Quality inspector jobs in New Castle, IN - 107 jobs

Join SMF - Where Your Career Takes Shape! At SMF, we don't just offer jobs-we build careers. As part of Etnyre International, we have a 50-year legacy in high-quality metal fabrication, serving industries like construction, power generation, agriculture, and mining. Our reputation as a top-tier supplier to Fortune 500 OEMs comes from our dedicated team members, cutting-edge technology, and commitment to excellence. With 200,000+ square feet of manufacturing capabilities across two locations, we handle everything from engineering and fabrication to finishing. Our recent partnership with Etnyre International has fueled even more growth and opportunity-and we want YOU to be a part of it! What We Offer - Total Rewards Package: ANNUAL BONUS for ALL team members ANNUAL Wage Increases to reward your dedication Competitive Pay Based on Experience $2.50/hour Shift Premium for 2nd shift 11 Paid Holidays + 3 Additional Paid Holiday Break Days Generous Paid Time Off (Vacation & Flex Time) Excellent Benefits Package: LOW-COST Medical, Dental, and Vision Insurance Company-Paid Life Insurance & Disability Coverage 401(k) with Employer Match & Profit Sharing Accident, Hospital, & Critical Illness Coverage Options Now Hiring: Quality Inspector (2nd Shift) Location: Anderson, SC Pay Range: $22.25 - $27.96/hour What You'll Do ️ Hands-on with manufacturing: support production, troubleshoot parts & fixtures Inspection pro: perform receiving checks, audits, weld certifications, and document results Metrology master: gauge repair, calibrations, and station verifications Keep it clean: maintain organized work areas for smooth operations Quality guardian: inspect rejected/reworked material, track non-conforming parts, and escalate issues Process evaluator: ensure proper gages at machine stations & recommend improvements Qualifications * Strong communication skills * Problem-solving mindset: define issues, collect data, draw valid conclusions Physical Requirements * Frequent climbing, bending, twisting * Ability to lift up to 55 lbs

**GE Aerospace Indianapolis** The Indianapolis site manufactures complex Aerospace components for a variety of applications. Join us on our growth and transformation journey in Indianapolis. **A few reasons to consider GE** + 10% pay differential for 2nd/3rd shift. + Healthcare Benefits eligible on day one of employment + 12 annual paid holidays; vacation eligible at day 30 of employment + Climate-controlled building out of the elements + Tuition reimbursement benefit + 401K with company match **Essential Responsibilities** + Weekend Shift Hours: 7am-7pm, Days: Friday, Saturday, Sunday + Use hand tools and measuring equipment to insure specifications are met + Work from complex product drawings, manuals, and specifications + Adherence to Operator Acceptance Procedures (OAP) + Review product documents and insure accuracy and work competion. + Inspect finished product and identify defects. + Set-up, operate, adjust, and troubleshoot all tools and equipment used in the inspection or assembly process. + Maintains accurate work records. + Willingness to support team concept and learn/perform other duties as required. + Maintains standards for 6S and tool control. + Recognizes process variation, adjusts accordingly while maintaining compliant work practices, and consistently produces conforming hardware. + Maintains productivity standards. + Willingness to work outside normal work hours to support assembly requirements. + Utilize precision measuring instruments to inspect parts. + Support our team concept and learn/perform other duties as required. + Communicate effectively and professionally with others. + Follow and promote safe work practices. + Support LEAN initiatives. + Lift light to medium weight material in an environment that may occasionally require crouching, stooping and/or flexible work positions. **Qualifications/Requirements** + High School Diploma or GED + Previous experience utilizing hand measurement gages such as mics, verniers, bore gages, calipers, height gages, and indicators. + One year of experience in a manufacturing environment + Familiarity with simple machine and tool operations + Understand how to identify and effectively use a variety of power and hand tools. + Read, understand and utilize procedures, detailed computerized build plans, and basic mathematical calculations. + Ability to perform precise and detailed work. + Communicate effectively and professionally with others within the team. + Follow and promote safe work practices. + Demonstrated ability to participate in a team environment. **Desirable characteristics** + Strong analytical and problem-solving skills + Ability to read, understand, and utilize procedures, sketches, and blueprints as well as perform basic mathematical calculations. + Working knowledge of precision measuring equipment. + Previous assembly and machine operator experience + Willingness to learn other production jobs _This role requires access to U.S. export-controlled information. Therefore, employment will be contingent upon the ability to prove that you meet the status of a U.S. Person as one of the following: U.S. lawful permanent resident, U.S. Citizen, have been granted asylee or refugee status (i.e., a protected individual under the Immigration and Naturalization Act, 8 U.S.C. 1324b(a)(3))._ **Additional Information** GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer (****************************************************************************************** . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). **Relocation Assistance Provided:** Yes GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

