Quality control analyst jobs in Pearland, TX - 187 jobs

1. Perform in-process and final inspections on fabricated parts, weldments, assemblies, and structural components. 2. Verify dimensions using calipers, micrometers, gauges, tapes, weld gauges, and other precision measuring tools, prepare reports. 3. Review and interpret engineering drawings, welding symbols, fabrication standards, and customer specifications. 4. Review NDE reports, prepare ncr when necessary. 5. Ensure products meet quality standards, customer requirements, and regulatory codes. QUALIFICATIONS: 1. High school education or equivalent. 2. Ability to use appropriate measuring and test equipment. 3. Product familiarity working in a similar environment. TRAINING REQUIRED: 1. Strong attention to detail, accuracy and problem solving skills. Ability to read and interpret engineering drawings and specifications. 2. Performing dimensional inspections. 3. Experience with NDT methods. (VT, MT, PT) 4. Experience working with ITPs, MTRs and fabrication quality documentation PPE AND SAFETY: 1. Follow all shop safety policies, including PPE requirements. 2. Reasonable accommodations are made to enable

We are searching for a Specialist in Quality Improvement with the Outpatient Fetal Center at The Pavilion for Women location- someone who works well in a fast-paced setting. In this position, you will work as part of the Quality & Outcomes Management (Q&OM) Team to achieve high quality, cost-effective health care throughout the Texas Children's Hospital System and maintain the necessary accreditation status for the organization (JCAHO, HCFA, NCQA, and other agencies, as needed). Think you've got what it takes? Qualifications Bachelor's degree in Nursing, Pharmacy, Social Sciences (Social Work), Respiratory Therapy, Health Information Management, or Business Administration 2 years of clinical and/or quality experience Certifications/Licenses: preferred CPHQ - Cert-Cert Prof Healthcare Qual RN - Lic-Registered Nurses or other clinical discipline Responsibilities Produces reports for quality improvement, guidelines, utilization, and outcomes, error-free and on time. Educates medical staff departments, administrative staff, and ancillary service departments regarding the tools of performance improvement, methods for measurement, analysis, and reporting to meet the standards of the JCAHO, HCFA, NCQA or other regulatory agencies. Provides medical staff and departmental staff teams with consulting and analysis services to support initiatives intended to achieve breakthrough or incremental process improvement in patient care, as measured by at least one improvement, worthy of storyboard, per area of responsibility per year. Produces guidelines and measures for medical management in a timely, efficient manner Provides Ongoing Professional Practice Evaluations, Focused Professional Practice Evaluations for areas of responsibility as defined by Joint Commission standards on time and error free. Provides opportunities and strategies for improvement of System entities and services as evidenced by at least two (2) improvements resulting from recommendations made. Participates in and coordinates committees Attends performance improvement, medical management and other System committees as scheduled. Prepares reports on Q&OM activities as needed for informing clinical, operations, and financial stakeholders, on time and error-free.

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

J oin Immatics and shape the future of cancer immunotherapy ; one patient at a time! Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics. Why Join Us? Innovative Environment: Help to pioneer advancements in cancer immunotherapy. Collaborative Culture: Be part of a diverse team dedicated to your professional growth. Global Impact: Contribute to therapies that make a lasting impact on patients globally. We are seeking a Senior Quality Control Analyst to join our Global Quality Operations team. In this role, the Senior Quality Control Analyst will be responsible for performing bioanalytical, cell-based, and molecular assays to support product release and stability testing within the Quality Control laboratory. The position will also play a key role in method transfer, qualification, and validation activities. FLSA Classification: Salary, Exempt Schedule: 8:00 AM - 5:00 PM; Monday to Friday; On-site Reports to: Quality Control Manager Location: 13203 Murphy Road Suite 100 Stafford, TX 77477 What You'll Do: As a Senior Quality Control Analyst, you will play a key role in supporting our Quality Control Operations: Conduct Tests and Analyze Results: Perform routine and non-routine testing on products and materials to verify compliance with established standards. Collaboration: Manage, in collaboration with other team members, purchasing, receiving, formulating, testing, release of materials and reagents, equipment and assay qualifications and validation. Quality Records: Lead quality documents and processes such as GxP deviations, lab investigations, OOS/OOE, CAPAs, change controls, etc. Documentation: Author and conduct periodic review of procedures. Conduct and document all activities consistent with cGMP/GxP, regulatory filings, and written procedures. Maintain data integrity and logs for equipment. Data Analysis: Ability to analyze complex data sets and interpret results accurately. Able to identity trend and deviations, and take initiative to troubleshoot issues Manage Laboratory Equipment: Perform and oversee the maintenance and calibration of laboratory equipment. Ensure Compliance: Involved in the creation of systems used in quality control to maintain compliance with regulations. Safety: Always demonstrate good safety practices and promote safety awareness. Secondary Functions: Train and support junior analysts. Transport controlled documents, QA-released QC materials and human biological samples. Assist with group tasks scheduling Maintain knowledge of internal procedures and current regulatory requirements Required Experience and Education: BA or BS in any science-related field Minimum five (5) years experience in a regulated laboratory environment MS degree or specialized skill set may substitute for 3 years Experience as a QC personnel in a related field. Experience in aseptic technique, cell culture and either flow cytometry or cell-based assays. Preferred Experience and Education: MS in Biology, Biological Sciences, Laboratory Science, Biochemistry, or Biomedical Science/Engineering Minimum five (5) years experience in a regulated laboratory environment Laboratory skills include a few of the following: visual inspection, flow cytometry, molecular and cell-based assays. Demonstrate technical competence and knowledge in method transfer and assay qualification/validation activities Excellent technical writing and troubleshooting/investigational skills. Demonstrate knowledge of cGMP/ICH/EU regulations and requirements. Experience writing GxP deviations, lab investigations, OOS/OOE, CAPAs, change controls, etc. Experience with LIMS and statistical software is a plus Competencies: Initiative Problem Solving Very detail oriented Strong analytical Technical writing, verbal communication, and interpersonal skills Ability to work Independently and manage multiple projects with aggressive timelines Work Environment: This position works in a typical office and lab environment with moderate noise levels and uses phone, computer, office equipment and supplies on a regular basis. Other duties performed while outside of office and lab building could involve exposure to manufacturing operations, along with outdoor conditions (including highway traffic) and temperatures. The percentage of working hours spent in a typical office and/or laboratory environment varies based on business needs. While performing the duties of this job, the employee may be occasionally exposed to moving mechanical parts, fumes or airborne particles, pathogens, and toxic or caustic chemicals. The employee can be occasionally exposed to wet and/or humid conditions, risk of electrical shock, sharps, or cuts, while performing tests. This position requires handling of human biological specimens including human peripheral blood and human T cell products, as well as laboratory chemicals Travel required: Less than 10% Minimal Physical demands: Communicating Verbally - expressing or exchanging ideas by means of the spoken word to impart oral information to others to convey detailed spoken instructions or other workers accurately, loudly or quickly. Hearing - the ability to hear, understand, and distinguish speech and/or other sounds one-on-one, group or conference, telephone, and other sounds. Keyboarding - entering data or text into a computer or other machine by means of a keyboard. Devices include a traditional keyboard, 10 key-pad, touch screens and others. Lifting - raising or lowering an object (up to 25 lbs) from one level to another (includes upward pulling). Carrying is to transport an object - usually by holding it in the hands or arms but may occur on the shoulder. Near Visual Acuity - clarity of vision at approximately 20 inches or less (working with small objects, reading small print, including the use of computers). Pushing - Exerting force upon an object so that the object moves away from the object. Pulling - Exerting force upon an object so that the object moves toward the force. Sitting - remaining in a sitting position for at least 50% of the time. Standing/Walking - remain on one's feet in an upright position at a workstation. Stooping - occasional bending the body downward and forward by bending the spine at the waist - requiring full use of the lower extremities and back muscles. Work authorization/security clearance requirements: Legal eligibility to work in the United States is required. Immatics participates in E-Verify and all new employees will be subject to the Department of Homeland Security requirements for employment Affirmative Action/EEO statement: Immatics is an equal opportunity employer. All employment decisions including the decision to hire, promote, discipline, or discharge, will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, national origin, ethnicity, marital status, age, physical or mental disability, medical conditions, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. What do we offer? At Immatics, we believe in investing in our team's health, safety and well-being. Here's what you can expect if you join Immatics Comprehensive Benefits: Competitive rates for Health, Dental, and Vision Insurance 4 weeks of Paid Time off, granted up front each year and prorated for first and last year of employment. Sick Time Off - 56 hours 12 Paid Holidays 100% Employer-Paid Life Insurance up to at 1x annual salary 100% Employer Paid Short- and Long-Term Disability Coverage 401(k) with Immediate Eligibility & company match… You are eligible for 401(k) plan participation as of your first paycheck. The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment. Partially paid Parental Leave for eligible employees. (3 weeks) Additional voluntary employee paid coverages including Accident, Hospital Indemnity, and Critical Illness Employee Paid Identity Theft Protection and Pet Insurance. Professional Growth: Opportunities to work with leading experts in the field of T-cell immunotherapy. Company provided learning and development opportunities Fast paced, high demand collaborative and dynamic environment.

