Quality assurance technician jobs in Round Rock, TX - 478 jobs

Job Posting Start Date 01-05-2026 Job Posting End Date 02-28-2026Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary Summary: The “Supplier Quality Technician” will be based in ……., reporting to …… In charge of engineering tests and technical functions related to the hold up of Supplier Quality Engineering. Responsibilities: Audits processes, tests and inspects products and/or develops, compiles and evaluates statistical data to define and maintain quality and reliability of products. Working from engineering drawings, specifications, schematics, diagrams, written descriptions, layouts or defined plans to perform complex engineering testing, checkout, First Article Inspection, root cause investigation, internal corrective actions and supplier correction actions. Interprets engineering drawings, schematic diagrams or formulas and confers with management or engineering staff to define quality and reliability standards. Selects processes to be audited from primarily the manufacturing areas and checks for a variety of features, including ESD (electro-static discharge) and handling practices, documentation, training and process integrity. Selects products for audits at specified stages in the production or post-production process, and tests products for variety of qualities such as dimensions, performance and mechanical, electrical or cosmetic characteristics. Records audit data, applying statistical quality control procedures. Evaluates data and writes reports to validate or indicate deviations from existing standards. Recommends modifications of existing quality or production standards, programs or reports to achieve optimum quality within limits of equipment capability. Prepares graphs or charts of data or enters data into computer for investigation. Download quality information from quality system to be used for QA reports. Explore engineering test results and implements process changes to resolve problems. Provides factory help to identify and resolve issues associated with purchased parts, materials and manufacturing. Qualifications: Typically requires an Associate's degree in electronics, military technical training or equivalent experience and training. Typically requires 4 years of related experience. What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Job CategoryQuality Is Sponsorship Available? NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

Job DescriptionSUMMARY A detail-oriented Laboratory Technician to manage and perform calibration, verification, and maintenance of measurement and test equipment used throughout our manufacturing operations. The ideal candidate will ensure all equipment remains within specified tolerances and complies with internal quality systems and external standards (e.g., ISO 9001, ISO/IEC 17025, or other applicable requirements). ESSENTIAL DUTIES AND RESPONSIBILITIES Perform calibration, verification, and functional checks on a variety of instruments and equipment (e.g., pressure, temperature, dimensional, electrical, torque, and flow devices) Maintain and update calibration records, certificates, and traceability documentation in accordance with internal quality procedures Identify and segregate equipment found out of tolerance Coordinate repairs or adjustments with internal teams or external vendors Develop and maintain calibration schedules to ensure on-time service for all equipment Support root cause analysis and corrective actions for measurement-related nonconformances Work with quality and engineering teams to define calibration requirements for new or modified equipment Ensure all calibration activities meet relevant standards (e.g., NIST traceability, ISO/IEC 17025, or customer-specific requirements) Assist in audit preparation and provide technical support during internal and external audits. Maintain a clean, organized calibration area and follow all safety protocols and environmental procedures EDUCATION AND EXPERIENCE Education: Associate's degree in Metrology, Engineering Technology, Physics, or related technical field (or equivalent experience) Experience: 5+ years performing calibrations or working in a metrology or testing environment Familiarity with measurement principles, uncertainty, and common standards for dimensional, electrical, or mechanical calibration Ability to interpret technical drawings, specifications, and equipment manuals Strong computer skills and experience with calibration management software (e.g., GAGEtrak, IndySoft, or similar) Excellent attention to detail, recordkeeping, and organizational skills Ability to work independently and manage multiple priorities in a manufacturing environment CERTIFICATES, LICENSES, REGISTRATIONS Individuals must be able to perform the duties of the job at a level as generally prescribed and learned by attaining the credentials below. ASQ Certified Calibration Technician (CCT) preferred ASQ Certified Quality Technician (CQT) preferred PHYSICAL DEMANDS Ability to lift and move equipment up to 50 pounds Work may involve standing for extended periods or using fine motor tools Typical work environment: laboratory and production floor MANAGEMENT DISCLAIMER TECO-Westinghouse's Management reserves the right to revise, change or modify the duties and responsibilities of this position at any time to meet business and organizational needs. This position description may not list all duties for this position. The incumbent in the position may be asked to perform other duties. This position description is not a contract for employment and either the incumbent or TECO-Westinghouse may terminate employment at any time, for any reason. Powered by JazzHR 2eMynjmPfm

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! Job Scope The Sr. Quality Assurance Technician is responsible for reviewing and verifying Device History Records (DHRs) to ensure compliance with internal procedures, FDA regulations (21 CFR Part 820), and ISO standards (e.g., ISO 13485). This role supports the release of intermediate materials and finished medical devices and ensures product quality and regulatory compliance. Job Responsibilities Inspect and verify product labels and insert, perform data review for material intermediate and component releases, label reconciliation in DHR, complete release documentation (release forms and status labels) Conduct review of documentation in accordance with released procedures, GxP standards (GDP, GMP) and production schedules Verify that all required production, inspection, and test documentation is complete and meets release criteria, including raw material status, calibration, etc. Attend interdepartmental meetings to support and coordinate product release, such as MRB. Identify and document any discrepancies or non-conformances found during DHR review, generating Non-Conformance Reports (NCs) as needed Log, file, maintain and archive various QA reports & records Maintain and track key performance metrics and assist other Quality Assurance personnel in data collection as needed Perform quality walkthroughs of manufacturing operations to drive continuous improvement and compliance Assist in continuous improvement of DHR review and related quality processes Participate in quality investigations (e.g., CAPA, NCs) related to DHR errors or product quality issues as needed Provide support during external audits and regulatory inspections, Other duties as assigned Education, Experience and Qualifications H.S. Diploma or equivalent required Associate's Degree in a life science or engineering or equivalent related experience preferred 3+ Years Experience in FDA regulated manufacturing environment, previous Quality experience preferred 3+ Years Experience with participating in formal audits preferred Good verbal and written communication skills in the English language Ability to interpret a variety of instructions in written oral form Computer skills (Microsoft Windows and Office programs), familiarity with Oracle preferred Working knowledge of GMP, GDP, and regulatory requirements (FDA, ISO 13485) Ability to apply sampling techniques Ability to manage and present data as it relates to product release Highly organized with proven time management and prioritization skills Ability to maintain attention to detail in a fast-paced environment Comfortable with routine work but able to switch back and forth between tasks Standard Physical Demands Vision (Color) on the job is required - Occasionally Standard Working Conditions Must work onsite at Luminex office - Constantly Work is normally performed in an office and a manufacturing environment - Constantly Possible exposure to biological or chemical hazard, extensive noise, and/or working with lasers - Occasionally Frequent use of personal computer, copiers, printers, and telephones - Frequently Frequent standing, walking, sitting, listening, writing, typing, and talking - Frequently Frequent work under deadlines, and in direct contact with others - Frequently Occasional lifting of 30 lbs. and climbing - Occasionally Travel Requirements 10% Domestic travel may be required Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation. The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.

We are seeking an analytical chemist with general laboratory experience including creation of standards/spiking mixes, sample preparation, and sample analysis as well as familiarity with GC/MS, FTIR, percent moisture determination, LC-MS/MS, HPLC-UV, and/or Raman analytical platforms. The focus of this role will be on providing technical support to Signature Science's quality assurance (QA) contracts for defense and homeland security programs as well as commercial proficiency testing (PT) programs, including HazMat PT, hemp/cannabis PT, and custom PT programs. The successful candidate will also support internal Signature Science quality programs through maintenance of the quality management system and QA laboratory support. Essential Duties and Responsibilities: Assist with planning and implementation of chemical analysis proficiency tests for methods such as gas chromatograph mass spectrometry (GC/MS), Fourier transform infrared spectroscopy (FTIR), percent moisture determination, liquid chromatography with tandem mass spectrometry (LC-MS/MS), high performance liquid chromatography - ultraviolet (HPLC-UV), and Raman. Activities include developing proficiency test plans, performing laboratory pilot testing, preparing and verifying proficiency test samples, and packaging samples for shipment. Perform laboratory activities related to the preparation and verification of proficiency test samples, as detailed below: o Creation of standards/spiking mixes, o Sample creation, o Sample extraction/dilution, and sample analysis, using techniques such as GC/MS, FTIR, percent moisture determination, LC-MS/MS, HPLC-UV, and Raman. Maintain laboratory equipment and laboratory records. Perform laboratory inventories, purchase laboratory supplies, and maintain appropriate purchasing records. Evaluate special study and proficiency test data, identify data trends and other issues, and help prepare reports. Lead or assist with the validation and/or verification of new methods Contribute to the development and revision of internal and external quality documents based on ISO/IEC 17025, ISO/IEC 17043, ISO 17034, and Clinical Laboratory Improvement Program (CLIP) standards, as applicable. Perform internal audits of Signature Science systems and procedures against relevant internal or external standards such as ISO/IEC 17025, ISO/IEC 17043, and ISO 17034. Regularly communicate with internal laboratory staff to help resolve laboratory or other quality-related issues. Other activities may include: o Assisting client laboratories in preparing for external ISO/IEC 17025 accreditation audits and attend assessments as an advocate for the client laboratory o Communicating with external laboratory staff to help resolve QA, PT, or other quality-related issues o Providing feedback and help prepare auditee corrective actions packets for submission to the accreditation body or certification body o Providing ISO/IEC 17025 training or training on other quality topics to clients o May serve as a task leader on one or more projects Required Knowledge, Skills & Abilities: General chemistry laboratory experience (e.g., creation of standards/spiking mixes, sample extraction/dilution, and sample analysis). Knowledge of and/or experience with GC/MS, FTIR, percent moisture determination, LC-MS/MS, HPLC-UV, and/or Raman analytical platforms. General quality management experience, preferably in an analytical laboratory setting. Proficiency in MS Word, MS Excel, and MS PowerPoint. Strong written and verbal communication skills. Proactive, self-starter Preferred knowledge, skills, and abilities include: Laboratory experience with GC/MS, FTIR, percent moisture determination, LC-MS/MS, HPLC-UV, and/or Raman analytical platforms. Experience assessing data for trends. Analytical laboratory auditing experience. Knowledge and experience with relevant quality standards, including ISO/IEC 17025, ISO/IEC 17043, ISO 17034, and/or CLIP. Ability to lead small teams and ensure accurate and timely submission of project deliverables. Education/Experience: Bachelor degree (or higher) in chemistry, biochemistry, or related field. At least 3 years experience performing analytical chemistry laboratory work Certificates and Licenses: None upon hire Clearance: Candidate must be able to obtain a Secret level security clearance. Supervisory Responsibilities: May serve as a task leader on one or more projects Working Conditions/ Equipment: Ability to work in varying conditions to include: traditional office environments with sedentary extended periods required for voluminous data analysis via office automation; Climate controlled laboratory environments requiring extended periods of standing when performing laboratory analyses, or during audits and SOP observation; Mobile laboratories, subject to wide ranges of temperature and humidity requiring extended periods of standing, stooping or kneeling in confined spaces; conference, classrooms or theaters that involve extended periods of standing for training delivery or command briefings; and outdoors in various weather and lighting conditions including heat, humidity, cold, snow, bright sun, and dark night. Exposure to various chemical and biological materials associated with an analytical lab or facility. Ability to wear required personal protective equipment (PPE) including gloves, coats or gowns, shoe cover, tyvek coveralls, safety glasses, respirators, and/or PAPRs. Subject to medical monitoring based on lab functions. The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor. Powered by ExactHire:190938

