Quality Technician Jobs in Littleton, CO

On site in Aurora, CO 80019 6 Month Contract to Hire $27/hr First year estimate $62,300, second year estimate $72,100 Benefits: Medical, Dental, Vision, 401K Day-to-Day An Engineering company specializing in custom conveyor systems design, commissioning, and integration is looking for a Quality Engineer to join their newer and expanding Quality Engineering team. We are looking for an Entry Level (0-2 years' experience) engineer with the goal of improving their professional skillsets in Quality assurance, including writing procedures and internal audits. You will be given the opportunity to learn and advance at the pace you set for yourself. You will work with tenured Engineers, Project Managers, Quality Assurance technicians who can pass on a deep level of knowledge in this space. Responsibilities include 75% Developing quality procedures, conducting root cause analysis, and implementing corrective actions. Other responsibilities include internal and supplier audits/Inspections, documenting work instructions/inspection plans/quality reports, analyzing data to identify trends, participating in new product development, and training employees on standards. This is a contract-to-hire position that will become permanent after 6 months. This company promotes internally, leaving plenty of room for advancement especially in this division which will be growing at a rapid pace as they continue to create process improvements. Candidates must pass a drug test. Must-haves Bachelor's Degree in Engineering GPA 3.0+ A passion to pursue a career in Quality Engineering in manufacturing 0-2 years of experience with Quality Engineering including development of QA standards, corrective actions Strong communication and ability to work with cross functional teams Proficiency with Measurement tools such as a micrometer and calipers Comfortable taking a background check and drug test Plusses Internship or Project Experience with Conveyer Systems Experience with root cause analysis in a manufacturing space

Our vision is to transform how the world uses information to enrich life for all . Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever. About our Team: The Global Quality (GQ) System Quality and Reliability Assurance (SORA) team at Micron plays a critical role in ensuring the quality and reliability of our products. Our team specializes in Returned Material Authorization (RMA) Failure Analysis (FA), working closely with engineers to analyze failures and improve product performance. We foster a culture of continuous improvement, collaboration, and technical expertise. Position Overview: As a QA Technician, you will be responsible for outgoing quality inspection and failure analysis activities. You will assist engineers in managing quality assurance tasks, performing quality inspections, conducting random audits, and supporting training efforts on production lines. Additionally, you will contribute to quality programs, audits, and 6S/ESD activities as needed. Responsibilities: Receive, verify, and prepare materials for testing. Perform bench-level testing, debug diagnostics, and isolate failing components. Conduct Automated Test Equipment (ATE) operations, including preconditioning and testing devices. Analyze failure data, summarize results, and track experiment progress. Develop and maintain documentation, provide training, and support technical expertise development. Minimum Qualifications: Experience in quality inspection, testing, or related technical roles. Strong understanding of debugging, diagnostics, and failure analysis techniques. Ability to interpret test results and collaborate with engineers to identify issues. Proficiency in handling testing equipment and documenting findings. Strong organizational and communication skills. Preferred Qualifications: Knowledge of ATE operations, firmware testing, and failure analysis tools. Experience working with quality programs, audits, and manufacturing processes. Familiarity with 6S/ESD compliance and best practices. Ability to train and mentor team members on processes and equipment usage. Prior experience in semiconductor or electronics manufacturing environments. The US base salary range that Micron Technology estimates it could pay for this full-time position is: $28.75 - $48.00 Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries of the position across all US locations. Within the range, individual pay is determined by work location and additional job-related factors, including knowledge, skills, experience, tenure and relevant education or training. The pay scale is subject to change depending on business needs. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Additional compensation may include benefits, discretionary bonuses and equity. As a world leader in the semiconductor industry, Micron is dedicated to your personal wellbeing and professional growth. Micron benefits are designed to help you stay well, provide peace of mind and help you prepare for the future. We offer a choice of medical, dental and vision plans in all locations enabling team members to select the plans that best meet their family healthcare needs and budget. Micron also provides benefit programs that help protect your income if you are unable to work due to illness or injury, and paid family leave. Additionally, Micron benefits include a robust paid time-off program and paid holidays. For additional information regarding the Benefit programs available, please see the Benefits Guide posted on micron.com/careers/benefits. Micron is proud to be an equal opportunity workplace and is an affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, citizenship status, disability, protected veteran status, gender identity or any other factor protected by applicable federal, state, or local laws. To learn about your right to work click here. To learn more about Micron, please visit micron.com/careers US Sites Only: To request assistance with the application process and/or for reasonable accommodations, please contact Micron's People Organization at hrsupport_************* or ************** (select option #3) Micron Prohibits the use of child labor and complies with all applicable laws, rules, regulations, and other international and industry labor standards. Micron does not charge candidates any recruitment fees or unlawfully collect any other payment from candidates as consideration for their employment with Micron.

Join CPI Card Group and become a part of a phenomenal team and work environment! CPI Card Group is a light manufacturuing company producing contact and contactless payment cards for our customers. CPI offers a full suite of solutions and the expertise in plastics manufacturing, personalization and fulfillment to provide a completely customized card package. We are currently looking for hard working production employees on all shifts to join our Littleton, CO facility. We offer an extensive benefits package for our employees including health insurance, time off, 401(k) matching, and more! The Quality Technician at CPI is responsible for the auditing, inspection and testing functions through-out the value stream. In addition, the Q.T. is charged with following up on any process and/or product non-conformances to assure they are brought to an effective solution while assisting with troubleshooting and supporting operations as required. Hourly rate - $23.30 Schedule: Monday-Thursday 4:00am-4:00pm Responsibilities Responsibilities: * Reads and interprets the shop floor documents (proof, job ticket, combo ticket) as well as applicable ISO, Association, and CPI internal specifications. Know where to locate standards in SharePoint * Complete Quality Release testing process including physical testing and visual inspection. Sets up and performs destructive and nondestructive tests on materials or product to measure performance, life or material characteristics * Observe, report, and document quality data information on checklists and in the shop floor data collection system as required * Initates quality hold and non-conformacnes based upon inspection results * Completes in-process audits in Finishing Qualifications Qualifications: * To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions * The candidate must be able to use a caliper and other hand tools. Prior experience is not required * The candidate must be able to interface with a PC by in putting and out putting data and using basic Microsoft Office Suite products. Keyboard input skills are necessary * High school diploma or equivalent (Preferred) * Elementary English proficiency communication skills necessary Physical Demand: * Work is primarily conducted standing or walking in a manufacturing environment and sitting in an office environment and often requires bending and stooping to observe product and/or manufacturing equipment * Manufacturing environment is noisy and may require ear protection * Work involves good eyesight, hand/eye coordination and excellent color vision to be able to ensure quality product * Work involves dealing with fine detail and constant human interaction Company Overview:CPI Card Group is a payment technology company and leading provider of credit, debit and prepaid solutions delivered physically, digitally and on-demand. CPI helps our customers foster connections and build their brands through innovative and reliable solutions, including financial payment cards, personalization and fulfillment, and Software-as-a-Service (SaaS) instant issuance. Learn more at ********************* Benefits:Competitive pay rates and an inclusive, empowering and rewarding culture.Solid benefits package including Medical, Dental, Vision, Long Term Disability, Short Term Disability, Life Insurance, Accident Insurance, Critical Illness Insurance, FSA, HSA, Vacation and Holiday Pay, Tuition Reimbursement and 401(k) with a competitive company match percentage. CPI is an Equal Opportunity Employer, including disability/vets. A complete background including drug screen is contingent upon hire.

