Quality control analyst jobs in Boulder, CO - 94 jobs

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.

EQUAL OPPORTUNITY EMPLOYER Corden Pharma 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. Corden Pharma embraces fair hiring practices. CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients, and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2,600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people's lives. Our network in Europe and the U.S. offers flexible and specialized solutions across five technology platforms: Peptides, Lipids, & Carbohydrates; Injectables; Highly Potent & Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients. SUMMARY Responsible for providing strong technical leadership and documentation support for development and manufacturing processes. Responsible for the planning and execution of multi-step syntheses from laboratory to full commercialization. Emphasis is on the creative application of a full range of literature and theoretical concepts from a diverse range of chemistry to the design and implementation of cost-effective processes for the manufacture of Corden pharmaceuticals. Works within a team-oriented environment with professionals from a variety of disciplines. Conducts research, analysis, synthesis, experimentation, and documentation for such purposes as process development, implementation, registration, validation, and process improvement. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned * Ensures that the chemistry is capable of meeting cost, yield, throughput, and QEH&S goals on assigned processes * Leads large and/or multiple teams to accomplish the peptide process development, transfer, or implementation of technology at a lab or plant scale * Develops and supports scalable peptide processes and provides technical expertise and support during lab and/or plant operations * Responsible for supplying management with specific project data to facilitate the budgeting process for the development, transfer and/or implementation of technology * Develops and executes procedures, processes, and methods for solutions to chemical and technical problems on lab and/or plant scale * Conducts research and development in order to improve manufacturing processes * Possesses an individual area of technical expertise, which others consult them for advice on * Adheres to GDP and SOPs in all aspects of work LEADERSHIP & BUDGET RESPONSIBILITIES Demonstrates a positive attitude. Supports a positive, healthy, and flexible work environment that encourages employees and coworkers to develop their full potential and expand their horizons. Leads team in the development, troubleshooting, transfer, and improvement of chemical and analytical processes. Gives regular reports to and actively solicits feedback from management. SAFETY & ENVIRONMENTAL RESPONSIBILITIES Every individual is personally responsible for the safety and environmental aspects of their activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience. 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. EDUCATION and/or EXPERIENCE Doctoral degree (PhD) in Organic Chemistry/Biochemistry, plus 5 years of experience; or equivalent combination of education and experience. Peptide experience required. LANGUAGE SKILLS Ability to read, analyze, and interpret common scientific and analytical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to write speeches and articles for publication that conform to prescribed style and format. Ability to effectively present information to top management, public groups, and/or boards of directors. MATHEMATICAL SKILLS Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent, and to draw and interpret bar graphs. REASONING ABILITY Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables. CERTIFICATES, LICENSES, REGISTRATIONS Domestic and international travel required. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, and sit. The employee is occasionally required to work with hands; reach above shoulder height; climb or balance; stoop, kneel, crouch, or crawl; and taste or smell. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. 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, the employee is frequently exposed to fumes or airborne particles and low levels of toxic or caustic chemicals. The employee is occasionally exposed to moving mechanical parts, outside weather conditions, and risk of electrical shock. The noise level in the work environment is usually moderate. CORE COMPETENCIES These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity. * Demonstrates a positive attitude * Maintains a well-documented record of work performed in a laboratory notebook, laboratory reports, and campaign reports * Experience in the synthesis and purification of peptides * Has working knowledge of all plant-scale unit operations, scale-up, and plant design considerations * Understanding of chemical reactivity, potential exotherms, cross reactivity, side products and waste streams, and especially for processes they support * Regularly seeks out new learning opportunities beyond basic skills that can result in innovative approaches to technical issues * Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple (not necessarily simultaneously) processes * Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements projects * Assumes reasonable risk in trying out new, self-generated ideas * Proactive approach to problem identification and resolution * Communicates effectively in writing and verbally within and across departments and to site management; updates are clear, selective, and effective * Ability to understand and apply statistical design of experiments and draw sound conclusions from the results; uses results when solving problems, or proposing improvements * Ability to provide leadership in all process chemistry aspects of manufacturing processes; leads teams in the development, transfer, troubleshooting, and improvement of chemical processes in interactive, interdisciplinary team environment * Seeks out opportunities to learn manufacturing needs and methods that facilitate substantial process improvements; acquires new skills in state-of-the art technology and applies it to their assignments * Demonstrates skills in negotiation and influencing others * Thorough working knowledge of regulatory issues in pharmaceutical manufacturing, including cGMPs, GDP, FDA, ICH, PSM, OSHA, EPA requirements, and process hazard analysis; can interpret regulatory laws, and propose, defend, and implement cost-effective solutions * Computer skills, in the areas of: Microsoft Office Products - Word, Excel, PowerPoint; statistical analysis programs, Chemdraw and SciFinder, Laboratory Information Management System, and business systems (SAP) * Develops special expertise in products and processes; acknowledged as an expert in one or more technical areas, both within and outside site * Creates clear, concise goals and strategies that support individual's development and the site's mission; actively participates in proposing and setting Process Chemist Group and Manufacturing Department goals * Routinely demonstrates a proactive approach to problem identification and resolution * Understands Corden's business goals and contributes technically to its strategy development * Interacts with management in developing project objectives and site strategies; advises management regarding technical opportunities and advances SALARY Actual pay will be based on your skills and experience. BENEFITS * 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service * Accident Plan * Critical Illness Insurance * Dental Insurance * Disability Insurance * Employee Assistance Program * Flexible Spending Account * Health Insurance PPO/HSA * Hospital Indemnity Plan * ID Theft Protection * Life Insurance * Paid Maternity/Paternity Leave * Tuition Reimbursement * Wellness Program * Vacation - Three Weeks 1st Year * Vision Insurance Job Extended to January 30, 2026