We are creating devices that enable a bi-directional interface with the brain. These devices allow us to restore movement to the paralyzed, restore sight to the blind, and revolutionize how humans interact with their digital world. Team Description: Join our innovative Equipment Quality Team, a dynamic collective of experts dedicated to maintaining the precision and efficacy of high-tech equipment in preclinical and manufacturing domains. Engage with the latest in biomedical devices, industrial instrumentation, and high-end technologies like lasers and RF systems. As pioneers who've crafted a robust equipment program from scratch, we champion creative problem-solving and strive to set industry benchmarks. Immerse yourself in a mission-critical role that propels safety and regulatory compliance to new heights, and become part of a collaborative force driving the future of biomedical quality. Job Description and Responsibilities: Neuralink is seeking an Equipment Quality Technician with a strong knowledge of applied metrolog. This technician will calibrate, repair, and perform preventative maintenance on equipment in the quality program. In addition, they will troubleshoot and repair instruments and systems. This role requires participation in cross-functional teams and some travel. Additionally, you will be expected to: Calibrate and perform preventive maintenance on any instrument or device in the equipment quality program with little to no supervision Provide the technical expertise for assisting management in developing work procedures and protocols Assist in the design, fabrication, check-out, start-up, and acceptance of new or modified equipment Determine and requisition parts required for maintenance repairs Adhere to cGxP guidelines, SOPs, and safety rules/regulations Assist management with determining work schedules and project costs Work closely with cross-functional team members in regards to continuous improvement activities, solving problems, and improving overall product quality Explain calibration issues and processes to customers and management when needed Required Qualifications: Ability to comprehend and apply manuals and schematics for maintenance and troubleshooting Proficiency in using hand tools, physical/dimensional test instruments, and electronic test instruments Able to work in a dynamic, fast-paced environment Strong interpersonal skills: ability to work with colleagues and cross-functional teams in a professional and organized manner Competence in operating computing hardware and standard software Minimum of 1 year of experience related industrial instrumentation/calibration experience and/or training, or equivalent combination of education and experience Willingness to assist with other Quality Engineering activities such as facilities, equipment, and facilities validation Preferred Qualifications: Experience in PMEL, TMDE, Metrology, Calibration, Instrumentation, Validation, or Biomedical Equipment Associates or Bachelors Degree in Science, Technology, Engineering, Mathematics or military training in calibration Relevant experience working in a highly regulated (e.g., GMP, GCP, GLP) environments Expected Compensation: At Neuralink, your base pay is one part of your total compensation package. The anticipated hourly rate for this position is expected to be within the below range. Your actual base pay will be determined by your job-related skills, experience, and relevant education or training. Texas Hourly Range: $20 - $34/Hr USD What We Offer: Full-time employees are eligible for the following benefits listed below. An opportunity to change the world and work with some of the smartest and most talented experts from different fields Growth potential; we rapidly advance team members who have an outsized impact Excellent medical, dental, and vision insurance through a PPO plan Paid holidays Commuter benefits Meals provided Equity (RSUs) *Temporary Employees & Interns excluded 401(k) plan *Interns initially excluded until they work 1,000 hours Parental leave *Temporary Employees & Interns excluded Flexible time off *Temporary Employees & Interns excluded

At Niagara, we're looking for Team Members who want to be part of achieving our mission to provide our customers the highest quality most affordable bottled water. Consider applying here, if you want to: Work in an entrepreneurial and dynamic environment with a chance to make an impact. Develop lasting relationships with great people. Have the opportunity to build a satisfying career. We offer competitive compensation and benefits packages for our Team Members. Plant Quality TechnicianResponsible for executing corporate and plant specific Food Safety, Quality and Laboratory requirements. The QA Technician reports to QA Manager. In the absence of the Quality Assurance Technician, the QA Manager or designate will assume the job duties. Essential Functions Ensure all parameters of food safety and quality are being adhered to and maintained throughout the facility. Assist with batching chemicals/ingredients for production. Calibrate lab and line equipment for accurate results. Collect in-process and finished product samples. Conduct standardized qualitative and quantitative testing to ensure it meets specifications. Perform aseptic testing for microbial contamination. Follow protocols for documenting testing results. Recognize deficiencies and initiate proper follow-up. Identify and isolate product that does not meet standards. Aid in troubleshooting deficiencies and non-conformances. Review food safety and quality records. Actively participate in plant teams (HACCP, Safety, etc.) Conduct other duties as assigned by management. Please note this job description is not designed to contain a comprehensive list of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without prior notice. Qualifications Minimum Qualifications: 0 Years - Experience in Field or similar manufacturing environment 0 Years - Experience in Position 0 Years - Experience managing people/projects *experience may include a combination of work experience and education Must read, write and communicate in English. Must be able to work 12 hour shift (days or nights) on a rotating schedule Must follow GMP Policy - wear company issued shirt, hat, safety glasses, earplugs and hairnet in production areas. Able to lift up to 50 lbs. Able to work under pressure in a very fast paced environment Preferred Qualifications: 2 Years- Experience in Field or similar manufacturing environment 2 Years - Experience working in Position 2 Years - Experience managing people/projects *experience may include a combination of work experience and education Competencies This position embodies the values of Niagara's LIFE competency model, focusing on the following key drivers of success: Lead Like an Owner Makes safety the number one priority Keeps alert for safety issues and escalates immediately Effectively prioritizes tasks based on department goals Shows respect to others and confronts interpersonal issues directly Prioritizes resolution of customer issues effectively Responds promptly and honors commitments to internal and external customers InnovACT Makes recommendations to continuously improve policies, methods, procedures, and/or products Demonstrates adaptability by reacting appropriately to unexpected changes in situations or circumstances Increases performance through greater efficiency Find a Way Seeks to develop technical knowledge through learning from other experts Understands interdepartmental impact of individual decisions and actions Seeks solutions rather than placing blame Empowered to be Great Consistently looks for ways to improve one's self through growth and development opportunities Communicates clearly and promptly up, down, and across Communicates effectively to manage expectations Education Minimum Required: High School Diploma Preferred: Associate's Degree Certification/License: Required: N/A Preferred: HACCP Foreign Language Required: Full Professional Proficiency Preferred: None Required Benefits Our Total Rewards package is thoughtfully designed to support both you and your family: Regular full-time team members are offered a comprehensive benefits package, while part-time, intern, and seasonal team members are offered a limited benefits package. Paid Time Off for holidays, sick time, and vacation time Paid parental and caregiver leaves Medical, including virtual care options Dental Vision 401(k) with company match Health Savings Account with company match Flexible Spending Accounts Expanded mental wellbeing benefits including free counseling sessions for all team members and household family members Family Building Benefits including enhanced fertility benefits for IVF and fertility preservation plus adoption, surrogacy, and Doula reimbursements Income protection including Life and AD&D, short and long-term disability, critical illness and an accident plan Special discount programs including pet plans, pre-paid legal services, identity theft, car rental, airport parking, etc. Tuition reimbursement, college savings plan and scholarship opportunities And more! *********************************************** * *Los Angeles County applicants only** Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers, the California Fair Chance Act, and any other applicable local and state laws. Any employment agency, person or entity that submits a résumé into this career site or to a hiring manager does so with the understanding that the applicant's résumé will become the property of Niagara Bottling, LLC. Niagara Bottling, LLC will have the right to hire that applicant at its discretion without any fee owed to the submitting employment agency, person or entity. Employment agencies that have fee agreements with Niagara Bottling, LLC and have been engaged on a search shall submit résumé to the designated Niagara Bottling, LLC recruiter or, upon authorization, submit résumé into this career site to be eligible for placement fees.