Join our dynamic Quality Assurance team at our Organic Dairy Processing facility in Platteville, CO. Be a part of a 2024 Top Workplace USA! Purpose: The Quality Assurance Lab Technician is responsible for in-process and finished product quality testing, maintaining accurate and complete records, and alerting management to any potential quality issues. Shift 6pm -6am Thurs - Sat and alternating Wednesdays OR Sunday - Tuesday and alternating Wednesdays Essential Responsibilities: All plant personnel have the responsibility to monitor and report any deviations from our Food Safety and Food Quality (HACCP & SQF) programs to your immediate supervisor. Assist in all in-bound and finished product milk processing including but not limited to: Customer Service, working with our Laboratory and Product Information Management System, Tanker/Silo Inventory Control, administrative assistant duties. Competency in Microsoft Windows and Office products. Responsible for performing process control testing in a manufacturing environment. Maintain accurate and complete laboratory testing result records. Maintain Good Manufacturing Practices, Good Laboratory Practices and Safety Procedures. Communicate any potential quality issues to QA Management. Professional communication and customer service skills in working with multiple departments and external partners. Other Required Responsibilities: Laboratory testing result data entry. Member of HACCP team. Other quality department responsibilities as deemed necessary. Knowledge & Experience: High School Diploma or equivalent. Bachelor's degree in Dairy Manufacturing, Food Science, Microbiology, or related field preferred. Experience in dairy laboratory testing procedures preferred. Knowledge of laboratory testing methods. Detail oriented and team member. Strong, honest work ethic with ability to handle multiple tasks daily. Good communication skills. Physical Requirements: Must be able to sit for extended periods of time; Must be able to stand or walk for more than 50% of the shift. Must be able to bend, stoop, kneel or crawl; reach grasp and lift, push, pull up to 50 lbs. regularly and up to 80 lbs. occasionally. 6pm - 6am Sun - Tue and alternating Wed OR Thurs - Sat and alternating Wed

The world's most revolutionary biopharma companies are partnering with Agilent Technologies to advance the next frontier of medicine. Agilent continues to invest in capacity and expansion of its Colorado operations. Join our team of professionals dedicated to the development and commercialization of nucleic acid therapeutics for life changing, lifesaving medicines. The Quality Control Laboratory Technician conducts checks, to ensure that laboratory reagents, instrumentation, glassware and peripheral laboratory components comply with corresponding GMP laboratory guidelines. Reports results to appropriate validation, engineering and or quality functions. Performs laboratory support activities to ensure that instrumentation relating to quality testing activities are maintained at best working conditions with minimum down time. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Performs routine inventory of laboratory supplies. * Orders supplies when needed or as requested. * Washes laboratory glassware and stores and organizes glassware appropriately. * Discards glassware that is broken or unusable. * Ensures proper storage of clean glassware * Performs daily calibration checks of laboratory equipment, including, but not limited to analytical balances, pH meters, water systems, and chemical fume hoods. * Oversees status of equipment maintenance and calibration in Regulatory Asset Manager (RAM). * Routinely verifies that all chemicals and reagents in the laboratory are within expiry. * Properly disposes of chemicals and reagents that are past expiry. * Coordinates and schedules vendor instrumentation maintenance, calibrations and qualifications. * Manages Purchase Orders. * Coordinates general maintenance of the laboratory in conjunction with the Facilities department. * Performs preventive maintenance and calibrations in conjunction with the Facilities Department. * Supports two laboratories across two sites located in Boulder, CO and Frederick, CO. * Responsible for procuring new instrumentation and initiating associated documentation through controlled document management system. * Supports a broad range of problems of varying scope and complexity. Qualifications * May require some higher education or specialized training/certification, or equivalent combination of education and experience * 1+ years of relevant experience for entry to this level * Prior experience in a GMP environment is preferred, but not required * Ability to read, understand, and follow Standard Operating Procedures * Organizational Skills and attention to detail are required to maintain an organized laboratory environment and manage the inventory of laboratory supplies * Ability to perform basic math calculations * Requires complete understanding of general and technical aspects of job * Demonstrated knowledge of analytical equipment and instrumentation, HPLC experience working in a GMP environment is preferred * Knowledge of FDA regulations and guidelines is preferred * Proven skills in coordinating and leading day to day tasks and working in collaboration to accomplish deadlines and objectives * Personal leadership skills and fosters working in a team environment * Knowledge of and skills in using computer software and hardware applications, including Microsoft Word and Excel Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least February 19, 2025 or until the job is no longer posted. The full-time equivalent pay range for this position is $25.03 - $39.11/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit ********************************* Travel Required: 25% of the Time Shift: Day Duration: No End Date Job Function: Quality/Regulatory

Starting Pay is $21.00 per hour Shift: Sunday - Thursday 9:00am - 6:00pm Maintains all aspects of Quality Assurance to ensure proper, safe and exceptional operation of the department. * 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. 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. Shamrock anticipates closing the application window for this job opportunity on or before December 31, 2025