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO) specializing in active pharmaceutical ingredients (APIs), excipients, drug products (DPs), and packaging. With around 3,000 employees worldwide, we help pharmaceutical, and biotech companies manufacture medicines with the ultimate goal of improving people's lives. Our network, spanning Europe and the U.S., provides flexible and specialized solutions across six technology platforms: Peptides, Lipids & Carbohydrates, Injectables, Highly Potent & Oncology, Small Molecules, and Oligonucleotides. We strive for excellence in supporting this network and are committed to delivering the highest quality products for patient well-being. Our People VisionWe strive for excellence. We share our passion. Together, we make a difference in patients' lives. SUMMARY Acts to drive and demonstrate the technology for the planning and execution of development and implementation of chemical processes. Ensures that the chemistry is sufficient to meet goals on process yields, throughputs, and QSHE requirements. ESSENTIAL DUTIES AND RESPONSIBILITIES Include the following. Other duties may be assigned: Familiarity with general TFF/ultra filtration setup, operation, and components Experience with lab and/or mid-large scale TFF/ultra filtration processing Knowledge of various types of TFF filtration methods and systems Understanding of key operating/scalable parameters for TFF/ultra filtration and ability to determine such parameters during process familiarization/optimization Provides technical support to lab or plant processes Works effectively in a team-oriented environment Presents work orally and in form of written development reports Adheres to GDP and SOPs in all aspects of work Independently plans and executes experiments, while working in a project team, toward development of viable commercial processes Demonstrates a clear understanding of technical issues and the requirements of a viable manufacturing process Executes procedures, processes, and methods for solutions to chemical and technical problems on a lab or plant scale Ensures that the chemistry is capable of meeting cost, yield, throughput, and QSHE goals on assigned processes Leads a team to accomplish the development, transfer, or implementation of technology at a lab or plant scale Develops and supports scalable processes and provides technical expertise and support during lab or plant operations LEADERSHIP & BUDGET RESPONSIBILITIES Demonstrates a positive attitude. Supports a positive, healthy, and flexible work environment that encourages employees and coworkers to develop their full potential and expand their horizons. This position has no supervisory responsibilities. Provides technical expertise to manufacturing. SAFETY & ENVIRONMENTAL RESPONSIBILITIES Every individual is personally responsible for the safety and environmental aspects of their activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience. QUALITY RESPONSIBILITIES Corden Pharma Colorado (CPC) is a manufacturer of a variety of pharmaceutical products. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable. This is critical as it is our mission to not place patients at risk due to inadequate safety, quality, or efficacy. CPC's Quality Management System, which incorporates cGMP, is designed to deliver this quality objective. Attainment is produced through the requisite participation and commitment of all staff across departments and at all levels within the company. cGMP is the part of Quality Management System ensuring products are consistently produced to accurate quality standards. Adherence to clearly defined procedures, in compliance with the principles of cGMP, is required when performing operations across Corden Pharma Colorado. 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. EDUCATION and/or EXPERIENCE Bachelor's Degree (BS) in Organic Chemistry and 5 years related experience and/or training; or equivalent combination of education and experience. TFF/Untra filtration experience is required; and Peptide and GMP experience is a plus. LANGUAGE SKILLS Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to develop bench scale laboratory procedures into step-by-step operating instructions for chemical operators. Ability to effectively present information to top management, public groups, and/or boards of directors. MATHEMATICAL SKILLS Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. REASONING ABILITY Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables. Ability to apply scientific methods to experimentally prove cause and effect. CERTIFICATES, LICENSES, REGISTRATIONS Domestic and international travel required. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, and sit. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision. 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, the employee is occasionally exposed to fumes or airborne particles and low levels of toxic or caustic chemicals. The noise level in the work environment is usually moderate. CORE COMPETENCIES These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity. Demonstrates a positive attitude Strong background in chemistry or a related scientific field Working knowledge of regulatory issues in Pharmaceutical Manufacturing including cGMPs, GDP, FDA, PSM, OSHA, and EPA requirements Communicates effectively in writing and verbally within the department Computer skills, in the areas of: Microsoft Office Products (Word, Excel, PowerPoint), Chemdraw, and SciFinder Ability to work interactively within a multi-functional team-oriented environment Takes initiative in setting own goals and work plans Hands-on organic chemistry laboratory experience Has a broad technical knowledge in Organic Chemistry and Process Improvement Methodology Maintains a well-documented record of work performed in a laboratory notebook, laboratory reports, and campaign reports Experience in the synthesis and purification of peptides (desired) Has working knowledge of all plant-scale unit operations, scale-up, and plant design considerations Understanding of chemical reactivity, potential exotherms, cross reactivity, side products, and waste streams, especially for processes they support Regularly seeks out new learning opportunities beyond basic skills that can result in innovative approaches to technical issues Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple (not necessarily simultaneous) processes Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements projects Assumes reasonable risk in trying out new, self-generated ideas Proactive approach to problem identification and resolution Communicates effectively in writing and verbally within and across departments and to site management; updates are clear, selective, and effective Ability to understand and apply statistical design of experiments and draw sound conclusions from the results; uses results when solving problems or when proposing improvements Ability to provide leadership in all process chemistry aspects of manufacturing processes; leads teams in the development, transfer, troubleshooting, and improvement of chemical processes in interactive, interdisciplinary team environment Seeks out opportunities to learn manufacturing needs and methods that facilitate substantial process improvements; acquires new skills in state-of-the art technology and applies it to their assignments Demonstrates skills in negotiation and influencing others SALARY Actual pay will be based on your skills and experience BENEFITS 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service Accident Plan Critical Illness Insurance Dental Insurance Disability Insurance Employee Assistance Program Flexible Spending Account Health Insurance PPO/HSA Hospital Indemnity Plan ID Theft Protection Life Insurance Paid Parental Leave Tuition Reimbursement Wellness Program Vacation - Three Weeks 1st Year Vision Insurance EQUAL OPPORTUNITY EMPLOYER Corden Pharma 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. Corden Pharma embraces fair hiring practices. This post will expire February 13, 2026

Starting compensation: $21.00 per hour (plus a $1.50 shift differential) Shift Days: Sunday to Thursday Shift Hours: 2:30 PM to Close Shamrock anticipates closing the application window for this job opportunity on or before December 31, 2026 Maintains all aspects of Quality Assurance to ensure proper, safe and exceptional operation of the department. Essential Duties: * Audits products for quality and safety prior to sending out to customers. * Audits incoming raw materials for supplier specifications, quality, and food security. * Reviews incoming ingredients for allergen checks and quality standards. * Responsible for compliance with all regulations. Food Safety - plant in proper sanitary condition at all times, including allergen control, pest control, guidelines followed. * Fills out necessary paperwork for product audits and HACCP documents. * Reviews HACCP documents prior to handing paperwork to QA Supervisor/Manager. * Work with operational teams daily with paperwork, quality checks, and HACCP procedures. * Ensure adherence to all standard work processes, including the Production Sanitation processes. * Aides in plant training requirements and training frequencies. Work with QA Supervisor/ Manager to ensure plant training requirements and frequencies are met. Conduct plant training sessions as needed. * Maintain understanding of processes and functional interdependencies. Recognize and escalate, as needed, those issues identified as risks to, or opportunities to improve, plant performance. * Must be able to work within timelines and in pressure situations. * Other duties may be assigned. Qualifications: * High School Diploma or GED preferred * Meat Protein Experience * HACCP certified, preferred 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 work for us? Benefits are a major part of your overall compensation, and we believe offering them at an affordable cost is not only the right thing to do, but it helps keep you and your family healthy. That's why Shamrock Foods pays for the majority of your health insurance, allowing you to take home more of your paycheck. And it doesn't stop there - our associates also enjoy additional benefits such as 401(k) Savings Plan, Profit Sharing, Paid Time Off, as well as our incredible growth opportunities, continued education, wellness programs. Equal Opportunity Employer Shamrock Foods Company is an Equal Opportunity Employer. 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.

