Quality control analyst jobs in Four Corners, TX

Have you ever thought about being part of a company that reimagines chemistry every day to build a better world? That's the purpose of Indorama Ventures, and we want you with us on this journey! We are looking for innovative, collaborative professionals who are ready to embrace the challenge of working in a company that is constantly expanding internationally. We value flexibility, partnership, and believe that the impact of our actions goes far beyond the chemical industry. Here, diversity matters. Our work environment is inclusive, diverse, and guided by respect, ethics, and equal opportunities for all. What we're looking for: Indorama Ventures- Indovinya is currently looking for a dynamic individual to work as a Research Chemist I located at our The Woodlands, Texas facility. In this role, you will be responsible to work with Research Scientists to evaluate existing and new chemistries, processes, or applications related to Indorama products. This position is focused on the laboratory working on directed experiments in a safe manner. The lab work may include glassware reactors, Parr reactor reactions, etc. Also, the work could include application specific testing for areas such as agricultural, oilfield, paints/coatings, personal care, etc. What will be expected from you? Maintain an awareness of the literature and other sources of information to remain current with developments in the area of functional products of interest to the Corporation. Work to complete projects in the US project pipeline. Set up and execute laboratory to meet both internal and external customer expectations. Set up and execute laboratory work to as outlined by R&D scientist. Analyzing samples by analytical methods or applications testing. Keep neat and orderly notebooks containing a record of all work performed. Maintain other records as necessary to support patent applications for innovative products. Maintain orderly laboratory space. Follow all safety and training requirements. Manage and optimize all process under your responsibility taking into consideration Quality, Legality and Food Safety (if applicable) and client needs on Indorama's products and services. Guarantee all documentation under your responsibility updated and available for consulting. Support R&D Lab Manager with properly managing the lab resources Interact with TS&D team to improve the lab, lab methods, etc. Work in cross functional /cross discipline teams as needed What are we looking for in the ideal candidate? BS in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering required. BS in other science field plus 2+ years in Research laboratory work Associates Degree with 5+ years in Research laboratory work 0-3 years' experience (more 3 years' experience preferred) in: R&D laboratory preferred. Surfactants knowledge in laboratory or application use strongly preferred. Use and knowledge of Parr Reactors preferred. Computer literacy w/ databases, word processing, spreadsheets Excellent organizational and communications skills Demonstrated presentation skills preferred. Experience in chromatography, spectroscopy, wet analysis, or other analytical techniques preferred. Formulation experience in Agricultural, Home Care, or Coatings preferred. English with Bilingual Portuguese or Spanish strongly preferred. What do we offer? A competitive compensation package, including: • Health insurance • WellHub / TotalPass • Life insurance • And other exclusive benefits The division you'll be joining is a global leader in the chemical industry. We offer a broad portfolio of solutions and high delivery standards to markets such as Crop Solutions, Home and Personal Care, Coatings, Energy & Resources, and Performance Products. Here, you can make a difference. Join us!