The Quality Control Technician conducts routine and specialized quality control testing on textiles, products, and finished goods, ensuring accuracy through detailed data collection and analysis. They participate in field testing to assess real-world performance, identify and report quality issues, and support continuous improvement initiatives. Responsibilities and Duties: Perform routine and non-routine quality control tests on textiles, products, and finished goods. Collect, record, and analyze quality and performance data; maintain detailed records and documentation. Participate in field testing of textiles and components, across a range of conditions (e.g., temperature) and seasons to simulate real-world usage. Identify and report quality deviations, inconsistencies, or failures and, as requested, work with other departments to address root causes. Calibrate and maintain testing equipment to ensure accuracy and reliability. Follow established protocols and quality standards. Support continuous improvement initiatives and recommend adjustments to processes and materials where applicable. Perform other duties as assigned to support Ametrine goals and objectives. Required Skills/Abilities: Execute with precision and maintain a sharp eye for detail throughout every stage of a project. Ability to notice small differences or inconsistencies and a thoroughness in following procedures and recording data. Strong computer skills, specifically in Excel and SharePoint/File Management. Comfortable working outdoors and in varying environmental conditions. Reliable and dependable. Ability to work independently and manage multiple testing schedules and priorities. Excellent communication and documentation skills. Take the initiative and have a self-starter mindset, prioritizing tasks and driving projects forward with minimal oversight. Approach challenges with curiosity, adaptability, and a strong sense of self-motivation. Step up and contribute as needed, maintaining a collaborative mindset without ego or rigid role boundaries. Education and Experience: High school diploma or equivalent required Driver's License Other Requirements: May require domestic travel. General work hours - 2nd Shift (1:30pm-12:00am), Monday through Thursday; flexibility to work evening and night hours and weekends when required; sometimes with short notice. Physical Requirements: Ability to sit, stand, walk, and move around the office and production environment for extended periods. Occasional lifting of materials, tools, or equipment that may exceed 25 lbs. Ability to perform fine motor tasks (e.g., using a computer, handling small parts, assembling prototypes). Visual acuity to read technical documents and to inspect prototypes or components. Frequent exposure to noise, machinery, and manufacturing tools. Will require working both indoors and outdoors in a variety of environments. The work environment is generally fast-paced, and the employee may be required to shift between team collaboration, independent work, and meeting tight deadlines. Depending on the location and project needs, the employee may be required to wear PPE such as safety goggles, gloves, or hearing protection.

Thalle Construction Co., Inc. ("Thalle") is currently seeking a Quality Control Technician. Our ideal candidate will be a team player who is highly motivated with a strong work ethic and efficient with a high level of professionalism and confidentiality. Thalle, established in 1947, is a heavy civil construction company with a corporate office in Hillsborough, NC and a regional office in Alvarado, Texas. Thalle has construction projects throughout the South East, Texas, and New Jersey with growth nationwide. Our diverse and expansive project scope of heavy civil infrastructure projects includes dams, reservoirs, locks, DOT roadway construction and bridges, large diameter utilities, landfills, mass excavation, wastewater, on-demand emergency services. We are a proud representative of Tully Group (******************* The Tully Group is one the nation's largest privately held, family-owned construction firms with their corporate office in New York City and long history of heavy civil projects in the Metro New York Area and New Jersey. Safety is our TOP priority! Thalle offers a competitive salary package with a full range of benefits, including Major Medical, Dental, Vision, Short and Long-Term Disability, generous PTO, paid company holidays, Life Insurance, and 401K with a company match, and more! Compensation is based on experience and qualifications. Thalle is an Equal Opportunity Employer, E-Verify and Drug Free Workplace. Location: Austin, Texas Job Title: Quality Control Technician Salary: Competitive compensation package based on experience. Essential Duties and Responsibilities: * Responsible for overall quality control (QC) of the project. * Assist with implementation of Project QA/QC Program and monitor for compliance. * Review and understand contract specifications, scope of work, and exclusions outlined in the contract and related industry standards. * Conduct inspections of workmanship and materials. * Administer the overall quality and assurance program. * Act in all quality assurance and control matters for the Company. * File reports and photo documentation * Attend contractor QA/QC meetings and monitor issues and concerns noted in the meeting minutes.. * Conduct business with 100% integrity and professionalism Education and/or Work Experience Requirements: * Bachelor's degree in Civil Engineering or Construction Management preferred * 1-3 years of heavy civil construction experience, preferably in dam, reservoir, landfill, wastewater treatment plants preferred. * Experience and knowledge of Army Corp of Engineer projects. * Proficiency in Microsoft Outlook, Word and Excel * Superior analytical and problem solving skills * Organization and planning skills * Strong oral, consultative and written communication skills * Ability to interface effectively with all levels of management * Ability to establish trust and interface effectively with Owners and Customers Physical Requirements: * Ability to safely and successfully perform the essential job functions consistent with the ADA, FMLA and other federal, state and local standards, including meeting qualitative and/or quantitative productivity standards. * Ability to maintain regular, punctual attendance consistent with the ADA, FMLA and other federal, state and local standards * Must be able to lift and carry up to 50 lbs * Must be able to talk, listen and speak clearly on telephone Apply to this job