Job Description The job of the Quality Control Technician is to ensure compliance with cGMP requirements and company procedures while providing support to the QC team and throughout the QA and Operations departments. Additionally, this role is responsible for coordinating QC sample preparation and external laboratory shipments in relation to Environmental Monitoring activities and other required sampling. This role will work closely with the Production team and report quality data to department management, as needed. Duties/Responsibilities: Maintain retention materials and disposal when required. Assist with review and release of raw materials, API, excipients, and sterile supplies. Coordination of Biohazard waste destruction. Perform sampling and inspection of in-process and finished products. Assists with Environmental Monitoring and microbiological sample evaluation activities. Coordination of submitting samples for testing with third party vendors on their respective web portals or paper submissions. Logbook and controlled document generation. Assist with investigations and develop and implement corrective and preventive actions geared toward continuous process improvements. Review GMP documents including production environmental monitoring forms, room and equipment logs, etc. Support quality management system activities including document control and training program management. Other duties and tasks, as assigned. Required Skills/Abilities: Excellent independent judgement, written communication, verbal communication, and interpersonal skills. Strong attention to detail. Familiarity with Good Manufacturing Practices and FDA Regulations. Proficient in using Microsoft Word, Excel, PowerPoint, Outlook. Education and Experience: 1-3 Years as a Quality Control Technician Pharmaceutical, Medical Device, or biotechnology industry experience, preferably in support of manufacturing. Associate degree in the sciences or equivalent experience preferred. Physical Requirements: Ability to work in a clean room setting Prolonged periods of sitting at a desk and working on a computer. Must be able to lift up to 15 pounds at times. 7:00 am to 3:30 pm, Monday through Friday

RESEARCH CHEMIST TECHNICIAN Rocky Mountain Scientific Laboratory Department:Advanced Chemistry & Chemical Processing Group Yes Travel:Yes Schedule:Full-time Description of Business Environment: Peace is often associated with passivity. At Rocky Mountain Scientific Laboratory, we associate peace with strength, courage, and action. We know that enabling peace to prevail is not for the faint of heart, which is why we built our company foundation on the core values of Integrity, Gratitude, Mission Driven, and Grit. We pride ourselves in providing unequaled services and technologies in the field of applied energetics to our customers. Our experts possess extensive knowledge and capability in energetic materials and military systems enabling them to offer analytical characterization, modeling & simulation, design, system integration, prototyping, test engineering, and proof-of-concept production services covering a wide range of applications. Our strengths lie in our ability and relentless determination to get the job done quickly and affordably. RMSL is an Equal Employment Opportunity (EEO), Affirmative Action employer and welcomes all qualified applicants. All qualified applicants will receive fair and impartial consideration for employment without regard to race, color, religion, sex, age, disability, veteran status, national origin or other legally protected status. An applicant with a disability or a disabled veteran can request reasonable accommodation to apply for one of our positions. Specific Job Description: RMSL is a growth company with an outstanding job opportunity for a Research Chemist Technician. This position will report to the Advanced Chemistry & Chemical Processing Group Manager. The Research Chemist Technician will be an integral part of a small cross functional team working on exciting development projects with cutting-edge technology. In this role, the ideal candidate will have a strong background in Chemistry with experience in organic and/or inorganic synthesis. This role will be a part of an integrated team focused on the development of novel energetic systems, energetic material scale-up processes, development of ammunition and armaments, testing and analysis of energetic materials. This individual must demonstrate innovation, an understanding of the fundamentals of engineering, an ability to learn, out-of-the-box thinking and creativity. Duties Include: Assist in the synthesize energetic materials and scale-up process Characterize novel energetic materials using a variety of analytical methods (DSC, TGA, SDT, TAM, Particle Size Analyzer, GC-FID, ARSST, UV-VIS-NIR, FTIR and Raman spectroscopy) and material sensitivity characterization (BAM friction, impact, and ESD testing) Ability to handle hazardous materials with strict adherence to safety process requirements Assist in the design of experiments and test series that result in safe and efficient collection of data Installation, maintenance, and operation of specialized instrumentation and testing equipment Project engineering tasks such as report writing, technical presentations (at customer and public meetings), and technical deliverables tracking Required Skills: Problem solver that can work in a fast-paced team environment on projects Hands-on experience with energetic materials Proficient in standard laboratory practices Exercises creative thinking and innovation Strong verbal and written communication skills Physical requirements: Must be able to sit for extended periods of time; must be able to lift up to 50 lbs.; must have the ability to see near and far and work with a computer monitor on a daily basis Required to bend, sit, stand and lift to perform job effectively Highly Beneficial Skills: Familiar with general explosive effects and chemistry Experience in one or more of the following areas Additive manufacturing (AM) Energetic material or hazardous material synthesis Laboratory and pilot plant scale-up of energetic or hazardous materials LabRAM operation Knowledge of basic-intermediate chemistry and/or chemical engineering Minimum Qualifications: Must have an AS, BS and/or MS in Chemical Engineering or Chemistry Ability to obtain security clearance Ability to obtain CO State Blasters Permit Benefits: Medical insurance Dental insurance Vision insurance 401(k) with matching Disability insurance Life insurance Paid time off Professional development Flexible schedule

