Quality control inspector jobs in Thornton, CO - 150 jobs

The Quality Control Technician at our 503B outsourcing facility is responsible for ensuring that all products meet the highest standards of quality and safety before they reach our clients. This role involves performing various tests and inspections on raw materials, in-process samples, and finished products, and environmental monitoring in cleanroom environments. The Quality Control Technician will work closely with production, quality assurance, and other teams to identify and resolve any quality issues, maintain accurate documentation, and support continuous improvement initiatives. This position requires a strong understanding of Good Manufacturing Practices (GMP), FDA regulations, and 503B guidelines, along with excellent attention to detail and analytical skills. Responsibilities Conduct routine testing and inspection of raw materials, in-process samples, and finished products to ensure compliance with established quality standards and specifications. Perform environmental monitoring, including sampling of air, surfaces, and personnel in cleanroom environments, ensuring adherence to GMP regulations. Maintain accurate and detailed records of all quality control activities, including test results, deviations, and corrective actions. Collaborate with production and quality assurance teams to investigate and resolve any quality issues or non-conformances. Operate and maintain laboratory equipment, ensuring proper calibration and function according to standard operating procedures (SOPs). Participate in the validation and qualification of new equipment, processes, and methods to ensure consistent quality and reliability. Assist in the development and revision of SOPs, work instructions, and other quality-related documents. Ensure timely and accurate completion of all required documentation and reports, maintaining compliance with FDA regulations and 503B guidelines. Support internal and external audits by providing necessary documentation and responding to audit findings in a timely manner. Stay current with industry trends, regulatory updates, and best practices related to quality control and 503B outsourcing facilities. Assist in the training and mentoring of new quality control staff, ensuring adherence to company policies and procedures. Work closely with the Quality Assurance team to implement and monitor quality improvement initiatives. Conduct stability testing and data analysis to ensure product integrity over specified shelf life. Physical Requirements Must possess 20/20 vision (with or without correction) and be able to pass vision and colorblindness test Qualifications TRAINING (e.g. Professional Qualifications, On-the-job Training, Education) An equivalent combination of education, training, and experience may substitute. High School Diploma or equivalent College degree preferred Exceptional attention to detail Current Good Manufacturing Practices (cGMP) Experience Preferred Good Documentation Practices (cGDP) experience preferred Cleanroom experience & experience wearing Personal Protective Equipment (PPE) preferred Excellent verbal and written communication skills Experience with Microsoft Office Suite (Word, Excel) and ability to utilize various software programs Strong work ethic and ability to work effectively as a team The Quality Control Team provides critical support to the Production Team. This is a 100% on-site position. Reliable transportation and punctuality are required Must be able to lift items repeatedly (lifting as a team for heavier items) Must be able to work in a variety of positions and locations such as sitting, standing, squatting, kneeling, reaching, and walking, for prolonged periods of time Must be able to wear required PPE for extended periods of time Position requires handling of laboratory chemicals or hazardous materials Must be able to use necessary equipment such as computers, scanners, or other technology devices as assigned Travel As part of your job duties, travel may be required. If applicable, you will be compensated at the current IRS mileage reimbursement rate.