Who we are: Electra is reinventing iron production to tackle the nearly 10% of global carbon dioxide emissions produced from iron and steelmaking. Its patented process uses chemistry and renewable energy to transform a variety of grades of iron ore into environmentally responsible pure iron at scale. By maximizing the value of Earth's resources and minimizing our environmental footprint and carbon emissions, Electra is forging a green future from the ground up. With a collaborative culture and passion for disrupting the status quo, careers at Electra offer challenge, reward, and the opportunity to bring to market solutions that dramatically improve the health of the planet. What you will do: The Quality Technician II will perform several selective types of inspection events, complete and maintain related documentation, and assist in implementing an inspection process using a continuous improvement approach. Key Responsibilities: Perform several types of inspection events: Incoming, First Article Inspections (FAI), in process assembly, raw material receiving, and special inspection request Process nonconforming material reports and work with internal parties review the nonconformance Interface with Quality Engineers for clarification and improvement of inspection techniques Process inspection records through designated systems Conduct inspections in accordance with established AQL requirements by lot Maintain work areas and equipment in a clean and orderly condition Review production drawings against product provided by internal and external suppliers Maintain measurement equipment in good working order while ensuring calibration status is active Collect and compile inspection data to generate reports as necessary Inspection of reworked product in accordance with internal procedures Encourage a culture of quality and continuous improvement throughout the organization Coordinate relevant activities, inspection requests, and priority scheduling with all departments Read, understand, and comply with all workplace heath and safety policies, safe work practices, and company policies and procedures Perform other duties as assigned by supervisor What we need you to bring to the team: Associate's degree in a related field of study in a technical discipline; or an equivalent combination of related education and experience 1-2 years of industry experience working in a quality role in a manufacturing setting (excludes internships, co-ops, and other school projects) Strong inspection tool experience - calipers, gauge pins, micrometers, height gauge, CMM, Vision systems. Keyence systems experience a plus. Experience with lean manufacturing principles and continuous improvement initiatives Strong foundation in reading and understanding engineering drawings & diagrams Quality System Standards experience (ISO9001, ISO13485, IATF16949, AS9100, 21 CFR 820) Basic understanding and application of GD&T and tolerance stack-ups Ability to adapt to multiple and/or changing projects simultaneously and the ability to thrive in a continuous improvement environment Ability to work independently as well as collaboratively as needed Excellent interpersonal, relationship-building, and communication skills Excellent troubleshooting and problem-solving skills Experience with, or ability to quickly learn, Microsoft Office suite of programs including Word, Excel, PowerPoint, Outlook, OneDrive, and SharePoint What we want you to bring to the team: 3+ years of industry experience working in a quality role in a manufacturing setting (excludes internships, co-ops, and other school projects) Physical Requirements: Ability to stand/sit for extended periods of time Ability to lift up to 50 pounds Ability to operate hand tools Compensation: The anticipated starting pay range for this position is $20.50 to $26.00 per hour and may be more or less depending upon skills, experience, and education. Benefits for you: 100% paid premiums across all medical, dental, vision, telemedicine, short-term disability, long-term disability, and basic life insurance plans Generous PTO $150 per month in employer HSA contributions (health savings account) Benefits for your family: 100% paid premiums across all medical, dental, vision, and telemedicine plans $300 per month in employer HSA contributions (heath savings account) 12 weeks of paid parental leave and flexible return-to-work options Benefits for your future: 401(k) with up to 5% matching contributions which vest 100% on day one Eligibility for incentive stock options

This position will report to the Supplier Quality Supervisor. This position will require close collaboration with the Supplier Quality, Inventory Control, and Supply Chain teams to ensure the highest standards of compliance, safety, and quality are maintained. Why Join Leiters Health? Are you passionate about making a real impact in the pharmaceutical industry? Do you thrive in a collaborative, innovative environment where your skills and ideas are valued? Look no further - Leiters Health is seeking talented individuals like you to join our dynamic team! At Leiters Health, we're not just another pharmaceutical company - we're pioneers in the field, dedicated to delivering high-quality compounded sterile products and outsourced solutions to healthcare providers nationwide. Our commitment to excellence and patient safety is at the core of everything we do. Innovative Culture: Be part of a forward-thinking company that encourages creativity, welcomes fresh ideas, and fosters an environment of continuous improvement. Meaningful Work: Contribute to a purpose-driven organization dedicated to providing critical medications and healthcare solutions that positively impact patients' lives. Professional Development: Access ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry. Cutting-Edge Technology: Work with state-of-the-art facilities and advanced technologies, staying ahead of the curve in pharmaceutical manufacturing. Collaborative Environment: Join a team of passionate individuals who are dedicated to teamwork, support, and mutual success, fostering a culture of inclusivity and collaboration. Who We're Looking For: We're seeking enthusiastic individuals who are driven, adaptable, and passionate about contributing to a mission-driven organization. Whether you're an experienced professional or just starting your career, Leiters Health provides an environment where your skills and talents will be recognized and appreciated. Sound like you? Apply today! Essential Functions: Inspect and verify the quality of raw materials, components, and packaging materials upon receipt to ensure they meet established specifications and regulatory requirements. Review and verify incoming material documentation, including Certificates of Analysis (COA), Certificates of Compliance (COC), and other relevant documentation to ensure completeness and accuracy. Inspect, review, and release incoming items intended for production use in accordance with raw material specifications. Communicate and collaborate with Supply Chain and Inventory Control to ensure appropriate items in inventory are available, appropriately qualified, documented, and released for approved use. Communicate with Supplier Quality when nonconforming materials are identified during incoming inspection. Request and obtain vendor/manufacturer certificates of analysis/conformance/sterility for incoming raw materials. Initiate and investigate deviations as applicable. Perform sampling of active pharmaceutical ingredients (API) and excipients in a cleanroom environment and submit samples for laboratory testing in accordance with internal specifications. Track and monitor all API and excipients due for retesting and submit samples for laboratory retesting in accordance with internal specifications. Safely operate pallet jack and forklift when transferring materials in the warehouse as needed. Adhere to all safety protocols and ensure the inspection area is kept clean, organized, and in compliance with GMP and safety guidelines. Work in a team or independently to release incoming materials. Other duties as assigned. Supervisory Responsibilities: None Experience and Necessary Skills: Minimum of 1-2 years of experience in quality or incoming inspection, preferably in a regulated manufacturing environment (pharmaceutical, medical device, or cGMP). Familiarity with material testing methods and quality procedures. Inventory management and warehouse experience desired. Excellent communication skills and ability to collaborate with cross-functional teams. Strong organizational skills and attention to detail with the ability to manage multiple tasks efficiently. Detail-oriented with a strong ability to identify nonconformance and resolve issues in a timely manner. Proficiency with Microsoft Office Suite (Word, Excel, etc.) and ERP software. High School Diploma or equivalent required. Associate or bachelor's degree in a scientific field preferred. 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. Ability to stand for extended periods and lift up to 30 lbs. Ability to work in a cleanroom environment, adhering to gowning and sanitation procedures. Ability to use personal protective equipment (PPE) as required. Verbal, written and oral English proficiency required. Understanding of 503B regulatory requirements, cGMP standards, and USP guidelines is a plus! Proficient written, verbal and oral English communication skills are required. Proficiency with Microsoft 365 tools including Outlook, Microsoft, and Excel. Must pass English Competency Test. Physical Requirements: Ability to stand or sit for extended periods of time. Ability to lift, push and pull up to 50 pounds periodically. Ability to maintain a gowning qualification, if applicable. Must have 20/20 near range vision and proficient color perception, with or without correction, if applicable. Benefits: 100% employer paid medical plan. Dental & Vision insurance options including FSA & HSA 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.