Join TBK Bank! At TBK Bank, a subsidiary of Triumph, we're a team of passionate, driven, collaborative, solutions-minded people who want to make a difference in the lives of our customers and communities. Our mission is to do well and to do good at the same time. We accomplish this by working together, because at the end of the day, TBK means striving for excellence, while delivering with humility. We thrive on providing exceptional customer service, and we look for friendly professionals dedicated to helping customers achieve their financial goals. Position Summary: TBK Bank, SSB seeks a qualified individual to support the Credit Compliance Team in carrying out policies and procedures to ensure compliance with all regulatory and policy guidelines. ESSENTIAL DUTIES & RESPONSIBILITIES Knowledge in all regulations and bank policies governing lending and credit areas of the Bank, including: Real Estate Lending HMDA Flood Insurance CIP/Beneficial Ownership Applicable Fair Lending and consumer lending regulations Perform monthly HMDA data scrub for accuracy for annual file submission to regulatory agencies. Participate in monthly review of new loans in a flood zone, vendor reports and loans coded in a flood zone. Participate in verifying loans in a standard flood area met regulatory and procedural guidelines. Participate in performing annual review of all loans in a flood zone. Perform reviews and audits of Bank practices at the direction of management. Final review of all loans post-closing to ensure accuracy. Learn and fully understand relevant Bank policies and procedures, as well as relevant regulatory guidance, in an effort to properly identify errors. Utilize and navigate Bank programs to identify documentation and/or booking errors. Effectively communicate quality control findings with appropriate person for follow-up. Adhere to Triumph's core values and promote the team culture. Perform other projects or duties as assigned. EDUCATION & EXPERIENCE High school diploma or general education degree (GED) required Typically requires one to two years of related banking experience SKILLS & ABILITIES REQUIRED Strong organization, interpersonal, communication skills Resourceful and research-minded Strong critical thinking and problem-solving skills Attention to detail and mental concentration Commitment to accuracy Strong time-management skills and ability to self-manage to meet deadlines WORK ENVIRONMENT The work environment characteristics described here maybe encountered while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Moderate noise (i.e. business office with computers, phone, and printers, light traffic). Ability to work in a confined area. Ability to sit at a computer terminal for an extended period of time. Occasional stooping or kneeling may be necessary. While performing the duties of this job, the employee is regularly required to stand, sit, talk, hear and use hands and fingers to operate a computer keyboard and telephone. Specific vision abilities are required by this job due to computer work. Light to moderate lifting is required. Regular, predictable attendance is required. Compensation Range Hourly: $17.36 - $23.80 We offer Medical, Dental, Vision, Paid Time Off, 401k and much more. Go on. Do it. Apply Today!

JOB TITLE: Quality Control Technician DEPARTMENT: Quality Assurance DIRECT SUPERVISOR: Director of QA GENERAL JOB DESCRIPTION: Scheduled hours for this position can vary depending on the needs of the company at the time. Shifts will generally be scheduled for four 10 hour shifts, from 1:00 - 11:30 pm Tuesday and Wednesday, and 4:00 am - 1:30 pm Saturday and Sunday. MAJOR DUTIES AND RESPONSIBILITIES: Responsible for carrying out policies and procedures as implemented by EB including GMPs, food safety, and quality to always keep facility “audit ready” Report violations to Production Lead or Supervisor, if repeat violations occur report to QA & Production Managers. Responsible for verifying policy, procedure and standard compliance through monitoring and documentation This includes but is not limited to Net Weight, Metal Detection, QC Checks, Retention Sample Log, Hold Log, Label Verifications & Misc. Paperwork that may be needed. Responsible for implementing corrective actions for non-compliance to policy and procedure and standards variance. Pulls retention samples and stores them in appropriate places with appropriate information logged. Inspects equipment at the beginning of production day & throughout the day for cleanliness and safe use. Other projects as assigned. Reports any food safety or quality issues immediately to Management. MINOR DUTIES: Places out of spec items on hold as needed. Identifies quality and food safety issues. Performs GMP training to new hires & refresher training as needed. QUALIFICATIONS: Food manufacturing experience preferred Able to stand for 4 hours at a time Attention to detail Comfortable correcting peers Outlook, Word and Excel preferred Bilingual (English and Spanish) preferred but not required RESPONSIBLE FOR FOOD SAFETY: Yes Pay Rate: $21.00 - $23.50 DOE WORK SETTING: In-person ABILITY TO COMMUTE/RELOCATE: Thornton, CO 80023: Reliably commute or planning to relocate before starting work (Required) WORK LOCATION: ONE LOCATION

Final QC Inspector FLSA STATUS: Non-Exempt DEPARTMENT: Quality SUPERVISOR: Quality Engineering Supervisor DIRECT REPORTS: None. This position is responsible for inspecting, testing, and sampling assembled parts or products for defects, wear, and deviations from specifications. The Final QC Inspector will conduct tests and inspections of products or processes to evaluate quality and performance, utilizing precision measuring instruments and test equipment. Minimum Qualifications Education: High school diploma, GED, or equivalent qualification preferred. IPC/WHMA-A-610 or 620 certification preferred. Experience: Prior experience in quality inspection, Knowledge: Knowledge of IPC 610 and 620, ability to read and understand customer requirements and simple customer assembly drawings Extensive knowledge of components, connectors, terminals and mating connectors for fixture construction Skills: Ability to read wiring diagrams and engineering drawings, use of multi-meter, complex test equipment, force gages and calipers Must be able to read, write and speak English Must be able to recognize discrepancies on drawings and in customer requirements and bring them to the attention of leads, supervisors and/or management Job Responsibilities Conduct basic signature testing of cables, test beeping, terminal and solder inspection, simple high voltage and ground impedance testing. Perform data entry and complete associated paperwork, including inspection logs. Conduct complex high voltage and ground impedance testing and generate new signature profiles for assemblies. Write first article inspection reports and complete RMA evaluations. Perform simple fixture repair and construction. Organize existing assembly files and fixture database. Audit shelf-life, hazardous communication (hazcom), and calibration logs. Calibrate Cirris Signature Testers. Evaluate new complex assemblies and develop inspection plans. Work closely with Manufacturing to identify and resolve issues with new assemblies. Train new inspectors and acquire information/components for future inspection requirements. Collaborate with Engineering and Account Management on workflow needs. Perform general area cleanup and organization. Attend appropriate training and administrative meetings. Work with other departments to achieve company goals. Utilize communication skills necessary to execute company directives. Perform soldering, termination, plugging of connectors, heat shrinking, and comply with ESD assembly requirements. Other responsibilities, initiatives and ad-hoc projects as required. Internal and External Relationships Internal: Works closely with the Quality Engineering Supervisor, Manufacturing, Engineering, and Account Management teams to ensure product quality and process efficiency. Collaborates with production staff to identify and resolve quality issues. External: Interacts with customers and suppliers as needed to address quality concerns, ensure compliance with specifications, and support continuous improvement initiatives. May communicate with third-party testing agencies when required. Physical Requirements The physical demands described here are representative of those that must be met to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand, walk, and sit for extended period and must have the capability to lift up to 25 pounds. They must perform repetitive tasks and they must also have the ability to see details clearly at close range (within a few feet) and have precise coordination of fingers for grasping, manipulating, or assembling small objects. Overtime may be required based on production demands. The working environment is a standard manufacturing environment. The noise level in the work environment is usually low to moderate. Pay: $21-26/hr (varies based on experience)