Core Hours: Monday - Friday, 8:00 am - 5:00 pm Purpose and Scope Provide direct supervision of a team of analysts responsible for the testing and release of Tolmar products in support of manufacturing timelines. Essential Duties & Responsibilities Prioritize workload to meet timelines while ensuring on-time delivery of all projects, testing and action items. Take ownership of tasks and results from initiation to completion to meet commitments and proactively address outcomes. Escalate and communicate items which arise per the timelines specified in the department escalation strategy. Execute all business and department goals and initiatives on time. Ensure adherence for compliance with all processes and procedures including training completions, QE and CAPA due dates, notebook and logbook audits, archiving, schedules, internal assessments. Issue all Certificates of Analysis within 2 business days of last test completion. Generate, monitor and report weekly team and analyst KPIs. Supervise the testing and release of Tolmar products, cleaning samples, EM, Bioburden, Endotoxin, raw materials, and stability samples. Strive to balance workload across all sites and teams to ensure adequate resource allocation. Partner with the scheduler to schedule all testing and reviews, review the weekly schedule and ensure company and department targets are met in the shortest possible cycle time. Provide assistance, training and leadership for direct reports through utilization of the OTD resources. Create, revise and monitor training progress utilizing training matrices for immediate functional areas, and collaborate with team on remediation of training gaps for site training matrix. Set and communicate clear expectations for analysts including providing regular feedback and coaching, monitoring progress and fostering employee development to align individual and team performance with organization goals. Create and revise developmental plans to help employees grow their skills and advance their careers. Monitor and discuss progress of employee's performance, growth and development in one on ones utilizing the career ladder and KPIs. Establish sample priorities for QC scheduler, submit schedule tickets as needed and ensure adherence to ship dates. Partner with the investigations team and the scheduler to ensure all actions for QEs are completed in 24 hours, second analyst testing is completed in less than 5 business days and QEs are closed on time (less than 45 business days). Support and execute all potential 3-day field alert investigations and actions expeditiously. Submit document change requests for all document updates and minimize document revisions for routine updates where possible. Ensure all samples logged into the LIMS system are submitted correctly. Identify, and complete cost savings initiatives and facilitate continuous improvement. Participate in leadership development activities and take an active role during department and company activities. Aid in setting procedure and ensure that all operations and functions (including the laboratory) are in full FDA, cGMP compliance and staff is properly trained. Utilize senior analysts to assist in training, document updates, laboratory investigations, projects, or advanced technical issues. Conduct and coordinate laboratory investigations, and all associated actions. Review and approve technical reports, test methods, specifications and procedural documents and ensure overall validity of the analytical results and review stability reports. Participate in project teams, company and department meetings, third party audits, and regulatory audits. Monitor departmental spending to stay within the established budget. Demonstrate leadership aptitude in technical functions and people management. Ability to perform designated duties under minimal supervision and support departmental management in all aspects of organizational functions. Accountable for maintaining an atmosphere of teamwork, cordiality and respect towards co-workers. Accountable for meeting departmental and compliance timelines. Participate in required annual hazardous waste training. Hazardous waste involvement may include, but is not limited to, container and tank management and inspections, generation of hazardous waste as a part of production or sampling processes and transfer of hazardous waste between lab procedure area, satellite accumulation and storage. Respond to spills per the Chemical Spill Procedures. Participate in the interview and selection process for candidates, as required. Perform other duties as required by business demands. Knowledge, Skills & Abilities Possesses a strong sense of purpose and drive to meet deadlines without sacrificing quality. Balances the need for speed with a commitment to accuracy and quality, completing tasks thoughtfully and effectively Expert knowledge in analytical testing of drug substances and formulations for Chemistry or Microbiology. Ability to perform designated duties under minimal supervision and support departmental management in all aspects of organizational functions. Proficient with computer systems for sample tracking, laboratory equipment, raw data handling and storage. Knowledge in analytical method validation and instrument qualification. Thorough knowledge of government regulations of drugs and medical devices as they apply to laboratory work. Technical leadership when working on complex problems within a technical scope in which analysis of situations or data requires an in-depth evaluation of various factors. Exceptional interpersonal and organizational skills that lead directly to the advancement of others and of the QC department. Ability to supervise a team of analytical professionals that is fully compliant with current Good Manufacturing Practices. Knowledge of analytical troubleshooting and product investigation. Effective oral and written communication. Proficient in the use of analytical laboratory instruments such as HPLC, FTIR, GPC, GC, and UV-Vis spectrophotometers, CCIT, Endotoxin, MODA,. Ability to prepare, review, conduct and assess analytical method validations, feasibility and suitable for use. Ability to coordinate activities to assure customers' needs are met in terms of sample analysis cycle time. Core Values The Quality Control Supervisor is expected to operate within the framework of Tolmar's Core Values: Center on People: We commit to support the well-being of our patients. We are committed to treating our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together. Are Proactive & Agile: We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes. Act Ethically: We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace. Constantly Improve: We are committed to a collaborative & proactive effort to improve our products, systems, processes, and services by reducing waste, increasing efficiency & improving quality. Are Accountable: We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future. Education & Experience Bachelor's degree in science, preferably in Chemistry or Biochemistry, or Microbiology. Six or more years' experience in an analytical laboratory environment with at least five years in a pharmaceutical GMP setting. Supervisory or team lead experience is preferred. Working Conditions Laboratory setting. Will be exposed to solvents, bio-hazardous materials, hazardous waste, and pharmaceuticals. Must be adaptable to shifting priorities and operate with a sense of urgency while maintaining high quality to meet important timelines in a high throughput lab. Business demands present a need to work extended hours. On call weekend support will be required with a minimum of 8 on call weekends each year. Compensation and Benefits Annual pay range $100,000 - $105,000 depending on experience Bonus Eligible Benefits information: careers/employee-benefits Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience. Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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.

Join SEAKR Engineering, a leading-edge provider of advanced electronics for space applications. Pushing the boundaries of technology on a mission to change the world for the better from space. Job Description SEAKR is looking for a motivated Lead, Quality Control Receiving Inspector (QCRI) who has experience inspecting high-reliability Mechanical and EEE (electrical) components. A successful candidate will have a technical aptitude with analytical problem-solving skills, the ability to work in a team environment, and effective time management skills for efficient task prioritization. The QCRI reports to the Receiving Inspection Supervisor within the Supply Chain division. Job responsibilities include… Verifying documentation, materials, and products meet the PO and engineering drawing requirements Performing basic dimensional inspections using micrometers, calipers, feeler gages, etc. Performing basic electrical inspections such as continuity testing in accordance with engineering drawing requirements Managing multiple receipts simultaneously, in different physical and electronic locations Navigate SEAKR's Enterprise Resource Planning (ERP) tool to support review, routing, and disposition non-conforming product and/or electronic inventory transactions Tracking and documenting arrival reports Processing and managing supplier RMAs Create, document, and implement inspection criteria and procedures Maintain an active role on internal continuous improvement teams Provide CMM testing and reporting as required Review and edit documentation as required. Able to work independently and as a team, along with Property, Supply Chain (Buyers), SQE's, QE's and other department/teams as required. Cover and report team duties in absence of the RI Supervisor when required. Qualifications A High School Diploma or GED is required. Candidate will have a minimum of 6 years of experience in product assurance, preferably in an inspection role (receiving, in-process, or final QA/QC related to electronics manufacturing). The candidate will also be able to satisfy the following: Must be able to pass IPC J-STD and IPC-A-610 inspection certification testing, including vision testing Must have a basic knowledge of dimensional inspection tools Must have the ability to interpret and apply engineering documentation (e.g., dimensioned drawings, SCDs, commercial datasheets) Must have a strong attention to detail to support strict adherence to work instructions or inspection procedures Have good attendance Work independently, and as a team. Preferred skills & experience include: CMM programming and/or operational experience; Proficient knowledge in GD&T Familiarity with AS9102 FAI requirements Training/Certification to requirements for electronic assemblies (e.g., J-STD-001, IPC-A-610 or similar) Experience operating inspection or test equipment (e.g., XRF, X-Ray or similar) Proficiency with an Enterprise Resource Planning (ERP) system (e.g., Kronos, IFS, Oracle, SAP, etc.) Additional Information Compensation: Base pay range is $23-30/hour, depending on qualifications. SEAKR has very rich medical, dental and vision insurance plans, along with a generous 401(k) retirement plan. In addition to base salary, employees are eligible for a year-end bonus. SEAKR offers a variety of paid leave, such as vacation, sick, bereavement, and FMLA. Schedule: This position will be onsite during regular M-F workdays with 9-hour shifts, with every other Friday off. SEAKR is an Equal Opportunity Employer - All your information will be kept confidential according to EEO guidelines. US Citizenship Required Applications will be accepted until 1/30/26

