range (or hiring range) represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting. This position may be eligible for overtime compensation, depending on the level. Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave, health plans and retirement contributions that add to your bottom line. Total Compensation Calculator (******************************************************* URL=****************************** The University of Colorado (CU) is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing non-discrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply, including protected veterans and individuals with disabilities. The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at ******************************** (******************************************************* URL=********************************) . The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students, and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees. CU Anschutz strongly encourages vaccination against the COVID-19 virus and other vaccine preventable diseases (******************************************************* URL=*********************************************************************************** . If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety sensitive job duties, you must enroll in the occupational health medical surveillance program (******************************************************* URL=************************************************************************************* . Application Materials Required: Cover Letter, Resume/CV, List of References : Health Care : Hybrid Department: U0001 -- Anschutz Med Campus or Denver - 20174 - SOM-MED-Clinical Immunology : Full-time : Aug 8, 2025 : Ongoing Posting Contact Name: Timothy Lovato Posting Contact Email: ***************************** (******************************************************* URL=*****************************) Position Number: 00838151jeid-39a112912c33414fabe75855b28accde The University of Colorado does not discriminate on the basis of race, color, national origin, sex, age, pregnancy, disability, creed, religion, sexual orientation, gender identity, gender expression, veteran status, political affiliation, or political philosophy. All qualified individuals are encouraged to apply.

UXO Quality Control Specialist This identifies the major responsibilities of this position. It does not include all aspects of the position such as potential additional duties requested by supervisors/managers and the requirement for flexibility in helping others for the Company's overall benefit. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. JOB SUMMARY Manage the site quality program under the auspice of the company Quality Assurance Manager. DUTIES AND RESPONSIBILITIES Responsible for implementing and enforcing all quality requirements in the Project Work Plan. Ensure operations produce a quality product while adhering to federal and state regulations. Inspect procedures and policies for compliance to industry standards. Evaluate methods and means for cost effectiveness. Reduce waste, duplicated effort, and product failure. Ensure operations adhere to the project work plan. Conduct workforce training on ordnance. Inspect safety procedures and training programs to maximize time and effectiveness. Conduct stakeholder feedback. Communicate negative trends of production or quality to the project manager. Communicate major deficiencies to the Quality Manager and Project Manager. Coordinate efforts with SUXOS to streamline operations through experience and teamwork. Serves as site liaison to the on-site USACE Safety Representative. MINIMUM QUALIFICATIONS, SKILLS, AND EDUCATIONAL REQUIREMENTS Graduate of a qualified explosive ordnance disposal (EOD) school with at least eight years combined military and commercial UXO experience. As an exception, a UXOSO may be a graduate of a qualified UXO school and have at least eight years commercial UXO experience, as required by DDESB TP18. Current 40-Hour HAZWOPER certification IAW 29 CFR 1910.120 Current 29 CFR 1910.120 HAZWOPER Physical Member of American Society for Quality (ASQ) ASQ Certified Quality Auditor (CQA), preferred, or in training for certification Ability to obtain a Secret Clearance Broad understanding of the Foreign Corrupt Practices Act (FCPA) Ability to work outside normal work hours at short notice as dictated by workload Ability to work away from primary work location in excess of normal workday Ability to travel outside the US Outstanding verbal and written communication skills; ability to interpret and explain company policy concerning MEC safety practices to executives, managers, employees, and clients Intermediate user level of computer systems; Microsoft office software (word, excel, outlook), inventory databases, and documentation control systems Valid Driver License Acknowledgment Selected candidate will be responsible for the satisfactory execution of these duties, responsibilities and functions. Duties and responsibilities may change from time to time without these changes being specified in this and that this job description in no way states or implies that these are the only duties to be performed when filling this position. We are committed to a merit-based hiring process that values individual skills, qualifications, and performance. Our hiring practices comply with all applicable federal, state, and executive orders, including the recent Executive Order on Equal Opportunity Hiring.

