Quality control analyst jobs in Texas - 686 jobs

The CBP Aircraft Quality Control Inspector is responsible for ensuring that assigned aircraft are maintained within required specifications of 14 CFR Parts 43, 91 and 125 and other FAA and DOD regulations, OEM instructions and CBP directives as required and are airworthy before operation. Principal Accountabilities: * Inspect the work of Aircraft Mechanics performing maintenance repairs and modifies aircraft structures, aircraft engines, electrical, avionics and aircraft sub-systems. * Apply technical knowledge and expertise in determining proper equipment installation and operation. * Apply comprehensive technical expertise to assist the maintenance department to solve complex problems by interpreting technical documentation such as; blueprints or manufactures' manuals. * Make entries in aircraft logs and records and is responsible for providing guidance and technical expertise to lower level technicians throughout all aircraft modifications and/or maintenance efforts. * Perform the receiving, in-process, final quality, flight safety inspections and functional operational tests during organizational, intermediate and depot level maintenance, modification and repair of military tactical aircraft systems or associated components. * Approve or reject work accomplished by field team members to ensure compliance with customer specifications, standards and technical data. * Review and approve locally developed procedures and solutions to complex repair situations. * Perform analysis of defects and interprets quality control rejection and failure trends. * Monitor safety, training, and certification requirements. * Using checklists, perform daily work site Safety Inspections and Foreign Object Damage Inspections. * Monitor tool control programs, inspects and maintains records to ensure that measuring and test equipment meets calibration requirements. * Maintain Quality, Safety, Training and Certification Records. * Coordinate with the Customer Quality Assurance Representative concerning quality matters, mandatory inspection points and final acceptance inspection of contract end items or services. * Inspect forms and records related to aircraft maintenance. * The inspector monitors' the maintenance departments program, such as but not limited to, engine oil consumption, logs and records processes, hydraulic contamination, NDI, electrical static discharge, employee certification programs, confined space entry, tool control, foreign object damage, material control receiving inspections, weight and balance, fall protection and safety programs. * The inspector assists in the development and maintenance of ground and flight operation standard operating procedures, quality plan and safety plans. Assists maintenance in briefing and debriefing functional check flights. * Possess knowledge of basic computer skills sufficient to use Government computer system to access various technical references for airframe repairs and Government training requirements. * Document maintenance as per Quality Assurance (QA) and established regulatory requirements. * Comply with work order timekeeping system procedures. * Maintain high state of cleanliness and utilize a clean-as-you-go process when executing maintenance duties. * Perform weekly Foreign Object Damage (FOD) walk-downs. * Maintain situational awareness, stay cognitive-focused, and mitigate risks. * Comply with processes and procedures as per DHS/DOD documents and publications. * Immediately report missing, lost, found, or unattended tools to the supervisor. Maintain and control tools IAW tool control policy and instructions. Inventory and inspect tools on a regular basis to identify when to replace worn or broken tools and report the need for replacement tools to the supervisor. * Clean work area as necessary, assuring all hazardous materials are properly stored; Handle hazardous materials, expired materials and wastes in accordance with applicable laws and regulatory requirements. * Comply with safety rules and procedures and perform work in a manner that enhances the safety of the work area. Promptly report accidents, injuries, safety, violations, and/or unsafe practices or procedures to supervisor. * Perform weekly break room and smoking area cleaning duties. * Perform other duties as assigned. Minimum Requirements: * Must be able to obtain and maintain a CBP Background Investigation Suitability clearance. Note: US Citizenship is required to obtain a CBP Background Investigation Suitability clearance. * High School Diploma or equivalent is required. * Five (5) years of experience in rotary wing aircraft. * Valid Airframe and Power Plant (A&P) License required. * Valid FAA Inspection Authorization (IA) required. * Ability to obtain a Government flight line driver's license. * Possess a valid United States driver's license. * Possess the experience and ability to provide technical support to structural/mechanical engineers and customers alike, must possess excellent organizational skills in prioritizing workload to meet aircraft delivery schedule. * Ability to read and interpret data is required. * Ability to read, write, speak and understand English. Physical Requirements/Working Environment: * Capable of performing tasks that frequently require: lifting, reaching, bending, walking, pulling, sitting, standing, crouching, stooping, kneeling, and stretching for prolonged periods of time. * Must be capable of performing tasks in cramped, awkward, and strained positions and/or climbing up and down ladders, work platforms, scaffolding, and aircraft structures. * Must be capable of carrying items up to 40 pounds or, for heavier objects, must seek assistance of other workers or weightlifting devices. * Must be capable of wearing cumbersome personal protective equipment for HAZMAT operations. * May be required to work night shifts. * May work in Aircraft maintenance hangar or outside. * Some domestic travel may be required. Amentum is proud to be an Equal Opportunity Employer. Our hiring practices provide equal opportunity for employment without regard to race, sex, sexual orientation, pregnancy (including pregnancy, childbirth, breastfeeding, or medical conditions related to pregnancy, childbirth, or breastfeeding), age, ancestry, United States military or veteran status, color, religion, creed, marital or domestic partner status, medical condition, genetic information, national origin, citizenship status, low-income status, or mental or physical disability so long as the essential functions of the job can be performed with or without reasonable accommodation, or any other protected category under federal, state, or local law. Learn more about your rights under Federal laws and supplemental language at Labor Laws Posters.

Fabricate, repair, and maintain various tools, dies, and fixtures used in the manufacturing process Interpret engineering drawings, blueprints, and specifications to create precise tooling components Operate manual machining equipment, such as lathes, milling machines, and grinders Perform inspections and quality checks to ensure compliance with specifications and standards Assist with aircraft structures III work, including assembly, installation, and repair tasks as needed 5 + years of experience as a Machinists or Tool Maker 5 + years of experience operating manual mill and manual lathe machines 5 + years of experience reading and understanding engineering drawings, blueprints, schematics, and specifications 5 + years of experience working with precision measuring tools Knowledge of aircraft structures III and related processes

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 Title Construction SSHO/QC Education Bachelor's Degree or Equivalent Career Level Experienced (Non-Manager) Category Construction Salary Grade Date Needed By Job Type Full-time Travel Job Description Site Safety and Health Officer/Quality Control (SSHO/QC) The SSHO/QC is responsible for managing the daily QC responsibilities of specific projects to ensure the project is constructed in accordance with the established standards. The role will include direct oversight and review of the entire project from design to completion. The CQCM will work closely with project managers, construction superintendents, the client's representative on site, and other key personnel. This position also has the overall responsibility to implement safety, health and environmental programs and procedures within the worksite in pursuit of a zero-incident culture. Maintain best practices designed to enhance and improve regulatory compliance, as well as minimize industrial injuries/illness, workers' compensation costs, property damage and other general liability losses. Responsibilities Participate in the Post Award Kick-off, Partnering, Preconstruction, Design Development, and Coordination and Mutual Understanding Meetings. Implement the "Three Phase of Control" plan. Ensure that no construction begins before the DOR has finalized the design for that segment of work, and construction submittals are approved as required. Inspect all work and rework, using International Conference of Building Officials certified QC specialists as applicable, to ensure its compliance with contract requirements. Maintain a rework log. Immediately stop any segment of work, which does not comply with the contract requirements and direct the removal and replacement of any defective work. Prepare daily QC reports. Ensure that Contractor Production Reports are prepared daily and align with the daily QC reports. Hold weekly QC meetings with the Commissioning Authority, DOR (or representative), Superintendent and the Contracting Officer/CE on site; participation shall be suitable for the phase of work. Ensure that design and construction submittals are reviewed and approved, as required by the contract, prior to allowing material on site and work to proceed with these items Maintain a submittal register Update As-built drawing daily, maintaining up-to-date set on site. Maintain a testing plan and log. Certify and sign statement on each invoice that all work to be paid under the invoice has been completed in accordance with contract requirements. Perform punch-out and participate in Pre-final and Final Acceptance Inspections. Submit list of deficiencies to the Contracting Officer for each inspection. Correct all deficiencies prior to the Final inspection. Notify Contracting Officer prior to final inspection to establish a schedule a date acceptable by the Contracting Officer. Ensure that all required key, operation and maintenance manuals, warranty certificates, and the As-built drawings