Role and Responsibilities This position is responsible for performing quality control laboratory testing on incoming, in-process and finished products and assisting in laboratory operations and method validation activities. The focus of the position is compliance with regulatory activities and company procedures as they relate to the laboratory department. Responsibilities include: Conduct analytical testing per Standard Operating Procedures (SOPs) and regulatory requirements including potency, material identification, particulate and dissolution. Maintain daily use, maintenance and cleaning logs for laboratory areas, equipment and utensils. Complete routine preventative maintenance of laboratory equipment to ensure accuracy of results. Prepare Certificates of Analysis for Quality review. Perform data entry, trending and record organization. Support in drafting and reviewing procedures, change controls, risk assessments, deviations and CAPA. Participate in test method and equipment validations. Ensure compliance to federal and state laws, as well as company standards and specifications. Assists the Laboratory Manager as needed.

Job DescriptionBuild Your Career. Elevate the Customer Experience. Make an Impact. At Advocate Roofing, our associates have the opportunity to grow both personally and professionally while contributing to a fast-moving, people-focused organization. Every team member plays a role in delivering an experience that exceeds expectations - for our customers and for each other. We're seeking a driven, technically skilled Quality Control Specialist to join our team. This role is the frontline presence of our Construction Department, ensuring work is completed to standard, customer concerns are addressed quickly, and communication flows seamlessly between the field and our internal teams. If you take pride in craftsmanship, thrive in problem-solving, and enjoy interacting directly with customers, this position offers the autonomy, responsibility, and impact you're looking for. Key Responsibilities Customer-Facing Duties Visit job sites where customers require in-person interaction with a construction representative. Represent the construction department when requested by Sales or other teams to be the "face of construction" on-site. Conduct job site investigations when there are construction issues that cannot be resolved without on-site assessment. Diagnose problems and help identify appropriate corrective actions. Self-perform fixes when you're capable of resolving the problem. Collaborate with Customer Success, Construction, Sales, or Leadership teams to respond to escalated or unclear issues. Repair & Documentation Create detailed work orders for any required repairs, ensuring: Clear, actionable instructions for the contractor. Step-by-step description of what needs to be completed. Specification of any required materials to complete the job. When capable, self-perform minor repair, to reduce delays and streamline resolution. Internal Collaboration Attend virtual meetings to communicate findings and support planning. Respond promptly to internal and job-related communications. Provide timely updates, risk alerts, and follow-up insights. Field Ownership & Accountability Uphold company standards and professionalism on every job site. Act as the primary communicator between field conditions and the office team. Escalate safety or timeline-impacting issues with urgency and clarity. What We're Looking For Experience in residential construction, roofing, siding, and gutters. Strong diagnostic and problem-solving skills. Excellent communication and documentation abilities, interacting with customers with clear communication is paramount in this role Technically sound, and able to perform repairs in roofing & siding Great customer service skills Requirements: Valid Driver's License with a clean driving record Ability to work 40 hours a week; Monday through Friday during specified hours; some overtime may be needed High school diploma or equivalent Excellent customer service skills Ability to lift 45 lbs Attention to detail with excellent communication and interpersonal skills. Ability to work outside and continuously stand/walk for extended periods of time Ability to work independently and confidently The Benefits Customizable medical, dental, vision, life, and long-term disability insurance plans to suit your needs Comprehensive 401(k) retirement plan Employee Assistance Program Abundant paid time off 9 paid holidays per year Monthly communication stipend Year-round team-building events and social outings Company Truck Program Performance-based incentive trips Employee Referral Program Robust technology and tools to help you thrive in your role Annual sales training and development programs Career path growth/leadership opportunities Opportunities to volunteer and give back to causes that are important to you through our Advocate Cares program. Advocate Construction is an equal-opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. #ZR

Eurofins Scientific is a network of independent companies 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 laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. With more than 20 U.S. locations, Eurofins Built Environment Testing offers Industrial Hygiene (IH) and Indoor Air Quality (IAQ) services to protect health in built environments. Clients include consultants, industry, real estate, healthcare, government, and homeowners. Services cover a wide range of tests, including asbestos (PLM/TEM), mold, bacteria, VOCs, allergens, Legionella, radon, lead, silica, and more. Job Description The PLM Analyst (Polarizing Light Microscope) prepares and analyzes environmental samples according to scientific methodology in compliance with company Quality Assurance programs and SOP's. Sample analyses include but are not limited to air/bulk asbestos samples. The analyst will validate and review data for accuracy and will upload laboratory data into the LIMS that ultimately generates required reports to clients. Schedules sample workload according to due dates and sample hold times. Analysts will be trained according to current methodologies using job specific testing and equipment. Analyst responsibilities include, but are not limited to, the following: Login, prepare, and analyze environmental samples for asbestos. Accurately enters and reports sample descriptions and analytical data using LIMS. Performs independent QC analysis for other analysts' work. Performs analysis of reference materials, proficiency samples. And other quality control samples as needed. Maintains client service and provides technical support as needed. Assists the QA manager in development, implementation and collection of QA processes for the different analytical tests. Performs and completes all analytical testing QA related tasks as needed. Assists in pursuing, receiving and maintaining necessary laboratory accreditations. Co-ordinates projects according to their rush status and due time for timely delivery. Assists co-workers on analytical questions, as necessary. Follows company policies and procedures and ensures that coworkers are doing the same. Manages and disposes analyzed samples as needed. Trains new asbestos or other analytical testing Analysts as needed. Performs root cause analysis and determines and implements corrective actions for errors and issues as necessary. Maintains all equipment properly and co-ordinates services of all equipment used in the laboratory, as needed. Communicates available capacity to Lab Manager. Supports departments within the lab (login, asbestos, metals, pollen/spores) when appropriate and as needed. Other responsibilities as deemed necessary by the Supervisor/Manager Preparation/Analysis of bulk samples by Polarized Light Microscopy (PLM) in accordance with the laboratory's Standard Operating Procedures Perform all analyses and quality control measures in accordance with the laboratory's Standard Operating Procedures Perform equipment maintenance and calibration in accordance with the laboratory's Standard Operating Procedures Maintain a clean and safe work area Enter data into the LIMS as specified and report data to the client, verbally and electronically Store and dispose of client samples in accordance with the laboratory's Standard Operating Procedures Qualifications Degree in Geology or similar is preferred At least 1-3 Years Laboratory Experience Computer and software proficient Ability to multitask In order to perform analysis, candidate must be able to distinguish colors Authorization to work in the United States indefinitely without restriction or sponsorship Professional working proficiency in English is a requirement, including the ability to read, write and speak in English. Additional Information This role is full-time and the candidate must be able to work, Tuesday - Saturday 1:00pm - 9:00pm, Training will be conducted Monday - Friday. Compensation Range : $20 - $27 per hour, based on experience. Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Company description: 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 laboratories work with the biggest companies in the world to ensure :40 the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It 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. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2023, Eurofins generated total revenues of EUR 6.515 billion, and has been among the best performing stocks in Europe over the past 20 years. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