Description The Quality Inspector role offers the opportunity to ensure excellence across manufacturing and inspection processes, supporting compliance, quality standards, and customer specifications. This position plays a key role in delivering high-quality products and services while collaborating with Engineering, Project Management, Procurement, and Manufacturing teams. Quality Inspectors drive continuous improvement, identify non-conformances, and help create a culture of safety, accountability, and operational excellence. This role provides hands-on experience with inspection tools, blueprints, and technical drawings, with increasing responsibility based on experience level. It offers the chance to mentor and develop team members, influence process improvements, and contribute directly to the success and efficiency of manufacturing operations. RK Company Overview As a second-generation, family-owned enterprise, RK Industries, LLC (RK) offers a diverse range of construction, manufacturing, advanced fabrication and building services. Led by Rick and Jon Kinning, RK represents seven distinct lines of business that work together to provide seamless project collaboration. Our exclusive building methodologies, accredited safety standards and professional execution allow us to turn our customers' greatest concepts into reality. The Quality Inspector will be responsible for ensuring that all manufacturing and inspection activities align with established quality standards, process documentation, and customer specifications. This role plays a key part in cross-functional teams including Engineering, Project Management, Procurement, and Manufacturing teams. The Quality Inspector upholds organizational performance by driving compliance, identifying non-conformances, and contributing to continuous improvement initiatives. Role Responsibilities Provide overall supervision for assigned project processes, including achieving performance metrics for safety, quality, delivery, and productivity. Drive the application of Lean Manufacturing tools and concepts to achieve measurable and sustainable improvements for assigned project processes. Train, mentor, and grow production team members to build a high performing and engaged workforce. Supervise manufacturing personnel, ensuring alignment, engagement, development, and retention of talent. Promote a culture of safety, accountability, continuous improvement, and operational excellence consistent with RK Mission Critical values. Identify opportunities for process efficiency and waste reduction. Accountable for the supervision of assigned project processes, including adherence to safety requirements, and standard work instructions. Coordinate with the Production Manager to provide tactical input on manufacturing support and execution. Participate in the development and implementation of manufacturing processes, including hazard analysis, safety procedures, and team member skill assessments. Perform these and other comparable related duties as instructed by the management team. Qualifications Quality Inspector-1: Includes All of the above plus: High school diploma or GED required; additional vocational or technical training preferred. 2+ years of related experience, preferably in a manufacturing or construction environment. Receives direct supervision in performing technical responsibilities. Familiar with basic inspection tools and techniques. Ability to follow detailed instructions and work in compliance with standard procedures. Understands acceptance criteria and is aware of internal and external quality expectations. Actively supports team goals and production timelines. Displays judgment and initiative in resolving issues and making recommendations. Willingness to contribute to continuous improvement efforts. Proficient in Microsoft Office 365 and capable of navigating ERP systems. Brings energy to a team under the general supervision of an experienced professional or manager. Quality Inspector-2: Includes All of the above plus: Associate degree or equivalent combination of education and experience. 4+ years of quality experience in manufacturing or construction, with increasing responsibility. Reads and interprets blueprints, diagrams, technical drawings, and models independently. Able to perform majority of installer tasks independently while meeting quality and delivery expectations. Strong understanding of industry standards such as NFPA 70 (NEC), NECA, and NEMA. Experience managing non-conformances and supporting corrective/preventive action processes. Effective communicator with strong documentation and reporting skills. Strong attention to detail and commitment to quality. Able to design and deliver basic training on inspection protocols or tools. Demonstrates initiative, problem-solving ability, and independent judgment in evaluating quality issues. Effectively balances workload while consistently meeting deadlines and shifting demands. Proactively collaborates with team members to meet production goals. Understands continuous improvement initiatives and is willing and able to make contributions. Quality Inspector-3 (Exempt): Includes All of the above plus: Senior-level Inspector responsible for complex installation requirements, troubleshooting, and team leadership. 6+ years of quality experience in manufacturing or construction, with increasing responsibility. Demonstrated ability to independently perform complex inspections and resolve quality issues. Proven experience identifying process gaps and suggesting effective improvements. Working knowledge of ISO 9001 principles and quality management systems. Excellent problem-solving skills with a proven ability to collaborate with engineering, project management, and production teams to effectively resolve complex related challenges and plan upcoming projects. Reads and interprets advanced blueprints and manages job requirements independently. Leads, trains, mentors, develops, and drives a quality team. Demonstrates deep understanding of methods, tools, standards, and quality assurance. Actively supports lean manufacturing principles and continuous improvement initiatives. Minimum Physical Requirements and Accountability Work outside, inside, and in dusty, noisy and hazardous areas. Work in high places, tight places, confined spaces and/or other adverse locations. Climb, balance, squat, kneel and crouch for extended periods. Ability to lift, move, and/or carry 50 lbs. Comply with all company policies and procedures. All employees are accountable for safety and health and are empowered to stop work if an unsafe condition is present. Employees should immediately notify their supervisor so that the hazard may be corrected. What Sets RK Industries Apart Safety: Our unmatched culture of safety is our foremost core value, guiding everything we do each day: Health, Safety, & Environmental Awards: Whether in Construction, Manufacturing, Fabrication, or Service, RK Industries is highly recognized and accredited throughout the industry: Accreditations & Recognition Benefits: RK Industries offers competitive benefits to support your growth and well-being: Benefits & Rewards Philanthropy: RK Industries not only builds our community through our projects, but also invests in it by supporting local services for over a decade through the RK Foundation: RK Foundation Development: Through RK University, we provide hands-on training and development opportunities that empower employees to advance their careers and grow within the company, to include leadership and technical learning opportunities, we well as our accredited apprentice program: RK University & RK Apprenticeship Program Applications are accepted on an ongoing basis. RK Industries, LLC is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability, protected veteran status or any other status protected by applicable law