**Job Details** Mead, CO Type** Full Time **Salary Range** $22.00 - $29.00 Hourly **Description** The Quality Technician IV position requires 75% of tasks to be completed outdoors with the remaining 25% to be computer based tasks in an office environment. It involves hands on calibration and management of the calibration system. Sampling chemicals for analytical testing is also a critical responsibility. **Job Responsibilities** + Verifying and calibrating production measurement equipment including but not limited to, digital scales, thermal couples, pressure transmitters, RTD's, pressure gauges (analog), solvent flow meters, standards. + Maintaining calibration schedules, records and database. + Manage quarterly scale calibrations with outside contractor. + Manage calibrations with third party calibration vendor. + Assist engineering with PO submission for process monitoring equipment. + Sampling chemicals for testing and verifying they meet specifications. + Assist with preparing final cylinder preparations and quality approval. + Report nonconforming materials and equipment to appropriate individuals. + Assist in failure investigations including material and equipment disposition. + Assist with inventory approval status for raw materials and expired materials. + Act as the quality representative in pre-production meetings. + Perform work in accordance with published BSC safety protocols and policies. + Perform visual inspections of chemical materials. + Perform visual inspection of cylinders and the application of tamper-evident seals. + Issue production batch records. + Projects and additional tasks as assigned. **Education** + High School Diploma or general education degree (GED) + Must pass a basic math and reading assessment **Qualifications** **Qualifications** + Prior calibration experience preferred. + Familiarity with digital scales, thermal couples, pressure transmitters, RTD's, pressure gauges (analog), solvent flow meters, standards preferred. + Minimum of 1 year working in a manufacturing environment. + Willingness to obtain ASQ Calibration Technician Certification. + Willingness to obtain fork lift certification. + Extreme attention to detail. + Strong communication skills. Interface effectively with personnel from all levels of the organization. + Proficiency in MS Office, Outlook, and ERP systems. + Prioritize multiple work items with minimal oversight. **Supervisory Responsibilities:** **None for this position** **Language Skills:** Read, interpret, and write documents such as operating procedures, work instructions, and routine reports and correspondence. **Mathematical Skills:** Ability to calculate figures and amounts such as proportions, percentages, chemical formularies, and volumes. Ability to apply concepts of basic algebra and geometry. Ability to comprehend and apply statistical techniques. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory and factor analysis. **Physical Requirements:** While performing the duties of this job, the employee is frequently required to stand; walk; use hands to finger, handle, or feel; and talk or hear. The employee is occasionally required to sit; reach with hands and arms; climb or balance; and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Must pass a physical examination. **Working Conditions:** While performing the duties of this job, the employee is often exposed to wet and/or humid conditions, moving mechanical parts, fumes or airborne particles, toxic or caustic chemicals, outside weather conditions, and extreme cold. The noise level in the work environment is usually moderate. Boulder Scientific Company is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you have a disability and are unable to apply for a position through the website provided, call BSC at ************ to ask for assistance.

With a passion for life Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers. Are you looking for an inspiring career? You just found it. Steritec Products Inc., a member of the Getinge Group, manufactures sterilization and cleaning medical device consumables using ink technology. We manufacture and print highly specialized proprietary inks that undergo specific color changes when exposed to different sterilization conditions in hospital and industrial/pharmaceutical sterilizers. We are located in the beautiful Inverness Business Park in Englewood, CO. We offer a generous benefit package (medical, dental, vision, life, LTD, 401(k) as well as PTO, company-paid holidays and much more) all effective first day of employment! This QC InspectionTechnician position is an on-site, full-time, non-exempt position. Hours are Monday - Friday, 2:15pm - 10:45pm (with some flexibility). Position Summary: The Quality Control Inspection Technician is responsible for the performance of all in-coming, in-process, and finished product inspection, verification and acceptance criteria decisions, including the following: Essential Job Functions: 1. Operation and use of calipers, micrometers and other measurement equipment and tools. 2. Operation of any other equipment necessary to assure that components and products meet specifications. 3. Performance of receiving methods for all in-coming items. 4. Performance of inspection methods for all in-coming components. 5. Performance of inspection methods for all screen printing, lamination, cutting, and packaging components and assemblies. 6. Performance of First Article inspection methods. 7. Inspection acceptance criteria decisions for all in-coming and in-process components and assemblies. 8. Non-Conforming Item Report processing. 9. Verification of Device History Record. 10. Verification of minor Corrective Actions. 11. Verification and inspection of correct performance of TADs and Reworks. 12. Reviews all required production labels. 13. Other QC duties as designated by the QA Manager. 14. Approve proofs for "out of house" artwork. Essential Job Requirements: EDUCATION * Minimum High School diploma. EXPERIENCE * Knowledge of medical devices. Production line experience and/or Quality background. Experience working as an inspector preferred. REQUIRED SKILLS * Excellent written and verbal communications skills. * Strong customer service focused work ethic and attention to detail. * Professional interpersonal skills necessary to interact with external customer and internal contacts. * Demonstrated time management and organizational skills; ability to work independently and as part of a + team. Strong computer skills including MS Office applications are required QUALITY REQUIRMENTS * Build Quality into all aspects of their work by maintaining compliance to all quality requirements. * Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function). * Must have the education and experience to understand and comply with U.S. and Worldwide medical device regulations (As applicable to your job function). * Attend all required Quality & Compliance training at the specified interval. * Adopt the "Beyond Compliance Quality Culture" in the work environment; always meet and exceed requirements. PHYSICAL REQUIREMENTS * Ensures environmental consciousness and safe practices are exhibited in decisions. * Duties are performed in an office environment. * Requires manual coordination and vision to operate PC and telephone. * Hearing necessary to receive and reply to outside contacts and employees. * Ability to speak clearly in order to communicate with outside contacts and employees in person and on the telephone. * Must be willing to work in a sitting position for long periods of time. * Some bending, stooping, reaching and lifting (up to 30 pounds) is required. * Willingness to frequently move to various locations within and outside of the building. All job requirements are subject to possible modification to reasonably accommodate individuals with disabilities. Some requirements may exclude individuals who pose a direct threat or significant risk to the health and safety of themselves or other employees. This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position. Employees will be required to follow any other job-related instructions and to perform other job-related duties requested by their supervisor in compliance with Federal and State Laws. Requirements are representative of minimum levels of knowledge, skills and/or abilities. To perform this job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently. Continued employment remains on an "at-will" basis. Salary Range: $25 - 30/ hour DOE About us With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries. Benefits at Getinge: At Getinge, we offer a comprehensive benefits package, which includes: * Health, Dental, and Vision insurance benefits * 401k plan with company match * Paid Time Off * Wellness initiative & Health Assistance Resources * Life Insurance * Short and Long Term Disability Benefits * Health and Dependent Care Flexible Spending Accounts * Commuter Benefits * Parental and Caregiver Leave * Tuition Reimbursement Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process. Nearest Major Market: Denver