The 2nd Shift Quality Control Inspector is responsible for performing in-process and final inspections of sheet metal components to ensure compliance with drawings, specifications, and customer requirements. This position plays a key role in maintaining product quality, preventing defects, and supporting a culture of operational excellence. Key Responsibilities * Perform in-process, first-article, and final inspections using standard metrology tools (calipers, height gauges, micrometers, pin gauges, thread gauges, etc.) * Verify part conformance to engineering drawings, tolerances, and work instructions * Read and interpret blueprints, GD&T, and manufacturing specifications * Document inspection results accurately in quality records, travelers, and digital systems * Identify nonconformances * Conduct surface finish, weld quality and dimensional inspections as required * Collaborate with production operators and supervisors to resolve quality issues * Maintain a clean, organized, and safe work environment * Support continuous improvement initiatives Qualifications * Required: * 1+ years of experience in quality inspection, preferably in sheet metal fabrication or manufacturing * Ability to read and interpret blueprints * Proficiency with standard inspection tools * Strong attention to detail and accuracy * Ability to work independently on 2nd shift * Basic computer skills for data entry and documentation * Preferred: * Experience with FAIRs & ISO 9001 environments * Knowledge of welding inspection (visual weld criteria, AWS standards) Physical Requirements * Ability to stand for extended periods * Ability to lift up to 40 lbs. * Frequent bending, reaching, and handling of materials

Job Description QC Specialist I As a QC Specialist I in the Health Care Services industry, you will play a critical role in ensuring the quality and safety of our products. You will be responsible for preparing data packets and Certificates of Analysis for product release as well as maintaining accurate records and communicating any issues or concerns to the appropriate parties. Your attention to detail and commitment to quality will be essential in this role. Why Join Leiters Health? Are you passionate about making a real impact in the pharmaceutical industry? Do you thrive in a collaborative, innovative environment where your skills and ideas are valued? Look no further - Leiters Health is seeking talented individuals like you to join our dynamic team! At Leiters Health, we're not just another pharmaceutical company - we're pioneers in the field, dedicated to delivering high-quality compounded sterile products and outsourced solutions to healthcare providers nationwide. Our commitment to excellence and patient safety is at the core of everything we do. Innovative Culture: Be part of a forward-thinking company that encourages creativity, welcomes fresh ideas, and fosters an environment of continuous improvement. Meaningful Work: Contribute to a purpose-driven organization dedicated to providing critical medications and healthcare solutions that positively impact patients' lives. Professional Development: Access ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry. Cutting-Edge Technology: Work with state-of-the-art facilities and advanced technologies, staying ahead of the curve in pharmaceutical manufacturing. Collaborative Environment: Join a team of passionate individuals who are dedicated to teamwork, support, and mutual success, fostering a culture of inclusivity and collaboration. Who We're Looking For: We're seeking enthusiastic individuals who are driven, adaptable, and passionate about contributing to a mission-driven organization. Whether you're an experienced professional or just starting your career, Leiters Health provides an environment where your skills and talents will be recognized and appreciated. Sound like you? Apply today! Qualifications: Bachelor's degree in a scientific field 1+ years of experience in a quality control role Strong attention to detail and ability to follow procedures Excellent communication and interpersonal skills Ability to work independently and as part of a team Experience in the Health Care Services industry Knowledge of FDA regulations and guidelines Experience with laboratory testing equipment Certification in quality control or related field Responsibilities: Prepare data packets and Certificates of Analysis for product release. Maintain accurate records of all quality control activities Communicate any issues or concerns to the appropriate parties Ensure compliance with all relevant regulations and standards Participate in continuous improvement initiatives to enhance quality and efficiency Benefits: Smart healthcare coverage options that rewards wellness (and puts money back in your pocket! Flexible Spending & Health Savings Accounts (FSA & HSA) available Dental & Vision insurance Employer Paid Life Insurance & Employee Assistance Program Short Term & Long-Term Disability Insurance Up to 4% 401K Matching (100% vested on day one!) Generous Paid Time Off Options - vacation, sick, paid leave and holidays! $5,250 Annual Tuition Reimbursement after 6 months $1,000 Referral Bonus Program with no limit Eligible for annual bonus program Shift: Monday-Friday 1st Timeline: We will be accepting applications on an ongoing basis until position is filled. We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law. *Please note that we do not work with third-party recruiters or agencies for this position. If you are a qualified candidate and wish to apply for this job, please do so directly through our official application process. We appreciate your understanding and cooperation in this matter.