THE COMPANY Built for Heroes and based in Florence, Texas, Staccato is on a mission to proudly serve those who protect and embody American freedoms. As the inventors of the 2011 platform-the World's Best Shooting Pistols-Staccato manufactures its handguns and ammunition in America at their headquarters in Florence, TX. The Staccato 2011 has been approved for on- or off-duty carry by over 1,600 U.S. law enforcement agencies in just five years, including elite teams such as U.S. Marshals Special Operations Group, the Texas Rangers and Miami Dade Special Response Team. With a spirit of American ingenuity and commitment to its family of owners, Staccato guarantees its guns for life, and guarantees supply of its 9mm ammunition to subscribers of its ammo service. Staccato Ranch serves as the place where Staccato unites its family of patriots to celebrate freedom and elevate heroes every day. Staccato was ranked one of the Fastest Growing Private Companies in the Southwest by Inc. Over 25% of our team members are veterans and 100% are patriots. We strive relentlessly to achieve our best every day and are focused on continuous improvement and progress in everything we do. THE MISSION Build the World's Best Shooting Handguns, so everyone can experience shooting excellence. THE POSITION We are seeking a hands-on, hard-working, detail-oriented individual to join our team in an intermediate-level role, building the Best Shooting Handguns in the World. Reporting to the Quality Manager, the successful candidate will possess an exceptional working knowledge of mathematical concepts, excellent visual awareness, and the ability to work with minimal supervision while performing in-depth inspections. Ultimately, the ideal candidate can efficiently monitor the integrity and quality of products without impeding production rates. JOB DESCRIPTION/DUTIES Primary duties will involve conducting specialized coating inspections at various stages, including in-process, post-process, and outplant phases. Additionally, you'll be responsible for meticulously documenting all aspects of these inspections. Secondary duties will involve conducting first article inspections, in-process manufacturing inspections, and various dimensional inspections of Staccato products. Inspecting products according to established Quality and Safety standards. Read and interpret drawings for dimensional callouts. Monitor testing procedures and processes to ensure tests are performed according to item specifications, protocols, and standard test methods. Interpret test results and compare them to the specifications and control limits in place while providing recommendations on the appropriateness of data. Complete documentation is necessary to support testing procedures. Ensure equipment is calibrated, validated, and maintained properly and ensure safety during equipment operation. Assist with any Quality concerns and report management concerns. Various tasks to support facility operations (Quality or Production) QUALIFICATIONS In addition to general team member expectations, this role requires explicitly the following: An associate's Degree of Science in an associated field is a plus but not mandatory; it may be substituted with a technical quality certificate, Six Sigma, Lean, or Continuous Improvement certification (ASQ, QMS, etc.). Proficiency in Microsoft Office (specifically Word, Excel, and Outlook) Experience with gauging equipment (calipers, micrometers, drop indicators, hardness testers, optical comparators, etc.) is preferred. Experience with coordinate measuring machines is highly desired. Experience with drawings and interpreting dimensional callouts is a plus. Experience with following processes and documenting results from inspection is preferred. Experience in process auditing is preferred. Prior Quality Control experience is preferred. Understanding of traceability is preferred. We offer a competitive and attractive compensation and benefits package, including health insurance, a 401(k) plan, paid vacation, and holidays. In addition, as a Staccato team member, you enjoy discounts on Staccato products. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, or national origin.

Job DescriptionAbout Base Base is America's next-generation power company. We're rebuilding the foundation of modern civilization-electricity-by deploying a vast network of distributed batteries that is transforming today's fragile, centralized grid into a resilient and abundant system. We are engineers, operators, and creatives solving some of the most complex, interdisciplinary challenges of our time. About the Role We are looking for a manufacturing quality technician to join our team. This role focuses on continuous monitoring of the quality of our parts and processes throughout our manufacturing lines. You will conduct product-level testing and measurement, work with manufacturing and supplier engineering teams to identify and root cause manufacturing problems, validate new parts and processes, and manage non-conforming material. What You'll Do Perform measurements and testing of incoming material as part of our incoming quality control process Execute our manufacturing quality control plan by regularly testing parts and auditing processes and equipment Identify and manage non-conforming material throughout the manufacturing process, including quarantining of material, repair, and disposition Identify and investigate process abnormalities and excursions, working with process and equipment engineering teams to root cause issues and implement corrective actions Conduct process trials and design of experiments (DoEs) with cross-functional engineering teams to validate process and part improvements What You'll Bring 2+ years of experience working in a manufacturing or test lab environment or equivalent educational background in Mechanical/electrical engineering or similar. Ability to understand and interpret mechanical and electrical drawings and schematics. Working knowledge of geometric dimensioning and tolerancing (GD&T) and the ability to measure part features accordingly. Experience with CMMs, pCMMs or other high-precision dimensional metrology equipment and associated metrology software (PC-DMIS, Polyworks, etc.) strongly preferred Experience with various dimensional, mechanical, and electrical test and measurement tools (calipers, micrometers, force gauges, digital multimeters, etc.) Ability to work with and interpret data to drive action utilizing basic statistical analysis Our Values First Principles Thinking: Question assumptions. Principles > rules. Operate at Base Pace: Focus on what matters, act quickly, and learn by doing. Give & Get Feedback: Be direct, be humble, and maintain a growth mindset. Everyone's an Owner: Follow through on commitments and own results. Strong Opinions, Loosely Held: Drive clarity and make calls with imperfect information. Committed to the Mission: Rebuilding the grid is a big challenge. We work hard because we care deeply about the impact we're creating. We work in-person. It's not a 9-to-5. We are all-in. Fun & Optimism Coexist with Grit: Collaboration and celebration coincide with the intensity of building real things. Do the best work of your life at Base.

Enviromedica is a natural health and wellness company, founded in 2007. Inspired by nature and ancestral health, we make premium foundational products to support whole body nutrition and help people achieve optimal health. We take great pride in our products and every ingredient is obtained from the highest quality sources. We provide an environment focused on personal and professional growth, impacting our community and helping others. Join our growing team! Requirements: Hard Skills B.S. in chemistry, biology or related scientific discipline. This education can be substituted by an associate degree and 3+ years occupying a comparable position. Technical writing of SOPs, work instructions, and reports. Basic computer literacy: Microsoft Word and Excel, and use of printers and scanners, or equivalent. Hands-on experience on: Conducting sampling and inspection of ingredients, packaging components, and finished product. Preparing testing samples and associated process paperwork. Using the following equipment: pH meter, viscometer, moisture analyzer, FTIR, and microscope. Performing specific gravity measurements, environmental monitoring, and microbiology testing. Conducting batch record review. Supporting the Document Control function. Following written instructions and established processes to carry out routine tasks. 2+ years of experience working in a GMP environment. Technical writing of SOPs, work instructions, and reports. Basic computer literacy: Microsoft Word and Excel, and use of printers and scanners, or equivalent. Soft Skills Outstanding people skills. Self-starting, highly motivated, and entrepreneurial attitude. Ability to, Solve conflict in a conciliatory way. Adjust to a constantly changing and fast paced environment. Meet tight deadlines. Work with other departments and to support team projects. Prioritize work load's according to evolving company needs. Creative thinking Ability to work independently. Accuracy and close attention to detail. Strong analytical judgement. While working, only 15% of the time corresponds to conducting lab activities. This position requires a significant amount of walking. This position offers the ability to grow professionally by learning and doing. No relocation assistance is provided at this time. Benefits We offer an encompassing benefits package including Medical, Dental, Vision, 401k, PTO and 8 paid Holidays per year.