What Quality Control contributes to Cardinal Health Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Control is responsible for the analysis or inspection of materials, components, products or processes for compliance with specifications and standards. Job Summary The Technician II, Quality Control performs varied product inspections or analysis generally of finished goods components, incoming materials or new products, by observing, measuring and recording data using applicable measurement tools. Compiles and inputs data, documents and process findings and interprets results. Completes applicable documents needed for the release of product to the field. This job follows demonstrates knowledge of testing methods, product usage, and applicable procedures according to regulations, and standards and adheres to established policies and procedures but also participates in the establishment of future inspection procedures. Schedule/ Location: Onsite in Aurora, CO. 40 hours. Saturday through Tuesday; 10-hour shifts. Approximate hours between 10:00 am and 8:00 pm. Holidays as needed. Overtime as needed with little to no notice. Candidate must be flexible to work different days, schedules and/or hours based on business needs. Responsibilities Operates analytical equipment, performs analytical tests, interprets results, and documents findings in accordance with SOPs and regulatory requirements. Responsible for analysis of raw materials, drug substance, in-process, and drug product testing. Responsible for test/procedures to be performed as well as documentation and reporting requirements. Interact regularly with manufacturing and service functions to establish quality standards for raw material, work in process, and finished products. Ensures results are consistent with acceptable test parameters and reports abnormal findings from analytical tests to the QC supervision. Champion Quality, cGMP compliance, and EHS/Radiation Safety practices. Follows/mentors GDP/cGMP requirements. Actively partner with plant management and personnel in troubleshooting quality deficiencies and implement corrective measures to eliminate quality problems. Assists in the release of the final product in compliance with cGMP. Assures quality events are complete and accurate and resolved in a timely manner that meets the expectations of applicable quality agreements. Able to challenge, appropriately, the design, conduct, and reporting of cGMP activities including metrics and annual reporting. In that context, has the knowledge of the production process of the product. Understands technical/release product issues and evaluates their potential impact on product quality and compliance. Provides ideas for continuous improvement of the cGMP Quality Management System. Escalates complex issues to management in a timely manner. Prioritizes and ensures work is delivered in an efficient way. Performs other job duties as assigned. Qualifications High School diploma, GED or equivalent, or equivalent work experience, preferred 1-3 years of experience, preferred 0 - 3 years of relevant experience with wet chemistry, TLC, analytical instrument maintenance, troubleshooting and qualification preferred Work well with others and understand how to be successful in a team environment. Detail-oriented, organized, able to multi-task, a self-starter, and self-motivated. Proficient in Microsoft Word and Microsoft Excel and possess strong technical writing skills. Strong communication skills. Ability to lift up to 40 lbs. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus Performance Expectations Demonstrates a commitment to the organization's mission, vision, and values supporting organizational decisions and behaviors. Contributes to the development and implementation of systems and processes ensuring strategic goal attainment. Works as part of a team with others and shows respect and values diversity toward others. Demonstrates efforts to discovering, meeting, and advocating for the customer's needs. Takes actions to continually improve quality and safety in daily work. Actively participates in improving work processes to meet and exceed expectations. Identifies opportunities for improvement based on process observations, outcome measures, and feedback. Reports errors in a timely and appropriate manner. Takes initiative and is accountable for areas of responsibility meeting regulatory requirements including, but not limited to, maintaining required trainings as appropriate to position requirements. The ability to act calmly and patiently when working under pressure and/or conditions of stress. Maintains integrity, composure, communicates with honesty, transparency, clarity and promotes alternative perspectives Physical/ Mental Requirements The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms; balance; stoop, kneel, crouch or crawl; talk or hear; and taste or smell. The employee must occasionally lift or move up to 40 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus. Work Environment The primary work environment consists of a professional office environment within a radiopharmaceutical manufacturing facility as well as the laboratory setting. The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory groups. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he/she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate. What is expected of you and others at this level Applies acquired knowledge and skills to complete standard tasks Readily learns and applies new information and methods to work in assigned area Maintains appropriate licenses, training and certifications Works on routine assignments that require some problem resolution Works within clearly defined standard operating procedures and/or scientific methods Adheres to all quality guidelines Works under moderate degree of supervision Work typically involves regular review of output by work lead or supervisor Refers complex unusual problems to supervisor Anticipated hourly range: $20.20 per hour - $28.80 per hour Bonus eligible: No Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being. Medical, dental and vision coverage Paid time off plan Health savings account (HSA) 401k savings plan Access to wages before pay day with my FlexPay Flexible spending accounts (FSAs) Short- and long-term disability coverage Work-Life resources Paid parental leave Healthy lifestyle programs Application window anticipated to close: 04/26/2025 *if interested in opportunity, please submit application as soon as possible. The hourly range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply. Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law. To read and review this privacy notice click here

On site in Aurora, CO 80019 6 Month Contract to Hire $27/hr First year estimate $62,300, second year estimate $72,100 Benefits: Medical, Dental, Vision, 401K Day-to-Day An Engineering company specializing in custom conveyor systems design, commissioning, and integration is looking for a Quality Engineer to join their newer and expanding Quality Engineering team. We are looking for an Entry Level (0-2 years' experience) engineer with the goal of improving their professional skillsets in Quality assurance, including writing procedures and internal audits. You will be given the opportunity to learn and advance at the pace you set for yourself. You will work with tenured Engineers, Project Managers, Quality Assurance technicians who can pass on a deep level of knowledge in this space. Responsibilities include 75% Developing quality procedures, conducting root cause analysis, and implementing corrective actions. Other responsibilities include internal and supplier audits/Inspections, documenting work instructions/inspection plans/quality reports, analyzing data to identify trends, participating in new product development, and training employees on standards. This is a contract-to-hire position that will become permanent after 6 months. This company promotes internally, leaving plenty of room for advancement especially in this division which will be growing at a rapid pace as they continue to create process improvements. Candidates must pass a drug test. Must-haves • Bachelor's Degree in Engineering GPA 3.0+ • A passion to pursue a career in Quality Engineering in manufacturing • 0-2 years of experience with Quality Engineering including development of QA standards, corrective actions • Strong communication and ability to work with cross functional teams • Proficiency with Measurement tools such as a micrometer and calipers • Comfortable taking a background check and drug test Plusses • Internship or Project Experience with Conveyer Systems • Experience with root cause analysis in a manufacturing space Compensation: $60,000 to $62,300 per year annual salary. [ If client has provided an exact salary, then no need to use a range; also, if the client has provided an hourly rate, then use same hourly language from the Contract/Contract-to-Hire section above. ] Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role include: [ description should be provided by the client since this is for a perm position- they will not receive IG benefits. If client does not provide it upon our request, we can insert something generic like "Benefit packages for this role may include healthcare insurance offerings and paid leave as provided by applicable law."]

Our vision is to transform how the world uses information to enrich life for all. Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever. About our Team: The Global Quality (GQ) System Quality and Reliability Assurance (SORA) team at Micron plays a critical role in ensuring the quality and reliability of our products. Our team specializes in Returned Material Authorization (RMA) Failure Analysis (FA), working closely with engineers to analyze failures and improve product performance. We foster a culture of continuous improvement, collaboration, and technical expertise. Position Overview: As a QA Technician, you will be responsible for outgoing quality inspection and failure analysis activities. You will assist engineers in managing quality assurance tasks, performing quality inspections, conducting random audits, and supporting training efforts on production lines. Additionally, you will contribute to quality programs, audits, and 6S/ESD activities as needed. Responsibilities: * Receive, verify, and prepare materials for testing. * Perform bench-level testing, debug diagnostics, and isolate failing components. * Conduct Automated Test Equipment (ATE) operations, including preconditioning and testing devices. * Analyze failure data, summarize results, and track experiment progress. * Develop and maintain documentation, provide training, and support technical expertise development. Minimum Qualifications: * Experience in quality inspection, testing, or related technical roles. * Strong understanding of debugging, diagnostics, and failure analysis techniques. * Ability to interpret test results and collaborate with engineers to identify issues. * Proficiency in handling testing equipment and documenting findings. * Strong organizational and communication skills. Preferred Qualifications: * Knowledge of ATE operations, firmware testing, and failure analysis tools. * Experience working with quality programs, audits, and manufacturing processes. * Familiarity with 6S/ESD compliance and best practices. * Ability to train and mentor team members on processes and equipment usage. Prior experience in semiconductor or electronics manufacturing environments. The US base salary range that Micron Technology estimates it could pay for this full-time position is: $28.75 - $48.00 Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries of the position across all US locations. Within the range, individual pay is determined by work location and additional job-related factors, including knowledge, skills, experience, tenure and relevant education or training. The pay scale is subject to change depending on business needs. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Additional compensation may include benefits, discretionary bonuses and equity. As a world leader in the semiconductor industry, Micron is dedicated to your personal wellbeing and professional growth. Micron benefits are designed to help you stay well, provide peace of mind and help you prepare for the future. We offer a choice of medical, dental and vision plans in all locations enabling team members to select the plans that best meet their family healthcare needs and budget. Micron also provides benefit programs that help protect your income if you are unable to work due to illness or injury, and paid family leave. Additionally, Micron benefits include a robust paid time-off program and paid holidays. For additional information regarding the Benefit programs available, please see the Benefits Guide posted on micron.com/careers/benefits. Micron is proud to be an equal opportunity workplace and is an affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, citizenship status, disability, protected veteran status, gender identity or any other factor protected by applicable federal, state, or local laws. To learn about your right to work click here. To learn more about Micron, please visit micron.com/careers US Sites Only: To request assistance with the application process and/or for reasonable accommodations, please contact Micron's People Organization at hrsupport_************* or ************** (select option #3) Micron Prohibits the use of child labor and complies with all applicable laws, rules, regulations, and other international and industry labor standards. Micron does not charge candidates any recruitment fees or unlawfully collect any other payment from candidates as consideration for their employment with Micron.

Join CPI Card Group and become a part of a phenomenal team and work environment! CPI Card Group is a light manufacturuing company producing contact and contactless payment cards for our customers. CPI offers a full suite of solutions and the expertise in plastics manufacturing, personalization and fulfillment to provide a completely customized card package. We are currently looking for hard working production employees on all shifts to join our Littleton, CO facility. We offer an extensive benefits package for our employees including health insurance, time off, 401(k) matching, and more! The Quality Technician at CPI is responsible for the auditing, inspection and testing functions through-out the value stream. In addition, the Q.T. is charged with following up on any process and/or product non-conformances to assure they are brought to an effective solution while assisting with troubleshooting and supporting operations as required. Hourly rate - $23.00 Schedule: Monday-Thursday 4:00am-4:00pm Responsibilities Responsibilities: Reads and interprets the shop floor documents (proof, job ticket, combo ticket) as well as applicable ISO, Association, and CPI internal specifications. Know where to locate standards in SharePoint Complete Quality Release testing process including physical testing and visual inspection. Sets up and performs destructive and nondestructive tests on materials or product to measure performance, life or material characteristics Observe, report, and document quality data information on checklists and in the shop floor data collection system as required Initates quality hold and non-conformacnes based upon inspection results Completes in-process audits in Finishing Qualifications Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions The candidate must be able to use a caliper and other hand tools. Prior experience is not required The candidate must be able to interface with a PC by in putting and out putting data and using basic Microsoft Office Suite products. Keyboard input skills are necessary High school diploma or equivalent (Preferred) Elementary English proficiency communication skills necessary Physical Demand: Work is primarily conducted standing or walking in a manufacturing environment and sitting in an office environment and often requires bending and stooping to observe product and/or manufacturing equipment Manufacturing environment is noisy and may require ear protection Work involves good eyesight, hand/eye coordination and excellent color vision to be able to ensure quality product Work involves dealing with fine detail and constant human interaction Company Overview: CPI Card Group is a payment technology company and leading provider of credit, debit and prepaid solutions delivered physically, digitally and on-demand. CPI helps our customers foster connections and build their brands through innovative and reliable solutions, including financial payment cards, personalization and fulfillment, and Software-as-a-Service (SaaS) instant issuance. Learn more at ********************* Benefits: Competitive pay rates and an inclusive, empowering and rewarding culture. Solid benefits package including Medical, Dental, Vision, Long Term Disability, Short Term Disability, Life Insurance, Accident Insurance, Critical Illness Insurance, FSA, HSA, Vacation and Holiday Pay, Tuition Reimbursement and 401(k) with a competitive company match percentage. CPI is an Equal Opportunity Employer, including disability/vets. A complete background including drug screen is contingent upon hire.