The Shamrock Students Professional Internship Program is an 11-week program focused on hands-on training in a variety of opportunities throughout the Shamrock Foods Company enterprise. As a Shamrock Student, you will be a part of a cohort of interns focused on real projects that impact the business. In addition to the work, you will do to support your department, you'll get to know your fellow interns through a variety of collaborative projects and events. Essential Duties: * Provide support for the Gold Canyon Meat Company's quality assurance team in an accurate and timely manner * Document and verify tare weights for all packaging SKUs to support compliance, labeling, and inventory accuracy. * Conduct receiving inspections with accurate digital logs and photo documentation to ensure traceability and quality compliance. * Review and improve the seafood returns process, identifying gaps and recommending workflow enhancements to increase efficiency and ensure food safety compliance. * Other duties as assigned Qualifications: * 1+ year(s) educational experience and currently pursuing a degree from an accredited college or university with a focus on Food Science, Food Technology, Nutrition, Dietetics, Microbiology, Agricultural Science, Food Engineering, or related studies * Maintains a minimum GPA of 3.0 * Must live in or near Commerce City, CO * Strong written and oral communication skills * Strong sense of urgency and accountability * Demonstrates expertise in Microsoft Office suite (Excel, Outlook, Word) * Ability to learn and act in a fast-paced environment * Effective task management * High level of motivation and adaptability * Great attitude and desire to learn and grow Pay for the role is weighted between $20-23 per hour. Shamrock anticipates closing the application window for this job opportunity on or before December 31, 2026 Corporate Summary: At Shamrock Foods Company, people come first - our associates, our customers, and the families we serve across the nation. A privately-held, family-owned and -operated Forbes 500 company, Shamrock is an innovator in the food industry and has been since being founded in Arizona in 1922. Our Mission: At Shamrock Foods Company, we live by our founding family's motto to 'treat associates like family and customers like friends.' Why intern for us? Shamrock Foods Company is committed to a program that goes beyond your typical internship experience, giving interns the opportunity to start their career path. We offer great training and growth for college students to help interns apply their education towards solving business problems and working on hands-on projects in a workplace environment. Our interns are more than a temporary associate; they become part of our family. Equal Opportunity Employer At Shamrock Foods Co all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status, sexual orientation, gender identity or any other basis protected by applicable law.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description The Manager of Quality Assurance is responsible for providing quality assurance leadership and guidance throughout the DPT network of laboratories. Under the direction of the Director of Regulatory Affairs and Quality Assurance, this position, in tandem with RA/QA Management and Senior Operations Management, will assist with ensuring that DPT's laboratories are inspection-ready at all times, compliant with regulations, and adhering to company lab programs. This position works closely and collaboratively with the other functional areas throughout the network of laboratories. Routine Department Operations and Quality Assurance Focus: Manages assigned personnel activities within the RA/QA department (e.g., timecards, time off); collaborate with Director RA/QA in employee performance evaluations. Coaches, reviews, manages, and terminates assigned staff. Sets goals for assigned employees. Counsels assigned Quality Systems Specialists regarding problems / issues encountered in daily activities. Identifies continuous improvement opportunities and coordinate actions to improve processes; proactively manage critical issues of a quality nature. Identifies, coordinates and/or implements tools and process improvements to promote efficiency and process improvements through the organization. Creates and maintains relationships with other managers within the Eurofins DPT network that is productive and promotes teamwork and change. Consults on quality-related questions and issues from internal and external clients. Supports the company and department in meeting its goals and initiatives. Serves as a liaison for the organization to outside vendors, clients and auditors. Performs duties in compliance with all applicable regulatory and accrediting agencies. Supports the Director of RA/QA in Executing organizational and department initiatives Preparing materials as requested by Executive Management (trending data, Management Review, customer-specific meetings) Provides perspective and Subject Matter Expertise on the interpretation of Clinical Laboratory Regulatory requirements that impact the Company's operations and regulatory compliance. Provides Quality Management support for QMS-related activities across our network of laboratories. Assists in designing and developing overall corporate quality system. Reviews and approves quality event investigations (including corrective action plans) to ensure thorough and high-quality records. Ensures laboratory practices are aligned and consistent across the organization, taking best practices into account helping to maintain audit-readiness throughout the organization, preparing laboratories for key inspections as well as internal and external audits. Oversees that new actions implemented as a result of customer complaints or deviations are to be rolled out to all laboratories. Trends Quality Management System timeline through the lifecycle of items (deviations, complaints, corrected reports, SCARs, CAPAs, etc.) for Operations Senior Management. Oversees training policies and procedures to ensure compliance with regulations and standards. Performs duties and tasks in a timely and compliant manner, ensuring accurate documentation and conclusions. Represents Eurofins DPT for client and regulatory-based audits/inspections. Qualifications TRAVEL REQUIREMENTS 5-15% travel to DPT locations, based on organizational need. Ability to meet STAT travel requests to host 2-5 unplanned regulatory audits annually. MINIMUM REQUIREMENTS Bachelor of Science degree in a medical-related field; Medical Technologist license is strongly preferred. 15+ years laboratory operations experience. 5+ years auditing experience. WORK EXPERIENCE REQUIREMENTS Technical knowledge of CLIA/CAP/FDA/OPTN laboratory regulations. Significant bench testing experience. Solid experience with QA programs, root cause analysis and implementation of actions. POTENTIAL ENVIRONMENTAL FACTORS All laboratories carefully maintain all hazardous materials. All employees must abide by Eurofins DPT's Safety and Exposure procedures. This includes using the provided safety clothing and equipment. For a list of potential chemical hazards, see appropriate SDS sheet. Additional Information Compensation: $100,000-$120,000 Schedule : Monday - Friday 8:00am - 4:30pm What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.