**Have you ever thought about being part of a company that reimagines chemistry every day to build a better world?** That's the purpose of Indorama Ventures, and we want you with us on this journey! We are looking for innovative, collaborative professionals who are ready to embrace the challenge of working in a company that is constantly expanding internationally. We value flexibility, partnership, and believe that the impact of our actions goes far beyond the chemical industry. Here, diversity matters. Our work environment is inclusive, diverse, and guided by respect, ethics, and equal opportunities for all. **What we're looking for:** Indorama Ventures- Indovinya is currently looking for a dynamic individual to work as a Research Chemist I located at our The Woodlands, Texas facility. In this role, you will be responsible to work with Research Scientists to evaluate existing and new chemistries, processes, or applications related to Indorama products. This position is focused on the laboratory working on directed experiments in a safe manner. The lab work may include glassware reactors, Parr reactor reactions, etc. Also, the work could include application specific testing for areas such as agricultural, oilfield, paints/coatings, personal care, etc. **What will be expected from you?** + Maintain an awareness of the literature and other sources of information to remain current with developments in the area of functional products of interest to the Corporation. + Work to complete projects in the US project pipeline. + Set up and execute laboratory to meet both internal and external customer expectations. + Set up and execute laboratory work to as outlined by R&D scientist. + Analyzing samples by analytical methods or applications testing. + Keep neat and orderly notebooks containing a record of all work performed. Maintain other records as necessary to support patent applications for innovative products. + Maintain orderly laboratory space. + Follow all safety and training requirements. + Manage and optimize all process under your responsibility taking into consideration Quality, Legality and Food Safety (if applicable) and client needs on Indorama's products and services. + Guarantee all documentation under your responsibility updated and available for consulting. + Support R&D Lab Manager with properly managing the lab resources + Interact with TS&D team to improve the lab, lab methods, etc. + Work in cross functional /cross discipline teams as needed **What are we looking for in the ideal candidate?** + BS in Chemistry, Chemical Engineering, Material Science, Biochemistry, or Polymer Chemistry/Engineering required. + BS in other science field plus 2+ years in Research laboratory work + Associates Degree with 5+ years in Research laboratory work + 0-3 years' experience (more 3 years' experience preferred) in: + R&D laboratory preferred. + Surfactants knowledge in laboratory or application use strongly preferred. + Use and knowledge of Parr Reactors preferred. + Computer literacy w/ databases, word processing, spreadsheets + Excellent organizational and communications skills + Demonstrated presentation skills preferred. + Experience in chromatography, spectroscopy, wet analysis, or other analytical techniques preferred. + Formulation experience in Agricultural, Home Care, or Coatings preferred. + English with Bilingual Portuguese or Spanish strongly preferred. **What do we offer?** A competitive compensation package, including: - Health insurance - WellHub / TotalPass - Life insurance - And other exclusive benefits The division you'll be joining is a global leader in the chemical industry. We offer a broad portfolio of solutions and high delivery standards to markets such as Crop Solutions, Home and Personal Care, Coatings, Energy & Resources, and Performance Products. **Here, you can make a difference.** **Join us!** We're Indovinya, a top producer of chemical intermediates and surfactants. Our extensive portfolio is designed to meet our customers' most diverse needs. As producers of solutions used for crops, oil and gas, coatings, home and personal care, and other applications, we are present in the daily lives of millions worldwide. Through our increasingly sustainable chemistry, designed to meet the needs of each of our customers carefully, we want to transform our operations and products into something increasingly relevant for the planet. We are part of Indorama Ventures Public Company Limited, one of the world's leading petrochemical producers, and are present globally with manufacturing in Europe, Africa, Americas, and Asia-Pacific. With 18 plants, seven R&D centers, and an experienced management team, we have a strong track record of environmental stewardship. Our expertise lies in innovative, eco-friendly chemistry. Today, Indovinya emerges as a more robust and strategic company dedicated to driving new business opportunities while prioritizing the well-being of countless individuals as employees, customers, suppliers and mainly the communities close to our operations worldwide.

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. Protomer is a recently -acquired, wholly owned subsidiary of Eli Lilly and Co. based in Pasadena, CA. The team operates as a group within Lilly Research Laboratories (LRL). LRL is focused on the discovery and development of new therapeutics for the treatment of a plethora of diseases. The scientists in LRL work cross-functionally between therapeutic target area disciplines, including Diabetes, Heart Failure, Renal, Neuroscience, ASCVD, Incretins and Insulins. The team at Protomer is working on responsive biotherapeutics that can be controlled using small molecule modulators. Protomer team is based in Pasadena and the research labs are located in Pasadena. We are currently expanding the team to advance several programs, including glucose sensing insulins (GSIs), and are looking for a research associate with experience in biochemistry, synthesis, bioconjugations, and purification/characterization of therapeutic compounds of interest. The ideal candidate will have a bachelor's or master's degree in chemistry, chemical engineering, biochemistry, biology, or a related field, as well as in-depth understanding of basic biochemistry and chemistry techniques and experience with development, validation, and implementation of experiments in a biomedical research setting. The applicant must be a fast-learning, task-oriented, and self-motivated person who can perform detailed work with minimal supervision. A requirement of this role is to work well as a great teammate in a fast-paced research setting. The applicant will be responsible for assisting Protomer's senior chemists with synthesis, bioconjugation, purification, and characterization of compounds of interest. The successful candidate will actively engage and present in team meetings and is expected to contribute to the team's progress and success. Responsibilities: * Work closely with senior scientist to accomplish team objectives and research milestones * Purify and characterize compounds using HPLC, FPLC, and various biochemical methods * Introduce and maintain innovative technologies with respect to peptide therapeutics, including developing and implementing assays and maintaining critical instruments. * Perform data analysis. Critically evaluate data and results and troubleshoot experiments. * Demonstrable ability to function independently, work within a team-oriented lab environment, and work within cross-functional project teams. * Maintain accurate record keeping, perform independent data analysis, and report data in written and oral formats and retain excellent electronic lab notes. * Perform work in compliance with Lilly Research Policies. Basic Qualifications: Undergraduate degree in chemistry, biochemistry, chemical engineering with working knowledge of standard biochemistry or chemistry lab techniques. Additional Skills/Preferences: * Academic or industry research experience * Proven ability to work in a flexible, team-oriented environment. * Experience with standard biochemistry techniques. * Strong communication skills and experience presenting data in a team environment. * Strong relationship-building and interaction skills with peers and management. 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 $69,000 - $179,300 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

PRIMARY DUTIES AND RESPONSIBILITIES: * Perform and/or assist with analytical testing of raw materials, in-process samples, and finished products. * Utilize analytical laboratory instrumentation with supervision. * Comply with cGMP regulations and follow all standard operating procedures. * Peer review data generated by other technicians. * Maintain and troubleshoot laboratory equipment and analytical instrumentation within level of experience. ASSOCIATED DUTIES AND RESPONSIBILITIES: * Perform and/or assist with equipment calibrations and qualifications. * Other related duties as required. REQUIRED SKILLS, ABILITIES, AND QUALIFICATIONS: * Bachelors degree in chemistry or related discipline. * 2-5 years' experience in a chemistry laboratory. * 2- 5 years' experience with analytical instrumentation, such as HPLC, GC, CE, ICP, FTIR, TOC, MS, and dissolution apparatus. * Ability to follow standard operating procedures. * Strong communication skills, both written and verbal. * Ability to organize, prioritize and effectively perform concurrent tasks with minimal supervision. * Strong attention to detail. * Desire and ability to work in a positive team environment. At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer. We offer medical, dental, vision and company matching 401K. All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.