are correct and complete, in accordance with the contract, and submitted to the Contracting Officer. Assure that all applicable tests special inspections, and observations required by the contract are performed. Coordinate all factory and on-site testing, Testing Laboratory personnel, QC Specialists, and any other inspection and testing personnel required by this Contract. Notify the Contracting Officer of any proposed changes to the QC plan. Retain a copy of approved submittals at project site, including Contractor's copy of approved samples. Update the Performance Assessment Plan as described in the UFGS section 01 31 19.05 20 POST AWARD MEETINGS and discuss monthly at QC meeting. Coordinate training of Government maintenance personnel with the eOMSI Preparer to assure training materials and training classes are accurate and provide instruction and documentation on critical elements of the products, materials, and systems in the constructed facility. Create and implement the requirements of the Health and Safety Plan (HASP or APP Accident Prevention Plan) Evaluate personnel performing tasks Determine that all personnel are properly trained, qualified, equipped, and physically protected from the site and operational hazards. Effectively implement LPS's site specific safety and health program Initiate and authorize a "Stop Work" order for any imminent S&H concerns; Lead daily safety meetings Conduct and document site training related to site-specific hazards Specify proper levels of PPE, per the requirements of the HASP In conjunction with the Site Supervisor, investigate and report in a timely manner any injuries, illnesses, accidents, incidents, or near misses, and ensure that proper procedures are followed through the investigation Conduct visitor orientation, daily safety inspections, and weekly safety audits. Properly complete the requisite safety and health related forms to capture required safety and health data. Provide the Site Supervisor with task hazard data for any new tasks or any tasks that significantly change during the conduct of site operations Assess each task and assess the effective implementation of the safety and health provisions required by the HASP Skills and Qualifications Bachelor's Degree in Engineering, architecture, or construction management and 5 years QCM experience on USACE, NAVFAC, DoE, or DoD projects (10 years' experience as QCM will be considered in lieu of education). Complete the course entitled "Construction Quality Management (CQM) for Contractors" and maintain a current certificate. Familiar with requirements of USACE EM 385-1-1, and experience in the areas of Activity Hazard Analysis (AHA), Accident Prevention Plans (APP) and safety compliance. 3-5 years of experience as a SSHO to include industrial, construction safety, and environmental protection. 30 Hr. Construction Safety Course with required yearly professional development hours CPR/FA training Understanding of FAR/DFAR requirements. Must possess and retain a valid driver's license Must be able to acquire and retain valid base access (if applicable) Must be able to pass a Federal Background Check Supervisory Responsibilities none Classification This is a full-time exempt position that reports to the Project Manager. Physical Demands Individuals must have the ability to lift 30 pounds. Must be able to remain in a stationary position at least 50% of workday and capability to move within the field. Any person in this position needs the ability to operate any field equipment used within the Construction Industry. There is a requirement to traverse multiple terrain types in outdoor weather conditions along with the ability to position self in a stoop, kneel, or crouch position. Individuals must be able to wear full construction PPE and have ability to enter confined spaces. # of Hires Needed 1 Exemption Type Exempt