Job Description GENERAL DESCRIPTION The Quality Control Technician I is responsible for inspecting and testing our products to ensure conformance with PCI standards and design specifications that are detailed on the pour sheet. This position is critical to ensuring the quality and safety of our products. Salary range $24.50/ hr - $27.00/ hr. Based on experience. WHY WORK FOR US? At Wells, we empower our team members to deliver an exceptional client experience. Our employees are talented problem solvers that shine in preconstruction, engineering, operations, and project management. They bring innovative solutions that yield outstanding results. In the design and construction industry, we focus on honesty and hard work to build trust that lasts beyond individual projects. Our team is consistently working to improve building processes and raise industry standards. We meet our partners' needs through collaborative efforts that ensure safe and certain results, reducing risks along the way. Together, we help businesses and individuals succeed and change our communities for the better. WHAT WE HAVE TO OFFER Wells values our employees and is committed to providing a competitive and comprehensive benefits package. Please note that the benefits listed here are for non-union employees. Benefits for union employees are covered under separate collective bargaining agreements which can be obtained through their union business agent or their HR representative. Health, dental and vision insurance Paid premiums for short- and long-term disability, and life insurance Wellness Incentives Paid holidays Flex spending for medical and daycare Health savings account (HSA) 401(k) plan with profit sharing Access to Nice Healthcare Employee Assistance Program Paid Time Off (PTO) Wishbone Pet Insurance Critical Illness Benefit Plan Accident Insurance Plan Voluntary Hospital Indemnity Plan Other benefits include Health and Family Care leave for both union and non-union employees. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES Performs pre-pour inspections including dimensions of member, position of reinforcement, location of tensioning strand, and quality of forming. Post-pour inspection of cast product Perform wet and hardened required testing on the materials used in the manufacturing of product. Prepares concrete specimens for testing. Regularly performs test for slump, temperature, unit weight, air content, and cylinder strength. Involved with tensioning of cable to record elongations and ensure cable is tensioned as designed. Perform cylinder strength tests to ensure they meet intended strength. Conduct aggregate gradations and sieve analysis. Compliance with safety policy and procedures. Maintains complete Quality Control documentation for inspections and testing performed. Identify and record quality issues and works with Production to resolve those issues. Acts in professional manner that demonstrates the individual has good character and can be trusted by all employees. Complete special projects as requested and performs other duties as assigned. Willingness to work outside all year long (Location Specific) EDUCATION, SKILLS, AND ABILITIES REQUIRED High School Diploma or GED. Must have interpersonal communication skills to interact with co-workers, supervisors, and managers. Experience with Microsoft Office. Must be able to solve problems quickly and efficiently. General math skills, be able to read a tape measure. Strong attention to detail and organizational skills. Knowledge of safety procedures that need to be followed. Ability to work with others to get the project completed efficiently. Must be motivated and self driven to complete a task. Understand and accepts changes that are implemented to become best in Class. PHYSICAL REQUIREMENTS/ ADA ESSENTIAL FUNCTIONS Physically able to lift up to 75 lbs, occasionally. Physically able to push, pull, lift, bend, climb, kneel, twist, squat, crawl and use hands/forearms repetitively and frequently. Ability to move around for up to 12 hours per day. Ability to work from ladders, scaffolding, swing stages and man lifts at various heights frequently. WORKING CONDITIONS Moderate to high risk of exposure to unusual elements. Moderate to high risk of safety precautions. Moderate to high exposure to production environment. Wet, hot, humid, and wintry conditions (weather related) (plant specific) Ability to work outside year-round (plant specific) This position profile identifies the key responsibilities and expectations for performance. It cannot encompass all specific job tasks that an employee may be required to perform. Employees are required to follow any other job-related instructions and perform job-related duties as may be reasonably assigned by his/her supervisor. “ Equal Opportunity Employer, including Veterans and Individuals with Disabilities . ” Wells participates in E-Verify and will provide the federal government with your I-9 Form information to confirm you are authorized to work in the U.S.

