Quality assurance specialist jobs in Houston, TX

Air Quality Consultant - Houston, TX (Hybrid 2-3 days on-site) We are seeking an experienced Air Quality Consultant with strong technical expertise in air quality and environmental compliance. This hire will join our client's team in Houston - they are a leading environmental consulting firm with expertise across various project types. This role requires leading complex projects, managing client relationships, and delivering results while driving business growth. The ideal candidate combines technical knowledge, project management skills, and the ability to mentor team members. Key Responsibilities: Lead multiple environmental projects from planning through execution, ensuring timely delivery, budget adherence, and quality outcomes. Serve as the primary point of contact for clients, maintaining strong relationships and identifying opportunities for expanded services. Develop project proposals, schedules, and resource plans, ensuring alignment with client expectations. Oversee project budgets, monitor performance metrics, and ensure financial targets are met. Provide technical guidance and review deliverables, ensuring compliance with regulatory requirements. Mentor junior staff, foster collaboration, and support team professional development. Conduct regular project meetings, communicate updates to stakeholders, and proactively address challenges. Maintain knowledge of federal, state, and local environmental regulations to advise clients strategically. Support business development efforts by contributing to proposals, identifying new opportunities, and assisting with client acquisition. Ensure all project work follows safety protocols and quality standards. Qualifications: Bachelor's degree in engineering, environmental science, or related field, with 7+ years of project management experience in consulting. Proven experience in air quality permitting, compliance, or related environmental services. Strong leadership, organizational, and communication skills. Demonstrated ability to manage multiple projects, budgets, and client relationships simultaneously. Technical writing and proposal development experience preferred.

**Job Category:** Lift Maintenance PL Administers the Inspection and Quality Control of aircraft completions, maintenance and modifications functions in accordance with part 145 repair station and regulatory requirements. _To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Other duties may be assigned to this position as needed._ + Direct, plan and layout the details of inspection standards, methods and procedures used by the repair station in complying with all applicable regulations, manufacturer's specifications, and instructions. + Coordinate with the FAA Certificate Holding District Office and other Federal Aviation Administration offices regarding repair station issues. + Serve as the primary contact with the FAA and final authority to approve aircraft for return to service all articles maintained or altered by the repair station. + Ensures preventive maintenance, repair, modifications and other maintenance of aircraft, components and related equipment complies with 14 CFR, manufactures specifications, Company policy and procedures as well as other methods accepted by the FAA and OSHA when accomplishing maintenance. + Assist when necessary to meet completion and production schedules and produce the quality maintenance. + Verify that each part or component is effective for the aircraft on which it will be installed. + Adhere to material handling and control procedures specified in RSQCM and by the equipment manufacturers. Oversee parts and material receiving inspection. + Assure the preliminary, hidden damage, in-progress, and final inspections of all articles maintained or altered by the repair station are completed and results recorded as outlined in this manual and the RSQCM. + Ensure that all department internal company forms, maintenance records, documents, work orders, etc. are completed, including performing maintenance computer system transactions as required. + Maintain and utilize RSQCM and aircraft manuals. + Make revisions as necessary to the documents of the repair station including but not limited to the Supervisory and Inspection Personnel Roster and Inspector Stamp Roster. + Administer recurrent training, including required FAA AMT training, and keep necessary licenses and certifications up-to-date. + Ensure proper calibration of required tooling. + Evaluate the area and equipment that will be utilized to ensure that safety is not compromised before performing any maintenance action; apply safety first at all times. + Fosters the Company's core values and culture throughout the work environment. + Screens, interviews and makes recommendations for hiring potential employees. Coaches and provides leadership, direction, motivation and supervision of direct reports. Appraises performance, provides performance feedback, takes corrective actions and oversees training and development of staff. + Performs other duties as assigned or required **REQUIRED KNOWLEDGE, SKILLS AND ABILITIES** _The requirements listed below are representative of the knowledge, skill, and/or ability necessary to perform this job._ EDUCATION and/or EXPERIENCE. + Specialty training beyond high school in Aviation with a FAA Mechanics and A/P Certificate with at least 3 years of previous experience. + Strong understanding of FAA regulations and standards as they pertain to Part 43, 65, 91 and 145 as well as inspection methods, techniques, and equipment used to determine the quality or airworthiness of an article undergoing maintenance, repair, or alterations + Ability to write technical documents and manuals. + Able to work both in a team setting and individually. PREFERRED EDUCATION and/or EXPERIENCE + Quality Assurance/Inspection experience in General Aviation, Corporate or Airline environment + Inspection Authorization + Quality Management in an aerospace/aviation repair station environment preferred + Experience with General Aviation piston aircraft + Superior communication skills, both written and verbal + Excellent electrical and mechanical troubleshooting skills. + Previous supervisory experience. REGULATORY + Possess a stable employment history. + Able to pass an FAA required 10 year work history review and pass criminal background and fingerprint checks. + Willing to submit to and pass FAA and Company mandated random drug and alcohol tests. + Must have and maintain a valid Driver's License and a clean driving record. LANGUAGE SKILLS Ability to read, write and communicate in English. Able to analyze, and interpret general business periodicals, 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 groups of managers, clients, customers, and the general public. REASONING/PROBLEM SOLVING 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. DECISION MAKING Makes decisions daily on use of resources, performance and budgets. Decisions could require additional expenditure of resources if not sound decisions. **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._ + Able to stand, walk, use hands to finger, handle and feel, reach with hands/arms up to 20% of the time. + Able to climb or balance, stoop, kneel, crouch and crawl up to 20% of the time. + Able to lift up to 50 pounds at least 20% of the time. + Able to lift or move 75 pounds at least 10% of the time. + