Quality control inspector jobs in Castle Rock, CO - 140 jobs

Civil Technology Inc. (CTI) is seeking a qualified Field Quality Control Manager to support work to modify and upgrade Baggage Handling Systems (BHS) at Denver International Airport (DEN). This role is instrumental in ensuring the BHS scope is completed as designed and expected, and will work closely with another quality inspector to review design documents and inspect field installation of the BHS system. We are specifically looking for a professional with hands-on experience inspecting electrical systems and process control systems for conveying/transport systems. Prior BHS experience is ideal-however, experience from industrial manufacturing environments manufacturing facilities can translate extremely well to this role. This position will primarily be on the day shift, with flexibility required as construction activities may drive off-hour and night inspections. Key Responsibilities Review project documents including construction drawings, submittals, shop drawings, and approved installation methods related to the BHS installation. Verify BHS components received onsite are supplied and installed in accordance with construction documents, shop drawings, submittals, RFIs, and Certificate of Compliance requirements. Perform shop inspections when needed to confirm compliance and readiness for installation. Verify electrical installation is completed in accordance with approved documents and related RFIs, including: Main power and control power Motors, conveyors, and BHS control systems Inspect and validate process control systems supporting BHS operations, including control devices and logic-driven conveying systems. Perform required site inspections and complete Quality Control Inspection Reports in ACC. Prepare Quality Reports in ACC for night shift inspections, ensuring required inspection scope is understood and executed by night inspectors. Meet with DEN QA representatives, attend quality follow-up inspections, and prepare Quality Reports in ACC. Attend meetings and inspections with DEN Operations (Log Plan) and prepare special reports for distribution with the project team. Perform inspections to document construction progress and re-inspect open structural, electrical, and mechanical issues, tracking status and resolution in ACC. Participate in planned temporary mock-up installations, including conveyor system electrical and control device installation. Provide extensive coordination between contractor personnel/activities and owner representatives to ensure BHS systems are installed correctly and operate as expected. Communicate clearly and professionally (written and verbal) to support issue resolution and maintain alignment across the team. Support other quality-related activities as requested. Preferred Experience Previous work experience with baggage handling systems (BHS) (highly preferred) Strong background inspecting: Electrical systems for conveying and transport systems Process control systems and logic-driven equipment In lieu of direct BHS experience, applicable experience from industrial/manufacturing conveying systems, including: Bottle/can manufacturing facilities (Pepsi, Coca-Cola, Coors, etc.) Automated production lines with process control and sequencing logic Experience supporting manufacturing plants and operations Aviation experience (preferred) Experience working on large, complex, active facilities requiring detailed coordination and communication Work Location & Requirements Work is located 100% onsite at Denver International Airport (DEN) Must be able to pass all required background checks for airport badging and access Why Join CTI? High-Impact Work: Be part of transformational projects shaping Denver's infrastructure. Competitive Compensation: Strong salary and opportunities for growth. Family-Oriented Culture: Supportive, close-knit environment that values collaboration and communication. Tangible Benefits: Full benefits package, competitive 401(k) matching, certification support, and more. Big Impact, Small Team: Your contributions won't get lost in the crowd-they'll be recognized and appreciated. Commitment to Diversity: Certified SBE, M/WBE, DBE, and ESB; we value every voice. Cutting-Edge Projects: Work on complex, high-profile construction management efforts at DEN and beyond. Continuous Learning: Professional development and certification support are core to our culture. Small Business Advantage: Agility and entrepreneurial spirit with the resources and reach of legacy projects. Additional Benefits 401(k) with match Cell phone reimbursement Dental insurance Fuel discounts Health insurance Paid time off Professional development assistance Performance bonuses About Civil Technology Inc. Since 1989, Civil Technology, Inc. (CTI) has been pushing the boundaries of construction and program management in Denver for decades. We don't just manage projects-we elevate them. From pre-design to the final closeout, our team delivers unmatched expertise, ensuring every project not only meets but exceeds expectations.

We're seeking an experienced Certified Welding Inspector to join our team. Certified Welding Inspector (CWI) Pay Range: $28-$35 per hour Schedule: Monday-Friday, 7:30 AM-4:00 PM Benefits Include: Medical, Dental, and Vision Insurance Paid Time Off (PTO) 401(k) Disability Coverage Requirements: Active AWS Certified Welding Inspector (CWI) certification Minimum of 3 years of welding inspection experience Strong knowledge of AWS standards Aluminum welding inspection experience Interviews are being scheduled immediately, and we're looking to hire as soon as possible. Interested candidates are encouraged to apply or reach out for additional details.

