Quality control analyst jobs in Lawton, OK - 850 jobs

About Sorion Sorion is re-engineering how critical chemicals and materials are produced through a mechano-catalytic platform that replaces slow, high-energy, solvent-intensive steps with direct, high-efficiency solid-state processes. Our approach enables materials that are impractical to make by conventional means, unlocking entirely new possibilities for industry and the planet. If you want your work to become real products and help define the future of materials manufacturing, this is the place. Role description As R&D Engineering Technician at Sorion, you will build, operate, and maintain the hands-on infrastructure that enables rapid mechanochemistry R&D. You'll assemble custom milling systems, wire temperature-control rigs, execute high-quality experiments, and support the early build-out of our pilot plant. Your work will turn experimental ideas into reliable hardware and data-producing systems, directly increasing Sorion's scientific velocity and helping us scale from benchtop prototypes to production-ready unit operations. What you'll do Build and modify experimental equipment Assemble, wire, and validate modified ball milling systems, including integrating heaters, thermocouples, PID controllers, and motor drivers Build custom mechanical fixtures and enclosures (e.g. 80/20 aluminum framing + acrylic) Work with engineers to prototype and debug custom mechanochemical reactor systems Maintain and repair laboratory equipment to maximize uptime Execute experiments with reliability and precision Co-develop and refine SOPs with scientists and engineers to ensure efficient, high-quality experimental workflows Precisely and rigorously execute mechanochemical experiments including data collection Handle powders, reagents, and solvents safely and consistently Organize experimental materials, consumables, and records for efficiency and traceability Support pilot-scale unit operations Assist engineers during the build-out of Sorion's pilot line, contributing to rigging, wiring, troubleshooting, and validation Help bring new unit operations online and ensure they operate safely and as intended Shape culture and ways of working Maintain a clean, organized, safety-first workspace Collaborate across disciplines with low ego and high curiosity Play a critical role in defining Sorion's foundational culture as an early team member What you'll bring We're looking for a hands-on builder - whether you developed skills in industry, in school, or through personal projects. Ability to read and execute basic wiring diagrams for heaters, PID controllers, thermocouples, relays, and motor drivers Hands-on mechanical assembly expertise, including building rigs with 80/20, basic machining familiarity, and tool competence Proficiency in installing and using scientific equipment Ability to co-develop and follow SOPs with consistent execution Proficiency with spreadsheets for logging experimental data, tracking experimental data, and recording maintenance Safe handling practices for powders and solvents Ability to translate mechanical, chemical, and electrical requirements into actionable tasks when working with interdisciplinary team members Highly organized work style across both physical and digital environments Ability to thrive in an early-stage, high-ambiguity, fast-paced startup environment Low ego, high curiosity, and a relentlessly resourceful spirit Location On-site: Houston, TX Compensation Salary range: $80,000 - $110,000 per year USD At Sorion, we take care of our team with competitive pay, stock options, and great benefits so you can thrive at work and beyond. The salary range for this role is an estimate based on a wide range of compensation factors, inclusive of base salary only. Actual salary offer may vary based on (but not limited to) work experience, education and/or training, critical skills, and/or business considerations. Highly competitive equity grants are included in the majority of full time offers, and are considered part of Sorion's total compensation package. We cover 100% of health insurance premiums for full-time employees.

Mission: An Analyst primarily handles financial data and generates reports from data interpretation. They then share the results of the analysis with supervisor, who use it to make strategic changes and improvements. Is this for you? Here are some sp Controller, Analyst, Office, Business Services, Financial

Alutiiq Operations Services, LLC has an exciting opportunity for a Quality Control Technician supporting Tinker Air Force Base located in Oklahoma City, OK. The Quality Control Technician is responsible for keeping current on procedures, policies, in Control Technician, Quality Control, Technician, QC Manager, Quality Assurance, Equipment Maintenance, Manufacturing

About the job QC inspector QC inspectors must possess computer skills and be bilingual. (Pipe Yard) Responsibilities include inspecting incoming and outgoing materials, conducting cycle counts, and maintaining an updated inventory system. Loading and unloading tasks are also required. Qualification: Must have relevant experience. Package Details