Job DescriptionSalary: $20/hr - $33/hr Primus Aerospace is a leading manufacturing partner to aerospace, defense & space OEMs / Primes & Tier I suppliers. The company specializes in producing high-tolerance, complex geometry parts; machined out of standard and exotic metals. Primus works directly with all major aerospace manufacturers (e.g., Boeing, Lockheed, Northrop) to provide components to mission critical civilian and defense programs. Job Purpose: The Quality Inspector performs inspections of product against customer requirements and according to internal procedures while maintaining the timely flow of product and minimizing escapes and other non-conforming materials. Quality Inspector Key Responsibilities and Accountabilities: Perform First Piece, Lot and Final Inspections against customer requirements Conduct in-depth review and able to properly interpret acceptance criteria in accordance with customer purchase order & specifications, including industry standards Command of problem solving techniques such as; 8D, Fish-Bone, 5-why & facilitate Team Based Root Cause Corrective Action(s). Define detailed in-process & final inspection plans Audit in process inspection reports/checklist on the production floor Perform and fill out AS9102 First Article Inspections and Inspection Reports Compile and confirm the accuracy of customer required shipment paperwork Understand and follow internal inspection procedures and maintain inspection records Proper tool selection based on tolerance zones Understand and maintain the ERP system per company policies Keep current with industry inspection techniques, practices and required standards Understand and stay current with industry standard inspection equipment; including calipers, micrometers, bore gauges, height gauges, indicators, etc. and the calibration and maintenance of these instruments Understand and stay current with GD&T standards, terminology and inspection methodologies Be willing to perform other duties as assigned (Calibration, Audits, CAPA, Customer Complaints, RMAs, etc.) At least 3-5 years practical experience in bench inspections and general practices and methodologies Requirements Experience with AS9100 and AS9102 Working knowledge of Special Processes Minimum of 3-5 years practical experience working with bench inspection processes and in-process inspections Working knowledge of Geometric Dimensioning and Tolerancing (GD&T) Strong time management Ability to work independently and meet deadlines Experience working in a manufacturing environment Good verbal and written communication Experience working with MS Excel and Word We offer comprehensive benefits including: Paid Time Off 401(k) with employer match Quarterly Incentive compensation Paid Holidays Medical, dental, vision & life insurance Short- and long-term disability IMPORTANT NOTICE: To adhere to U.S. Government international trade regulations, applicant must be a U.S. Citizen, or lawful permanent resident of the U.S. At Primus Aerospace, we are proud to be an Equal Opportunity Employer. We are committed to creating an inclusive environment that supports, respects, and celebrates all individuals. #zr #cj

Job DescriptionDescription: A Quality Control/Floor Inspector assists the Chief Inspector with all things as required and needed in support of the Repair Station and operations. This person reports directly to the Chief Inspector. Key Duties and Responsibilities: Maintain a clean and orderly workspace. Work efficiently with the team to ensure a smooth workflow. Assist the Chief Inspector with logbook research as required. Perform aircraft inspections when not inspecting discrepancies or work orders. Assist the Chief Inspector with floor inspection items. Giving the “ok to close panels” and being the “backup” to ensure quality and safety of our products. Assist the Chief Inspector with returning aircraft to service after work is completed. Ensure that we are delivering a safe aircraft that meets our quality standards. Inspecting discrepancies once completed for proper repairs, correct paperwork, and correct sign-off of discrepancies. (Make sure accepted or approved procedures are used at all times). Other duties as assigned. Benefits Available with employment: Medical, Dental, Vision and Supplemental Plans Estimated application closing date: 10/31/25 Requirements: Qualifications Education Requirements: Must have High School Diploma or GED Must have an FAA approved Airframe and Powerplant license. Experience Requirements: Ability to work independently with minimal direction. Ability to understand technical publications and requirements. Clear understanding of FAA and Repair Station requirements. Assist with or undertake any other duties as assigned by key personnel. Ability to work with several individuals while showing independence in balancing and prioritizing requests. Three years business/corporate aircraft maintenance experience Other Requirements: Clean driving record. Able to pass a background check. Ability to pass a drug screening test. Occasionally required to lift up to 35 pounds. Must be able to sit, stand, kneel and climb ladders. Must be able to show up to work on time ready to work. Must have dependable transportation to and from work. Ideal Candidate Will Possess the Following Skills: Attention to detail. Sincere desire to assist others. Able to develop a friendly rapport. Persistence in the face of obstacles. Professional in appearance and mannerisms. A willingness to take on responsibilities and challenges. Being reliable, responsible, and dependable, and fulfilling obligations. Being pleasant with others on the job and displaying a good-natured, cooperative attitude. Being sensitive to others' needs and feelings and being understanding and helpful on the job. Guiding oneself with little or no supervision and depending on oneself to get things done IAW acceptable techniques and methods. Maintaining composure, keeping emotions in check, controlling anger, and avoiding aggressive behavior even in very difficult situations. An ability to guide oneself with little or no supervision, depending on oneself to get things done while following the requirements of the Repair Station. Accepting criticism and dealing calmly and effectively with high stress situations being open to change (positive or negative) and to considerable variety in the workplace.