: For over 75 years, Puffer-Sweiven has set the standard in equipment and services for process control, automation, safety, and reliability. We help process-intensive facilities run more efficiently and safely by delivering quality products, technical support, and knowledgeable staff to implement the needed process solutions - with the goal of exceeding customer expectations. Our dedication brings the most advanced products and services to our customers throughout the Central and Gulf Coast regions of Texas. Specialties: As an Emerson Impact Partner, we offer a broad base of superior solutions including the top product lines for a given application. Our specialties at Puffer-Sweiven include: Process Control & Safety Systems Control Valves & Regulators Isolation Valves & Actuation Oil & Gas Automation Reliability Solutions & Services Pressure Management Specialty Pumps & Rotating Equipment Instrumentation Maintenance & Repair Services Duties and Responsibilities: Inspection & Testing Perform incoming inspections of pressure relief valves to assess condition and identify defects. Verify dimensional accuracy, material specifications, and component integrity before and after repair. Oversee hydrostatic, pneumatic, and functional testing to confirm valve performance. Ensure that all repaired Valves meet all necessary specifications, both physical asset and documentation prior to shipment of the valve to customer; i.e. Final Inspection Repair Oversight Monitor repair activities to ensure adherence to approved procedures and OEM specifications. Validate calibration of tools, gauges, and test benches used in valve repair. Ensure replacement parts meet quality and certification requirements. May communicate with customers directly to discuss specific issues found. Maintain the work area and equipment in a clean and orderly condition. Required to work independent of supervision for after-hours call-outs. Compliance & Documentation Maintain detailed inspection records, test reports, and repair certifications. Ensure compliance with ASME, API, ISO, and other applicable standards. Support audits by regulatory bodies and internal quality teams. Continuous Improvement Identify recurring defects and recommend corrective/preventive actions. Collaborate with technicians and engineers to improve repair processes. Provide training and guidance on quality standards and inspection techniques. Inspects valve and/or actuation assets against inspection forms. Ensures compliance to repair procedures and standards. Initiate non-conformances for assets that fail inspections against inspection forms. Monitor status of open non-conformances and work with Supervisors and Managers to ensure timely action. Escalate Quality Issues to relevant leadership as necessary. Suggest quality and process improvements to leadership. Drive implementation of processes as required. Monitor and report out established KPI's relevant at final inspection, like First Pass Yield % (FPY). QUALIFICATIONS: Education / Experience / Skills Technical diploma or degree in Mechanical Engineering or related field. Minimum 3-5 years of experience in valve inspection, repair, or industrial equipment quality assurance. Strong knowledge of pressure relief valve standards (ASME Section VIII, API 576, NBIC). Proficiency in using precision measuring instruments (micrometers, calipers, gauges). Ability to work non standard hours/after hours. Familiarity with non-destructive testing (NDT) methods is a plus. Strong organizational skills with exceptional attention to detail are required. COMPETENCIES: Ability to safely use and maintain a large variety of tools and equipment, associated with the assembly of relief valves, including impact wrenches, electric and manual hand tools, lapping machines, and overhead cranes and forklifts. Ability to read customer specification sheets and basic dimensional drawings. Ability to read and interpret assembly manuals (i.e. Manufacturers' Spring charts), engineering drawings and technical specifications. Good computer skills. Ability to work independently or as a team member. Ability to work with minimum supervision. Attention to detail and strong analytical skills. Excellent documentation and reporting skills. Strong communication and teamwork abilities. Commitment to safety and regulatory compliance.