From a small family business to a multi-billion dollar global company, Sonoco has been changing the face of products and packaging since 1899 - all while keeping the heart of "People Build Businesses" alive. Our talented people are at the core of our growth, constantly reinventing the Sonoco wheel with brilliant solutions every year. Today we are a world leader in global packaging solutions with diversified operations in over 34 countries. We're extremely proud of our portfolio of brands, our achievements in sustainability and industrialization and the groundbreaking work accomplished by our people. Position: Quality Tech I for VIP Line Location: Portland, IN Pay: $22.30 hourly Shift: 1st shift; 7am-3:30pm Since 1989, ThermoSafe has been driven by a singular purpose: protecting the integrity of products that protect people. We're a global team of thinkers, builders, and doers-advancing thermal science and redefining what's possible in sustainable cold-chain innovation. From our labs to our manufacturing floors, and across every business function, ThermoSafe team members collaborate to design, produce, and deliver solutions that keep critical medicines safe worldwide. At ThermoSafe, curiosity drives progress and collaboration fuels innovation. Whether working in a lab, on a production line, or behind a spreadsheet, every employee plays a vital role in protecting patients and advancing global health. We value accountability, creativity, and diverse perspectives-empowering people to make real-world impact. Because at ThermoSafe, every degree-and every person-matters. Report to the Production Shift Supervisor and become ThermoSafe's unbreakable gatekeeper of quality on the VIP packaging line. You'll own first-piece sign-offs, precision measurements, product quarantine, dry-down studies, and relentless line walks-ensuring every gauge sheet, record, and panel meets flawless GMP standards while protecting the world's most temperature-critical shipments. What You'll Do * Safety is non-negotiable-#1 priority, every shift, no exceptions * Own first-piece approvals, weighing, measuring, quarantining suspect product, and supporting dry-down studies * Conduct line walks to verify every gauge sheet and production record is complete and GMP-perfect * Print labels, crush Excel work, handle communications, and nail end-of-shift Oracle inventory closeouts with the supervisor * Spot defects instantly, troubleshoot fast, and keep quality bulletproof * Keep product moving-pack out, stage, and flow finished goods all shift * Maintain a spotless, 5S-excellent, highly organized workspace * Jump in wherever needed-help other teams, get it done, no hand-holding * Live ThermoSafe's mission: obsess over quality, own safety, protect the customer What You Bring * Proven manufacturing experience (strongly preferred) and rock-solid attendance * "Make it happen now" urgency with zero tolerance for cutting corners * Eagle-eyed defect detection and fanatical attention to detail * Strong verbal and written communication skills * Ability to work independently while juggling multiple priorities * Reliable, committed, quality-obsessed, and a genuine team player * Physical stamina to lift/carry up to 49 lbs, stand full shifts, bend, stoop, twist, and grasp repetitively * Solid computer skills-Excel, email, label printing, Oracle transactions * Ability to read and execute manufacturing instructions precisely at high speed If you're wired for perfection and want every panel you touch to safeguard life-saving pharmaceuticals or mission-critical payloads-this is your line to own. Come be the quality shield that keeps the world's most important shipments safe. At Sonoco Products Company, we offer a comprehensive total rewards package, including competitive pay and benefits. *Benefits listed below are for employees located in the U.S. Specific benefits and wellbeing programs may vary depending on your location (within the U.S. or global), or if you are a union employee. Benefits * Medical, dental, and vision coverage for you and your dependents, including FSA and HSA options * 401(k) retirement plan with company match * Wellbeing tools and resources to support holistic health, including an Employee Assistance Program with a variety of services * Paid time off and holidays to recreate, rejuvenate and care for the health of yourself and family * Variety of company paid and voluntary employee-paid insurance plans including life, personal accident, and disability insurance * Tuition reimbursement We are an equal opportunity employer, and we strictly prohibit and do not tolerate discrimination against employees, applicants or any other covered persons because of race, color, religion, national origin or ancestry, sex, pregnancy, sexual orientation, marital status, gender identity or expression, age, disability, genetic information, veteran status, or any legally protected characteristic.

Starting Pay $23.000 increasing to $24.00 after completion of training. Shift and Schedule * 12 hour shift (7pm - 7am) * Continental schedule (2/2/3) The Quality Control Technician is responsible for inspecting and assessing the quality of injected plastic products to ensure they meet established company and customer standards during incoming quality control, in process quality control and outgoing quality control. They use a variety of precision tools and equipment to measure and test materials, as well as identify defects or deviations in the manufacturing process. Their insights drive continuous improvement initiatives within the production team, ensuring consistent product quality. Additionally, they collaborate with the manufacturing team and other departments to implement corrective actions and improve overall production standards. Responsibilities for this position include: * Perform incoming quality control inspections on components by interpreting, measuring, and verifying dimensions meet tolerances according to drawings using standard measuring tools and equipment. * Test raw materials using melt flow index tester and moisture analyzer. * Perform in process quality control on product during the manufacturing process for adherence to company and customer requirements using equipment and visually inspection. * Audit product and process for conformance to standards. * Interpret and report testing results and compare them to established specifications and control limits. Generate inspection reports and accept or reject finished goods. * Conduct routine and non-routine analyses of in-process materials, raw materials, and finished goods. * Record inspection and testing data into appropriate systems. Maintain accurate and up-to-date logs. * Review documentation for compliance and maintain traceability records. * Collaborate with production teams to address quality-related issues (product & process). * Familiar with computers, able to navigate excel, email, data entry, multiple operating systems, take photos of product and upload them to designated location. Requirements Requirements * Intelligence: Requires the ability to learn and understand relatively complex principles and techniques related to administrative and clerical duties; to make independent judgments without supervision; to acquire knowledge of topics related to primary occupation. * Verbal Aptitude: The ability to record and deliver information, explain procedures, and follow oral and written instructions. * Numerical Aptitude: Requires the ability to utilize mathematical formulas; add, subtract, multiply, and divide figures. * Physical lifting and movement: Ability to walk or stand 12 hours a day. Ability to lift, push, pull or move 35 pounds and stoop, bend, or reach above the shoulders. Qualifications: * High School Diploma or equivalent. * Good written and verbal communication skills required. * Able to make a decision based on data and standards. * Previous quality experience in a manufacturing environment is preferred. * High attention to detail and commitment to maintaining accurate documentation. * Ability to work collaboratively in a team environment and contribute to a positive, supportive at