Feeling stifled by your current job and team dynamic? Seeking more meaningful challenges and a work squad that's as committed as you are? You may be onto something here. Is your happy place in the lab or analyzing and verifying data at the computer? Do you dig working on your own but still like to be part of a team that's as tenacious as you are? Great, because we could really use someone with your instincts and drive. The Position: Quality Control Chemical Lab Analyst I With your lab experience and knack for paying attention to the details, you're not shy about speaking up when things don't look right. That's perfect because our team's mission is to evaluate the quality and safety of raw ingredients and uphold our high standards on behalf of patients who need compounded medications. You bring at least 3 years of hands-on HPLC experience and a strong background with other analytical techniques, ensuring accuracy and reliability in every result. You're also the type who takes constructive criticism as an opportunity to grow while consistently demonstrating professionalism. As a true team player, you know that collaboration is just as essential as independent focus, and you thrive in an environment where everyone pulls together toward a common goal. No stranger to lab analysis work, you're adept at taking on testing, data entry, documentation review, customer complaint calls or emails, investigative work, troubleshooting lab equipment issues, and communicating with vendors and interdepartmental groups in any given week. Plus, you can't help but strive for continuous improvement. When it comes to communication, you can handle yourself well - and when called for, you're not afraid to pick up the phone or speak to someone in person. You are mature and treat everyone with dignity and respect, using your intuition and instincts to determine the best path forward. Plus, you appreciate working independently because you are self-driven, decisive, and know how to prioritize your workload to honor commitments. That's why past coworkers or supervisors have praised you for being exceptionally diligent and dependable. Not into celebrity gossip? We get it - we prefer genuine connections, too. You'll appreciate that the minds you'll collaborate with are just as focused on getting the job done right, always. Don't worry, we're friendly and will make sure you feel comfortable with us quickly. You can bet we'll mix in some humor and keep things fun! We also think it's rewarding to learn and grow together, so we often embrace training and development opportunities - individually and as a team - to be lifelong learners. For work-life balance, you'll have options with hours and days in the office since this is a 100% onsite role. You'll also find that team managers engage on a human level and take a genuine interest in what you bring - professionally and personally. We believe that transparency and open communication build trust within the team, which helps minimize stress all around. The Company While our work requires a lot of focus and accuracy, we love how the friendly company culture creates a comfort level you don't find elsewhere. Are you craving a positive workplace that's a little less talk and a lot more action? If this sounds like you, then you sound like us. At PCCA, we're optimistic about the future of personalized medicine because we're proud to produce incredible products and services that enable pharmacists to improve patients' lives. Our values are more than just words on a wall - we walk the walk every day. And you'll find our benefits are just as great as the people you'll get to work with. Come share your intelligence and wit with our team. You could finish each day knowing that your keen eye and analytical expertise help protect patients who need personalized medicine for their unique health needs. The security and satisfaction might just leave you with more energy to enjoy your personal life.