QC Inspect I - Tulsa, OK . & Requirements: Previous Inspection experience is preferred, but not required. Education and Experience Requirements High School Diploma or GED required. 1 year quality inspection experience or 2 years GAC manufacturing experience required. 2 years manufacturing experience or equivalent aerospace experience preferred. Other Formal Inspection Training Program 90 Days required. Position Purpose: In a team oriented environment, perform all tasks in Initial Phase Manufacturing, Composites, Final Phase in a timely and efficient manner to ensure aircraft parts, sub-assemblies, major assemblies, and installations are built to type design data. Job Description Principle Duties and Responsibilities: Essential Functions: Perform inspection duties utilizing engineering drawings and orders, route cards, inspection travelers, work instructions, technical specifications, QA procedures and instructions, and other related documents. Perform preliminary and progressive inspections of aircraft structure and systems, verify functional operation, final inspections, inspect for FOD and verify paperwork. Witness, verify and document specified manufacturing process steps. Perform conformity/first article inspections to ensure compliance with FAA approved procedures. Ensure the proper use and storage of area tools and equipment. Conduct work in a manner that enhances own/other employees health and safety, product safety and promotes risk reduction; participate openly in safety-related event investigations, and immediately report workplace hazards and make suggestions for control; cooperate and contribute toward the overall success of the Safety program at the local level. Additional Functions: Provide technical support to manufacturing personnel. . Perform area inspections to ensure compliance with applicable standards and specifications. . Participate in continuous improvement activities. . Perform other duties as assigned Other Requirements: Working knowledge of shop mathematics, and CATIA or blueprint reading and interpretation. Competent in the use of basic shop tools and equipment. Aviation Personnel currently offers: .63 cents per mile up to $252.00 Travel Pay on your first check, Plus a $100.00 longevity Monthly bonus! Great benefits like: Holiday Pay, Vacation Pay, $250.00 referrals fees and FREE Direct Deposit. Cash Advances Available! Did you know Aviation Personnel GUARANTEES Highest pay package at every location we have openings? Please, give us a call @ 817-244-2125 We look forward to helping you find your next assignment; also please forward our information to your friends who might be interested as well.