Quality Control CMM Inspector (Night Shift) Shift: Night Shift (Monday - Thursday 4:30PM-3:00AM 10 hr. shift) As a Quality Inspector, you will play a crucial role in ensuring that our products meet or exceed customer specifications and quality standards. You will be responsible for inspecting machined parts, identifying defects, and verifying compliance with engineering drawings and the necessary part numbers and traceability numbers. Job Responsibilities: Perform in-process and final inspections on valve components, machined parts and detailed final assemblies. Perform receiving inspection on incoming product. Proficient in visual and dimensional inspections using all inspection tools for granite plate inspection. Interpret drawings, certifications, and industry specifications. The ability to apply GD&T. Trains and mentors less experienced inspectors. Create inspection reports and maintain accurate records of inspections and findings. Collaborate with production teams to address quality issues and provide feedback for process improvement. Performs other duties as assigned. Follow company instruction in record management including calibration, inspection, and test report. Able to lift to 50 pounds occasionally and be able to use forklift equipment Job requires walking through the campus 80% of time during shift, may be exposed to elements. May perform any other work-related functions as deemed necessary and appropriate by immediate supervisor or manager, as directed. . Skills & Abilities: Ability to interpret mechanical drawings of components and assemblies Knowledge of Geometric Dimensioning and Tolerancing (GDT) required Ability to read and interpret standards and specifications such as ASME, ANSI, NACE, etc. Proficient in MS Office Suite specifically MS Excel, and experience with ERP/MRP systems. Ability to work in a team-oriented environment that is fast paced and demanding. Must be self-directed, have excellent initiative and organizational skills. Exhibits a strong ability to handle multiple demands with a sense of urgency, drive, and energy. Works well meeting multiple deadlines with the ability to deliver on time. Excellent written and verbal communications skills. Core Qualifications: High School diploma or equivalent required. Minimum of five years QC inspection experience of raw material, machined parts, coating, and review of inspection and testing documentations. Minimum of 3 years of experience working in a machining and assembly environment Candidate must have Portable CMM (Faro, Romer) and/or Stationary CMM experience preferred Experience with nonconforming material control and ability to follow company specific instructions and directions. Experience with equipment calibration program. Experience with the review and approval of Certified Material Test Reports with respect to internal and national material specifications/standards. Experience with evaluation for acceptance of inspection and testing reports including Certificate of Conformance, Coating, Welding, Hardness Test, Heat Treat, Liquid Penetrant, Magnetic Particle Testing, Ultrasonic Testing, and Radiographic Testing.

SUMMARY/OBJECTIVE: Quality Control Associate at Allied Interior Solutions Inc., plays a crucial role in ensuring the precision and excellence of cabinet countertop production. The responsibilities include inspecting and verifying the quality of materials, processes, and finished products. ESSENTIAL FUNCTIONS: Reasonable accommodation may be made to enable individuals with disabilities to perform these essential functions. Conduct visual inspections and measurements during different stages of the production process. Use precision tools and equipment to assess the accuracy of cuts, edges, and dimensions. Identify defects or imperfections and collaborate with production teams to address and rectify issues. Record and document inspection results, maintaining detailed reports for quality assurance purposes. Collaborate with the Quality Control Supervisor to implement and enhance quality control procedures. Participate in continuous improvement initiatives to optimize production processes. KNOWLEDGE, SKILLS, AND ABILITIES (KSA): Knowledge: Understanding of stone countertop manufacturing processes. Familiarity with quality control tools and techniques. Skills: Attention to Detail: Ability to meticulously inspect materials and finished products. Analytical Thinking: Capability to analyze inspection results and identify trends or areas for improvement. Communication Proficiency: Effective communication with production teams and supervisors. Time Management: Skill in prioritizing tasks to meet quality control deadlines. Problem Solving: Ability to address and resolve quality issues efficiently. Teamwork and Collaboration: Capacity to work collaboratively in a manufacturing environment. WORK ENVIRONMENT: The work environment is a manufacturing facility, which may include exposure to dust, noise, and machinery. Safety precautions and personal protective equipment are provided. PHYSICAL DEMANDS: Ability to stand, walk, and move around the production area for extended periods. Lift and carry materials weighing up to 50 pounds. Use precision tools and equipment with dexterity. REQUIRED EDUCATION AND EXPERIENCE: High school diploma or equivalent. 1-2 years of experience in quality control or a related field. Familiarity with stone countertop manufacturing processes. Basic knowledge of quality control tools and techniques. PREFERRED EDUCATION AND EXPERIENCE: Associate degree in a relevant field. 2+ years of experience in stone countertop manufacturing quality control. Certification in quality control or a related discipline. AFFIRMATIVE ACTION/EEO STATEMENT: Allied Interior Solutions Inc. is committed to providing equal employment opportunities for all individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other characteristic protected by applicable law. We embrace diversity and encourage a work environment where differences are respected and valued. Other Duties: This job description should not be interpreted as an exhaustive list of responsibilities or as an employment agreement between the employer and employee. The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification and are subject to change as the needs of the employer and the requirements of the job change. Any essential functions of this position will be evaluated as necessary should an employee/applicant be unable to perform the functions or requirements due to a disability as defined by the Americans with Disabilities Act (ADA). Reasonable accommodation for the specific disability will be made for the employee/applicant when possible.