TAK Broadband is a leading end-to-end U.S. fiber broadband network construction contractor operating in 42 states. It builds more than just networks; it connects communities to new valuable digital opportunities. TAK offers comprehensive service solutions, from construction to drops to fulfillment. TAK's ecosystem of partners allows it to successfully complete every project starting from the first point of conception. This includes engineering teams, distributors, and more than 100 qualified construction crews with extensive experience across all ISP types and markets; over 300 experienced bury drop crews; and more than 700 professional technicians. We are seeking a Quality Control Technician to join our team in Houston, TX. In this role you will ensure timeliness, completeness and accuracy of work performed by technicians. You will perform inspections post-install to ensure compliance to client specifications and complete reviews to ensure proper restoration of the area. You will be meeting at this address each day before going out to the work site: 13805 West Rd STE 100. Houston, Tx 77041 Why TAK? * Full Time * Paid Weekly * Compensation: $16 - $20 per hour, DOE * Full Benefits Package (Medical, Dental & Vision) * Paid Time Off * 401(k) with Company Match! * 25K Company Paid Life Insurance * Independent Work & Team Collaboration * Career Development & Advancement Opportunities! The Role * Ensures timeliness, completeness and accuracy of work performed by technicians * Performs inspections post install to ensure compliance to client specifications * Completes reviews to ensure proper restoration of area * Captures photos and attach to the inspection report * Performs white line excavations and collects locate data * Verifies the system is complying with all safety requirements * Performs work in a safe manner, following all OSHA and company guidelines * Prioritizes, organizes and efficiently completes tasks to meet deadlines * Works in a variety of outdoor environments * Drives Company vehicles responsibly and safely * Conducts and attends meetings as needed Requirements * 2+ years of telecommunications (i.e. cable, internet, telephone, wireless) industry experience required * Experience with quality control and verifications * Experience calling in Bluestakes a plus * Experience with underground locates and the ability to use a compass for directional instructions * Basic mechanical aptitude, ability to utilize hand tools for intended purposes * Ability to travel daily around to various work sites and open to a variety of schedules * Excellent customer service, time management, problem-solving and troubleshooting skills * Ability to learn and operate testing equipment and software/programs * Ability to utilize hand tools, identify wire size/color and accurately utilize measuring devices * Ability to carry, climb, operate, and work upon an extension ladder (approximately 28 feet high and 75 pounds) * Ability to complete work indoors, outdoors, in tight spaces and elevated by bending, reaching, twisting, climbing, and working while standing up to 70% of the time * Ability to safely navigate various terrains, managing equipment and tools * A body weight of no more than 275 pounds to perform ladder work safely. Safety is our #1 Priority. If personal safety is not compromised, an accommodation may be available based on previous ladder experience in a similar role * Must provide a valid government-issued photo ID for verification; a driver's license is required if the role involves driving * Passing of all pre-employment requirements (MVR, Background Check, Drug Screen) The compensation and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, with or without notice, subject to applicable law. TAK 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, age, disability, genetic information, protected veteran status, or any other characteristic protected by law. We maintain full compliance with the Americans with Disabilities Act and are committed to providing equal access throughout our employment practices. Individuals with disabilities may request reasonable accommodations during the application and hiring process by contacting *****************************. Salary Description $16 - $20 per hour, DOE

**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.

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!

RESPONSIBILITIES: * Perform and/or assist with analytical testing of raw materials, in-process samples, and finished products. * Utilize analytical laboratory instrumentation with minimal 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. * Perform and/or assist with equipment calibrations and qualifications. * Other related duties as required. QUALIFICATIONS: * Bachelor's degree in chemistry or related discipline. * 2-5 years' experience in a pharmaceutical 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. 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.

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

Job Description Job Title: Quality Control Inspector Pay: $18.00 - $20.00 per hour We are seeking a detail-oriented Quality Control Inspector to ensure products meet quality standards and regulatory requirements in a fast-paced manufacturing environment. Responsibilities: Inspect raw materials, in-process, and finished products using calipers, micrometers, CMM, and vision systems Ensure compliance with ISO 9001, ISO 13485, CGMP, FDA, and HACCP standards Perform quality audits and document inspection results Analyze quality data and support corrective actions Collaborate with production teams to resolve quality issues Qualifications: Experience with precision measurement and inspection tools Knowledge of quality systems and manufacturing standards Strong attention to detail and documentation skills Apply today to help maintain high-quality, reliable products.