Responsible for ensuring that Bila Solar products meet all customer requirements, from incoming inspection of raw material to final inspection of finished goods. Responsible for understanding all production requirements (blueprints/work instructions/etc) and effectively verifying adherence to these standards. Responsible for documentation of inspection and initiating the non-conformance process if needed. About the Company Bila Solar is driving the next generation of American solar innovation, by transforming American solar production from our HQ in the heart of Indianapolis, Indiana - strengthening the domestic supply chain and creating advanced manufacturing jobs in clean energy. Led by highly-experienced industry veterans, we're among the first-to-market to offer US-made solar cells in a 550w dual-glass module that can deliver exceptional durability and top-tier performance. But, we're not stopping there. Our facility also produces an innovative, ultralight, 17-pound 520w module, designed for commercial rooftops and low-load-bearing structures, bringing solar to places traditional panels can't reach. Key Responsibilities: Support creation and revisions of documentation (SOP, Inspection instructions, data collection, etc.) Support the development of Quality and Operations-related inspections. Able to fill in for Quality operation resources as needed to relieve breaks or cover in absences (willingness to be involved in cross training) Collaboration in troubleshooting and Root Cause investigations (data collection, feedback, etc) Provide recommendations for process adjustments Become proficient in use of production and inspection gages (training plan developed) Support material control activities including, but not limited to, non-conforming material and hold material disposition activities Support the development of training plans for Quality inspectors as well as production resources as needed (training matrix development) Inspection of material with an understanding of the specifications and requirements Performing quality testing as needed with training support Defect identification and procedure adherence for resolution Reporting on quality issues and managing records of inspection and compliance data. Potential for internal audit activities (work instructions, SOPs, etc.) Skills: Must have excellent written and verbal communication skills. Strong computer skills, including Excel. Must have excellent organizational skills and attention to detail. Demonstrated problem solving skills. Excellent follow-up skills. Individual must be able to work with limited supervision and actively participate in a team-oriented, continuous improvement, manufacturing environment. Jobsite: Indianapolis, IN 46225 Benefits Competitive Salary: Competitive compensation based on experience and qualifications. Health Coverage: Health, dental, and vision insurance. Retirement Plan: Retirement savings plan (401k) with company match. Paid Time Off: Paid time off and holidays. Career Growth: Opportunities for career advancement and professional development. Application Process: If you're ready to make an impact as a Bila Solar Quality Inspector, please submit your resume detailing your relevant experience and qualifications. We are excited to review your application and explore how you can contribute to our team!

Job Description Responsible for ensuring that Bila Solar products meet all customer requirements, from incoming inspection of raw material to final inspection of finished goods. Responsible for understanding all production requirements (blueprints/work instructions/etc) and effectively verifying adherence to these standards. Responsible for documentation of inspection and initiating the non-conformance process if needed. About the Company Bila Solar is driving the next generation of American solar innovation, by transforming American solar production from our HQ in the heart of Indianapolis, Indiana - strengthening the domestic supply chain and creating advanced manufacturing jobs in clean energy. Led by highly-experienced industry veterans, we're among the first-to-market to offer US-made solar cells in a 550w dual-glass module that can deliver exceptional durability and top-tier performance. But, we're not stopping there. Our facility also produces an innovative, ultralight, 17-pound 520w module, designed for commercial rooftops and low-load-bearing structures, bringing solar to places traditional panels can't reach. Key Responsibilities: Support creation and revisions of documentation (SOP, Inspection instructions, data collection, etc.) Support the development of Quality and Operations-related inspections. Able to fill in for Quality operation resources as needed to relieve breaks or cover in absences (willingness to be involved in cross training) Collaboration in troubleshooting and Root Cause investigations (data collection, feedback, etc) Provide recommendations for process adjustments Become proficient in use of production and inspection gages (training plan developed) Support material control activities including, but not limited to, non-conforming material and hold material disposition activities Support the development of training plans for Quality inspectors as well as production resources as needed (training matrix development) Inspection of material with an understanding of the specifications and requirements Performing quality testing as needed with training support Defect identification and procedure adherence for resolution Reporting on quality issues and managing records of inspection and compliance data. Potential for internal audit activities (work instructions, SOPs, etc.) Skills: Must have excellent written and verbal communication skills. Strong computer skills, including Excel. Must have excellent organizational skills and attention to detail. Demonstrated problem solving skills. Excellent follow-up skills. Individual must be able to work with limited supervision and actively participate in a team-oriented, continuous improvement, manufacturing environment. Jobsite: Indianapolis, IN 46225 Benefits Competitive Salary: Competitive compensation based on experience and qualifications. Health Coverage: Health, dental, and vision insurance. Retirement Plan: Retirement savings plan (401k) with company match. Paid Time Off: Paid time off and holidays. Career Growth: Opportunities for career advancement and professional development. Application Process: If you're ready to make an impact as a Bila Solar Quality Inspector, please submit your resume detailing your relevant experience and qualifications. We are excited to review your application and explore how you can contribute to our team!

FULLBEAUTY Brands™ is the premier fashion and lifestyle destination for the plus size customer. We are an online and catalog marketplace offering a curated collection of the finest family of plus size brands and thousands of products. The Quality Inspector is an hourly / nonexempt position and is outside the scope of the Collective Bargaining Agreement (CBA). The Quality Inspector is responsible for performing audits and various administrative duties associated with these audits. The Quality Inspector is responsible for auditing hourly CBA work and documenting instances of non-conformance for review with Department Supervisors. PRIMARY RESPONSIBILITIES: Audit and monitor quality requirements in accordance with company quality assurance policies and customer specifications. Conduct visual inspection of merchandise through various stages of processing within Southeastern / Plainfield fulfillment centers. Document instances of non-conformance for review with management. Prepare reports and enter data into the Quality Databases / Files. Maintain quality reports, documents, and forms. Maintain 5S standards for audit areas, workspaces and resources. Research, identify, and conduct root cause analysis in addition to report findings and recommendations for corrective action and improvement to management. Assist management with special projects as requested. MINIMUM QUALIFICATIONS: High school diploma or equivalent. Associates degree is desired. At least one (1) year of recent experience as a Quality Inspector within a distribution or manufacturing environment desired. Required Skills Proven ability to perform basic math functions (i.e., addition, subtraction, multiplication, division and computing percentages). Understanding of basic statistics desired. Understanding of the primary phases of 5S, with experience in applying its various methodologies. Understanding of Standard Operating Procedures (SOPs) and Quality Processes Proven ability working in teams and one-on-one situations. Excellent interaction skills that involve communicating information in an effective and positive manner to both hourly associates and mid-management. Excellent written and verbal communication skills. Ability to use a personal computer and software relevant to the position. Demonstrated basic-intermediate level proficiency using Microsoft Word and Excel. Knowledge of Access desired. Certification in Quality Inspection or familiarity with quality management systems desired. Ability to work day, evening, and night shifts at Southeastern or Plainfield, including daily overtime and weekends as needed. Working Conditions & Physical Requirements Work Environment: Distribution Center Physical Requirements: Ability to sit, stand, bend, twist, reach, push, pull, lift, climb, and walk for up to 12 hours each workday. Ability to lift 40 lbs. occasionally. WHY JOIN FULLBEAUTY? Competitive Health Benefits (Medical, Dental & Vision) Employer HSA Contribution 401K Match Employee Assistance Program Hybrid Work Schedule (Corporate) Business Casual Attire Wellness Initiatives 30% Associate Merchandise Discount Across our Family of Brands Employee Discount on Travel, Cell Phone Plans and More Generous Paid Time Off Program Promote From Within Culture Commitment to Being an Equal Opportunity Employer Life Insurance Benefits Internal charity that supports FULLBEAUTY Brands' associates and their immediate family members during times of extreme hardship FULLBEAUTY Brands™ is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, sexual orientation, gender identity, disability or protected veteran status.