Temp Connect Staffing is actively recruiting skilled candidates for Quality Control positions in Houston, TX, and beyond! This job order has been posted as a waitlist to help pre-qualify candidates to be contacted when we receive new opportunities. Schedules: 1st, 2nd, or 3rd shifts Pay Range: $14.00 - $20.00 per hour (based on position availability) General Requirements: Recent experience in quality control or quality assurance in a production environment. Proficiency with measuring tools, inspection equipment (e.g., calipers, micrometers), and software (e.g., Microsoft Office or quality control software). Ability to identify problems, analyze potential solutions, and implement corrective actions to maintain product quality. Willing to submit to background and drug screenings. Ability to stand for extended periods. Must be reliable, punctual, and able to work in a fast-paced environment. Prior experience in positions such as Quality Control Inspector, Quality Control Analyst, Quality Assurance Technician, or Quality Control Coordinator is a big plus! Be 18 years or older. Benefits: Affordable Health and Dental Plans Referral Program Responsibilities may include: Examine incoming materials to ensure they meet specified quality standards before they enter the production process. Continuously check production lines to ensure products meet quality standards throughout the manufacturing process. Perform tests (e.g., visual inspections, measurements, and functional tests) on finished goods to ensure they meet specifications. Record and maintain accurate documentation of inspection results, testing procedures, and quality control findings. Detect and report any defects or deviations from quality standards, ensuring immediate corrective actions are taken. Ensure measurement tools and testing equipment are calibrated and maintained properly for accurate testing results. How to apply on jobs.connectstaffing.com: Attach a resume when you “quick apply” to a job OR if you don't have a resume, please complete a general application with us first at hrcenter.ontempworks.com/en/CNN. Afterward, you may “quick apply” to any job without a resume. All applicants meeting minimum requirements will receive an SMS text inviting them to participate in an AI-based interview. This gives you the chance to describe your relevant skills and experience so you may be fully considered for each opportunity.

The Quality Control Inspector 1 supports the organization in the development, maintenance and execution of a quality control program that will allow the business to continually improve. In addition, the Quality Control Inspector 1 will help ensure that the supply being delivered from vendors and the product being shipped to customers meets the expected standards and specifications. Duties and Responsibilities: Inspect raw materials, machined, welded, and coated parts ordered and received at TEI (TRENDSETTER ENGINEERING, INC) headquarters from vendors and internal machine shop for quality and accuracy. Verify parts received against engineering drawings, specifications, and manufacturing records. Prepare electronic inspection reports for incoming products. Maintain incoming inspection log. Issue, document, and follow up on NCR's. Manage calibrated measuring equipment and certificate log. As necessary, perform other duties, requiring the same level of skill & responsibility. Support any new quality initiatives as required. Be familiar with company HSE (Health, Safety, and Environmental) policies and procedures. Share knowledge & best practice across the company. All other duties as assigned. Qualifications: Associate degree or at least 5 years of previous experience related to quality control inspection, preferably within the oil & gas industry. Advanced skills in dimensional measurement and verification, utilizing all necessary tools. Proficient computer skills and knowledge of Share point and Microsoft 365 required. Ability to demonstrate initiative and assertiveness, plan and organize work in an efficient manner, and work well under stress and time pressures. Strong interpersonal and communications skills, both verbal and written

SHIFT: Day /OBJECTIVE The QC Inspector will be responsible for approving incoming, in-process, and finished materials for defects. The QC inspector will also be responsible for documenting inspection results, taking measurements, and tracking defects. ESSENTIAL FUNCTIONS Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions Reports to QC Lead person for daily activities Perform and document dimensional and visual checks of production parts and incoming goods. Responsible for notifying Quality Control Lead person, in addition to Manufacturing and Engineering, of non-conforming goods. Inspect customer-supplied inserts, per drawings supplied. Ring check and approve production tryouts to engineered tolerances. Inspection of buy-out materials. Make first-piece inspection and document ring checks. Shipping certifications. Log and verify traceability packets. Implement and practice Lean Manufacturing tools including 5S, increased productivity, and eliminate waste. Maintain a 5S checklist as it applies to your work area. Perform other related duties assigned by QA Manager or QC Lead person Other Requirements An annual vision examination is required. Must be able to use measuring devices. Must follow company safety procedures at all times. Must have average reading, writing, and mathematical skills. Must be able to visually inspect materials. Must be able to lift 50 lbs., 3 ft. high. Required Education and Experience High school diploma or equivalent, with 4-5 years of work-related experience. Work Environment This job operates in an office and manufacturing environment. This role routinely uses tools and other such equipment during the course of the job duties. Provided Personal Protective Equipment, as well as steel-toed boots or shoes, must be worn at all times. Physical Demands Moderate walking and climbing Physically able to conduct inspections and carry equipment used for inspections Must be able to lift up to 25 pounds at a time While performing the duties of this job, the employee is regularly required to, stand, sit; and stoop Regular, predictable attendance is required Position Type/Expected Hours of Work This is a full-time position, and hours of work and days are Monday through Friday. Occasional evening and weekend work may be required as job duties demand. Travel None EEO STATEMENT Utex Industries is an equal employment opportunity employer and shall make all employment-related decisions without regard to race, color, national origin, ancestry, religion, creed, age, sex, sexual orientation, marital status, military or veteran status, and/or any other status or condition protected by applicable federal, state, or local law. Other Duties Please note this job description is not designed to cover or contain a comprehensive listing 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 notice.

Job Description Quality Control Technician- PQC SEG Solar is expanding its horizons in the solar industry and seeking candidates to join our Quality Control Department. If you're passionate about contributing to a greener world, eager to grow professionally, and thrive in a collaborative environment, this opportunity is for you! As a Quality Control team member, responsibilities include: Performing visual inspections of solar modules at various stages of production Identifying and recording defects such as cracks, scratches, contamination, or misalignment Conducting EL image review and ensuring proper documentation Checking labeling, barcode placement, and ensuring traceability compliance Verifying proper application of materials (e.g., POE, EVA, backsheet, junction box) Ensuring that standard operating procedures (SOPs) and quality standards are followed Communicating defects and abnormalities to engineers or supervisors for corrective actions Completing inspection reports accurately and on time Collaborating with production staff to support continuous quality improvement Maintaining cleanliness and organization of the inspection station Following safety protocols and company policies at all times Other duties within the department, as needed Qualifications: High School Diploma or equivalent; previous experience in quality control, quality inspection, and in a manufacturing environment, a plus. Strong attention to detail and organizational skills. Strong communication (written and verbal), organizational, and interpersonal. Ability to multitask effectively and deliver under tight deadlines. Able to use Microsoft Office (Word, Excel, etc.) Able to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Able to work independently and in a team setting. Able to stand for long periods of time. Attention to detail and accuracy. Good manual dexterity and hand - eye coordination. Job Type: Full-time Physical Setting: Onsite Schedule: Ability to work 8-12-hour shifts; ability to work overtime and weekends (Saturdays) Ability to commute: Reliable transportation Benefits: 401(k) Health Insurance Vision and Dental Dental insurance Flexible spending account Paid Time Off Holiday Pay

We are seeking a Quality Control to join our team! You will conduct tests to determine the quality of materials and finished products as well as identify areas of improvement to increase efficiency. Responsibilities: Perform thorough examinations of all materials and finished metal products Conduct and report internal audits and evaluations Implement and improve quality control operating procedures Identify and troubleshoot equipment problems and defects Participate in routine visual inspections Maintain a clean and safe work environment Qualifications: Previous work experience in quality control in Metal Manufacturing Strong attention to detail Strong analytical and critical thinking skills Excellent written and verbal communication skills

As a Quality Inspector, you''be the focal point for all QA/QC assessment for our Flexible Pipe Systems business. Conducting qualitative risk assessments, root cause analysis and providing corrective actions. Supporting QMS system by creating, editing and reviewing documents to be aligned with global standards. As a Quality Inspector, you''be the focal point for all QA/QC assessment for our Flexible Pipe Systems business. Conducting qualitative risk assessments, root cause analysis and providing corrective actions. Supporting QMS system by creating, editing and reviewing documents to be aligned with Baker Hughes global standards. This is for a third shift position (9pm-5: 30am). Training will be on the first and second shifts until training is complete (training timeframe dependent on competencies) -(1st)5am-1: 30pm and (2nd)-1pm-9: 30pm. The plant runs 24/7 so they need coverage 7 days a weeks. The inspector will work a 8 hour shift for 4 to 6 days a week, as dictated by necessity of the plant. Must be available to work weekends, as necessary. Key responsibilities: •Inspecting parts, assemblies and subassemblies to required drawings and prints •Initiating non-conformance reports on all parts and assemblies that are not to drawing and print specifications. •Assuring that manufactured units meet quality control procedures, engineering specifications and customer requirements. •Initiating corrective action requests when conditions adverse to quality are repetitive in nature. •Partnering with manufacturing management and internal process teams to eliminate the causes of quality problems •Completing, inspecting and distributing all quality records and documents and performing specialized testing as required •Verifying tests as required on all components and completed assemblies. •1 x 12 hour shifts this year to provide 24/7 coverage from Monday to Sunday. •Candidate will start on day shift due to training then move to nights. Skills & Competencies: •Be able to read and correctly interpret prints / drawings and specifications •Display understanding of defects, problem-solving skills or an enthusiasm to learn and develop your skill set in a hands-on environment •Have excellent communication skills and the ability to be a valuable team player Work Environment: •Fast paced and noisy environment with constant movement. •Regular lifting and/or moving up to to 50 lbs. Qualifications: •Have a High School Diploma or equivalent level of education •Demonstrate proven experience in a Quality Technician or Inspection role Shifts: •2nd shift: Monday -Friday from 3pm - 3am (12 hour shift for 4 to 6 days a week) •Must be able to work some weekends

**KNOWLEDGE/ EXPERIENCE/SKILLS:** Typical Requirements: Two or more years of either applicable lab experience or relevant college coursework. Physically capable of working within a laboratory environment on a rotating days schedule. Computer literacy & mechanical aptitude. Strong attention to detail and ability to work independently or as part of a team. Basic skills with Microsoft Excel, Word, Outlook and PowerPoint. Experience with polymer analyses and testing with MFI, Extruder, and DSC is highly desirable. Familiarity with SQC, ISO 9001, ISO 17025 quality systems. **PRINCIPAL ACCOUNTABILITIES:** Accurate, efficient, and un-biased analysis of finished products in a timely manner is high priority. Accountability maintained through the management hierarchy. Control established through the timing & application of documented procedures/methods/protocols and oversight/supervision of activities. This position requires a high level of personal organization and discipline in conducting analyses and logging results on a routine basis. A significant number of inter-departmental activities are reliant upon the accuracy of data collected and reported by this position.