Eurofins Scientific is a network of independent companies providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. With over 50 laboratories and more than 40 service centers nationwide, Eurofins Environment Testing provides full-service environmental analysis across all 50 states. Our network supports public and private clients-including DoD, DOE, and municipalities-through robust logistics and continuous investment in people, technology, and infrastructure. We offer comprehensive testing for air, water, soil, sediment, tissue, and waste, covering a wide range of analytes including PFAS, metals, VOCs/SVOCs, dioxins/furans, radiochemicals, and more. Job Description Eurofins Environment Testing South Central is looking for a Laboratory Analyst for our Stafford, TX location. Responsibilities Include : Analyze samples from different matrix, to provide information on compounds or quantities of compounds present, according to EPA, ASTM and Standard Methods. Use analytical techniques and instrumentation, such as gas and high performance liquid chromatography (HPLC), ion chromatography, electrochromatography and spectroscopy. Document measurements of samples and Quality Control in logbooks interpret data and meet strict guidelines on documentation when recording data in the LIMS database. Calibrate instrumentation and other equipment. Maintain stock of laboratory chemicals and consumables. Report scientific results Develop techniques for the analysis of environmental samples Work collaboratively in cross-functional teams Other duties as assigned Qualifications Bachelor's degree in environmental science, chemistry, or related field. Proven analytical and mathematical skills Authorization to work in the United States indefinitely without restriction or sponsorship. Professional working proficiency in English is a requirement, including the ability to read, write and speak in English Additional Information This is a full-time position Monday to Friday 4 pm to 1 am with occasional overtime and weekends as needed. Training will be M-F 9 am to 6 pm. compensation: $20 - $25 / hour (DOE). Candidates within a commutable distance to Stafford, TX are encouraged to apply. Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. To learn more about Eurofins, please explore our website ****************** We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

**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.

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

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.

Pipe- Quality Control Inspector Inspector is responsible for ensuring the company is meeting the required specifications and tolerances in the manufacturing process by testing, measuring and validating products. Inspect goods during process and when they are finished. Verify calibration and working condition of measuring equipment against standards. Identify, mark, and segregate rejects and reworks. Test, measure, and validate products. Must operate heavy duty and standard forklift and overhead crane. Requirements and Qualifying skills: OCTG or Line Pipe Manufacturing environment; hot when weather is hot and cold when weather is cold. Working in greasy, dirty, noisy environment. Must have experience using micrometers, ovality and ultrasonic thickness gages. Must have basic arithmetic math skills and able to read measuring equipment. Must be able to push, pull and have good finger and hand dexterity with good hand-eye coordination. Good housekeeping; keeping work area orderly - materials, tool, and personal belongings. Clear and free of debris. Must be able to work (40-60 hours+) 6 AM to 6 PM Have reliable transportation to and from work. Basic computer skills Communication skills Bilingual (Spanish & English) (preferred)

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

BEYOND International Inc. is seeking a Lab Assistant / Chemical Technician to join our Chemical & Quality Department. This role is primarily focused on Quality Control and laboratory support, with opportunities to assist in R&D-related activities as experience grows. Key Responsibilities Primary Responsibilities (QC / Lab / Production - ~70%) Prepare samples for Quality Control testing Complete and maintain testing records, SOPs, test reports, and related documentation Inspect and track the stability of raw materials, in-process samples, and finished products Maintain laboratory and production instruments, including routine checks and basic maintenance Support raw material inventory management and monthly usage tracking Work safely and maintain a clean work area in accordance with standard lab and production practices Perform tasks that may require lifting up to 25 lbs and/or moving up to 50 lbs Secondary Responsibilities (R&D Support - ~30%) Assist the Lead Chemist and Chemical Engineer with new product research and development Support R&D sample preparation and stability tracking Conduct basic literature searches independently or as instructed Communicate effectively with internal teams and external vendors as needed Qualifications Required Legal authorization to work in the United States Minimum 1 year of chemical or laboratory-related experience Ability to reliably commute to Sugar Land, TX 77478 Proficiency in Microsoft Office (Word, Excel, Outlook) Ability to lift up to 25 lbs and/or move up to 50 lbs Preferred Degree in Chemistry or a related field Familiarity with ISO 13485 concepts (training will be provided) Experience in a production or laboratory environment Team-oriented, self-motivated, and flexible Ability to perform basic literature research independently Job Details Job Type: Full-time, on-site Schedule: 8-hour shift Pay: $15.00 - $18.00 per hour (based on experience) Work Location: Sugar Land, TX Benefits Health insurance Paid time off (PTO)