The QA Manager has responsibility for setting the direction for our quality approach across the delivery teams. Specifically, these responsibilities include: •Provides the technical leadership in the definition, development and maintenance of the testing environments •Provide Innovative test strategies and solutions to support successful product delivery •Mentor and guide members of the QA teams •Provides technical product and process guidance to other QA team members •Partners with Product Management and Delivery teams throughout the software lifecycle •Demonstrates agility, ability to foster and engage in healthy conflict, mentorship, ability to remove obstacles, and creates clarity from ambiguity •Stays abreast of quality practices and techniques evangelizes such with the greater team Qualifications Key Skills •Domain knowledge of the business in order to provide guidance to testers around what needs to be tested •Strong analytical abilities •Team building skills and coaching skills •Ability to mine and analyze test results •Automation scripting and framework skills Additional Information All your information will be kept confidential according to EEO guidelines

Would you like to join an innovative team driven by a bold vision - unleashing tools to accelerate breakthroughs in human health? Would you like to join an innovative team creating technology to power ground-breaking insights in academic, clinical, pharma and biotech research? It is an extraordinary time for Standard BioTools. Our technology is empowering customers to improve life through comprehensive health insight. We invite you to join a leading provider of indispensable life sciences tools that is accelerating global research on multiple frontiers of human health. At Standard BioTools, we are building a positive culture where our people can do the best work of their careers, informed and influenced by our core behaviors: • Keep customers front and center in all of our work • Be accountable and deliver on commitments • Drive continuous improvement • Be collaborative and work as one team: fostering communications in a learning, coaching, and helpful environment This position will report to the Manager, Quality Assurance and is responsible for completing onsite quality activities that support business operations, including product and material release. This position also supports other quality systems activities including customer complaints, CAPAs, supplier quality, nonconformances, training, document control, and audits. The individual in this role will be relied upon to ensure the compliance and effectiveness of the quality system for their role as defined in respective procedures. Key Job Responsibilities Attend standup meetings for manufacturing, lab, and QC Review and release of incoming materials Review analytical QC (aQC) and functional QC (fQC) activities Review testing and batch records associated with product release Review Equipment Maintenance and Calibration Records Monitor and approve non-conformance management steps File and maintain integrity of quality records Use electronic documentation systems (eDMS, eQMS) to process Change Orders and Quality events Create, revise and drive release of documents and templates Update databases and spreadsheets used to track, monitor, and report department activities Support internal and external audit activities Support quality issues and quality metrics related activities Conduct assay study review and release to support laboratory services Monitor and support development of training plans based on roles defined in procedures Support Customer Complaints Program Support CAPA Program Support Supplier Quality Program by monitoring performance and managing Supplier Corrective Actions and supplier self-questionnaires Participate in continuous improvement projects Comply with applicable regulatory requirements, company policies, operating procedures, processes, and task assignments. (e.g. 42CFR493, 21CFR820, ISO 9001, ISO 13485, ISO 15189) Other duties, as assigned Qualifications Education: Bachelor's or Associate's degree in a Scientific or Technical field preferred but not required. Skills and Experience: 2-5 years in Quality or Operations, preferably within a related regulated field (pharma or medical device) Desired experience with: Electronic document management Electronic Quality Management workflow Change control systems Good documentation practices Excellent attention to detail Intermediate knowledge of FDA CDRH, ISO, CAP and/or CLIA regulations. (e.g. 42CFR493, 21CFR820, ISO 9001, ISO 13485, ISO 15189) Strong computer skills with word processing, spreadsheets, and software tools in support of preparing technical documentation and metrics Ability to work independently while following Standard Operating Procedures (SOPs) Strong verbal and written communications Multitasks, prioritizes and meets deadlines in timely manner Attention to detail in preparation of materials and their review Work Environment Ability to be on site 4-5 days a week Work is in typical office environment and occasional work in a typical laboratory environment with personal protective equipment use required The work environment may include, but is not limited to, the following hazards: chemical, electronic, mechanical, biohazard waste, and infectious materials While performing the duties of this job, the employee is frequently required to stand and walk. The employee is regularly required to stoop, crouch, and twist. Occasionally the employee is required to kneel, squat, and sit As Somalogic (now Standard BioTools) is a Hazardous Waste Generator, this position performs hazardous waste duties in accordance with internal controlled documents, local, State and Federal regulations Salary Expectations: $50,000 - $70,000 Range for Role: $49,000.00-$70,000.00 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.

The International Rescue Committee (IRC) responds to the world's worst humanitarian crises, helping to restore health, safety, education, economic wellbeing, and power to people devastated by conflict and disaster. Founded in 1933 at the call of Albert Einstein, the IRC is one of the world's largest international humanitarian non-governmental organizations (INGO), at work in more than 40 countries and 29 U.S. cities helping people to survive, reclaim control of their future and strengthen their communities. A force for humanity, IRC employees deliver lasting impact by restoring safety, dignity and hope to millions. If you're a solutions-driven, passionate change-maker, come join us in positively impacting the lives of millions of people world-wide for a better future. JOB OVERVIEW: Under the direction of the Deputy Director, the Data and Quality Assurance Coordinator is responsible for ensuring data integrity through the development and implementation of data collection, monitoring, and reporting systems for IRC Denver. As a key member of the IRC Denver Program team this role serves as the lead for IRC Denver's database, data, and quality assurance. The position works collaboratively with local staff, and headquarters technical advisors to support high-quality data tracking and reporting. This role contributes to continuous quality improvement by identifying and developing program reports, dashboards, and tools that strengthen quality assurance, monitoring, and evaluation efforts across programs MAJOR RESPONSIBILITIES: Coordinate with the deputy director, program leads, office leadership, and relevant headquarters technical advisors to ensure effective data collection to support ongoing performance analysis and decision-making. Implement and maintain internal data control processes that align with donor, state, and organizational requirements. Conduct regular quality assurance and compliance reviews to ensure data accuracy, completeness, and program adherence to requirements. Recommend and support improvements to data collection, reporting processes, and workflows to enhance program quality and efficiency. Collaborate with program managers to conduct internal compliance reviews and data monitoring activities. Support staff in the development and implementation of program evaluation tools, including systems for tracking, collecting, and analyzing data for existing and new programs. Provide training and ongoing technical assistance to staff on data systems, tools, and best practices. Actively participate as a member of the team in program meetings, cross-functional collaboration, and staff development activities. Adhere to IRC policies and procedures, state and federal regulations, and donor guidelines. May support direct client services or projects, including but not limited to, intake and eligibility assessments, outreach and recruitment, and special focus groups. Perform other duties as assigned. JOB REQUIREMENTS: Bachelor's degree is preferred, or an equivalent combination of education and relevant work experience. Experience in refugee resettlement or other nonprofit work preferred. Minimum of two years of relevant experience, including work with data systems or databases. Advanced computer skills, including proficiency with database systems, computer-based reporting, Microsoft Office applications, and data visualization tools. Experience with Salesforce and/or ETO is strongly preferred. Experience working in a multicultural nonprofit or international setting with a diverse client base. Strong English language skills, both written and verbal. Demonstrated ability to manage multiple priorities, meet deadlines, and adapt to changing demands. Strong organizational, planning, time management, and logistical skills. Exceptional attention to detail. Sound judgment, ethical decision-making, and professionalism consistent with IRC values. Demonstrated commitment to IRC's mission and safeguarding principles to support the wellbeing of clients and staff. Working Environment: A combination of standard office environment, remote work, and ‘field' time within the service delivery area to perform the outlined responsibilities. May require occasional weekend and/or evening work. Compensation: ( Pay Range: $28 - $30 ) Posted pay ranges apply to US-based candidates. Ranges are based on various factors including the labor market, job type, internal equity, and budget. Exact offers are calibrated by work location, individual candidate experience and skills relative to the defined job requirements. PROFESSIONAL STANDARDS All International Rescue Committee workers must adhere to the core values and principles outlined in IRC Way - Standards for Professional Conduct. Our Standards are Integrity, Service, Equality and Accountability. In accordance with these values, the IRC operates and enforces policies on Safeguarding, Conflicts of Interest, Fiscal Integrity, and Reporting Wrongdoing and Protection from Retaliation. IRC is committed to take all necessary preventive measures and create an environment where people feel safe, and to take all necessary actions and corrective measures when harm occurs. IRC builds teams of professionals who promote critical reflection, power sharing, debate, and objectivity to deliver the best possible services to our clients. Cookies: *********************************************** US Benefits: We offer a comprehensive and highly competitive set of benefits. In the US, these include: 10 sick days, 10 US holidays, 20-25 paid time off days depending on role and tenure, medical insurance starting at $163 per month, dental starting at $6.50 per month, and vision starting at $5 per month, FSA for healthcare and commuter costs, a 403b retirement savings plans with immediately vested matching, disability & life insurance, and an Employee Assistance Program which is available to our staff and their families to support counseling and care in times of crisis and mental health struggles. Equal Opportunity Employer: IRC is an Equal Opportunity Employer. IRC considers all applicants on the basis of merit without regard to race, sex, color, national origin, religion, sexual orientation, age, marital status, veteran status, disability or any other characteristic protected by applicable law.