Who We Are: Delta, founded in 1971, is a global provider of power and thermal management solutions. Its mission statement, "To provide innovative, clean and energy-efficient solutions for a better tomorrow," focuses on addressing key environmental issues such as global climate change. As an energy-saving solutions provider with core competencies in power electronics and automation, Delta's business categories include Power Electronics, Mobility, Automation, and Infrastructure. Delta, founded in 1971, is a global provider of power and thermal management solutions. Its mission statement, "To provide innovative, clean and energy-efficient solutions for a better tomorrow," focuses on addressing key environmental issues such as global climate change. As an energy-saving solutions provider with core competencies in power electronics and automation, Delta's business categories include Power Electronics, Mobility, Automation, and Infrastructure. Delta, founded in 1971, is a global provider of power and thermal management solutions. Its mission statement, "To provide innovative, clean and energy-efficient solutions for a better tomorrow," focuses on addressing key environmental issues such as global climate change. As an energy-saving solutions provider with core competencies in power electronics and automation, Delta's business categories include Power Electronics, Mobility, Automation, and Infrastructure. About the role: The Quality Control Inspector is responsible for inspecting sheet metal parts, welded assemblies, and finished products to ensure compliance with engineering drawings, welding standards, and customer requirements. This role supports the manufacturing team by identifying nonconformities, ensuring corrective actions, and maintaining product quality throughout fabrication and welding processes. Key responsibilities: Perform dimensional inspections of sheet metal components using calipers, micrometers, height gauges, and other precision measurement tools. Conduct visual and dimensional weld inspections per AWS D1.1, ISO, or equivalent welding standards. Verify weld quality, including size, length, penetration, porosity, cracks, undercut, and overall workmanship. Review and interpret engineering drawings, specifications, and weld symbols to ensure product conformity. Perform in-process inspections during sheet metal fabrication (cutting, bending, stamping, drilling, assembly, etc.). Inspect surface finishes, powder coating/painting, and other secondary processes Document inspection results, prepare quality reports, and maintain records. Support root cause analysis and corrective/preventive actions (CAPA) Collaborate with production and engineering teams to resolve quality issues. Ensure inspection tools and gauges are calibrated and properly maintained. Follow all company safety, ISO 9001, and quality system procedures. Minium Qualifications: High school diploma or technical certification required, associate degree in a technical field preferred. 2+ years of experience in quality inspection within a sheet metal fabrication or welding environment. Experience with precision measurement tools (calipers, micrometers, height gauges, CMM experience a plus). Strong attention to detail and ability to work independently. Good communication and documentation skills. Preferred Qualifications: Strong knowledge of welding processes (MIG, TIG, spot welding) and common weld defects. Ability to read and interpret engineering drawings, GD&T, and weld symbols. Familiarity with AWS D1.1 or similar welding standards; welding inspection certification (CWI, WI) preferred. Understanding of ISO 9001 quality systems; IATF knowledge a plus. Benefit at Delta Electronics Americas: Life at Delta EEO Statement: Delta Electronics Americas is an Equal Opportunity Employer and is committed to compliance with all applicable federal, state, and local laws. Delta Electronics America is committed to fostering a diverse, inclusive, and respectful workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, age, marital status, national origin, disability, veteran status, or any other protected characteristic. The base salary range for this full-time position is 45k-55k per year. Actual pay will depend on factors such as location, skills, experience, market conditions, and business needs. This role may also be eligible for incentive pay, subject to the terms of the applicable plan. Eligible employees receive company-provided benefits in accordance with plan terms and eligibility requirements. Benefits include health coverage, wellness resources, retirement savings plan, paid time off, and other company‑sponsored programs; parental leave is provided in accordance with applicable law. About the role: The Quality Control Inspector is responsible for inspecting sheet metal parts, welded assemblies, and finished products to ensure compliance with engineering drawings, welding standards, and customer requirements. This role supports the manufacturing team by identifying nonconformities, ensuring corrective actions, and maintaining product quality throughout fabrication and welding processes. Key responsibilities: Perform dimensional inspections of sheet metal components using calipers, micrometers, height gauges, and other precision measurement tools. Conduct visual and dimensional weld inspections per AWS D1.1, ISO, or equivalent welding standards. Verify weld quality, including size, length, penetration, porosity, cracks, undercut, and overall workmanship. Review and interpret engineering drawings, specifications, and weld symbols to ensure product conformity. Perform in-process inspections during sheet metal fabrication (cutting, bending, stamping, drilling, assembly, etc.). Inspect surface finishes, powder coating/painting, and other secondary processes Document inspection results, prepare quality reports, and maintain records. Support root cause analysis and corrective/preventive actions (CAPA) Collaborate with production and engineering teams to resolve quality issues. Ensure inspection tools and gauges are calibrated and properly maintained. Follow all company safety, ISO 9001, and quality system procedures. Minium Qualifications: High school diploma or technical certification required, associate degree in a technical field preferred. 2+ years of experience in quality inspection within a sheet metal fabrication or welding environment. Experience with precision measurement tools (calipers, micrometers, height gauges, CMM experience a plus). Strong attention to detail and ability to work independently. Good communication and documentation skills. Preferred Qualifications: Strong knowledge of welding processes (MIG, TIG, spot welding) and common weld defects. Ability to read and interpret engineering drawings, GD&T, and weld symbols. Familiarity with AWS D1.1 or similar welding standards; welding inspection certification (CWI, WI) preferred. Understanding of ISO 9001 quality systems; IATF knowledge a plus. Benefit at Delta Electronics Americas: Life at Delta EEO Statement: Delta Electronics Americas is an Equal Opportunity Employer and is committed to compliance with all applicable federal, state, and local laws. Delta Electronics America is committed to fostering a diverse, inclusive, and respectful workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, age, marital status, national origin, disability, veteran status, or any other protected characteristic. The base salary range for this full-time position is 45k-55k per year. Actual pay will depend on factors such as location, skills, experience, market conditions, and business needs. This role may also be eligible for incentive pay, subject to the terms of the applicable plan. Eligible employees receive company-provided benefits in accordance with plan terms and eligibility requirements. Benefits include health coverage, wellness resources, retirement savings plan, paid time off, and other company‑sponsored programs; parental leave is provided in accordance with applicable law.