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

Tendeg LLC is an engineering-driven company that designs and builds high-performance antenna systems and precision structures for space missions. Our work supports communications, sensing, and data delivery in demanding orbital environments, with applications ranging from weather forecasting and Earth science to global connectivity, national security, and scientific exploration. Our hardware is flight-proven, with more than 25 antennas currently on orbit and a portfolio of deployable apertures that spans multiple sizes and frequency regimes. As we scale manufacturing to meet growing demand, we re building a team focused on disciplined execution, technical rigor, and delivering hardware that works. If you re interested in joining a growing team that designs and builds the infrastructure behind modern space missions, we d like to hear from you. Tendeg s Philosophy We encourage innovation and entrepreneurial energy. We are successful because we take a unique approach to solving problems. We look for creative thinkers and self-motivated people that can collaborate within our open team environment. TENDEG is an acronym for TENacious Design and Engineering Group. Obviously, tenacity is another trait we embrace. Title: Quality Inspector Position Type: Full-Time/Non-Exempt Pay Range: $30.00 - $35.10 Hourly (Salary to be determined by the education, experience, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data) Location: Louisville, CO (Onsite) Position Purpose: As a Quality Inspector II you will be responsible for inspecting electrical wiring harnesses, circuit boards, machine parts and mechanical assemblies used in Tendeg deployable antennas, ground support equipment, test equipment, and/or internal development tools. They work closely with engineers and other technicians to ensure that electrical and mechanical systems function efficiently and reliably, and document non-conformances when they occur. Job Responsibilities: Complies with established job safety practices, policies and procedures as specified in plant and corporate directives for the safe performance of the work assignment. Advises production when inspection results do not meet customer specifications and create non-conformance reports. Performs record keeping duties as required under the direction of the QA Manager. Initiates, reviews, and follows all standard operating procedures (SOPs) for area of responsibility. Conduct detailed inspections of aerospace components, structures, systems, and material certifications according to established standards and procedures. Perform visual and dimensional inspections using precision measuring instruments such as calipers, micrometers, and precision measurement equipment. Verify compliance with engineering drawings, specifications, and technical documents. Document inspection results accurately and thoroughly, including any deviations or non-conformities. Collaborate with engineers, technicians, and other team members to document and resolve quality issues. Participate in the development and improvement of inspection processes and procedures. Maintain a clean and organized work environment and ensure proper handling and storage of inspected components. Adhere to safety protocols and regulations at all times to ensure a safe working environment. Establishes and maintains effective work relationships within the department, the division, the group, and the company. Complies with environmental regulations when using, dispensing, or handling hazardous and non-hazardous materials and wastes. Perform other duties as assigned. Required Skills, Qualifications and Education: 3-6 years of experience High school diploma or equivalent; technical education or certification in aerospace technology, quality control, or a related field is preferred. Experience with GD&T, Zeiss CMM, FaroArm, Leica and Micro vu preferred. IPC-620, IPC-610 and J-STD 001 certifications are preferred but not necessary. Strong attention to detail and excellent observational skills. Proficiency in using precision measuring instruments and basic hand tools. Ability to interpret engineering drawings, specifications, and technical documents. Good communication skills and the ability to work effectively in a team environment. Willingness to learn and adapt to new technologies and inspection techniques. Commitment to maintaining high standards of quality and safety. Benefits: As we are growing and investing in our company, we invest in our team. We recognize employee contributions through competitive salaries and bonuses and take pride in taking care of our employees. Here is how we show our appreciation: Generous Paid Time Off Paid Parental Leave Medical/Dental and Vision Insurance Plans Tax Advantage Account (Flexible Spending Account) (FSA) Retirement Savings Plan-Traditional 401(k) Plan Employer Paid Short Term Disability and Basic Life, AD&D Additional Benefit Options Including Voluntary Life and Long Term Disability Employee Assistance Program (EAP) Company SWAG Dog friendly work environment Free company parking Break rooms fully stocked with snacks, drinks, and an espresso coffee machine "Must be a U.S. Person as defined by 22 CFR 120.62." Tendeg LLC is an Equal Employment Opportunity (EEO) employer. All qualified applicants are considered for employment without regard to race, religion, color, sexual orientation, age, disability, marital status, genetic information, national origin, veteran status and any other protected factor. #LI-TENDEG

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

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.