Donaldson is committed to solving the world's most complex filtration challenges. Together, we make cool things. As an established technology and innovation leader, we are continuously evolving to meet the filtration needs of our changing world. Join a culture of collaboration and innovation that matters and a chance to learn, effect change, and make meaningful contributions at work and in communities. Position Summary: The Quality Control Inspector is responsible for verifying product quality, conducting inspections and tests, and documenting results to ensure compliance with internal and external requirements. This role actively participates in problem-solving, root cause analysis, and continuous improvement efforts across the organization. Role Responsibilities: * Perform inspections and testing of products to ensure compliance with specifications and quality standards. * Read and interpret blueprints, engineering drawings, and bills of materials. * Document inspection results, including Certificates of Conformance and other quality records. * Investigate customer complaints and product returns, and implement containment measures. * Participate in root cause analysis and develop corrective and preventive actions. * Calibrate and maintain standard measuring equipment (gauges, calipers, tooling). * Support the Production Part Approval Process (PPAP) and ISO 9001 requirements. * Resolve nonconforming material using company resources and procedures. * Collaborate with production, engineering, and management to drive continuous improvement. * Adhere to all EHS and PPE policies while maintaining a safe and positive work environment. Minimum Qualifications: * High school diploma or GED with at least 1 year of quality control experience. * Knowledge of ISO 9001 or similar quality standards and quality techniques (e.g., SPC, PPAP). * Strong communication skills and proficiency with Microsoft Office. * Ability to work independently and in a fast-paced, team-oriented environment, including off-shifts or extended hours as needed. Preferred Qualifications: * Associate's degree or technical certification in quality, manufacturing, or related field. * 2+ years of quality control experience in a manufacturing environment. * Experience with ISO 9001 audits, SPC, PPAP, and root cause analysis. * Proficient with dimensional measurement tools, calibration, and interpreting blueprints. * Strong problem-solving skills with ability to support continuous improvement in a fast-paced environment. Immigration Sponsorship Not Available: * Donaldson will not offer immigration sponsorship or assume sponsorship of an employment visa for this position. * International relocation or remote work arrangements outside of the U.S. will not be considered. Keywords: Quality Assurance, Inspection, ISO9001 Equal Opportunity Employer, including Disability and Veterans Employment opportunities for positions in the United States may require use of information which is subject to the export control regulations of the United States. Hiring decisions for such positions are required by law to be made in compliance with these regulations. Applicants for employment opportunities in other countries must be able to meet the comparable export control requirements of that country and of the United States. Donaldson Company has been made aware that there are several recruiting scams that are targeting job seekers. These scams have attempted to solicit money for job applications and/or collect confidential information, Donaldson will never solicit money during the application or recruiting process. Donaldson only accepts online applications through our Careers | Donaldson Company, Inc. website and any communication from a Donaldson recruiter would be sent using a donaldson.com email address. If you have any questions about the legitimacy of an employment opportunity, please reach out to ******************************* to verify that the communication is from Donaldson. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

1st shift: 6:30 am - 3pm Starting pay $17/hr. (Temp to hire) After 90 days, $18/hr. Job Summary:We are seeking a detail-oriented and hands-on Quality Inspector who will also be responsible for performing rework on non-conforming products. This dual role involves inspecting products at various stages of production to ensure they meet quality standards, identifying defects, and performing corrective actions to bring products into compliance.Key Responsibilities:Quality Inspection: Conduct inspections of incoming materials, in-process components, and finished products. Record inspection results and maintain accurate quality documentation. Report and document non-conformances and collaborate with the production team to determine root causes. Assist in audits, process validations, and quality improvement initiatives. Rework & Repair: Perform hands-on rework on defective or non-conforming products based on established procedures or work instructions. Document rework activities, including materials used and time spent. Collaborate with engineering or quality teams to develop or update rework procedures. Ensure reworked items meet all quality standards before release. Qualifications: High school diploma or equivalent. 2+ years of experience in quality inspection, manufacturing, or a similar role. Experience with rework or repair of mechanical, electronic, or assembly-based products is a strong plus. Proficient in reading technical drawings, work instructions, and inspection documentation. Strong attention to detail and commitment to product quality. Basic computer skills for data entry and report generation. Working Conditions: This role may require standing for extended periods and working with small parts or tools. Use of personal protective equipment (PPE) may be required depending on the work environment. Occasional lifting of up to 30 lbs. #Indy

Title: Environmental Monitoring Technician Temp to perm potential 6am/8am start time - 8 hours a day Monday-Friday 3 positions on first shift Aseptic Technique/comfortable in clean rooms entry level microbiologist water collection GDP willingness to learn Background Qualifications: High School diploma required as minimum. Associates degree and/or related certification in Microbiological Sciences highly preferred. Experience with aseptic technique and/or working in aseptic environments. Ability to gown aseptically for Manufacturing and Aseptic Filling areas. As persons in this role are engaged in sampling and environmental monitoring during open manufacture of medicinal products, individuals must not be affected by an infectious disease nor have open lesions on any exposed surface of the body. Working hours will require flexibility with available work hours. Sufficient mobility to work in manufacturing processing areas is required. Major Position Activities & Responsibilities: Environmental monitoring of the aseptic area during production fills or weekly monitoring Must immediately notify supervisor if affected by infectious disease or open lesions on body, as individuals are not permitted to enter manufacturing areas or handle product if these conditions exist. Water collection and testing of WFI, Clean Steam, and the Deionized Water Performs media fill qualification and release in support of environmental monitoring program. Perform sampling activities in support of environmental investigations Maintenance of the cleanliness of the microbiology laboratory area, refrigerators, and incubators Handling of wastes including hazardous wastes. Attendance at mandatory annual hazardous waste training meeting(s). Demonstration of competency in training by passing test(s) administered by the company or consultant providing such training. Responsible for adhering to the Environmental, Health and Safety program. Performs special projects and other duties as assigned. As a part of the employees job requirements, the employee may be required to handle wastes including hazardous wastes. The employee must attend mandatory annual hazardous waste training meeting(s) and show a competency in that training by passing test(s) administered by the company or consultant providing such training.