TAK Broadband is a leading end-to-end U.S. fiber broadband network construction contractor operating in 42 states. It builds more than just networks; it connects communities to new valuable digital opportunities. TAK offers comprehensive service solutions, from construction to drops to fulfillment. TAK's ecosystem of partners allows it to successfully complete every project starting from the first point of conception. This includes engineering teams, distributors, and more than 100 qualified construction crews with extensive experience across all ISP types and markets; over 300 experienced bury drop crews; and more than 700 professional technicians. We are seeking a Quality Control Technician to join our team in Denver, CO. In this role you will ensure timeliness, completeness and accuracy of work performed by technicians. You will perform inspections post-install to ensure compliance to client specifications and complete reviews to ensure proper restoration of the area. Why TAK? * Full Time * Paid Weekly * Compensation: $20 - $22 per hour, DOE * Full Benefits Package (Medical, Dental & Vision) * Paid Time Off * 401(k) with Company Match! * 25K Company Paid Life Insurance * Independent Work & Team Collaboration * Career Development & Advancement Opportunities! The Role * Ensures timeliness, completeness and accuracy of work performed by technicians * Performs inspections post install to ensure compliance to client specifications * Completes reviews to ensure proper restoration of area * Captures photos and attach to the inspection report * Performs white line excavations and collects locate data * Verifies the system is complying with all safety requirements * Performs work in a safe manner, following all OSHA and company guidelines * Prioritizes, organizes and efficiently completes tasks to meet deadlines * Works in a variety of outdoor environments * Drives Company vehicles responsibly and safely * Conducts and attends meetings as needed Requirements * 2+ years of telecommunications (i.e. cable, internet, telephone, wireless) installation or construction industry experience (sales, call center and IT roles are not considered) * Experience with quality control and verifications * Experience calling in Bluestakes a plus * Experience with underground locates and the ability to use a compass for directional instructions * Basic mechanical aptitude, ability to utilize hand tools for intended purposes * Ability to travel daily around the Chicago metro area and open to a variety of schedules * Excellent customer service, time management, problem-solving and troubleshooting skills * Ability to learn and operate testing equipment and software/programs * Ability to utilize hand tools, identify wire size/color and accurately utilize measuring devices * Ability to carry, climb, operate, and work upon an extension ladder (approximately 28 feet high and 75 pounds) * Ability to complete work indoors, outdoors, in tight spaces and elevated by bending, reaching, twisting, climbing, and working while standing up to 70% of the time * Ability to safely navigate various terrains, managing equipment and tools * A body weight of no more than 275 pounds to perform ladder work safely. Safety is our #1 Priority. If personal safety is not compromised, an accommodation may be available based on previous ladder experience in a similar role * Valid driver's license with a satisfactory driving record (no suspensions or revocations) * Passing of all pre-employment requirements (MVR, Background Check, Drug Screen) The compensation and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, with or without notice, subject to applicable law. The Company expects to accept applications for this position until January 23, 2026 but encourages interested applicants to apply as soon as possible. TAK is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by law. We maintain full compliance with the Americans with Disabilities Act and are committed to providing equal access throughout our employment practices. Individuals with disabilities may request reasonable accommodations during the application and hiring process by contacting *****************************. Salary Description $20 - $22 per hour, DOE

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

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)

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

Job Description Inspection & Packaging Lead (3rd shift) This position reports directly to the Inspection and Packaging Supervisors as well as the VILP Manager. The role is responsible for general support of the Visual Inspection, Labeling, and Packaging of finished sterile compounds. The Lead is responsible for ensuring the accuracy for label reconciliation, document completeness and correctness of all product identification. 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 positivelyimpactpatients' lives. Professional Development: Access ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry. Cutting-EdgeTechnology: Work withstate-of-the-artfacilities 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! Essential Functions: Lead and perform the line/area clearance of the visual inspection or label, and packaging activities. Review of batch record during and end of visual inspection, label, and packaging activities. Assist Inspection & Packaging Supervisors in overseeing employees who are responsible for visual inspection/labeling/packaging of finished goods. Collaborate with Inspection & Packaging Supervisors to ensure timely visual inspection and labeling of products to meet scheduled batch release dates. Ensure that training on SOPs and processes remains current. Analyze Production efficiencies downtime and waste. Lead teams to improve the results. Write investigations and CAPA actions for non-conformances in the department. Work with QA to quickly resolve any variance or document errors so that product may be released on time. Lead Problem Solving activities. Assist with maintaining batch and label inventory and managing daily staffing for visual inspection and labeling. Other duties as assigned. Supervisory Responsibilities: Lead a team of Associates, providing direction, support, and training. Provide a positive and collaborative work environment through effective communication and accountability, escalating conflict promptly and fairly. Experience and Necessary Skills: 1-year previous leadership experience or comparable experience preferred. Minimum 1 years' experience in aseptic processing preferred. Knowledge of cGMP guidelines/standards. Bachelor's degree or relevant experience preferred. Demonstrated written and oral communications skills including strong presentation skills. Excellent organizational skills and results oriented. Strong results orientation. Strong Microsoft Office skills are essential, proficient in the use of spreadsheets and word processing programs Ability to effectively bring others together and reconcile differences. Able to lift up to 50 lbs. and stand for extended periods when required Must pass an eye exam confirming 20/20 near vision corrected (with contacts or glasses) or uncorrected Must pass an eye exam confirming the ability to accurately perceive color 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 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. Monday - Friday 1130pm to 8am