Job Posting Start Date 01-22-2026 Job Posting End DateFlex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world.A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but don't meet every bullet point, we encourage you to apply and join us to create the extraordinary.Job Summary To support our extraordinary teams who build great products and contribute to our growth, we're looking to add a Quality Lab Analyst located in Austin, TX. Reporting to the Quality Manager, the Quality Lab Analyst role will support medical device process confirmation testing in a FDA 21 CFR Part 820 & ISO 9001 regulated laboratory. This role is hands-on and focused on laboratory testing, data integrity, and documentation, ensuring accurate and timely support for product release. SHIFT G- 6am-6pm Th, Fri, Sat every other Wed What a typical day looks like: Perform routine and non-routine laboratory testing following approved SOPs and protocols. Prepare buffers, solutions, and test materials for PCT activities. Execute customer-defined test designs and accurately record lab results. Generate and maintain electronic and paper-based lab documentation in compliance with GDP. Operate laboratory equipment (precision balances, small volumes, vacuum systems, YSI). Support lab investigations (OOS/OOT), CAPAs, and audit readiness. Maintain lab readiness, inventory control, 5S, and GMP conditions. Collaborate with cross-functional teams and support continuous improvement initiatives. Adhere to EHS and Safety-First standards. The experience we're looking to add to our team: Bachelor's degree in Chemistry or related field. 2+ years of laboratory experience, preferably in medical or regulated environments. Strong attention to detail and experience with lab documentation systems (electronic and paper-based documentation systems) Comfortable working with small volumes, precise measurements, and lab equipment. What you'll receive for the great work you provide: Full range of medical, dental, and vision plans Life Insurance Short-term and Long-term Disability Matching 401(k) Contributions Vacation and Paid Sick Time Tuition Reimbursement Job CategoryQuality Is Sponsorship Available? NoFlex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. We're happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex.com and we'll discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

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

Research & Development - Method Development / Method Validation Chemist Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry and is the most respected name in our industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer. The position requires the performance of variety of task including development and validation of analytical method, work with HPLC (High Performance Liquid Chromatography), manage a variety of research projects, and qualitatively/quantitatively testing client samples. This position requires knowledge of commonly used concepts, practices, procedures, and instrumentation used in a chemistry laboratory. Research Scientist II manages projects with some supervision and reports to the lab supervisor. The Research Scientist II must be able to think and work independently, yet share ideas and work toward team goals. The ability to express thoughts in a clear concise manner both orally and written is also expected. Works to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities. Some highlights.. Attractive Relocation Package available! Great Benefits Excellent Work/Life Balance Fantastic work environment 100% Company-paid Medical and Dental Insurance 401K Retirement with Company Match This is a full-time role Work Schedule: Days and hours of work are Monday through Friday, 8:30 a.m. to 5 p.m. Flexible hours such as early, late and weekend shift may be required. Work Restrictions: Because of vital nature of this work, we do not allow medical marijuana cards and we do random drug testing on all of our employees. Essential Functions... Qualitatively and quantitatively test of client samples. Development and validation of analytical methods. Manage research projects and coordinate project related works between different departments of ARL. Write research protocol, project report and working instruction. Communication with client regarding the project/sample test status. Use HPLC, IC and LCMSMS. Position Requirements... A BS in chemistry or related science with 4+ years industrial experience in MDMV Chemistry in the bio-technology and/or Pharmaceutical space. PhD in chemistry with 4+ years industrial experience in MDMV Chemistry in the bio-technology and/or Pharmaceutical space preferred. or related science with 0-2 years industrial experience Communication Proficiency. Work Environment... This job operates in a laboratory environment. Physical Demands... This position often requires standing for prolong periods of time; dexterity in fingers and hands to perform complex and precise manipulations; ability to walk and stood; ability to lift and move up to 50 lbs; see in the normal visual range including the ability to distinguish colors and shades and hear in the normal audio range with or without correction. AAP/EEO Statement ARL Bio Pharma, Inc. provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law. ARL Bio Pharma, Inc. expressly prohibits any form of workplace harassment based on race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law. Improper interference with the ability of ARL Bio Pharma, Inc. employees to perform their job duties may result in discipline up to and including discharge. Further, the company takes affirmative action to ensure that applicants and employees are treated without regard to any of these characteristics.

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 - 5:30 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: Training Coordination and Collaboration Coordinate and manage team training activities in partnership with crossfunctional team members. Oversee the Quality Control training program to ensure all required training is scheduled, tracked, and completed. Organize, maintain, and archive training documentation in compliance with internal and external requirements. Support the design, development, and implementation of training curriculum to enhance team competency and performance. Testing and Analysis Perform routine and nonroutine testing on products and materials to verify compliance with established specifications and standards. Analyze complex data sets, identify trends and deviations, and take initiative to investigate and troubleshoot issues. Cross Functional Collaboration Collaborate with team members to manage purchasing, receiving, formulation, testing, and release of materials and reagents. Support equipment and assay qualification activities, including validation and periodic review. Quality Records Management Lead the creation, management, and closure of quality records, including GxP deviations, laboratory investigations, OOS/OOE events, CAPAs, and change controls. Documentation Author, revise, and conduct periodic reviews of procedures and controlled documents. Document all activities in accordance with cGMP/GxP standards, regulatory requirements, and internal procedures. Maintain data integrity and complete accurate equipment logs and records. Equipment Management Perform and oversee routine maintenance, calibration, and qualification of laboratory equipment to ensure operational readiness. Compliance Participate in developing and maintaining Quality Control systems to ensure alignment with regulatory and industry standards. Ensure all work practices meet regulatory, corporate, and departmental compliance requirements. Safety Consistently demonstrate safe laboratory practices and promote a strong safety culture within the team. Secondary Functions: Transport controlled documents, QA-released QC materials and human biological samples. Assist with tasks scheduling Maintain knowledge of internal procedures and current regulatory requirements Required Experience and Education: BA or BS in any science-related field Four (4) years of experience in a regulated laboratory environment MS degree or specialized skill set may substitute for 1 year Experience performing QC activity in a related field. Experience developing training material for GxP Quality Control processes. Preferred Experience and Education: MS in Biology, Biological Sciences, Laboratory Science, Biochemistry, or Biomedical Science/Engineering Five (5) years of experience in a regulated laboratory environment Laboratory skills include a few of the following: visual inspection, flow cytometry and cell counting. Molecular and cell-based assays. Qualification/Validation activities Technical writing and troubleshooting/investigational skills. Knowledge of cGMP/ICH/EU regulations and requirements. Experience with LIMS. 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.

**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!

Job DescriptionSalary: Quality Control Chemist About Rowe Casa: From the beginning, Rowe Casa Organics has been on mission to provide safe, natural, and non-toxic products that you can trust. In 2017, sisters Jill and Alicia embarked on a mission seeking greater health and wellness for their families. Frustrated by the lack of transparency and truly safe, effective options, Jill Rowe took matters into her own hands by making our very first product, Elderberry Immune Support. Today, Rowe Casa Organics produces over 300 products to help people thrive in their health, wellness, and lifestyle. From wellness necessities and household essentials to the finest of self-care, each product that we offer is crafted with the utmost quality, care, and love. About the Position: The Quality Control Chemist will be part of the Quality Department reporting to the QC Manager or designee. This position will be responsible of the analytical laboratory for testing samples of RCO products across all manufacturing facilities and logistics. Duties/Responsibilities: Perform laboratory analysis on all materials and samples. Perform tests on component samples, identify any contamination, conduct an analysis and initiate corrective measures. Perform tests on all incoming ingredients and document all records. Develop and prepare research papers and documents for all protocols. Perform audits on various environmental programs and perform reviews. Develop various testing processes for all raw materials and equipment. Monitor all finished products. Investigate all issues and prevent any GMP problems on samples. Maintain accurate records and perform tests on all activities conducted in the laboratory. Develop and document various analytical laboratory processes and prepare final reports. Any other duties and responsibilities required by Quality Management. Required Skills/Abilities: Bachelors degree (or equivalent) in chemistry, biochemistry, or another relevant field. Ability to plan and execute experimental protocols. Knowledge of laboratory tests, IR, UV, HPLC, etc. Proficient in methods and practices of microbiological analysis. Ability to prepare research papers and technical reports (is a plus). Analytical thinker with strong conceptual and research skills. Previous experience in a cGMP facility is a plus. Excellent laboratory skills. Ability to compile information Ability to work under pressure Excellent organizational skills and attention to detail Positive attitude Ability to adapt Physical Requirements: Prolonged periods sitting at a desk and working on a computer Must be able to lift up to 50 pounds at times Rowe Casa Organics is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, national origin, age, disability, or any other legally protected status.

Barcel USA takes pride in our people-centric culture - We Value the Person is our Core Belief. In addition to competitive pay and comprehensive benefits, we are committed to providing a safe and inclusive work environment that appreciates all dimensions of diversity, promotes personal and professional development opportunities and allows our associates to be their authentic selves. The Quality Control Operator ensures the products meet their respective specifications and quality standards by performing physicochemical analyzes, measurement testing, and monitoring steps of the production process. Responsibilities: - Product sampling and quality monitoring. * Physicochemical analysis of food products. * Measurement testing, such as finished product weight and oxygen level. * Critical Control Point (CCP) monitoring. * Maintenance of quality control records. * Compliance with the QA laboratory procedures. * Compliance with Good Manufacturing Practices (GMP), and Quality & Food Safety guidelines. * Support the 5S program in the manufacturing facility, keeping working areas, utensils, and equipment clean and organized. * Compliance with company safety rules and procedures, providing support to eliminate any unsafe conditions. * Support to all quality shifts, as needed. * Any other duties assigned by the management. Qualifications Qualifications: * Demonstrate strong communication and teamwork skills, consistently applying Grupo Bimbo's Golden Rule of Respect, Fairness, Trust, and Care in all interactions. * Ability to read and interpret pick lists and order documentation. * Strong attention to detail and accuracy. * Ability to work efficiently in a fast-paced environment. * Ability to lift and move items of varying weights. * Basic understanding of warehouse operations and inventory management. * Ability to follow safety guidelines and procedures. * Reliable and punctual with a strong work ethic. Physical Requirements: * Ability to stand and walk for extended periods. * Ability to lift and carry items up to 50 pounds. * Ability to bend, stoop, and reach as needed. * Ability to work in a warehouse environment with varying temperatures. Barcel USA LLC is an equal opportunity employer with a policy that provides equal employment opportunity for applicants and employees regardless of race, color, religion, disability, gender, age, national origin, sexual orientation, gender identity, marital status, pregnancy, veteran status, or any other classification protected by law. This policy applies to all aspects of employment, including recruitment, hiring, promotion, compensation, reassignment, layoff, discharge, education, training, and all other working conditions. We believe diversity drives innovation and success. We proudly welcome applications from individuals with disabilities, veterans, and women, and are committed to creating an environment where everyone can thrive.

Full-time Description At SPL, the work you do matters. Our teams provide trusted energy and environmental testing and measurement solutions that protect communities, support critical infrastructure, and safeguard the environment. With a nationwide footprint and opportunities for growth across multiple locations and disciplines, SPL is a place where you can build a career while making a real-world impact. We're searching for a motivated Laboratory Analyst I to join our night shift laboratory team in Midland, TX. In this role, you'll be actively engaged in daily laboratory operations, supporting critical testing through sample preparation, analytical testing, and accurate documentation within the Laboratory Information Management System (LIMS). You'll work hands-on with laboratory instrumentation, contribute to quality and compliance initiatives, and help maintain a safe, efficient, and well-organized laboratory environment. This position offers the opportunity to strengthen technical expertise, collaborate with an experienced team, and directly contribute to reliable, high-quality results that support essential laboratory operations. Please note: This is a full-time, onsite position following a Monday - Friday schedule from 3 PM to 12 AM CST. What You'll Do Perform sample preparation, analytical testing, and data entry in accordance with approved methods, SOPs, and quality standards Operate and maintain laboratory instruments, performing routine calibration, troubleshooting, and preventative maintenance Accurately document and review results within the Laboratory Information Management System (LIMS) or designated systems Support the laboratory's quality system by following Good Laboratory Practices (GLP), assisting with audits, corrective actions, and continuous improvement initiatives Adhere to safety and compliance protocols to maintain a safe and efficient laboratory environment Assist with general laboratory housekeeping, inventory management, and cross-training as needed Perform other duties as assigned Requirements What We're Looking For Associate's or Bachelor's Degree in Science or related area; equivalent experience may be considered in lieu of degree Professional laboratory experience strongly preferred, including hands-on use of laboratory instrumentation, standardized analytical methods, and analytical data interpretation Proficiency with Microsoft Office tools (Word, Excel, Outlook) and Adobe Acrobat Strong analytical, organizational, and problem-solving skills, with a high level of attention to detail Ability to manage multiple priorities and meet deadlines in a fast-paced setting What We Offer Competitive compensation Medical, dental, and vision coverage 401(k) with company match Employer-paid life, AD&D, and disability insurance Paid time off, sick leave, and paid holidays Paid parental leave Employee Assistance Program (EAP) Tuition reimbursement and professional development support Work Schedule & Travel Full-time, onsite position following a Monday - Friday schedule from 3 PM to 12 AM CST Flexibility to work beyond standard hours, including evenings and rotating weekends, as operational needs require Our Commitment to Diversity & Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future.

is Monday - Friday 4:00 AM - 1:00 PM Responsibilities: The Quality Analytical Chemist is an important role in Fruit of the Earth's continued success. This position requires time management skills. Attention to detail and strong analytical methods are required. Professionalism, flexibility, dependability and fast turn around are skills necessary for the day-to-day success of this position. Key Responsibilities: Oversee the development and validation of analytical methods. Ability to troubleshoot analytical instrumentation. Performs routine QC testing such as IR, viscosity, specific gravity, pH, titrations, and various wet chemistry. Responsible for calibration and validation of laboratory equipment and standards. Responsible for analysis of raw materials, in-process bulk, finished products, stability samples, and validation samples with minimal supervision. Monitors laboratory consumables and assist in removing expired reagents/test solutions. Insure proper training of laboratory technicians. Ensure all documentation forms are properly filled out and signed/dated. Follow required protocols, practices and SOPs. Conducting laboratory investigations for Out of Specification (OOS) results. Demonstrate a flexible approach to providing coverage for analytical testing as considered necessary by supervisor. Assist laboratory management in writing and revising SOPs, test methods and analytical specifications. Performs other duties and responsibilities as assigned by supervisor. Qualifications Necessary Qualifications: Four-year college degree in Chemistry or related field required. Minimum of 2-5 years of laboratory experience. Thorough knowledge and hands-on experience with HPLC, FTIR, UV/Visible Spectrophotometer and wet chemistry techniques. Knowledge of cGMP, cGLP, OSHA, TDOH and FDA rules and regulations. Strong understanding of quality control processes. Strong organizational, interpersonal, written and oral communication skills. Ability to meet and monitor deadlines and prioritize work. Self-motivated and detail oriented. Strong computer skills including Microsoft Office Suite. Flexible ability to take on additional tasks as needed. Additional Preferred Qualifications: Experience with TOC Analyzers. Able to develop and validate analytical methods. Experience with process validation testing. Experience with Empower software.

NIGHT SHIFT: Monday - Friday 8pm - 4:30am PathAdvantage Laboratory specializes in Gynecologic Anatomic and Clinical Pathology laboratory testing and services. We are looking for a motivated and energetic Molecular and Microbiology Technologist to join our team! This is an exceptional opportunity for an individual that is interested in becoming an integral part of a company with an outstanding reputation in DFW as well as having a friendly and cooperative spirit within the Clinical Laboratory. Candidates for this position should be talented, ambitious, discrete and show attention to detail, continuously striving to improve their professional careers as well as help the company grow. Molecular and Microbiology Laboratory Technologist Responsibilities: Under the general supervision of the Lab Manager, independently performs complex molecular-based procedures and analyzes results with a high degree of quality and in accordance with established laboratory protocols Perform routine quality control, calibration and maintenance in accordance with established laboratory protocols Operate complex equipment and computer programs related to the LIS system Record, analyze, and interpret test results; promptly report abnormalities Maintain a neat and clean work environment Participate in troubleshooting of Quality Controls and instrument failures Prioritize tasks to meet turnaround times Perform other miscellaneous job-related duties delegated by the Laboratory Manager Qualifications Molecular and Microbiology Technologist Requirements: Bachelor's degree from an accredited college or university in Medical Technology or related area of specialty with at least 1 year of clinical lab experience High level of attention to detail along with strong communication and organizational skills desired Outstanding Compensation Package and Benefits: Compensation commensurate with experience Health Insurance Dental Insurance Life Insurance Vision Insurance (Voluntary)