Job Description Summary: Manages product quality and shares concrete knowledge to fellow employees and customers by performing the following duties: Essential Duties and Responsibilities: · Performs ongoing ACI ASTM concrete and raw materials testing. Imports test data into appropriate spreadsheets or software. · Evaluates existing quality or production standards and procedures and recommends modifications to upper management. · Educates plant personnel on product quality, batching efficiency and Verifi utilization. · Educates ready-mix drivers on product quality and Verifi utilization. · Investigates and evaluates product anomalies at plants and jobsites. · Advises upper management on product issues arising from problems identified through technical support calls and visual inspections with plant personnel and customers. · Conducts audits and makes ongoing improvements to material handling procedures, batching and driver habits. · Visits job sites, attends pre-pour meetings, calls on customers, collects market and job information. Reviews Verifi data for product consistency. · Advises and assists plant personnel value-added products (i.e. fibers) and temperature control methods. · Assists in the laboratory with new product testing. · Completes all required paperwork (reports, forms, letters, etc.). Supervisory Responsibilities: This job has no direct supervisory responsibilities. Education and/or Experience: Degree from college, university or technical school and one to two years related experience and/or training; or equivalent combination of education and experience. Knowledge/Skills/Abilities/Experience · Current, valid state driver's license required. · Satisfactory driving and criminal record. · ACI Field Grade 1 Certification required, or ability to pass written and hands on test within 6 months of hire · Demonstrates effective communication skills (oral and written). · Demonstrates proficiency with simple math calculations including addition, subtraction, multiplication and division (especially percentages) as well as measurements. · Proficient in Microsoft Word, Excel · Demonstrates ability to successfully handle multiple tasks simultaneously. · Demonstrates ability to plan, organize and prioritize tasks. · Demonstrates ability to work independently with minimal supervision. · Demonstrates ability to identify and solve problems. Physical Requirements: · Frequent/occasional reaching, grabbing and pulling of testing equipment and material samples. · Frequent/occasional use of fingers, wrists and hands to enter data via computer keyboard. · Occasional lifting of up to 50 lbs. · Occasional/frequent climbing of steps and ladders. · Occasional/frequent stooping, squatting, bending, kneeling and twisting. · Occasional pushing and pulling. · Must be able differentiate colors. · Must be able to hear noises. Environmental Conditions (Personal protective equipment is provided where required or requested) · Exposure to elements of weather to include extremes in heat, cold, dust and moisture for limited periods. · Occasionally/frequently exposed to rough, muddy and icy walking surface conditions. · Intermittent exposure to high noise levels and vibration. · Occasional/frequent exposure to moving parts/pieces of equipment. · Frequent exposure to cement, concrete, admixtures, dust, diesel fuel, and other substances that may cause burns, be toxic or explosive if handled incorrectly. · Frequently exposed to water and wet conditions. Other key attributes · Strong interpersonal skills · Project management skills, especially follow-up and follow-through Powered by ExactHire:190864

Job DescriptionDescription: VulCan: At VulCan Packaging, we're not just making cans-we're building the future of beverage manufacturing right here in the heart of Austin. Our team is a vibrant mix of makers, thinkers, and doers-the real flavors of this city-who bring their unique talents and energy to everything we create. We're proud to be the only can manufacturer in North America using waterless technology-better for the planet, and safer for the people who power our production. Every day, our team tackles tough challenges with heart, hustle, and a shared passion for making the best products in the industry. We're dedicated to innovation, precision, and next-level customer service. And while our systems are designed for performance, it's our people who truly make us stand out. VulCan is redefining beverage packaging with high-performance innovations that elevate brands, enhance consumer experiences, extend shelf life, and set new industry standards in sustainability, functionality, and design. Role: The Quality Control Technician - Cans & Decorating is a hands-on, floor-based role responsible for inspecting both the physical quality of aluminum cans and the quality of decoration applied to them. This includes visual and structural inspection of cans, ink mixing, plate making, and mounting plates on cylinders to ensure finished products meet customer and internal specifications. This role focuses on quality control and execution on the production floor. It does not include quality assurance systems, audits, or certification ownership. The QC Technician works closely with the Quality Lead, Floor Leads, and the Graphics & Pre-Press Lead (Art Department) to identify issues early, prevent scrap, and keep production running smoothly. Responsibilities: Can Quality Control Perform in-process and finished product inspections on aluminum cans, including visual and basic structural checks (dents, scratches, coating issues, contamination, deformation, and overall can integrity). Verify cans meet customer and internal quality standards, document inspection results, and communicate issues promptly to the Quality Lead or Floor Leads. Escalate quality concerns quickly to prevent scrap, rework, or customer impact. Decorating & Print Quality Control Conduct in-process quality checks on decorated cans, inspecting color accuracy, registration, ink coverage, varnish appearance, and visual defects. Compare production output to approved customer samples and specifications and support first article approvals and decorator start-ups. Communicate decorating-related quality issues to Floor Leads and the Quality Lead. Ink Mixing Mix, adjust, label, store, and track inks according to formulas, standards, and job requirements. Maintain clean and organized ink mixing and storage areas, dispose of inks and solvents per safety and environmental guidelines, and support color matching efforts with Operators, Leads, and the Graphics & Pre-Press Lead. Plate Making & Cylinder Mounting Perform plate making for decorator jobs based on approved artwork and specifications. Verify artwork orientation and plate requirements, mount plates accurately onto decorator cylinders, inspect plates and cylinders for defects or wear, and ensure plates are properly labeled, staged, and tracked. Work closely with the Graphics & Pre-Press Lead and Quality Lead to resolve artwork or plate-related issues. Requirements: 1+ year of experience in quality control, manufacturing inspection, manufacturing, metal packaging, or printing environments Experience inspecting physical products for visual and structural quality Ability to color match and identify visual defects accurately Strong attention to detail and ability to spot defects quickly Comfortable working in a manufacturing / production floor environment Ability to stand, walk, bend, and reach frequently throughout the shift Ability to lift up to 50 lbs Willingness to work around noise, industrial equipment, inks, solvents, coatings, and moving machinery Ability to work in hot or cold conditions Ability to wear and use required personal protective equipment (PPE) Schedule & Flexibility Full-time, on-site role. Schedule flexibility may be required to support production needs, decorator start-ups, or job changeovers.