Donaldson is committed to solving the world's most complex filtration challenges. Together, we make cool things. As an established technology and innovation leader, we are continuously evolving to meet the filtration needs of our changing world. Join a culture of collaboration and innovation that matters and a chance to learn, effect change, and make meaningful contributions at work and in communities. Position Summary: The Quality Control Inspector is responsible for verifying product quality, conducting inspections and tests, and documenting results to ensure compliance with internal and external requirements. This role actively participates in problem-solving, root cause analysis, and continuous improvement efforts across the organization. Role Responsibilities: Perform inspections and testing of products to ensure compliance with specifications and quality standards. Read and interpret blueprints, engineering drawings, and bills of materials. Document inspection results, including Certificates of Conformance and other quality records. Investigate customer complaints and product returns, and implement containment measures. Participate in root cause analysis and develop corrective and preventive actions. Calibrate and maintain standard measuring equipment (gauges, calipers, tooling). Support the Production Part Approval Process (PPAP) and ISO 9001 requirements. Resolve nonconforming material using company resources and procedures. Collaborate with production, engineering, and management to drive continuous improvement. Adhere to all EHS and PPE policies while maintaining a safe and positive work environment. Minimum Qualifications: High school diploma or GED with at least 1 year of quality control experience. Knowledge of ISO 9001 or similar quality standards and quality techniques (e.g., SPC, PPAP). Strong communication skills and proficiency with Microsoft Office. Ability to work independently and in a fast-paced, team-oriented environment, including off-shifts or extended hours as needed. Preferred Qualifications: Associate's degree or technical certification in quality, manufacturing, or related field. 2+ years of quality control experience in a manufacturing environment. Experience with ISO 9001 audits, SPC, PPAP, and root cause analysis. Proficient with dimensional measurement tools, calibration, and interpreting blueprints. Strong problem-solving skills with ability to support continuous improvement in a fast-paced environment. Immigration Sponsorship Not Available: • Donaldson will not offer immigration sponsorship or assume sponsorship of an employment visa for this position. • International relocation or remote work arrangements outside of the U.S. will not be considered. Keywords: Quality Assurance, Inspection, ISO9001 Equal Opportunity Employer, including Disability and Veterans Employment opportunities for positions in the United States may require use of information which is subject to the export control regulations of the United States. Hiring decisions for such positions are required by law to be made in compliance with these regulations. Applicants for employment opportunities in other countries must be able to meet the comparable export control requirements of that country and of the United States. Donaldson Company has been made aware that there are several recruiting scams that are targeting job seekers. These scams have attempted to solicit money for job applications and/or collect confidential information, Donaldson will never solicit money during the application or recruiting process. Donaldson only accepts online applications through our Careers | Donaldson Company, Inc. website and any communication from a Donaldson recruiter would be sent using a donaldson.com email address. If you have any questions about the legitimacy of an employment opportunity, please reach out to [email protected] to verify that the communication is from Donaldson. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

Job Description We're looking to hire Quality Line Reference Technicians for our Fishers, Indiana site! Responsibilities: Perform in-process, visual, dimensional, functional, and packaging controls according to the control plan of the manufactured product Be the reference key-person for product quality within the shift with reference to the production lines to which they are dedicated Cooperate with the QC laboratory for the evaluation of the defects Monitor production lines status in coordination with the other functions, recording the control results and the other required information, Guarantee a high level of cleaning and tidiness of the work areas Initiate deviations and OOS and participate in the investigations and solving activities for the non-conformities that occur during the shift Support personnel training activities Qualifications: Basic computer application knowledge Prior experience in manufacturing or quality control Knowledge of device manufacturing/pharma Quality Management System processes and features Experience in healthcare device/pharma manufacturing environment. International travel may be required, based on business needs Ability to work weekends Stevanato Group is an Equal Employment Opportunity (EEO) employer. We believe that a diverse workforce is key to our success. We welcome applications from all members of society irrespective of age, sex, disability, sexual orientation, race, religion or belief It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Job Type: Full-time Benefits: 401(k) 401(k) matching Dental insurance Health insurance Life insurance Paid time off Retirement plan Vision insurance Schedule: 8 hour shift Experience: performing quality control test: 3 years (Required) healthcare environment (medical device or phrama): 3 years (Required) visually inspected products: 3 years (Required) Quality inspection: 3 years (Required) Work Location: In person