York Space Systems was founded to radically improve spacecraft affordability and reliability, transforming, and enabling next-generation space mission operations worldwide. Today, York is one of the most innovative aerospace companies, specializing in end-to-end customer solutions and the rapid production of spacecraft platforms. York's complete Space Segment Solution includes spacecraft production, payload integration, system integration & test, launch services, ground segment services, and mission operations, enabling customers to leverage York's existing technology solutions to get to orbit rapidly and responsively. The Quality Inspector II is primarily responsible for the physical inspection and documentation of the conformance of various material and components received in support of production. Typical daily responsibilities include dimensional inspection of components, creation of inspection documentation, review of vendor provided materials, support to non-conformance processes and engagement with supported teams including production, inventory and procurement. This role ensures compliance with industry best practices included in quality standards, customer requirements, and regulatory guidelines. The Quality Inspector II will analyze non-conformances, lead/support root cause and corrective action investigations, and work cross-functionally to improve product quality and process efficiency.KEY RESPONSIBILITIES Non-Conforming Material & Process Management Identify, document, and manage non-conforming material through quality processes. Support quality leadership in the management of material dispositions. This could include participating in non-conforming material investigations using problem-solving methods such as 8D, 5-Whys and Fishbone Diagrams. Support containment activities to minimize production disruptions and customer impact. Maintain and improve the non-conformance management system to ensure traceability, accuracy, and regulatory compliance. Quality System & Compliance Support compliance to quality standards, customer-specific requirements, and other applicable industry regulations. Participate in internal and external audits, including customer, regulatory, and third-party audits. Ensure proper documentation and records management related to non-conforming material and corrective actions. Support the creation of quality processes and procedures including material handling. Conduct or support training of quality processes and procedures to other teams. Conduct of Quality Inspections Using and maintaining measurement tools, systems and best practices complete inspections of various materials and components against engineering documentation and industry standards. Document completed inspections and initiate appropriate actions where non-conformance may be identified. This could include preparing detailed reports for engineering, quality, production or procurement. Ensure vendor compliance to any industry standards called out in purchasing contracts or documentation. This could include AS9102 FAI, IPC or Mil-Std requirements Process Improvement & Risk Mitigation Work with cross-functional teams to implement process improvements that reduce defects and enhance product quality. Participate in risk assessments related to non-conforming material and critical process deviations. Contribute to continuous improvement initiatives, such as Lean and Six Sigma and Kaizen projects, to enhance manufacturing efficiency and product reliability. QUALIFICATIONS AND EXPERIENCE High school diploma with a preferred technical certification or associate degree in a related field. 3-5 years of experience in quality inspection or manufacturing within the aerospace, defense, or related high-reliability industry. Knowledge of quality standards, and regulatory requirements. Experience with quality tools such as 8D, FMEA, SPC, and Six Sigma methodologies. Ability to interpret engineering drawings & specifications. Excellent communication and problem-solving skills with the ability to work cross-functionally. Proficiency in quality management systems (QMS), ERP systems, and data analysis tools. PREFERRRED QUALIFICATIONS Experience with AS9100, ISO9001 or AS9102 Quality Standards. Experience with industry standards including IPC-A-610, IPC/WHMA-A-620, J-Std-001, ASME Y14.5 and MIL-Standards. Hands-on experience with quality inspection and testing methods.