Your mission Ensure that every pair of shoes leaving production meets Zellerfeld's standards of quality, consistency, and innovation by conducting thorough checks, documenting findings, and driving improvements back into the product cycle. Key responsibilities Inspect shoes at different production stages (before washing and after finishing) Verify visual and structural quality of shoes, including patterns and details Document findings, track patterns of recurring issues, and maintain QC logs Report back to the product team with insights and suggestions for improvements Manage and process failed orders (documentation, reporting, resolution) Collaborate with production team to prevent defects and ensure timely corrections Your profile Experience in QC, production, or manufacturing environment (footwear/garment preferred but not required) Strong attention to detail and ability to spot inconsistencies Basic knowledge of documenting workflows and patterns Good communication skills for reporting and team feedback Organized, reliable, and proactive problem solver Based in Austin or surroundings. Why us? An innovative company with cutting-edge technology in the field of 3D printing. A dynamic and motivated team with flat hierarchies. Comprehensive training - prior knowledge is not necessarily required. Various development opportunities and long-term perspectives. About us Zellerfeld is revolutionizing the footwear industry with the world's first 3D-printing technology for fully customizable shoes. Our goal is simple: printed shoes on every foot. We're a passionate team of engineers, designers, and innovators, questioning the status quo and disrupting traditional manufacturing processes. Backed by founders, influencers, and celebrities who believe in our vision, we're committed to making a lasting, positive impact-not just on the footwear industry, but on the world.

Mars Petcare is seeking a Quality Technician to join our exciting pet food business at a manufacturing plant in Temple, Texas. We focus our attention on the unique needs of cats and dogs. That obsession with detail allows us to deliver precise, effective nutrition and help them become their magnificent best. As part of our overall total compensation package, Mars Petcare offers a competitive benefits package to all associates: Medical, Dental, Vision & Life Insurance, Short- & Long-Term Disability, and 401k match. Associates are also immediately eligible (based on hire date) for up to three weeks of vacation, 11 Paid Holidays per year, Sick Pay, Maternity & Parental Leave, and annual bonus earning potential, plus many other ancillary benefits not listed here. Shift: 223 Nights (7pm - 7:30am) What are we looking for? Food Science, Engineering, Chemistry, or equivalent BSc/ MSc degree is preferred. Knowledge of quality management system - FSSC22000, and quality program GMP/ Hygienic design, familiar with legal food safety requirements and food process technology. Problem-solving skills and systematic thinking Communication and influencing skills. What will be your key responsibilities? Drive the implementation of GMP on-site in compliance with the Mars GMP/ GHP standard, including GMP for production/ engineering and contractor, etc. Document control system management, including the Nexus system. Develop the quality system training material and training plan and follow the implementation. CAPA system follow-up to make sure all CAPA are not overdue. Prepare the management review report material. Verify the system procedure and regulation requirement compliance in the process. Coordinate change management assessment at the site level. Complete any other projects assigned by the Line Manager. What can you expect from Mars? Work with over 130,000 diverse and talented Associates, all guided by the Five Principles. Join a purpose-driven company where we're striving to build the world we want tomorrow, today. Best-in-class learning and development support from day one, including access to our in-house Mars University. An industry-competitive salary and benefits package, including a company bonus.

Job Posting Start Date 01-13-2026 Job Posting End Date 04-06-2026Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary To support our extraordinary teams who build great products and contribute to our growth, we're looking to add a Quality Technician located in Austin, TX. Shift: 6:00am-6:00pm Sunday, Monday, Tuesday and every other Wednesday What a typical day looks like: Audits processes, tests and inspects products and/or develops, compiles and evaluates statistical data to define and maintain quality and reliability of products. Working from engineering drawings, specifications, schematics, diagrams, written descriptions, layouts or defined plans to perform complex engineering testing, checkout, First Article Inspection, root cause research, internal corrective actions and supplier correction actions. Interprets engineering drawings, schematic diagrams or formulas and confers with management or engineering staff to define quality and reliability standards. Selects processes to be audited from primarily the manufacturing areas and checks for a variety of features, including ESD (electro-static discharge) and handling practices, documentation, training and process integrity. Selects products for audits at specified stages in the production or post-production process, and tests products for variety of qualities such as dimensions, performance and mechanical, electrical or cosmetic characteristics. Records audit data, applying statistical quality control procedures. Evaluates data and writes reports to validate or indicate deviations from existing standards. Recommends modifications of existing quality or production standards, programs or reports to achieve optimum quality within limits of equipment capability. Perform calibration on inspection tools e.g. micrometers, calipers height gages etc. Maintain gage track program, print list of gages due for calibration in the beginning of each month and follow up with calibration. Send gages out for calibration, maintain calibration records. Prepares graphs or charts of data or enters data into computer for research data. Download quality information from quality system to be used for QA reports. Research for engineering test results and implements process changes to resolve problems. Performs out of box audits (OBA) as required. Provides factory hold up to identify and resolve issues associated with purchased parts, materials and manufacturing. May be required to perform receiving inspection. Review at the beginning of the shift the Quality Auditors assistance and validated the Check List. Scrap disposition at MRB in less than 24 hours. Assure that the Customer implementation activities are in place. Meet the SSYMA requirements (boats, goggles, gloves, ear plugs). Review the SPC data and confirm the actions are effective. Validate the tooling and gauges are working properly (microscope, magnifier, etc). Qualifications: Requires a High School Diploma or equivalent, technical training, or equivalent experience. Typically requires a minimum of 4 years of related experience. What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Job CategoryQualityRelocation: Not eligible Is Sponsorship Available? NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