Ambu provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Objective: The objective of this position is to ensure that products manufactured at Ambu USNV meet established quality standards and specifications. This includes verifying that products are produced, documented, and tested according to these standards before they are released. Responsibilities and Essential Functions: * Conduct visual, dimensional, and functional inspections and tests on components and finished products across all work areas, ensuring compliance with established policies and procedures. * Record inspection and test data as prescribed by written instructions and procedures, following cGDP. * Prevent mix-ups, damage, deterioration, contamination, or other adverse effects to products during handling. * Operate all associated test and measurement equipment as instructed and documented in procedures. * Identify and segregate nonconforming products from the production line according to documented policies and procedures. * Follow the NCR procedure when a nonconformity is identified and participate in the NCR response team (NRT) by collecting and providing pertinent information. * Offer suggestions for enhancing quality, manufacturing, and safety, including recommendations for policies and procedures. * Follow gowning, PPE, and cleanliness procedures, and practice good personal hygiene to prevent contamination and maintain product integrity. * Notify supervision of issues or errors, providing immediate response. * Support the onboarding and training of new Quality Control Inspectors. * Work overtime as needed per company policy to meet production demand. * Perform other related duties and responsibilities as assigned. Authorities: * Halt manufacturing upon identifying nonconformities and request the initiation of NCRs. * Label nonconforming products accordingly. Qualifications: * High school diploma or equivalent. * At least one year of experience in Quality Inspections, Quality Assurance, or a related field, or one year of experience with Ambu products. * Technical degree preferred. * Experience in the medical device industry preferred. Required skills: * Strong attention to detail and organizational skills. * Proficient in reading inspection gauges/instruments (e.g., tape measure, Go/No Go gauges, calipers, etc.) and other measuring devices. * Basic math skills for addition, counting, and timekeeping. * Ability to follow directions and documented instructions accurately. * Capable of working independently according to specifications and procedures. * Effective communication and teamwork skills. * Legible handwriting and ability to perform written documentation in compliance with all document control procedures and GDP (Good Documentation Practices). * Ability to distinguish tone and color. * Ability to stand for extended periods as needed. * Ability to routinely lift, push, and/or pull up to fifty pounds. * Proficiency with Microsoft Office (Word, Excel, PowerPoint). * Must be able to read, write, and understand English. Work Environment: This is a manufacturing facility, so employees may be exposed to noise, chemicals, fumes, airborne particles, machinery, vibration, or other workplace hazards. These exposures are managed in compliance with current safety and health standards. Ambu Provided Training within the first six months: * Agile * Learning Management system

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Organization Overview: The Technician - QC in Indianapolis Active Pharmaceutical Ingredient (IAPI) group performs accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. The technician completes second person verification of other's results. The technician also participates in laboratory analytical investigations, equipment evaluations and qualification, and some quality system improvement initiatives by executing well-defined protocols and procedures. The technician shares technical information and best practice within plant sites or group. Responsibilities: Sample Analysis and Reporting * Verify (SPV) analytical data of other analysts within the lab as requested. * Accurately and safely perform analytical test methods or related support activities as per procedures or protocols. Uses technical knowledge in the review and interpretation of data for conformances to procedures, standards, protocols, and/or real-time recognition of aberrant data and results. * Perform data entry and reviews own work for accuracy in accordance with laboratory procedures, standards and GMP requirements. * May perform holistic review of data for release of data from the laboratory. Problem Solving * Recognizes when a deviation from test methods, procedures, et cetera has occurred and initiates analytical investigations and participates in a Root Cause Investigations. * Participates in investigations for deviations. * Assists in troubleshooting equipment and methods as required. Continuous Improvement Initiatives * Assist in improvement of quality systems by creating or revising worksheets and other lab documentation systems. * Identifies and communicates opportunities for improvement initiatives in daily work activities. * Reviews SOPs for executable as written. * Shares technical information and best practice within plant sites or group. Lab Operations * Assist with drafting protocols for non-routine testing or validation with appropriate guidance. * Assist in developing equipment qualification protocols with appropriate guidance. * Perform routine equipment calibrations or maintenance. * Comply with and assist with implementing safety standards. * Execute notification to management when required by procedures or standards. * Initiate lab deviations * Train and mentor others. Assist with developing training materials. Basic Requirements: * Associate's degree in a science field related to the lab (e.g., chemistry for Chem. Labs) or 1+ years of demonstrated relevant experience in a GMP analytical lab Additional Skills/Preferences: * Proficiency with computer systems LIMS, Empower, Excel, etc. * Ability to work in a lab environment, including wearing appropriate PPE and other safety required equipment and considerations. * Demonstrate strong math and documentation skills. * Demonstrate strong oral and written communication and interpersonal interaction skills. Additional Information: * Sunday-Thursday 8 Hour Evening to Night Shift. * Tasks may require repetitive motion and standing for long periods of time. * Must be able to lift at least 5 liters of liquid. * Overtime or weekend work required, as necessary. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $18.02 - $34.90 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Quality Control - Quality Technician The Quality technician I may be responsible for performing any of the following types of inspections: Incoming Inspections: evaluate incoming materials and components for conformance to specific criteria. Incoming inspections will be performed using dimensional, visual, and process related criteria to determine suitability for use. A base understanding of metrology, traceability, and product preservation is required for this function. In-process Inspections: evaluate product in various stages of the process either internally or after being processed by a third party. Accurate recordkeeping and an understanding of proper document control practices is essential to success in this role Final Inspections: evaluation of product prior to release for shipment to the customer. This will include assisting with completing and compiling documentation for First Article Inspection packets as well as production inspection records. Ability to interact with all areas of production to maintain efficient product throughput. Review production records for accuracy and compliance. Ability to work in clean room environment including adherence to gowning, cleanliness, and procedural standards. Work with a high level of precision and detail. Participation in auditor development program and ability to learn and master auditing practices and principles. Work in a team environment for an increased productivity and quality by ensuring quality and timely outputs while working with a continuous improvement mindset. Understand and follow all company policies and safety procedures. All other duties as assigned by the supervisor. PHYSICAL DEMANDS/WORK ENVIRONMENT Capacity to work indoors in an office, laboratory, and/or manufacturing environment. Ability to work in a stationary position for prolonged periods of time. Capability to lift objects or equipment weighing up to 40 pounds with or without reasonable accommodation. Physical aptitude to use basic hand tools in a laboratory and/or manufacturing environment. Ability to travel and/or attend meetings locally for trainings. MINIMUM REQUIREMENTS 2 Year technical degree or equivalent prior quality experience in a production environment working with multiple products/product lines. Available to work first shift with occasional overtime on evenings/weekends if needed. Intermediate computer and math skills including ability to use Excel and Microsoft Teams. Ability to evaluate requirements, understand technical documents, and keep thorough, organized records. Familiarity with reading part prints and detailed specification review. Ability to use hand tools and measuring devices such as calipers, micrometers, height gauges, surface roughness meters, Go/no-go gauges, pin gauges, comparators, borescopes, sight pipes, etc... Communicate effectively. Ability to perform multiple tasks while adhering to procedural guidelines with minimal supervision. Provia, Syteline, and Excel spreadsheets experience in a work environment a plus. Prior ISO Class 5 clean room experience a plus. Experience with Vision Systems, CMMs, Comparators, borescopes or Sight Pipes a plus. For internal use only: Quality001