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required Pratt & Whitney is working to once again transform the future of flight-designing, building and servicing engines unlike any the world has ever seen. And because transformation begins from within, we're seeking the people to drive it. So, calling all curious. Come ready to explore and you'll find a place where your talent takes flight-beyond the borders of title, a country or your comfort zone. Bring your passion and commitment and we'll welcome you into a tight-knit team that takes our mission personally. Channel your drive to make a difference into shaping an organization and an industry that's evolving fast to the future. At Pratt & Whitney, the difference you make is on display every day. Just look up. Are you ready to go beyond? What is my role type? In addition to transforming the future of flight, we are also transforming how and where we work. We've introduced role types to help you understand how you will operate in our blended work environment. We have an opportunity for a Quality Technical Team Member to be based in Columbus, GA. (onsite role) What You Will Do: Records for Blades and Disks: Input and store Columbus Forge LPA records. Maintain inventory and storage of Level 4 documentation records for Columbus Operations. Log and ballot Columbus Forge quality procedures, standard work, and forms for Columbus Operations. Check Level 4 documentation records in and out of SharePoint for maintenance by operational functional teams. Other duties as assigned. Compile and distribute results of the LPA audits to operational Business Unit Leaders. Run CAR status reports for Tier 4 meetings for Operations Leadership. Generate communication for Toolbox Talks delivered to employees to inform the workforce of key issue awareness. Process and Expedite Level 4 Documentation Ballots with operational teams. Process and expedite Level 1 through Level 3 documentation ballots with operational teams. Support Level 4 Documentation TPM with executing and expediting reviews and input, as requested. Perform 6s each shift Engage in process optimization to allow success of production/quality goals while achieving and maintaining cost savings Complete all training within the expected time given Qualifications You Must Have: HS diploma (or equivalent, e.g. G.E.D. in the US) or vocational/technical education in related discipline Minimum of 1 year of relevant work experience Qualifications We Prefer: Experience in manufacturing environment Quality assurance or quality control experience is a plus What We Offer: Medical, dental, vision and life insurance Short-term disability, long-term disability and parental leave 401(k) match Flexible spending accounts Employee assistance program Employee Scholar Program (No waiting period!) Paid time off including: 3 weeks of vacation, 5 personal sick days, 3 unpaid days for unique situations at supervisor discretion, and 12 paid government holidays Additional Information: Must be a U.S. Citizen. This position may require access to systems/tools that are restricted to individuals who possess US citizenship. What is my role type? In addition to transforming the future of flight, we are also transforming how and where we work. We've introduced role types to help you understand how you will operate in our blended work environment. This role is: Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance workers, as they are essential to the development of our engines. Candidates will learn more about role type and current site status throughout the recruiting process. For onsite and hybrid roles, commuting to and from the assigned site is the employee's personal responsibility. As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX 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 or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

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

Oversees logs and procedures and ensures Q.C. and Production are abiding by GMP and GLP company rules set forth by company SOPs. Ensuring things are made right in the first place is the best way of preventing out of specification products. ESSENTIAL DUTIES AND RESPONSIBILITIES: Includes the following, but other duties may be assigned as the company's needs dictate. Reviews and approves the Production filling batch records. Checks and audits the documents for accuracy and GMP compliance during and at the completion of filling. Checks and confirms that the correct components and compounding batch have been set-up and are being used on the appropriate packaging line. Reviews the data reported by the mechanics, machine operators, and line leads to ensure that the information is correct and entered appropriately. Responsible for placing compounded batches and finished goods that do not conform to company specifications into Quarantine status with applicable labeling. Reports any quality issues to Quality management and participates in investigations, as necessary. Performs daily housekeeping audits of the Production area logbooks and reports results to Quality management. Supports GMP training of employees. Participates in Quality System audits as directed by Quality management. Complies with Health, Safety, and Environmental responsibilities for the position. Inspects the production lines to ensure that both Production and Quality control personnel are following the required SOP to perform their jobs. QUALIFICATIONS: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE: High school diploma or GED (general education degree) and some college (science-based courses preferred). Minimum 6-months of hands-on experience as Quality audit/inspector in cGMP environment; preferably in pharmaceutical, biomedical, or medical device field (regulated industry). Experience with batch record keeping, CAPA initiation, and deviation investigation. Should have experience working on the floor of a manufacturing facility. LANGUAGE SKILLS: Fluent in reading, writing, and speaking the English language, as well as having experience with technical writing (knowing Spanish is a plus). Ability to read, analyze, and interpret professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from departmental manager/supervisor or other employees. MATHEMATICAL SKILLS: Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis. COMPUTER SKILLS: To perform this job successfully, an individual should have knowledge of Database software, Spreadsheet software and Word Processing software. REASONING ABILITY: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to sit, use hands to finger, handle or feel; and reach with hands and arms. The employee is occasionally required to stand, walk, talk or hear, and taste and smell. The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently exposed to fumes or airborne particles (herbal powders). The noise level in the work environment is usually quiet. Sunrider Manufacturing 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.

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.

**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!

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

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.