A detail-oriented Laboratory Technician to manage and perform calibration, verification, and maintenance of measurement and test equipment used throughout our manufacturing operations. The ideal candidate will ensure all equipment remains within specified tolerances and complies with internal quality systems and external standards (e.g., ISO 9001, ISO/IEC 17025, or other applicable requirements). ESSENTIAL DUTIES AND RESPONSIBILITIES Perform calibration, verification, and functional checks on a variety of instruments and equipment (e.g., pressure, temperature, dimensional, electrical, torque, and flow devices) Maintain and update calibration records, certificates, and traceability documentation in accordance with internal quality procedures Identify and segregate equipment found out of tolerance Coordinate repairs or adjustments with internal teams or external vendors Develop and maintain calibration schedules to ensure on-time service for all equipment Support root cause analysis and corrective actions for measurement-related nonconformances Work with quality and engineering teams to define calibration requirements for new or modified equipment Ensure all calibration activities meet relevant standards (e.g., NIST traceability, ISO/IEC 17025, or customer-specific requirements) Assist in audit preparation and provide technical support during internal and external audits. Maintain a clean, organized calibration area and follow all safety protocols and environmental procedures EDUCATION AND EXPERIENCE Education: Associate's degree in Metrology, Engineering Technology, Physics, or related technical field (or equivalent experience) Experience: 5+ years performing calibrations or working in a metrology or testing environment Familiarity with measurement principles, uncertainty, and common standards for dimensional, electrical, or mechanical calibration Ability to interpret technical drawings, specifications, and equipment manuals Strong computer skills and experience with calibration management software (e.g., GAGEtrak, IndySoft, or similar) Excellent attention to detail, recordkeeping, and organizational skills Ability to work independently and manage multiple priorities in a manufacturing environment CERTIFICATES, LICENSES, REGISTRATIONS Individuals must be able to perform the duties of the job at a level as generally prescribed and learned by attaining the credentials below. ASQ Certified Calibration Technician (CCT) preferred ASQ Certified Quality Technician (CQT) preferred PHYSICAL DEMANDS Ability to lift and move equipment up to 50 pounds Work may involve standing for extended periods or using fine motor tools Typical work environment: laboratory and production floor MANAGEMENT DISCLAIMER TECO-Westinghouse's Management reserves the right to revise, change or modify the duties and responsibilities of this position at any time to meet business and organizational needs. This position description may not list all duties for this position. The incumbent in the position may be asked to perform other duties. This position description is not a contract for employment and either the incumbent or TECO-Westinghouse may terminate employment at any time, for any reason.

Thalle Construction Co., Inc. (“Thalle”) is currently seeking a Quality Control Technician. Our ideal candidate will be a team player who is highly motivated with a strong work ethic and efficient with a high level of professionalism and confidentiality. Thalle, established in 1947, is a heavy civil construction company with a corporate office in Hillsborough, NC and a regional office in Alvarado, Texas. Thalle has construction projects throughout the South East, Texas, and New Jersey with growth nationwide. Our diverse and expansive project scope of heavy civil infrastructure projects includes dams, reservoirs, locks, DOT roadway construction and bridges, large diameter utilities, landfills, mass excavation, wastewater, on-demand emergency services. We are a proud representative of Tully Group (******************* The Tully Group is one the nation's largest privately held, family-owned construction firms with their corporate office in New York City and long history of heavy civil projects in the Metro New York Area and New Jersey. Safety is our TOP priority! Thalle offers a competitive salary package with a full range of benefits, including Major Medical, Dental, Vision, Short and Long-Term Disability, generous PTO, paid company holidays, Life Insurance, and 401K with a company match, and more! Compensation is based on experience and qualifications. Thalle is an Equal Opportunity Employer, E-Verify and Drug Free Workplace. Location: Austin, Texas Job Title: Quality Control Technician Salary: Competitive compensation package based on experience. Essential Duties and Responsibilities: Responsible for overall quality control (QC) of the project. Assist with implementation of Project QA/QC Program and monitor for compliance. Review and understand contract specifications, scope of work, and exclusions outlined in the contract and related industry standards. Conduct inspections of workmanship and materials. Administer the overall quality and assurance program. Act in all quality assurance and control matters for the Company. File reports and photo documentation Attend contractor QA/QC meetings and monitor issues and concerns noted in the meeting minutes.. Conduct business with 100% integrity and professionalism Education and/or Work Experience Requirements: Bachelor's degree in Civil Engineering or Construction Management preferred 1-3 years of heavy civil construction experience, preferably in dam, reservoir, landfill, wastewater treatment plants preferred. Experience and knowledge of Army Corp of Engineer projects. Proficiency in Microsoft Outlook, Word and Excel Superior analytical and problem solving skills Organization and planning skills Strong oral, consultative and written communication skills Ability to interface effectively with all levels of management Ability to establish trust and interface effectively with Owners and Customers Physical Requirements: Ability to safely and successfully perform the essential job functions consistent with the ADA, FMLA and other federal, state and local standards, including meeting qualitative and/or quantitative productivity standards. Ability to maintain regular, punctual attendance consistent with the ADA, FMLA and other federal, state and local standards Must be able to lift and carry up to 50 lbs Must be able to talk, listen and speak clearly on telephone

About Base Base is America's next-generation power company. We're rebuilding the foundation of modern civilization-electricity-by deploying a vast network of distributed batteries that is transforming today's fragile, centralized grid into a resilient and abundant system. We are engineers, operators, and creatives solving some of the most complex, interdisciplinary challenges of our time. About the Role We are looking for a manufacturing quality technician to join our team. This role focuses on continuous monitoring of the quality of our parts and processes throughout our manufacturing lines. You will conduct product-level testing and measurement, work with manufacturing and supplier engineering teams to identify and root cause manufacturing problems, validate new parts and processes, and manage non-conforming material. What You'll Do Perform measurements and testing of incoming material as part of our incoming quality control process Execute our manufacturing quality control plan by regularly testing parts and auditing processes and equipment Identify and manage non-conforming material throughout the manufacturing process, including quarantining of material, repair, and disposition Identify and investigate process abnormalities and excursions, working with process and equipment engineering teams to root cause issues and implement corrective actions Conduct process trials and design of experiments (DoEs) with cross-functional engineering teams to validate process and part improvements What You'll Bring 2+ years of experience working in a manufacturing or test lab environment or equivalent educational background in Mechanical/electrical engineering or similar. Ability to understand and interpret mechanical and electrical drawings and schematics. Working knowledge of geometric dimensioning and tolerancing (GD&T) and the ability to measure part features accordingly. Experience with CMMs, pCMMs or other high-precision dimensional metrology equipment and associated metrology software (PC-DMIS, Polyworks, etc.) strongly preferred Experience with various dimensional, mechanical, and electrical test and measurement tools (calipers, micrometers, force gauges, digital multimeters, etc.) Ability to work with and interpret data to drive action utilizing basic statistical analysis Our Values First Principles Thinking: Question assumptions. Principles > rules. Operate at Base Pace: Focus on what matters, act quickly, and learn by doing. Give & Get Feedback: Be direct, be humble, and maintain a growth mindset. Everyone's an Owner: Follow through on commitments and own results. Strong Opinions, Loosely Held: Drive clarity and make calls with imperfect information. Committed to the Mission: Rebuilding the grid is a big challenge. We work hard because we care deeply about the impact we're creating. We work in-person. It's not a 9-to-5. We are all-in. Fun & Optimism Coexist with Grit: Collaboration and celebration coincide with the intensity of building real things. Do the best work of your life at Base.