From a small family business to a multi-billion dollar global company, Sonoco has been changing the face of products and packaging since 1899 - all while keeping the heart of “People Build Businesses” alive. Our talented people are at the core of our growth, constantly reinventing the Sonoco wheel with brilliant solutions every year. Today we are a world leader in global packaging solutions with diversified operations in over 34 countries. We're extremely proud of our portfolio of brands, our achievements in sustainability and industrialization and the groundbreaking work accomplished by our people. Position: Quality Tech I for VIP Line Location: Portland, IN Pay: $22.30 hourly Shift: 1st shift; 7am-3:30pm Since 1989, ThermoSafe has been driven by a singular purpose: protecting the integrity of products that protect people. We're a global team of thinkers, builders, and doers-advancing thermal science and redefining what's possible in sustainable cold-chain innovation. From our labs to our manufacturing floors, and across every business function, ThermoSafe team members collaborate to design, produce, and deliver solutions that keep critical medicines safe worldwide.At ThermoSafe, curiosity drives progress and collaboration fuels innovation. Whether working in a lab, on a production line, or behind a spreadsheet, every employee plays a vital role in protecting patients and advancing global health. We value accountability, creativity, and diverse perspectives-empowering people to make real-world impact. Because at ThermoSafe, every degree-and every person-matters. Report to the Production Shift Supervisor and become ThermoSafe's unbreakable gatekeeper of quality on the VIP packaging line. You'll own first-piece sign-offs, precision measurements, product quarantine, dry-down studies, and relentless line walks-ensuring every gauge sheet, record, and panel meets flawless GMP standards while protecting the world's most temperature-critical shipments. What You'll Do Safety is non-negotiable-#1 priority, every shift, no exceptions Own first-piece approvals, weighing, measuring, quarantining suspect product, and supporting dry-down studies Conduct line walks to verify every gauge sheet and production record is complete and GMP-perfect Print labels, crush Excel work, handle communications, and nail end-of-shift Oracle inventory closeouts with the supervisor Spot defects instantly, troubleshoot fast, and keep quality bulletproof Keep product moving-pack out, stage, and flow finished goods all shift Maintain a spotless, 5S-excellent, highly organized workspace Jump in wherever needed-help other teams, get it done, no hand-holding Live ThermoSafe's mission: obsess over quality, own safety, protect the customer What You Bring Proven manufacturing experience (strongly preferred) and rock-solid attendance “Make it happen now” urgency with zero tolerance for cutting corners Eagle-eyed defect detection and fanatical attention to detail Strong verbal and written communication skills Ability to work independently while juggling multiple priorities Reliable, committed, quality-obsessed, and a genuine team player Physical stamina to lift/carry up to 49 lbs, stand full shifts, bend, stoop, twist, and grasp repetitively Solid computer skills-Excel, email, label printing, Oracle transactions Ability to read and execute manufacturing instructions precisely at high speed If you're wired for perfection and want every panel you touch to safeguard life-saving pharmaceuticals or mission-critical payloads-this is your line to own. Come be the quality shield that keeps the world's most important shipments safe. At Sonoco Products Company, we offer a comprehensive total rewards package, including competitive pay and benefits. *Benefits listed below are for employees located in the U.S. Specific benefits and wellbeing programs may vary depending on your location (within the U.S. or global), or if you are a union employee. Benefits Medical, dental, and vision coverage for you and your dependents, including FSA and HSA options 401(k) retirement plan with company match Wellbeing tools and resources to support holistic health, including an Employee Assistance Program with a variety of services Paid time off and holidays to recreate, rejuvenate and care for the health of yourself and family Variety of company paid and voluntary employee-paid insurance plans including life, personal accident, and disability insurance Tuition reimbursement We are an equal opportunity employer, and we strictly prohibit and do not tolerate discrimination against employees, applicants or any other covered persons because of race, color, religion, national origin or ancestry, sex, pregnancy, sexual orientation, marital status, gender identity or expression, age, disability, genetic information, veteran status, or any legally protected characteristic.

Donaldson is committed to solving the world's most complex filtration challenges. Together, we make cool things. As an established technology and innovation leader, we are continuously evolving to meet the filtration needs of our changing world. Join a culture of collaboration and innovation that matters and a chance to learn, effect change, and make meaningful contributions at work and in communities. Position Summary: The Quality Control Inspector is responsible for verifying product quality, conducting inspections and tests, and documenting results to ensure compliance with internal and external requirements. This role actively participates in problem-solving, root cause analysis, and continuous improvement efforts across the organization. Role Responsibilities: Perform inspections and testing of products to ensure compliance with specifications and quality standards. Read and interpret blueprints, engineering drawings, and bills of materials. Document inspection results, including Certificates of Conformance and other quality records. Investigate customer complaints and product returns, and implement containment measures. Participate in root cause analysis and develop corrective and preventive actions. Calibrate and maintain standard measuring equipment (gauges, calipers, tooling). Support the Production Part Approval Process (PPAP) and ISO 9001 requirements. Resolve nonconforming material using company resources and procedures. Collaborate with production, engineering, and management to drive continuous improvement. Adhere to all EHS and PPE policies while maintaining a safe and positive work environment. Minimum Qualifications: High school diploma or GED with at least 1 year of quality control experience. Knowledge of ISO 9001 or similar quality standards and quality techniques (e.g., SPC, PPAP). Strong communication skills and proficiency with Microsoft Office. Ability to work independently and in a fast-paced, team-oriented environment, including off-shifts or extended hours as needed. Preferred Qualifications: Associate's degree or technical certification in quality, manufacturing, or related field. 2+ years of quality control experience in a manufacturing environment. Experience with ISO 9001 audits, SPC, PPAP, and root cause analysis. Proficient with dimensional measurement tools, calibration, and interpreting blueprints. Strong problem-solving skills with ability to support continuous improvement in a fast-paced environment. Immigration Sponsorship Not Available: · Donaldson will not offer immigration sponsorship or assume sponsorship of an employment visa for this position. · International relocation or remote work arrangements outside of the U.S. will not be considered. Keywords: Quality Assurance, Inspection, ISO9001 Equal Opportunity Employer, including Disability and Veterans Employment opportunities for positions in the United States may require use of information which is subject to the export control regulations of the United States. Hiring decisions for such positions are required by law to be made in compliance with these regulations. Applicants for employment opportunities in other countries must be able to meet the comparable export control requirements of that country and of the United States. Donaldson Company has been made aware that there are several recruiting scams that are targeting job seekers. These scams have attempted to solicit money for job applications and/or collect confidential information, Donaldson will never solicit money during the application or recruiting process. Donaldson only accepts online applications through our Careers | Donaldson Company, Inc. website and any communication from a Donaldson recruiter would be sent using a donaldson.com email address. If you have any questions about the legitimacy of an employment opportunity, please reach out to ******************************* to verify that the communication is from Donaldson. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.