Amarillo Gear Company LLC As a part of the global industrial organization Marmon Holdings-which is backed by Berkshire Hathaway-you'll be doing things that matter, leading at every level, and winning a better way. We're committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone's empowered to be their best. SCOPE: The Tool Specialist will provide assistance with CNC machine tooling (tool bodies, inserts, endmills, grinding wheels, etc.) and hand tooling (wrenches, hardware, etc.) for the manufacturing plant. They will be responsible for organizing, inventorying, and repairing tooling in the tool crib, ordering special tooling, sending off tooling to be repaired, setting up and maintaining tool setup package carts for various work-centers, and assisting with part changeover at various CNC machines. They will work with different departments to improve production flow and on-time delivery throughout the entire manufacturing plant. EDUCATION REQUIREMENTS/ EXERIENCE: * 2+ years of hands-on programming experience preferred * Ability to write and understand machine code preferred * Inventory experience * Be comfortable in a fast-paced environment * Some experience with CAD/CAM software, such as Autodesk Fusion * Strong communication and documentation skills, with the ability to communicate with machinists on machine processes * Highly proficient in Microsoft Office (Excel, Word, Access, PowerPoint, etc.) * Mathematically inclined RESPONSIBILITIES: * Ensure each CNC machine has all the tooling required to manufacture various parts ahead of time to help production flow smoothly through the shop. * Coordinate tool tests with the CNC Programmer and report CNC programming changes that need to be made to improve tool life and part quality. * Clean up extra unused tooling at each work-center and inventory it to be sharpened or reused. * Set up tool packages for CNC machine changeovers to ensure CNC operators have all tooling they need to perform quick changeovers. * Inventory current tooling used at work-centers (such as custom-made boring heads) to help identify where spare tooling will be required to help production flow. * Assist the CNC operators in part changeover duties in pit-crew style changeovers to help the changeover go quicker and smoother. * Help complete program changes/transfers when CNC Programmer needs support. * Perform other duties, as assigned. REQUIRED PHYSICAL DEMANDS: * Standing for more than 1 hour, walking more than 100 ft., reach above, at or below shoulders, climb stairs, bend, stoop, and/or squat, grasping, hand/wrist twisting, lifting of up to 50lbs. Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law. We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to ******************, and please be sure to include the title and the location of the position for which you are applying.

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.

Lab Analyst I - Early Phase Clinical Research- ICON San Antonio- Full Time/Permanent ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Lab Analyst I to join our diverse and dynamic team. As a Lab Analyst I at ICON, you will be responsible for conducting routine laboratory tests and analyses to support clinical research studies. You will play an essential role in maintaining accurate data, adhering to standard procedures, and contributing to the overall success of the laboratory operations. Title: Lab Analyst I Location: On-Site San Antonio TX USA Job Type: Full Time-Permanent Shift/Schedule: M-F 11 AM-7 PM What You Will Be Doing: * Performs and reports routine and special laboratory tests on clinical trial specimens to aid in subject safety and in accordance to protocol requirements, under general supervision. * Detect abnormalities as indicated in protocol. * Performs specimen processing and testing independently to include waived and moderate complexity testing. Analyzes test results and assumes accountability for accuracy. * Operates, maintains, and troubleshoots laboratory instrumentation and equipment and makes minor repairs as necessary and knows when to notify lab management. * Understands, performs, and practices quality control management to include running controls, evaluating data, documentation of data, and taking corrective action as required. Communicates any relevant QC information to Supervisor or Manager. * Must cross-train to other laboratory sections as needed. * Calculates, enters, and/or verifies results of laboratory procedures. * Utilizes the Laboratory Information System and eSource system. * Provides notification and documentation of critical laboratory values obtained to Principal Investigator. * Participates in the evaluation, development, and implementation of new or updated testing procedures and protocols. * Must complete all required compliance and regulatory tasks and follow all applicable policies and procedures. * Your Profile: * Associate or bachelor's degree in medical laboratory science. * MT/MLT/ASCP required (Clinical Lab Scientist license) * Minimum 2 years in a laboratory environment, preferably in a clinical pathology laboratory or related industry. * Proficient in laboratory techniques like coagulation and hematology testing * Good communication skills and the ability to work effectively in a team environment. What ICON can offer you: Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: * Various annual leave entitlements * A range of health insurance offerings to suit you and your family's needs. * Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. * Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being. * Life assurance * Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply

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.

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: Bachelor's 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.

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.