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.

Core Hours Tuesday - Saturday, 7:00 am - 3:30 pm Purpose and Scope Performs routine testing of raw materials, cleaning samples, bulk intermediate and finished product, and/or stability samples, according to established regulatory protocols and procedures. Essential Duties & Responsibilities Prioritizes tasks and performs job duties with minimal guidance from management. Works to complete tasks in an efficient manner, and is a productive member of the department. Performs analyses on a variety of samples using intermediate preparation techniques and analysis methods. Employee will be trained and become proficient in the intermediate preparation techniques and analysis methods. Actively contributes to short-term team objectives, focusing on routine tasks while ensuring consistency and quality. Develops and implements strategies to overcome daily challenges and improve workflows. Applies intermediate technical skills and a foundational understanding of cGMP, organizational structure, and departmental processes to complete standard work assignments. Takes the initiative to support projects and actions demonstrating a continuous improvement mindset. Delivers high-quality work on a consistent basis, meeting deadlines and maintaining reliability in daily tasks. Proactively develops actionable solutions based on an understanding of the problem, collaborating with team members when necessary to ensure the solution is effective and aligns with organizational goals and regulatory requirements. Demonstrates strong focus and concentration to complete tasks with minimal mistakes, maintaining quality under pressure, and ensuring focus during work to support infrequent preventable errors. Takes responsibility for individual contributions and accepts accountability for performance. Actively participates in team activities, challenges, and shared responsibilities (such as T-cards, archival, etc.), showing enthusiasm and a can-do attitude to inspire others, while maintaining professionalism. Overcomes challenges with a positive attitude, staying focused on the goal even in the face of setbacks Models good laboratory stewardship by maintaining a clean, orderly and safe work environment and proactively restocks low inventory items and routine lab supplies. At the direction of management, trains junior analysts in analysis methods and lab techniques. Accountable for documenting all activities and maintaining records according to good documentation practices. Accountable for proper use, care and maintenance of instrumentation. Provides detailed accounts of testing performed to investigators. Under the direct supervision of an investigator, may perform investigational testing. Makes scientific recommendations to management/technical writers regarding QC procedures. Completes tasks on time and works to eliminate repeat errors. Follows all procedures applicable to job functions to ensure high quality of work. Responsible for ensuring that company and regulatory data integrity guidelines are consistently followed. Accountable for maintaining an atmosphere of teamwork, cordiality and respect towards co-workers and is willing to assist co-workers in the completion of tasks. Performs intermediate method transfers. Represents the department by providing accounts of testing performed and results of method transfer activities and assists with troubleshooting aberrant method transfer results, if necessary. Interacts respectfully with all other employees both inside and outside of the department and members of management and shows interest in others' input and reasoning. Appropriately resolves differences of opinion. Upon delegation, may be responsible for representing the QC chemistry laboratory when communicating with outside departments and vendors. Identifies issues and escalates those issues to the department senior leadership or management as appropriate. Participates in required annual hazardous waste training. Hazardous waste involvement may include, but is not limited to container and tank management and inspections, generation of hazardous waste as a part of production or sampling processes and transfer of hazardous waste between lab procedure area, satellite accumulation and storage. Respond to spills per the Chemical Spill Procedures. Performs additional duties as assigned. Knowledge, Skills & Abilities Knowledge of a government regulated pharmaceutical laboratory environment, preferably for drugs or medical devices including cGMP, GLP and ICH and their application to laboratory testing and review processes and procedures. Intermediate understanding of the use of USP, NF and other compendia. Ability to use and maintain analytical laboratory instruments such as HPLC, FTIR, GPC, GC, Dissolution and UV-Vis spectrophotometers. Effective written and oral communication skills. Knowledge of computer systems for sample tracking, laboratory equipment, chromatography, raw data handling and storage. Ability to interpret, understand and follow analytical procedures/calculations and scientific principles. Core Values This position is expected to operate within the framework of Tolmar's Core Values: Center on People: We commit to support the well-being of our patients. We are committed to treating our employees and those we serve as valued partners. By placing people at the heart of our actions, we actively engage, invigorate, acquire knowledge, and grow together. Are Proactive & Agile: We embody a culture of engagement and action. With a hands-on approach, we fearlessly adapt to change. We anticipate, respond swiftly and efficiently to ignite a spirit that propels us towards extraordinary outcomes. Act Ethically: We are committed to consistently conducting our business in an ethical, compliant, and socially aware manner, in line with our purpose of positively impacting lives. We actively cultivate diversity, equity, inclusion & sustainability in our workplace. Constantly Improve: We are committed to a collaborative & proactive effort to improve our products, systems, processes, and services by reducing waste, increasing efficiency & improving quality. Are Accountable: We think, act, and communicate with honesty, transparency, and clarity in alignment with our core values. We don't compromise our values for near term gain. We take accountability & ownership of our work, actions, successes, and setbacks. We strive to deliver our best as we shape the future. Education & Experience Bachelor's degree in scientific discipline, preferably in Chemistry or Biochemistry. Two or more years of experience in a QC analytical laboratory position in the pharmaceutical industry. Experience with chromatography software. Working Conditions Laboratory setting. Will be exposed to solvents, bio-hazardous materials, hazardous waste, and pharmaceuticals. Must be adaptable to shifting priorities and operate with a sense of urgency while maintaining high quality in order to meet important timelines in a high throughput lab. Business demands may present a need to work extended hours. Compensation and Benefits Pay: $36.00 - $37.00 per hour, depending on experience, plus shift differential following training Benefits summary: careers/employee-benefits Tolmar compensation programs are focused on equitable, fair pay practices including market-based base pay and a strong benefits package. The final compensation offered may vary from the posted range based on the selected candidates qualifications and experience. Tolmar is an Equal Opportunity Employer. We do not discriminate on the basis age 40 and over, color, disability, gender identity, genetic information, military or veteran status, national origin, race, religion, sex, sexual orientation or any other applicable status protected by state or local law. It is our intention that all qualified applicants be given equal opportunity and that selection decisions are based on job-related factors. Qualifications EducationBachelors of Chemistry (required) Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