Ambu provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Objective: The objective of this position is to ensure that products manufactured at Ambu USNV meet established quality standards and specifications. This includes verifying that products are produced, documented, and tested according to these standards before they are released. Responsibilities and Essential Functions: * Conduct visual, dimensional, and functional inspections and tests on components and finished products across all work areas, ensuring compliance with established policies and procedures. * Record inspection and test data as prescribed by written instructions and procedures, following cGDP. * Prevent mix-ups, damage, deterioration, contamination, or other adverse effects to products during handling. * Operate all associated test and measurement equipment as instructed and documented in procedures. * Identify and segregate nonconforming products from the production line according to documented policies and procedures. * Follow the NCR procedure when a nonconformity is identified and participate in the NCR response team (NRT) by collecting and providing pertinent information. * Offer suggestions for enhancing quality, manufacturing, and safety, including recommendations for policies and procedures. * Follow gowning, PPE, and cleanliness procedures, and practice good personal hygiene to prevent contamination and maintain product integrity. * Notify supervision of issues or errors, providing immediate response. * Support the onboarding and training of new Quality Control Inspectors. * Work overtime as needed per company policy to meet production demand. * Perform other related duties and responsibilities as assigned. Authorities: * Halt manufacturing upon identifying nonconformities and request the initiation of NCRs. * Label nonconforming products accordingly. Qualifications: * High school diploma or equivalent. * At least one year of experience in Quality Inspections, Quality Assurance, or a related field, or one year of experience with Ambu products. * Technical degree preferred. * Experience in the medical device industry preferred. Required skills: * Strong attention to detail and organizational skills. * Proficient in reading inspection gauges/instruments (e.g., tape measure, Go/No Go gauges, calipers, etc.) and other measuring devices. * Basic math skills for addition, counting, and timekeeping. * Ability to follow directions and documented instructions accurately. * Capable of working independently according to specifications and procedures. * Effective communication and teamwork skills. * Legible handwriting and ability to perform written documentation in compliance with all document control procedures and GDP (Good Documentation Practices). * Ability to distinguish tone and color. * Ability to stand for extended periods as needed. * Ability to routinely lift, push, and/or pull up to fifty pounds. * Proficiency with Microsoft Office (Word, Excel, PowerPoint). * Must be able to read, write, and understand English. Work Environment: This is a manufacturing facility, so employees may be exposed to noise, chemicals, fumes, airborne particles, machinery, vibration, or other workplace hazards. These exposures are managed in compliance with current safety and health standards. Ambu Provided Training within the first six months: * Agile * Learning Management system

QUALITY_CONTROL - QUALITY_TECHNICIAN_I PURPOSE * This role is to provide quality inspection, continuous improvement, and general quality support within the organization. This position requires attention to detail, ability to understand and follow established processes, and product evaluation skills. A successful candidate will be competent in reading and understanding basic blueprints and completing routine inspections. ESSENTIAL DUTIES * The Quality Technician may be responsible for performing any of the following types of inspections: * Incoming Inspections: evaluate incoming materials and components for conformance to specific criteria. Incoming inspections will be performed using dimensional, visual, and process related criteria to determine suitability for use. A base understanding of metrology, traceability, and product preservation is required for this function. * In-process Inspections: evaluate product in various stages of the process either internally or after being processed by a third party. Accurate recordkeeping and an understanding of proper document control practices is essential to success in this role * Final Inspections: evaluation of product prior to release for shipment to the customer. This will include assisting with completing and compiling documentation for First Article Inspection packets as well as production inspection records. * Ability to interact with all areas of production to maintain efficient product throughput. * Review production records for accuracy and compliance. * Ability to work in clean room environment including adherence to gowning, cleanliness, and procedural standards. * Work with a high level of precision and detail. * Participation in auditor development program and ability to learn and master auditing practices and principles. * Work in a team environment for an increased productivity and quality by ensuring quality and timely outputs while working with a continuous improvement mindset. * Understand and follow all company policies and safety procedures. * All other duties as assigned by the supervisor. PHYSICAL DEMANDS/WORK ENVIRONMENT * Capacity to work indoors in an office, laboratory, and/or manufacturing environment. * Ability to work in a stationary position for prolonged periods of time. * Capability to lift objects or equipment weighing up to 40 pounds with or without reasonable accommodation. * Physical aptitude to use basic hand tools in a laboratory and/or manufacturing environment. * Ability to attend meetings locally for trainings. MINIMUM REQUIREMENTS * 2 Year technical degree or equivalent prior quality experience in a production environment working with multiple products/product lines. * Available to work first shift with occasional overtime on evenings/weekends if needed. * Intermediate computer and math skills including ability to use Excel and Microsoft Teams. * Ability to evaluate requirements, understand technical documents, and keep thorough, organized records. * Familiarity with reading part prints and detailed specification review. * Ability to use hand tools and measuring devices such as calipers, micrometers, height gauges, surface roughness meters, Go/no-go gauges, pin gauges, comparators, borescopes, sight pipes, etc... * Communicate effectively. * Ability to perform multiple tasks while adhering to procedural guidelines with minimal supervision. * Provia, Syteline, and Excel spreadsheets experience in a work environment a plus. * Prior ISO Class 5 clean room experience a plus. * Experience with Vision Systems, CMMs, Comparators, borescopes or Sight Pipes a plus. For internal use only: Quality001