Quality Control Inspector - 26000006Description What We Are Looking For We need a detail-oriented individual to perform visual, mechanical, functional, and dimensional inspections on various medical device products using specialized test equipment. Your responsibilities will include conducting timely quality reviews of device history records to ensure proper batch disposition and release. As a key member of our Quality Control Team, you'll serve as a reviewer and approver for both products and documentation, ensuring full compliance with customer specifications and regulatory requirements. Join our growing team where your attention to detail can make a real difference in the quality of life-saving medical devices! Onsite This role has an onsite work schedule requiring the person to be in the onsite location 5 days a week. What's in it for You! Competitive Pay: $21. 00 - $23. 00 per hour. Our employees are the best part of our company. We want you to feel valued, appreciated, and included. Because of this, we make sure your hard work is recognized. Paid Leave (US ONLY): Enjoy time away from work with Company paid holidays and a flexible working schedule through our paid time off (PTO) policy. Yep, you read that correctly. We are a Company that values you and makes sure you take time for yourself. 401(k): Prepare for a secure retirement with our 401k plan, which includes an employer matching contribution. Comprehensive Health & Wellness Plans: We offer a comprehensive benefit package that includes medical, dental and vision coverage, company-paid short-term and long-term disability insurance, as well as company-paid basic life insurance that supports you during your career with us. We believe that taking care of our employees is essential, and these benefits reflect our commitment to your health, security, and peace of mind. Global Team: With our state-of-the-art corporate headquarters in Rock Hill, South Carolina, our global team has a presence across more than 15 countries worldwide. Experience a workplace comprised of talented individuals who are passionate about serving our customers and each other. Innovative Culture: Innovation is at the heart of what we do! Since our founding in 1986 by Chuck Hull, the inventor of 3D printing, we have continuously pushed the boundaries of what is possible with additive manufacturing. When you join 3D, you will have the opportunity to work with cutting edge technology in an innovative and collaborative culture!Talent Development: At 3D Systems, we invest in talent programs to support employees with opportunities to grow, contribute, develop, and thrive in their careers. Connection & Engagement Opportunities: We strive to cultivate an environment where our diverse global workforce can connect and thrive. Our Employee Resource Group program, Employee Recognition program, and 3D Gives Back program, are just a few examples of how you will be empowered to build connections, celebrate wins, and make a meaningful impact. What You Will Do Perform inspection tasks using various test instruments and equipment to measure values and verify functional operation of components. Determine product acceptability and recommend disposition of defective items according to established procedures. Generate Non-conformance Reports for products found outside specifications and communicate with quality/development. engineers regarding product and documentation defects. Complete all tasks accurately and on-time with meticulous attention to detail. Review and resolve documentation discrepancies with manufacturing/operations personnel to facilitate timely product release. Make final disposition decisions and prepare certificates of compliance/analysis based on comprehensive documentation review. Build quality into every aspect of the material release process by maintaining strict compliance with all quality requirements. Participate actively in continuous improvement initiatives, problem-solving, and professional development. Qualifications What You Will Bring Educational Requirements High School Diploma or GED required. Experience Required Previous experience in Quality Control, manufacturing, or production environment required Technical proficiency with precision measuring tools including calipers, micrometers, and pin gauges Working knowledge of Microsoft Word and Excel for documentation and data analysis Ability to work across multiple software platforms and systems Strong attention to detail with demonstrated ability to perform repetitive tasks with accuracy Capability to manage multiple tasks and competing priorities in a fast-paced environment Ability to work effectively both independently and in team settings Strong written and verbal communication skills for effectively documenting issues and communicating with engineers This position serves the Quality Control Group, which includes the need to review technical information from aerospace and defense customers. Preferred Experience Experience with Coordinate Measuring Machines (CMM) is a plus. Applications accepted online through January 30, 2026 #LI-MP1 3D Systems is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, color, ethnicity, religion, sex, age, sexual orientation, genetic information, marital status, gender identity or national origin or because he or she is an individual with a disability or a disable veteran, Armed Forces service medal veteran (referred to collectively as "protected veterans"). The Company also provides applicants with equal employment opportunities without regard to pregnancy, childbirth, medical needs arising from pregnancy or childbirth, and related medical conditions including, but not limited to, lactation. Primary Location: US-CO-LittletonWork Locations: USA-CO-Littleton 80127Job Level: Entry LevelTravel: NoType of Position: EmployeeJob Posting: Jan 12, 2026, 4:07:29 PM

Summit Interconnect is the premier electronics manufacturer in the US, located in Aurora, Colorado. Specializing in printed circuit board (PCB) assembly, we build the latest application designs from leading technology companies. From satellites and rocket payload to cutting-edge medical devices, we are known for our speed, service, and impeccable commitment to quality. We are continuously innovating our processes and systems to stay on the cutting edge of printed circuit board assembly manufacturing. Our vision is to have the best employees working to provide an outstanding service experience, and the coolest technology solutions for our customers. We look forward to you joining the team! Position Summary Execute the inspection of electronic assemblies according to industry specific standards. Ensure that the specifications of the established quality standards are met on all out-going products. Assist the Quality Assurance Manager, Production Manager and other company leadership with quality related functions as required. What you will do…. Inspect Printed Circuit Boards (PCBs) and Printed Circuit Boards Assembly (PCBAs) using microscope and magnifying tools following supplied data from customer and IPC-A-610 guidelines. Complete customer Certificates of Compliance (C of C) as required. Ability to separate good and non-conforming product during inspection process. Log inspection findings into electronic logs. What you need… High school diploma or equivalent. Minimum experience of 1 year in Electronic PCB Assembly. Minimum experience of 1 year in Quality Control. Understanding of quality concepts including sampling plans and continuous improvement Good working knowledge and understanding of PCBA manufacturing processes. Ability to read and interpret drawings, prints and component datasheets. Familiarity with basic measuring instruments tools and gauges (calipers, micrometers, etc.) Proficient with Microsoft office (Excel, Word, etc.). Excellent communication skills both written and verbal. (Including ability to read, understand and explain GMP, process procedures and other necessary documentation). Positive attitude to changes. Self-motivated with a team attitude. Be able to work scheduled and extra hours as required. Attention to detail. Preferred Proficient with IPC-A-610 standard (CIS preferred) Location: 20100 E 32nd Pkwy, #225 Aurora, CO 80011 Compensation : -$19.00-$20.00 /hour DOE +shift differential Schedule: Monday-Friday 11:00am-7:30pm Benefits Advanced Assembly has an excellent benefits program. We believe in taking care of our employees. We also have fun with regular company events, BBQ's, employee recognition awards, and performance- based bonus plans. Competitive Benefits Include: Medical Dental Vision EAP (free employee assistance programs) 401(k) plan Life Insurance Paid Time Off (PTO) Seven (7) paid holidays a year Candidates must pass background and drug testing. ITAR Compliance Notice This position requires compliance with the International Traffic in Arms Regulations (ITAR). Under ITAR, candidates must be a U.S. citizen, U.S. lawful permanent resident (e.g., "Green Card" holder), asylee, or refugee as defined by 8 U.S.C. 1324b(a)(3). Applicants who do not meet this requirement may not be eligible for employment in this position. Summit Interconnect is an Equal Opportunity Employer We are committed to fostering an inclusive and diverse workplace where everyone is valued and respected. We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status, or any other legally protected characteristic. tation, gender identity, national origin, age, disability, genetic information, veteran status, or any other legally protected characteristic.

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.