Job Description 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)

SEAKR is looking for a motivated Lead, Quality Control Receiving Inspector (QCRI) who has experience inspecting high-reliability Mechanical and EEE (electrical) components. A successful candidate will have a technical aptitude with analytical problem-solving skills, the ability to work in a team environment, and effective time management skills for efficient task prioritization. The QCRI reports to the Receiving Inspection Supervisor within the Supply Chain division. Job responsibilities include… * Verifying documentation, materials, and products meet the PO and engineering drawing requirements * Performing basic dimensional inspections using micrometers, calipers, feeler gages, etc. * Performing basic electrical inspections such as continuity testing in accordance with engineering drawing requirements * Managing multiple receipts simultaneously, in different physical and electronic locations * Navigate SEAKR's Enterprise Resource Planning (ERP) tool to support review, routing, and disposition non-conforming product and/or electronic inventory transactions * Tracking and documenting arrival reports * Processing and managing supplier RMAs * Create, document, and implement inspection criteria and procedures * Maintain an active role on internal continuous improvement teams * Provide CMM testing and reporting as required * Review and edit documentation as required. * Able to work independently and as a team, along with Property, Supply Chain (Buyers), SQE's, QE's and other department/teams as required. * Cover and report team duties in absence of the RI Supervisor when required.

Inspection & Packaging Lead (3rd shift) This position reports directly to the Inspection and Packaging Supervisors as well as the VILP Manager. The role is responsible for general support of the Visual Inspection, Labeling, and Packaging of finished sterile compounds. The Lead is responsible for ensuring the accuracy for label reconciliation, document completeness and correctness of all product identification. 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 positivelyimpactpatients' lives. Professional Development: Access ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry. Cutting-EdgeTechnology: Work withstate-of-the-artfacilities 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! Essential Functions: Lead and perform the line/area clearance of the visual inspection or label, and packaging activities. Review of batch record during and end of visual inspection, label, and packaging activities. Assist Inspection & Packaging Supervisors in overseeing employees who are responsible for visual inspection/labeling/packaging of finished goods. Collaborate with Inspection & Packaging Supervisors to ensure timely visual inspection and labeling of products to meet scheduled batch release dates. Ensure that training on SOPs and processes remains current. Analyze Production efficiencies downtime and waste. Lead teams to improve the results. Write investigations and CAPA actions for non-conformances in the department. Work with QA to quickly resolve any variance or document errors so that product may be released on time. Lead Problem Solving activities. Assist with maintaining batch and label inventory and managing daily staffing for visual inspection and labeling. Other duties as assigned. Supervisory Responsibilities: Lead a team of Associates, providing direction, support, and training. Provide a positive and collaborative work environment through effective communication and accountability, escalating conflict promptly and fairly. Experience and Necessary Skills: 1-year previous leadership experience or comparable experience preferred. Minimum 1 years' experience in aseptic processing preferred. Knowledge of cGMP guidelines/standards. Bachelor's degree or relevant experience preferred. Demonstrated written and oral communications skills including strong presentation skills. Excellent organizational skills and results oriented. Strong results orientation. Strong Microsoft Office skills are essential, proficient in the use of spreadsheets and word processing programs Ability to effectively bring others together and reconcile differences. Able to lift up to 50 lbs. and stand for extended periods when required Must pass an eye exam confirming 20/20 near vision corrected (with contacts or glasses) or uncorrected Must pass an eye exam confirming the ability to accurately perceive color 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 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. Monday - Friday 1130pm to 8am

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.