A large school district in Thornton, CO is looking to add a QA/QC Coordinator to their team. This person will assist with all construction quality assurance and control of projects happening that fall under the bond they were awarded. This person will be responsible for drawing reviews, coordinating reviews amongst trades (i.e., HVAC, plumbing, electrical). They will facilitate project walk throughs, participate in construction and design meetings, facilitate contractor meetings and act as the district coordinator. This role is salaried, however is contingent on the bond work/timeline (estimating 4-7 years). There is an opportunity for a permanent opening once this project is completed. They are able to pay between 63k - 74k. They offer continuing education, PERA Pension plan, and a well-rounded team with great teamworking culture. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements - 4+ years of commercial or public sector construction experience - 4+ years in drawing reviews - Firm HVAC knowledge (specifically within commercial or public sector construction) Ability to read and interpret blueprints and specification - Bachelor's degree in quality control, construction management, business administration, or related field - Certified PMP

Role and Responsibilities Belmar Select Outsourcing is an FDA registered 503B Outsourcing Facility with a location in Lakewood, CO and Golden, CO. We supply high quality hormone-replacement products to prescribers nationwide. We are rapidly growing our Quality Assurance Team. If you have an eye for detail, a positive attitude and enjoy a rapidly growing & fast-paced environment, this is the career for you! This position reports to the Quality Assurance Training Manager. Depending on skills, experience, and desire to learn, the Quality Assurance Training Assistant will be placed in a specialty area with opportunities for growth and cross training. The Quality Assurance Training Assistant will perform a variety of activities serving multiple manufacturing facilities, including but not limited to the following: Wed-Sat shift from 7:00am -5:30pm. This will include a 15% shift differential RESPONSIBILITIES Key Responsibilities: Certified Trainer training and support on the production floor. Daily check of Batch Production Records for correct training documentation. Assisting with the administration of personnel qualifications and requalifications for new hires and existing personnel. Preparing new hire training paperwork. Assisting with new-hire and existing employee module training. Ensuring personnel sign for training in ACE after training events such as classes, presentations, OJTs, proficiency observations, skills assessments, Group Trainings, etc. Assisting with one-on-one retraining when necessary for deviations, investigations, requalification failures, etc. Working with department supervisors and managers to schedule on-the-job training, performance assessments, qualifications, requalifications, etc. Digital uploads of all qualifications/requalifications into the Learning Management System. Filing training documents into training binders. Auditing of new hire training to ensure all required documentation has been completed. Tracking Belmar Select Outsourcing and Green Mountain Pharmaceuticals personnel qualifications and requalifications including vision screenings, annual GMP, and GDP training. Scheduling new hire and existing personnel vision screenings, etc. with approved vendors. Working with department supervisors and managers to build training schedules for new hires. Assisting with Group Training presentations and class training when needed. Writing or assisting with training deviations. Must be professional at all times. Performs other duties as assigned. PHYSICAL REQUIREMENTS Onsite position (not remote) Ability to stand for long periods of time. Ability to bend, lift, push and pull. Required to wear personal protective equipment and work in a cleanroom environment for extended periods of time. Prolonged periods of sitting at a desk and working on a computer

Job DescriptionRoles & Responsibilities - Using hands to fulfill orders in a timely and efficient manner - Ensure daily quality and minimum standards are met - Pay close attention to detail to avoid errors - Work with match media mailing to ensure accurate order delivery - Meet daily production goals while maintaining high-quality standards - Keep work area clean and organized - Follow all safety guidelines and procedures Satisfies customers according to company standards of quality and output by prepping, scanning, inspecting, compiling, assembling and binding documents. Is required to be cross trained and demonstrates the skill set for scan to file to include traditional copy, oversize, color, mail outs and on-site functions. • Achieves customer satisfaction by consistently prepping, scanning, inspecting, compiling, and assembling projects accurately in a timely manner. • Meets deadlines by working at a quick and steady pace while maintaining quality/error free work. • Achieves Time Productive statistics by meeting standards established by the facility. • Meets company production standards by achieving the Impressions per Hour (IPH) rate in accordance with standards established. • Maintains optimal machine performance by correcting simple machine problems (clearing jams, refilling toner, replacing machine oil, etc.) and having a working knowledge of machine codes to report in the event of equipment failure. • Completes all paperwork in a timely, accurate and legible manner by reading and writing in English. • Troubleshoots problems by communicating effectively and promptly to manager. • Prevents assembly errors by maintaining an organized work station. Minimum Qualifications Qualifications: - Ability to work with hands and complete repetitive tasks for extended periods - Attention to detail and strong organizational skills - Ability to work independently or as part of a team - Ability to meet daily production goals while maintaining high-quality standards - Previous experience in fulfillment or related field preferred - Familiarity with match media mailing preferred - Ability to lift up to 50 lbs. Working Conditions: - This is a seasonal project-based position that requires standing, bending, and lifting for extended periods. - Work schedule may vary depending on production needs, and some overtime may be offered. - The work environment may be noisy and require the use of personal protective equipment. - If you are interested in this position and meet the qualifications, please submit your resume and a cover letter highlighting your relevant experience. Required Skills fulfillment Work Authorization US Citizen Green Card