The primary responsibility of a QC is to inspect palletized product in the production warehouse. The QC must report all product made incorrectly and create a path forward to get the product repaired prior to the palletized product going into a prime bin location. Important Personal Skills Able to work outside in environmental conditions which at times include extreme heat or extreme cold Wear all required Personal Protective Equipment (PPE) without restriction and pass any medical examination associated with the use of said PPE. Lift 55 pounds floor to waist Push and pull 30 pounds horizontally Carry 20 pounds while walking Climb stairs and ladders Stand/walk 12 hours per day Extend arms through normal range of motion while standing and squatting. Job Tasks Responsible for handling finished product. Performs quality control activities. Performs scrap and exception handling. Assist in repairing pallets with quality issues. Ensures clean workspace and performs housekeeping activities. Supports P&S Operations in checking all pallets prior to offload for any Quality issue. Reports all anomalies to management/inventory at the end of shift. Train Short Service Workers Participate in all LPS activates Any other duties that may be assigned to complete the task. Qualification and Experience Must possess a valid driver's license 18 years or older and legally able to work in the U.S. Stable work history with good references from past employers Speak, write, and read in fluent English, hear, and have good vision High school diploma/GED required Pass a drug screen, physical, and background check Benefits: Medical, Dental, and Vision Insurance 401k (4% matching) Short-Term/Long-Term Disability Life Insurance Vacation Pay Holiday Pay (starting on the first day of employment) TALKE USA, INC. 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. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

BEYOND International Inc. is seeking a Lab Assistant/Chemical Technician for our Chemical & Quality Department. The assistant/technician will support production, products quality control test, regular lab & production instruments maintenance etc. Responsibilities: Assist the Lead Chemist and Chemical Engineer in new product research and development (R&D) Prepare sample for Quality Control test, complete the testing records, maintain protocols, SOPs, test reports and related documents, have good documentation practice Inspect and track the stability of raw materials, R&D products and finished products Work safely and maintain a clean work area in accordance with production requirement and standard lab practices (May lift up to 25 lbs and/or move up to 50 lbs) Maintenance of the raw material inventory and monthly usage Maintain lab equipment and perform test apparatus verifications/calibrations Effectively communicate with colleagues, customers and outside vendors Qualifications: Have a legal job status in the United States (H1B sponsored if approved by supervisor) Chemistry and other related degree preferred (0-2 years experience required) Attention to quality including familiarity with ISO 13485 concepts Familiar with production environment and laboratory procedures Proficiency in Microsoft Office (Word, Excel, Outlook) Be able to do literature search independently or as instructed Team oriented, self-motivated and flexible to working overtime when needed Job Type: Full-time Pay: $13.00 - $18.00 per hour Benefits: Health insurance Paid time off Schedule: 8 hour shift Ability to commute/relocate: Sugar Land, TX 77478: Reliably commute or planning to relocate before starting work (Required) Application Question(s): Familiarity with ISO 13485 concepts and procedures Experience: Chemical engineering: 1 year (Required) Work Location: In person

TempToFT Must be available to be on call. Must have active TWIC Card. Must be able to pass DISA Drug Screening and background. This position goes in to plants, water, and road sides cleaning up chemical spills and doing preventative cleaning. Hazmat is an additional 5 an hr. On call is a minimum of 4 hours pay. 18.00