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

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

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

Responsibilities: Verify electronic scrap materials against provided documentation Check part numbers, serial numbers, quantities, and general condition Ensure accuracy and completeness of inspection records Provide clear, timely inspection reports with photographic evidence Follow client-specific verification and traceability requirements High availability and flexible job scheduling preferred Ability to lift and move boxes and electronic equipment as required during inspections (25lbs aprox) Technical & Industry Experience: 1-3 years basic quality inspection experience in Electronics Technician / Quality Inspector / IT Hardware Technician. Candidates should have 1-3 years of experience in quality control, warehouse inspections, or similar operational roles Exposure to electronic scrap or end-of-life IT equipment inspections is a plus, but not mandatory Strong attention to detail with the ability to accurately verify part numbers, serial numbers, and quantities Familiarity with networking hardware, electronic components, or IT equipment Experience with inventory verification and documentation review Ability to use MS Word and Excel to submit inspection reports and photo evidence within required timelines (typically within 24 hours after job completion) Ability to work independently and follow detailed client instructions Flexibility in scheduling and availability for short-notice inspections. Job Type: 1099 Contractor Project Duration: CURRENT PROJECT: begins soon as we hire; Recurrent, several days per month Note: This is a 1099 contract role - project duration may vary based on client needs Shift Hours: CURRENT PROJECT: 8 hours each day (days will be flexible). Note: As a 1099 contractor, project schedules may vary depending on site availability Location: Must be able to travel to Colorado Springs, Colorado and nearby areas (exact CLIENT address can ONLY be shared once contractor joins) Compensation: $20.00 - $25.00 per hour About Us Since 1984, Pro QC International goes above and beyond the traditional roles of quality control. We assist clients to put better quality products on the market by resolving quality and production related challenges and reducing supply chain risk and cost. Pro QC offers solutions in over 88 countries. We manage our global operations from 18 Offices Worldwide. Our clients range from small start-ups to multinational companies in the Americas, Europe, Asia, the Middle East and Africa. Join Our Team We are always looking for talented candidates in Asia, Americas, Europe, Middle-East, and Africa. At Pro QC, we value quality over quantity. We value professionalism, dependability, and teamwork. We believe in building trusted partnerships that are earned through conscious efforts. In our strive for excellence, we are passionate about delivering quality solutions to organizations around the world. Leveraging an ever-expanding, interconnected group of people from diverse backgrounds, Pro QC offers an attractive and unique opportunity as part of a global family. Our Vision: To nurture the trust of our customers and our team through dynamic interactions, creative supply chain solutions, and integrated partnership.

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.

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

An Industrial Engineering company specializing in custom industrial mechanical systems is looking for a Quality Inspector to join their first shift (6:00am - 2:30pm) team in Aurora, CO. The company is growing its quality division and will be looking for either an Entry or mid-level inspector with the goal of improving their professional skillsets in Quality Inspection procedure creation. You will be given the opportunity to learn and advance at the pace you set for yourself. You will work with a Senior Quality Inspector, Quality Engineer, Manufacturing teams, and Management to ensure quality of custom built electromechanical mechanical systems. Responsibilities include 75% quality measurement procedures/measurements, reading and interpreting blueprints/ weld symbols, and implementing corrective actions. Other 25% responsibilities include documenting work /following inspection plans/quality reports, and other administrative actions. The Company is well established in its industry and offers room for advancement, and you will be coming into a growing division. This is a 6 month contract to hire position, and will turn into a permanent position in the next 6 months. Candidates must pass a drug test. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements 1+ year of Quality experience Experience reading blueprints or part diagrams Experience utilizing a tape measure and other quality measurement tools Strong communication and ability to work with cross functional teams Comfortable taking a background check and drug test

About Us LR Associates, LLC is a Veteran owned federal government contractor providing facilities management and other services to various government customers. We support our customers with highly skilled personnel and provide customized solutions to accomplish the mission. We are seeking Full Time Custodial Workers, Supervisors, Quality Control Inspectors and Floor Techs. We are looking for highly motivated individuals who have experience in janitorial work, floor tech experience or janitorial supervisory experience. Responsibilities Clean designated building areas (dusting, sweeping, vacuuming, mopping, cleaning ceiling vents, restroom cleaning, pull trash etc.) Clean Locker Rooms and Showers Strip Wax Floors (Buffer Experience) Supervise custodial teams or conduct Quality Control Inspections on premises. Carry out all assigned cleaning tasks and special projects Notify management of occurring deficiencies Stock, maintain and resupply Restrooms Must follow all health and safety regulations requirements Requirements Must pass Federal Government background check (mandatory for access to USAFA facilities) Ability to work flexibile schedules, including evenings, weekends and holidays. Strong communication and interpersonal skills for working with diverse groups of people. Ability to stand, walk, lift and move equipment for extended periods. Must be a dependable team player who can take direction and adapt quickly. Prior experience in facilities or custodial support preferred but not required. Why Work With Us? Be part of a Veteran-owned company supporting the U.S. Air Force Academy mission. Flexible part-time hours based on event scheduling Gain experience in event support, facilites management and governement operations. Opportunity to work in a unique and highly professional environment. Equal Opportunity Employer/Vet/Disability