Join our dynamic Quality Assurance team at our Organic Dairy Processing facility in Platteville, CO. Be a part of a 2024 Top Workplace USA! Purpose: The Quality Assurance Lab Technician is responsible for in-process and finished product quality testing, maintaining accurate and complete records, and alerting management to any potential quality issues. S hift 6pm -6am Thurs - Sat and alternating Wednesdays OR Sunday - Tuesday and alternating Wednesdays Essential Responsibilities: All plant personnel have the responsibility to monitor and report any deviations from our Food Safety and Food Quality (HACCP & SQF) programs to your immediate supervisor. Assist in all in-bound and finished product milk processing including but not limited to: Customer Service, working with our Laboratory and Product Information Management System, Tanker/Silo Inventory Control, administrative assistant duties. Competency in Microsoft Windows and Office products. Responsible for performing process control testing in a manufacturing environment. Maintain accurate and complete laboratory testing result records. Maintain Good Manufacturing Practices, Good Laboratory Practices and Safety Procedures. Communicate any potential quality issues to QA Management. Professional communication and customer service skills in working with multiple departments and external partners. Other Required Responsibilities: Laboratory testing result data entry. Member of HACCP team. Other quality department responsibilities as deemed necessary. Knowledge & Experience: High School Diploma or equivalent. Bachelor's degree in Dairy Manufacturing, Food Science, Microbiology, or related field preferred. Experience in dairy laboratory testing procedures preferred. Knowledge of laboratory testing methods. Detail oriented and team member. Strong, honest work ethic with ability to handle multiple tasks daily. Good communication skills. Physical Requirements: Must be able to sit for extended periods of time; Must be able to stand or walk for more than 50% of the shift. Must be able to bend, stoop, kneel or crawl; reach grasp and lift, push, pull up to 50 lbs. regularly and up to 80 lbs. occasionally.

Starting Pay is $21.00per hour Shift: Sunday - Thursday 4:15am - 1:30pm Maintains all aspects of Quality Assurance to ensure proper, safe and exceptional operation of the department. * 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. 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. Shamrock anticipates closing the application window for this job opportunity on or before December 31, 2025

**_What Quality Control contributes to Cardinal Health_** Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications. Quality Control is responsible for the analysis or inspection of materials, components, products or processes for compliance with specifications and standards. **_Job Summary_** The Technician II, Quality Control performs varied product inspections or analysis generally of finished goods components, incoming materials or new products, by observing, measuring and recording data using applicable measurement tools. Compiles and inputs data, documents and process findings and interprets results. Completes applicable documents needed for the release of product to the field. This job follows demonstrates knowledge of testing methods, product usage, and applicable procedures according to regulations, and standards and adheres to established policies and procedures but also participates in the establishment of future inspection procedures. **_Schedule/ Location:_** + Onsite in Aurora, CO. + 40 hours. Saturday through Tuesday; 10-hour shifts. Approximate hours between 10:00 am and 8:00 pm. + Holidays as needed. Overtime as needed with little to no notice. Candidate must be flexible to work different days, schedules and/or hours based on business needs. **_Responsibilities_** + Operates analytical equipment, performs analytical tests, interprets results, and documents findings in accordance with SOPs and regulatory requirements. + Responsible for analysis of raw materials, drug substance, in-process, and drug product testing. + Responsible for test/procedures to be performed as well as documentation and reporting requirements. + Interact regularly with manufacturing and service functions to establish quality standards for raw material, work in process, and finished products. + Ensures results are consistent with acceptable test parameters and reports abnormal findings from analytical tests to the QC supervision. + Champion Quality, cGMP compliance, and EHS/Radiation Safety practices. + Follows/mentors GDP/cGMP requirements. + Actively partner with plant management and personnel in troubleshooting quality deficiencies and implement corrective measures to eliminate quality problems. + Assists in the release of the final product in compliance with cGMP. + Assures quality events are complete and accurate and resolved in a timely manner that meets the expectations of applicable quality agreements. + Able to challenge, appropriately, the design, conduct, and reporting of cGMP activities including metrics and annual reporting. In that context, has the knowledge of the production process of the product. + Understands technical/release product issues and evaluates their potential impact on product quality and compliance. + Provides ideas for continuous improvement of the cGMP Quality Management System. + Escalates complex issues to management in a timely manner. + Prioritizes and ensures work is delivered in an efficient way. + Performs other job duties as assigned. **_Qualifications_** + High School diploma, GED or equivalent, or equivalent work experience, preferred + 1-3 years of experience, preferred + 0 - 3 years of relevant experience with wet chemistry, TLC, analytical instrument maintenance, troubleshooting and qualification preferred + Work well with others and understand how to be successful in a team environment. + Detail-oriented, organized, able to multi-task, a self-starter, and self-motivated. + Proficient in Microsoft Word and Microsoft Excel and possess strong technical writing skills. + Strong communication skills. + Ability to lift up to 40 lbs. + Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus **_Performance Expectations_** + Demonstrates a commitment to the organization's mission, vision, and values supporting organizational decisions and behaviors. Contributes to the development and implementation of systems and processes ensuring strategic goal attainment. + Works as part of a team with others and shows respect and values diversity toward others. + Demonstrates efforts to discovering, meeting, and advocating for the customer's needs. + Takes actions to continually improve quality and safety in daily work. Actively participates in improving work processes to meet and exceed expectations. Identifies opportunities for improvement based on process observations, outcome measures, and feedback. + Reports errors in a timely and appropriate manner. Takes initiative and is accountable for areas of responsibility meeting regulatory requirements including, but not limited to, maintaining required trainings as appropriate to position requirements. + The ability to act calmly and patiently when working under pressure and/or conditions of stress. Maintains integrity, composure, communicates with honesty, transparency, clarity and promotes alternative perspectives **_Physical/ Mental Requirements_** The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. + While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms; balance; stoop, kneel, crouch or crawl; talk or hear; and taste or smell. The employee must occasionally lift or move up to 40 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus. **_Work Environment_** + The primary work environment consists of a professional office environment within a radiopharmaceutical manufacturing facility as well as the laboratory setting. The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory groups. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he/she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate. **_What is expected of you and others at this level_** + Applies acquired knowledge and skills to complete standard tasks + Readily learns and applies new information and methods to work in assigned area + Maintains appropriate licenses, training and certifications + Works on routine assignments that require some problem resolution + Works within clearly defined standard operating procedures and/or scientific methods + Adheres to all quality guidelines + Works under moderate degree of supervision + Work typically involves regular review of output by work lead or supervisor + Refers complex unusual problems to supervisor **Anticipated hourly range:** $20.20 per hour - $28.80 per hour **Bonus eligible:** No **Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental and vision coverage + Paid time off plan + Health savings account (HSA) + 401k savings plan + Access to wages before pay day with my FlexPay + Flexible spending accounts (FSAs) + Short- and long-term disability coverage + Work-Life resources + Paid parental leave + Healthy lifestyle programs **Application window anticipated to close:** 04/26/2025 *if interested in opportunity, please submit application as soon as possible. The hourly range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity. _Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._ _Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._ _To read and review this privacy notice click_ here (***************************************************************************************************************************