Job Description : For over 75 years, Puffer-Sweiven has set the standard in equipment and services for process control, automation, safety, and reliability. We help process-intensive facilities run more efficiently and safely by delivering quality products, technical support, and knowledgeable staff to implement the needed process solutions - with the goal of exceeding customer expectations. Our dedication brings the most advanced products and services to our customers throughout the Central and Gulf Coast regions of Texas. Specialties: As an Emerson Impact Partner, we offer a broad base of superior solutions including the top product lines for a given application. Our specialties at Puffer-Sweiven include: Process Control & Safety Systems Control Valves & Regulators Isolation Valves & Actuation Oil & Gas Automation Reliability Solutions & Services Pressure Management Specialty Pumps & Rotating Equipment Instrumentation Maintenance & Repair Services Duties and Responsibilities: Inspection & Testing Perform incoming inspections of pressure relief valves to assess condition and identify defects. Verify dimensional accuracy, material specifications, and component integrity after and after repair. Oversee hydrostatic, pneumatic, and functional testing to confirm valve performance. Ensure that all repaired Valves meet all necessary specifications, both physical asset and documentation prior to shipment of the valve to customer; i.e. Final Inspection Repair Oversight Monitor repair activities to ensure adherence to approved procedures and OEM specifications. Validate calibration of tools, gauges, and test benches used in valve repair. Ensure replacement parts meet quality and certification requirements. May communicate with customers directly to discuss specific issues found. Maintain the work area and equipment in a clean and orderly condition. Required to work independent of supervision for after-hours call-outs. Compliance & Documentation Maintain detailed inspection records, test reports, and repair certifications. Ensure compliance with ASME, API, ISO, and other applicable standards. Support audits by regulatory bodies and internal quality teams. Continuous Improvement Identify recurring defects and recommend corrective/preventive actions. Collaborate with technicians and engineers to improve repair processes. Provide training and guidance on quality standards and inspection techniques. Inspects valve and/or actuation assets against inspection forms. Ensures compliance to repair procedures and standards. Initiate non-conformances for assets that fail inspections against inspection forms. Monitor status of open non-conformances and work with Supervisors and Managers to ensure timely action. Escalate Quality Issues to relevant leadership as necessary. Suggest quality and process improvements to leadership. Drive implementation of processes as required. Monitor and report out established KPI's relevant at final inspection, like First Pass Yield % (FPY). QUALIFICATIONS: Education / Experience / Skills Technical diploma or degree in Mechanical Engineering or related field. Minimum 3-5 years of experience in valve inspection, repair, or industrial equipment quality assurance. Strong knowledge of pressure relief valve standards (ASME Section VIII, API 576, NBIC). Proficiency in using precision measuring instruments (micrometers, calipers, gauges). Ability to work non standard hours/after hours. Familiarity with non-destructive testing (NDT) methods is a plus. Strong organizational skills with exceptional attention to detail are required. COMPETENCIES: Ability to safely use and maintain a large variety of tools and equipment, associated with the assembly of relief valves, including impact wrenches, electric and manual hand tools, lapping machines, and overhead cranes and forklifts. Ability to read customer specification sheets and basic dimensional drawings. Ability to read and interpret assembly manuals (i.e. Manufacturers' Spring charts), engineering drawings and technical specifications. Good computer skills. Ability to work independently or as a team member. Ability to work with minimum supervision. Attention to detail and strong analytical skills. Excellent documentation and reporting skills. Strong communication and teamwork abilities. Commitment to safety and regulatory compliance.

/OBJECTIVE The QC Inspector will be responsible for approving incoming, in-process, and finished materials according to Internal and Customer requirements. The QC inspector will also be responsible for creating and documenting inspection results, taking measurements, and tracking non-conforming product. ESSENTIAL FUNCTIONS Reports to QC Leadperson and/or Supervisor for daily activities and workload. Perform and document dimensional and visual checks of production parts and incoming goods and creating inspection reports to internal and customer requirement. Responsible for notifying Quality Control Leadperson and/or Supervisor, in addition to Manufacturing and Engineering personnel, of non-conforming goods. Inspect customer supplied material, per specified drawings. Inspecting and gathering product documentation, final document packets, material heat reports as required. Inspection of buy-out materials. Make First Article inspection and document inspection results. Log and verify traceability packets. Implement and practice Lean Manufacturing tools including 5S, increased productivity, and eliminating waste. Maintain 5S checklist as it applies to your work area. Perform other related duties assigned by QA Manager or QC Leadperson or QC Supervisor. Other Requirements An annual vision examination is required. Must have experience with the use of measuring instruments in the completion of dimensional inspections. (Calipers, micrometers, CMM, Pi tapes, Optical comparators, etc.) Must follow company safety procedures at all times. Must have average reading, writing, and mathematical skills. Must be able to visually inspect materials and manufactured products. Must be able to lift 50 lbs., 3 ft. high. Required Education and Experience High school diploma or equivalent, with 2-3 years of work-related experience. Work Environment This job operates in an office and manufacturing environment. This role routinely uses tools and other such equipment during the course of the job duties. Provided Personal Protective Equipment, as well as steel-toed boots or shoes, must be worn at all times Physical Demands Moderate walking and climbing Physically able to conduct inspections and carry equipment used for inspections Must be able to lift up to 25 pounds at a time While performing the duties of this job, the employee is regularly required to, stand, sit; and stoop Regular, predictable attendance is required Position Type/Expected Hours of Work This is a full-time position, and hours of work and days are Monday through Friday. Occasional evening and weekend work may be required as job duties demand. Travel None EEO STATEMENT Utex Industries is an equal employment opportunity employer and shall make all employment-related decisions without regard to race, color, national origin, ancestry, religion, creed, age, sex, sexual orientation, marital status, military or veteran status, and/or any other status or condition protected by applicable federal, state, or local law. Other Duties Please note this job description is not designed to cover or contain a comprehensive listing 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 notice.