RESEARCH CHEMIST/CHEMICAL ENGINEER Rocky Mountain Scientific Laboratory Department:Advanced Chemistry & Chemical Processing Group Yes Travel:No Schedule:Full-time Description of Business Environment: Peace is often associated with passivity. At Rocky Mountain Scientific Laboratory, we associate peace with strength, courage, and action. We know that enabling peace to prevail is not for the faint of heart, which is why we built our company foundation on the core values of Integrity, Quality, Agility, and Grit. We pride ourselves in providing unequaled services and technologies in the field of applied energetics to our customers. Our experts possess extensive knowledge and capability in energetic materials and military systems enabling them to offer analytical characterization, modeling & simulation, design, system integration, prototyping, test engineering, and proof-of-concept production services covering a wide range of applications. Our strengths lie in our ability and relentless determination to get the job done quickly and affordably. RMSL is an Equal Employment Opportunity (EEO), Affirmative Action employer and welcomes all qualified applicants. All qualified applicants will receive fair and impartial consideration for employment without regard to race, color, religion, sex, age, disability, veteran status, national origin or other legally protected status. An applicant with a disability or a disabled veteran can request reasonable accommodation to apply for one of our positions. Specific Job Description: RMSL is a growth company with an outstanding job opportunity for a Research Chemist. This position will report to the Advanced Chemistry & Chemical Processing Group Lead. The Research Chemist/Chemical Engineer will be an integral part of a small cross functional team working on exciting development projects with cutting-edge technology. In this role, the ideal candidate will have a strong background in Chemistry/Chemical Engineering with experience in organic and/or inorganic synthesis. This role will be a part of an integrated team focused on the development of novel energetic systems, energetic material scale-up processes, development of ammunition and armaments, testing and analysis of energetic materials. This individual must demonstrate innovation, an ability to learn, out-of-the-box thinking and creativity. Duties Include: Develop novel synthesis and scale-up processes Characterize novel energetic materials using a variety of analytical methods Formulation optimization of propellants, pyrotechnics, and explosive formulations Handling and testing of energetic materials, armaments, and weapon systems Integrate energetic materials in to end articles such as ammunition and munitions. Ability to handle materials with strict adherence to safety process requirements Design of experiments and test series that result in safe and efficient collection of data Design, source selection, installation, maintenance, and operation of specialized instrumentation and testing equipment Assistance with company compliance in restricted information security regulations Project engineering tasks such as report writing, technical presentations (at customer and public meetings), and technical deliverables tracking Required Skills: Problem solver that can work in a team environment on fast pace projects Hands-on experience with energetic materials Proficient in standard laboratory practices Exercises creative thinking and innovation Strong verbal and written communication skills Physical requirements: Must be able to sit for extended periods of time; must be able to lift up to 50 lbs.; must have the ability to see near and far and work with a computer monitor Required to bend, sit, stand and lift to perform job effectively Highly Beneficial Skills: Familiar with general explosive effects and chemistry Experience in one or more of the following areas Continuous Synthesis Armament and munition development Energetic material synthesis and formulation Laboratory and pilot plant scale-up of energetic materials Knowledge of basic-intermediate chemistry and/or chemical engineering Experience with chemical formulation development Minimum Qualifications: Must have a BS or higher in Chemistry or Chemical Engineering Ability to obtain security clearance Ability to obtain CO State Blasters Permit Benefits: Medical insurance Dental insurance Vision insurance 401(k) with matching Disability insurance Life insurance Paid time off Professional development Flexible schedule

Job Description Summit Interconnect is the premier electronics manufacturer in the US, located in Aurora, Colorado. Specializing in printed circuit board (PCB) assembly, we build the latest application designs from leading technology companies. From satellites and rocket payload to cutting-edge medical devices, we are known for our speed, service, and impeccable commitment to quality. We are continuously innovating our processes and systems to stay on the cutting edge of printed circuit board assembly manufacturing. Our vision is to have the best employees working to provide an outstanding service experience, and the coolest technology solutions for our customers. We look forward to you joining the team! Position Summary Execute the inspection of electronic assemblies according to industry specific standards. Ensure that the specifications of the established quality standards are met on all out-going products. Assist the Quality Assurance Manager, Production Manager and other company leadership with quality related functions as required. What you will do…. Inspect Printed Circuit Boards (PCBs) and Printed Circuit Boards Assembly (PCBAs) using microscope and magnifying tools following supplied data from customer and IPC-A-610 guidelines. Complete customer Certificates of Compliance (C of C) as required. Ability to separate good and non-conforming product during inspection process. Log inspection findings into electronic logs. What you need… High school diploma or equivalent. Minimum experience of 1 year in Electronic PCB Assembly. Minimum experience of 1 year in Quality Control. Understanding of quality concepts including sampling plans and continuous improvement Good working knowledge and understanding of PCBA manufacturing processes. Ability to read and interpret drawings, prints and component datasheets. Familiarity with basic measuring instruments tools and gauges (calipers, micrometers, etc.) Proficient with Microsoft office (Excel, Word, etc.). Excellent communication skills both written and verbal. (Including ability to read, understand and explain GMP, process procedures and other necessary documentation). Positive attitude to changes. Self-motivated with a team attitude. Be able to work scheduled and extra hours as required. Attention to detail. Preferred Proficient with IPC-A-610 standard (CIS preferred) Location: 20100 E 32nd Pkwy, #225 Aurora, CO 80011 Compensation: -$19.00-$20.00 /hour DOE +shift differential Schedule: Monday-Friday 11:00am-7:30pm Benefits Advanced Assembly has an excellent benefits program. We believe in taking care of our employees. We also have fun with regular company events, BBQ's, employee recognition awards, and performance- based bonus plans. Competitive Benefits Include: Medical Dental Vision EAP (free employee assistance programs) 401(k) plan Life Insurance Paid Time Off (PTO) Seven (7) paid holidays a year Candidates must pass background and drug testing. ITAR Compliance Notice This position requires compliance with the International Traffic in Arms Regulations (ITAR). Under ITAR, candidates must be a U.S. citizen, U.S. lawful permanent resident (e.g., "Green Card" holder), asylee, or refugee as defined by 8 U.S.C. 1324b(a)(3). Applicants who do not meet this requirement may not be eligible for employment in this position. Summit Interconnect is an Equal Opportunity Employer We are committed to fostering an inclusive and diverse workplace where everyone is valued and respected. We provide equal employment opportunities to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, veteran status, or any other legally protected characteristic. tation, gender identity, national origin, age, disability, genetic information, veteran status, or any other legally protected characteristic.