This description is intended to be illustrative of the major duties performed by the employee assigned to this position. Performs other duties as assigned. This position reports to the Quality Manager. The role is responsible for performing quality activities and maintaining a quality laboratory environment in a sterile pharmaceutical manufacturing facility. The candidate should have an understanding of raw material requirements, laboratory environments, and cGMP requirements. The position requires an individual who works independently and in a team environment, with attention to detail, and maintains communication with other functional areas and sites. Why Join Leiters Health? Are you passionate about making a real impact in the pharmaceutical industry? Do you thrive in a collaborative, innovative environment where your skills and ideas are valued? Look no further - Leiters Health is seeking talented individuals like you to join our dynamic team! At Leiters Health, we're not just another pharmaceutical company - we're pioneers in the field, dedicated to delivering high-quality compounded sterile products and outsourced solutions to healthcare providers nationwide. Our commitment to excellence and patient safety is at the core of everything we do. Innovative Culture: Be part of a forward-thinking company that encourages creativity, welcomes fresh ideas, and fosters an environment of continuous improvement. Meaningful Work: Contribute to a purpose-driven organization dedicated to providing critical medications and healthcare solutions that positively impact patients' lives. Professional Development: Access ongoing training, mentorship, and growth opportunities to expand your skills and advance your career within a rapidly growing industry. Cutting-Edge Technology: Work with state-of-the-art facilities and advanced technologies, staying ahead of the curve in pharmaceutical manufacturing. Collaborative Environment: Join a team of passionate individuals who are dedicated to teamwork, support, and mutual success, fostering a culture of inclusivity and collaboration. Who We're Looking For: We're seeking enthusiastic individuals who are driven, adaptable, and passionate about contributing to a mission-driven organization. Whether you're an experienced professional or just starting your career, Leiters Health provides an environment where your skills and talents will be recognized and appreciated. Sound like you? Apply today! Essential Functions: Responsible for performing daily quality functions including: Performing environmental monitoring of personnel and clean rooms. Incubation, enumeration, and verification of agar plates. Review analyses carried out through in-house and contract labs and file data.

Job Details Mead, CO Full Time $22.00 - $29.00 HourlyDescription The Quality Technician IV position requires 75% of tasks to be completed outdoors with the remaining 25% to be computer based tasks in an office environment. It involves hands on calibration and management of the calibration system. Sampling chemicals for analytical testing is also a critical responsibility. Job Responsibilities Verifying and calibrating production measurement equipment including but not limited to, digital scales, thermal couples, pressure transmitters, RTD's, pressure gauges (analog), solvent flow meters, standards. Maintaining calibration schedules, records and database. Manage quarterly scale calibrations with outside contractor. Manage calibrations with third party calibration vendor. Assist engineering with PO submission for process monitoring equipment. Sampling chemicals for testing and verifying they meet specifications. Assist with preparing final cylinder preparations and quality approval. Report nonconforming materials and equipment to appropriate individuals. Assist in failure investigations including material and equipment disposition. Assist with inventory approval status for raw materials and expired materials. Act as the quality representative in pre-production meetings. Perform work in accordance with published BSC safety protocols and policies. Perform visual inspections of chemical materials. Perform visual inspection of cylinders and the application of tamper-evident seals. Issue production batch records. Projects and additional tasks as assigned. Education High School Diploma or general education degree (GED) Must pass a basic math and reading assessment Qualifications Qualifications Prior calibration experience preferred. Familiarity with digital scales, thermal couples, pressure transmitters, RTD's, pressure gauges (analog), solvent flow meters, standards preferred. Minimum of 1 year working in a manufacturing environment. Willingness to obtain ASQ Calibration Technician Certification. Willingness to obtain fork lift certification. Extreme attention to detail. Strong communication skills. Interface effectively with personnel from all levels of the organization. Proficiency in MS Office, Outlook, and ERP systems. Prioritize multiple work items with minimal oversight. Supervisory Responsibilities: None for this position Language Skills: Read, interpret, and write documents such as operating procedures, work instructions, and routine reports and correspondence. Mathematical Skills: Ability to calculate figures and amounts such as proportions, percentages, chemical formularies, and volumes. Ability to apply concepts of basic algebra and geometry. Ability to comprehend and apply statistical techniques. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory and factor analysis. Physical Requirements: While performing the duties of this job, the employee is frequently required to stand; walk; use hands to finger, handle, or feel; and talk or hear. The employee is occasionally required to sit; reach with hands and arms; climb or balance; and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Must pass a physical examination. Working Conditions: While performing the duties of this job, the employee is often exposed to wet and/or humid conditions, moving mechanical parts, fumes or airborne particles, toxic or caustic chemicals, outside weather conditions, and extreme cold. The noise level in the work environment is usually moderate.