Must be able to work the assigned schedule. No flexible days and times. It is Mon-Friday, if Overtime available they will advise in advance. This is a 1st shift role. 7a to 330p M-F. Some OT may be available but not the standard. No flex schedules candidate will be responsible for using their hands to fulfill orders, ensuring that daily quality and minimum standards are met. The role involves attention to detail and working with match media mailing. Key Responsibilities: - Using hands to fulfill orders in a timely and efficient manner - Ensure daily quality and minimum standards are met - Pay close attention to detail to avoid errors - Work with match media mailing to ensure accurate order delivery - Meet daily production goals while maintaining high-quality standards - Keep work area clean and organized - Follow all safety guidelines and procedures Qualifications: - Ability to work with hands and complete repetitive tasks for extended periods - Attention to detail and strong organizational skills - Ability to work independently or as part of a team - Ability to meet daily production goals while maintaining high-quality standards - Previous experience in fulfillment or related field preferred - Familiarity with match media mailing preferred - Ability to lift up to 50 lbs. Working Conditions: - This is a seasonal project-based position that requires standing, bending, and lifting for extended periods. - Work schedule may vary depending on production needs, and some overtime may be offered. - The work environment may be noisy and require the use of personal protective equipment. - If you are interested in this position and meet the qualifications, please submit your resume and a cover letter highlighting your relevant experience. Shift timings 7:00 am to 3:00 pm (Mon- Fri) Job Type: Temp $16.50 per hr Roles & Responsabilities Satisfies customers according to company standards of quality and output by prepping, scanning, inspecting, compiling, assembling and binding documents. Is required to be cross trained and demonstrates the skill set for scan to file to include traditional copy, oversize, color, mail outs and on-site functions. Achieves customer satisfaction by consistently prepping, scanning, inspecting, compiling, and assembling projects accurately in a timely manner. Meets deadlines by working at a quick and steady pace while maintaining quality/error free work. Achieves Time Productive statistics by meeting standards established by the facility. Meets company production standards by achieving the Impressions per Hour (IPH) rate in accordance with standards established. Maintains optimal machine performance by correcting simple machine problems (clearing jams, refilling toner, replacing machine oil, etc.) and having a working knowledge of machine codes to report in the event of equipment failure. Completes all paperwork in a timely, accurate and legible manner by reading and writing in English. Troubleshoots problems by communicating effectively and promptly to manager. Prevents assembly errors by maintaining an organized work station Minimum QualificationsQualifications: - Ability to work with hands and complete repetitive tasks for extended periods - Attention to detail and strong organizational skills - Ability to work independently or as part of a team - Ability to meet daily production goals while maintaining high-quality standards - Previous experience in fulfillment or related field preferred - Familiarity with match media mailing preferred - Ability to lift up to 50 lbs. Working Conditions: - This is a seasonal project-based position that requires standing, bending, and lifting for extended periods. - Work schedule may vary depending on production needs, and some overtime may be offered. - The work environment may be noisy and require the use of personal protective equipment. - If you are interested in this position and meet the qualifications, please submit your resume and a cover letter highlighting your relevant experience. Required SkillsfulfillmentWork Authorization US Citizen Green Card

Job Description Document Specialist Company: REFIJET is a premier US provider of aggregated lender auto-refinancing. We provide a comprehensive, full-service process that assists consumers in identifying and obtaining the best refinance loan for which they qualify We are a fast-growing financial services company which has quickly achieved a leadership position in its industry and is regularly recognized as an innovator in its space and are consistently named as Lending Trees #1 automotive finance source. We have been named one of Denver's Best Companies to Work for, three consecutive years. We have ambitious growth plans for 2024 and 2025. We are based in beautiful Denver, Colorado with professional offices just 15 minutes from downtown Denver Job Summary We are seeking an Administrator and Document Specialist. This role will include general administrative duties associated with automobile loans and gap insurance, gathering and checking complex documents and ensuring customer provides all relevant documentation. This is an opportunity to work with a fast-moving vibrant company in a true team environment, that is fast paced, energetic truly collaborative, highly ethical and fun. Key Responsibilities Verifying accuracy of information for generating loan documents. Preparing and sending loan documents securely Calling customers on the phone to walk them through signing and returning loan documents Collecting information from financial institutions relevant to the customer account. Fielding customer service calls relevant to the loan processing. Skills and Knowledge Detail oriented Knowledge of the Spanish language would be highly desirable Great work ethic and integrity Good communication skills Friendly personality Computer proficiency and good typing skills Qualifications and Experience: Previous experience in Financial Services, particularly the mortgage loan processing field, in an administrative role would be advantageous. What we offer: Full training Great Benefit package including: Competitive base salary and bonus Health, Dental and Vision Insurance plus Life Insurance 401(k) Plan Life insurance Paid Time Off True potential for advancement, we always endeavor to promote from within.