About Us We are a leading sheet metal fabrication company in Denver, CO, specializing in high-quality precision parts for the industrial, commercial, and automotive markets. We are committed to delivering superior products through disciplined processes, teamwork, and continuous improvement. Position/Job Summary: 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 Location: Denver, CO Shift: 2nd Shift (Typical hours: 4:00 PM - 12:30 PM, Monday-Friday) Department: Quality Control Employment Type: Full-Time What we offer: Health Benefits: Medical, dental, and vision coverage. Company paid for Life insurance, short-term and long-term disability insurance. Additional Benefits: Paid time off, Floating Holidays, Volunteer time off, and sick time off (depending on state of employment). 401k Plan Employee Perks: Discounts on products and services. Equal Opportunity Employer/Veterans/Disabled This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before the employer can take any action against you, including terminating your employment. Employers can only use E-Verify once you have accepted a job offer and completed the Form I-9.

Duties and Responsibilities: Work effectively with the Quality, Operations, and R&D departments to perform all work accurately, with a sense of urgency and a positive attitude. Activities include the following: In-Process and Final Device Inspection and Test : Support Manufacturing as the QC inspector for clean-room & packaging inspection activities. Perform and document in-process and final inspection/test of devices and sub-assemblies. Provide inspection/test assistance to R&D, Operations and Quality Engineering in support of design and process verification/validation activities. Receiving Inspection and Test : Perform and document receiving inspection/test of device components & raw materials in accordance with drawings/specifications. Maintain accurate & timely records of inspection activities and recording such activities in the QC Receiving Log. Non-Conforming Materials : Identify, segregate and quarantine non-conforming materials resulting from inspection activities. Initiate NCRs and notify the workstream owner in a timely manner. Execute and record disposition activities in accordance with approved NCRs. Microbiological Monitoring : Participates in periodic microbiological and particulate testing of the cleanroom and products as required. Returned Goods Authorization : Perform timely inspections and maintain accurate records of all returned TriSalus products through the RGA process. Correctly dispositions returned product as defined in approved procedures. Quality Record maintenance : Receive, verify, scan and physically file Quality Records in an organized manner as needed. Shipping QC : Verify TriSalus products and associated paperwork are accurate and complete prior to shipment. Audit Assistance : Help retrieve, review, organize and re-file documentation during all TriSalus site audit activities (internal, FDA, ISO registrar). GP Dynamics : Transfer released materials in the ERP software for material management as needed. Training Record support : Enter complete training/certification records into the eQMS as needed. General : Perform other quality inspection, test or administration activities as assigned. Qualifications Education & Certifications: High School diploma. Advanced education or certifications a plus. Work Experience: 2+ years of Quality Control / Inspection experience in a medical device or similar technical product manufacturing company. Experience working with sterile disposable products in a cleanroom environment a plus. Knowledge, Skills & Abilities: Able to read and interpret engineering drawings, specifications and detailed technical documents. Able to read and follow quality procedures and detailed work instructions (QLPs/OPs). Able to perform component and product inspection/testing using tools such as microscopes, calipers, micrometers, pin gauges, depth gauges, pull force test systems and vision measuring systems. (Sufficient knowledge to select and use the correct measurement tool for the required inspection accuracy. Able to accurately document results of inspections using good documentation practices. Able to understand and apply inspection sampling plans, such as C=0 or ANSI Z1.4. Able to utilize basic math skills. Able to use MS Word and MS Excel. Must possess strong attention to detail. Possess good communication skills and able to interact with peers in a professional manner. Possess knowledge and application of US and international standards for quality management (FDA 21 CFR 820, ISO 13485). Demonstrates excellent critical thinking skills. Ability to adapt to and rapidly learn new processes. Strong verbal and written communication skills and confidence in making inspection related decisions. Participates as a member of cross functional technical teams to support process improvements, special projects and investigations as needed. Approaches work tasks with a positive attitude and seeks feedback on performance to continually improve. Physical Requirements: Ability to safely and successfully perform the essential job functions consistent with the ADA, FMLA and other federal, state and local standards, including meeting qualitative and/or quantitative productivity standards. Must be able to lift and carry up to 30 lbs. Ability to maintain regular, punctual attendance consistent with the ADA, FMLA and other federal, state and local standards.

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.

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