Arlington Regular MERIEUX NUTRISCIENCES As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years. If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us! YOUR DAY TO DAY LIFE We are looking for a Microbiology Lab Technician in 330 Westway Place, Suite 400, Arlington, TX 76018 USA. Your mission will be to: Main activities: ● Prepare sample for analysis by recording, weighing, and blending ● Write identification onto plates so that client and sample number can be tracked ● Pipette sample solution into tubes or plates according to the analysis process being performed ● Pour the agar into plates or tubes to begin the growth process ● Collect plates and place them in the incubator for the specified amount of time and temperature ● Prepare media and broth for use in pathogen testing as required ● Ensure that media and materials are prepared for the next testing sequence ● Maintain knowledge of Laboratory Information Management System (LIMS) that is required to complete job responsibilities ● Set up equipment and materials needed for analysis ● Read plates and tubes, as required, to determine the number of organisms in the sample ● Support corporate quality and continuous improvement process ● Perform necessary housekeeping duties in a timely manner, keeping the work areas and equipment clean and sanitized ● Must participate in cleaning schedule and maintain retain samples as required ● Adhere to all safety policies ● Responsibility to support laboratory management in the implementation maintenance, and improvement of the management system ● Perform other related tasks as needed YOUR PROFILE Knowledge: Profile (required education/qualification and professional background): Associates degree or equivalent work experience and 1+ year relevant work,. The incumbent must have a basic knowledge of science to accurately perform testing procedures and obtain accurate results. A basic knowledge of personal computers is useful to accurately enter testing data and results. A basic knowledge of laboratory safety procedures and policies is necessary to ensure a safe working environment. Planning skills are useful to maintain supplies of analysis materials and ensure analysis is completed within specified time. Required skills: Time management skills, ability to prioritize samples and tasks in a fast-paced environment. Attention to detail. Analytical skills are essential to complete analysis procedures and determine the concentration of the microorganism. A general knowledge of the Laboratory Information Management System is required to process client data. Physical dexterity is required for manipulating samples. Work Environment: The incumbent works in a laboratory setting with proper lighting and temperature control. Occasional exposure to laboratory fumes, chemicals, and materials will occur when in the laboratory. Safety equipment of gloves, laboratory coat and eyeglasses may need to be worn depending on the testing process. The incumbent may use the autoclave daily to complete the analysis process. Continuous lifting of analysis materials weighing up to 50 pounds are necessary to transport media materials. The incumbent can expect extended time spent in a standing position. The incumbent should be able to detect slight variation in shades of colors. Schedule: Tuesday thru Saturday, 12:30 - 9pm Full Time Eligible Benefits Overview: Comprehensive medical, dental, and vision insurance plans. Generous paid time off (PTO) package to support work-life balance following state and local ordinances. Optional 401(k) plan with employer matching contributions. The information above provides a general overview and may vary based on specific job responsibilities, location, or other factors. Details will be clarified during the hiring process. Pay: $17 - $18.50/hr WHY JOIN US? * Because you would contribute to an inspiring Public Health purpose, supported by long-term and visionary shareholders. * Because you would have an impact on our strategic pillars that build on 50 years of experience and expertise. * Because you would be part of a community of an enthusiastic and skilled group of people who love co-building together and serving a purpose bigger than them. * Because you would be welcome as you are, in a diverse and open-minded environment that is rich in our singularities and differences. * Because you would grow in an international group of more than 8200 fantastic team members, with plenty of opportunities to learn and share. Ready for the journey? To apply please click on 'Apply now' button