Job Description The Quality Control Specialist is a critical member of the team, ensuring the production and distribution of high-quality, sterile pharmaceutical products in compliance with FDA regulations, cGMP guidelines, and USP standards. This role involves conducting rigorous testing, inspections, and documentation throughout the manufacturing process to verify product integrity, sterility, and accuracy. Key responsibilities include performing laboratory analyses, environmental monitoring, and equipment calibration; reviewing and maintaining quality control records; and collaborating with cross-functional teams to identify and address quality issues. The specialist must remain updated on regulatory changes and implement continuous improvement initiatives to enhance operational quality and efficiency. Duties/Responsibilities: Works effectively and efficiently in a team environment. Conduct routine and non-routine viable, non-viable and surface environmental monitoring in all classified areas of the facility, as needed Incubation and enumeration of samples related to environmental monitoring processes, as needed. Conduct morphology assessment on appropriate samples at the conclusion of the incubation term, as needed. Perform review and release of raw materials, API, and excipients. Coordinates third party sample submission. Demonstrates the ability to perform detail-oriented work with a high degree of accuracy. Conduct investigations pertaining to OOS/OOT of raw materials, in-process, and finished product results with production personnel and/or supplier. Assists with all aspects of the quality system, such as change control, investigations, CAPA, and validation systems to ensure compliance and timely completion of assigned activities. Compiling data for quarterly report review. Review and release of finished product testing results. Generation of Certificate of Analysis and Finished Good Forms for batch release. Participate in product development meetings and represent Quality Control. Assist with the development, management and improvement of quality system processes and procedures to ensure compliance with applicable laws, regulations, and company standards in support of cGMP for pharmaceutical compounding. Lead/support audits (internal and external) to ensure compliance to CGMP regulations and internal procedures. Performs other duties as assigned. Required Skills/Abilities: Excellent verbal and written communication skills. Excellent interpersonal and customer service skills. Excellent sales and customer service skills. Excellent organizational skills and attention to detail. Excellent time management skills with a proven ability to meet deadlines. Strong analytical and problem-solving skills. Strong supervisory and leadership skills. Ability to prioritize tasks and to delegate them when appropriate. Ability to function well in a high-paced and at times stressful environment. Proficient with Microsoft Office Suite or related software. Education and Experience: BS/BA in Microbiology, Chemistry, or a relevant field/or equivalent experience. 2-5 years of Quality Control experience. Experience in a cGMP environment. Previous pharmaceutical experience. Familiarity with 21 CFR Part 11/210/211. Experience with aseptic manufacturing environments. Comfortable in a fast-paced, small company environment and able to adjust workload based upon changing priorities. Physical Requirements: Demonstrates ability to walk and stand for prolonged periods of time. Demonstrates ability to sit/ stand at a desk and working on a computer. Must be able to lift up to 15 pounds at times. Timeline: We will be accepting applications on an ongoing basis until position is filled.

At Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the world today, and for generations to come. Our pioneering and inventive spirit has enabled us to be at the forefront of many technological advancements in our nation's history - from the first flight across the Atlantic Ocean, to stealth bombers, to landing on the moon. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work - and we have an insatiable drive to do what others think is impossible. Our employees are not only part of history, they're making history. Northrop Grumman Space Sector has an exciting career opportunity for a Documentation Specialist - 3. The Threat Modeling Center is responsible for the development and delivery of high fidelity threat modeling products in support of MDA and MDA's Missile Defense System. **This position is on-site at Schriever Space Force Base.** The **Threat Documentation Specialist** **3** requires a detailed-oriented person responsible for the development of technical documents containing graphs, charts, maps, large tables and technical details of threat scenarios used in the Missile Defense Agency's (MDA) Missile Defense System (BMDS) ground tests and other events. Must have excellent written, verbal, and interpersonal communication skills, and the ability to follow established processes and procedures. Must be a motivated team player with a can-do attitude and a willingness to ask questions and learn. Must be able to adapt to rapid changing project requirements and meet firm product schedule delivery dates. Must be able to understand and translate technical intelligence and engineering parameters into layman's terms. Will also serve as the final quality control checkpoint for documents for delivery including technical content and proper classification markings. **Basic Requirements:** + Bachelor's degree and 5 years of related experience, or a Master's degree and 3 years of related experience, or a PhD and 1 years of related experience. + Must be familiar with template-based document production tools such as Adobe Framemaker + Experience with Linux and LaTeX + Must be familiar in Microsoft Office products, including Word, PowerPoint and Excel + Must have basic understanding of the DoD Guide for Marking Classified Documents and of proper procedures for tracking, storing and cataloging classified documents + Must be self-motivated, able to work in a dynamic team environment + Must be detailed oriented and able to analyze documents for erroneous or technical anomalies + Applicants must have a current active in-scope U.S. Government DoD issued Secret security clearance at the time of application and is required to start. **Preferred Requirements:** + Previous experience with technical writing in a Modeling and Simulation area is preferred + Understanding of basic ballistic missile and air breather system characteristics a plus + Background in intelligence or a related career field or area of study a plus + Ability to obtain DoD Top Secret Clearance \#NGSpace \#COSpace \#NGFeaturedJobs Primary Level Salary Range: $77,800.00 - $116,800.00 The above salary range represents a general guideline; however, Northrop Grumman considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions. Depending on the position, employees may be eligible for overtime, shift differential, and a discretionary bonus in addition to base pay. Annual bonuses are designed to reward individual contributions as well as allow employees to share in company results. Employees in Vice President or Director positions may be eligible for Long Term Incentives. In addition, Northrop Grumman provides a variety of benefits including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business. The application period for the job is estimated to be 20 days from the job posting date. However, this timeline may be shortened or extended depending on business needs and the availability of qualified candidates. Northrop Grumman is an Equal Opportunity Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO and pay transparency statement, please visit *********************************** U.S. Citizenship is required for all positions with a government clearance and certain other restricted positions.

Role and Responsibilities Belmar Select Outsourcing is an FDA registered 503B Outsourcing Facility with a location in Lakewood, CO and Golden, CO. We supply high quality hormone-replacement products to prescribers nationwide. We are rapidly growing our Quality Assurance Team. If you have an eye for detail, a positive attitude and enjoy a rapidly growing & fast-paced environment, this is the career for you! This position reports to the Quality Assurance Training Manager. Depending on skills, experience, and desire to learn, the Quality Assurance Training Assistant will be placed in a specialty area with opportunities for growth and cross training. The Quality Assurance Training Assistant will perform a variety of activities serving multiple manufacturing facilities, including but not limited to the following: RESPONSIBILITIES Key Responsibilities: Certified Trainer training and support on the production floor. Daily check of Batch Production Records for correct training documentation. Assisting with the administration of personnel qualifications and requalifications for new hires and existing personnel. Preparing new hire training paperwork. Assisting with new-hire and existing employee module training. Ensuring personnel sign for training in ACE after training events such as classes, presentations, OJTs, proficiency observations, skills assessments, Group Trainings, etc. Assisting with one-on-one retraining when necessary for deviations, investigations, requalification failures, etc. Working with department supervisors and managers to schedule on-the-job training, performance assessments, qualifications, requalifications, etc. Digital uploads of all qualifications/requalifications into the Learning Management System. Filing training documents into training binders. Auditing of new hire training to ensure all required documentation has been completed. Tracking Belmar Select Outsourcing and Green Mountain Pharmaceuticals personnel qualifications and requalifications including vision screenings, annual GMP, and GDP training. Scheduling new hire and existing personnel vision screenings, etc. with approved vendors. Working with department supervisors and managers to build training schedules for new hires. Assisting with Group Training presentations and class training when needed. Writing or assisting with training deviations. Must be professional at all times. Performs other duties as assigned. PHYSICAL REQUIREMENTS Onsite position (not remote) Ability to stand for long periods of time. Ability to bend, lift, push and pull. Required to wear personal protective equipment and work in a cleanroom environment for extended periods of time. Prolonged periods of sitting at a desk and working on a computer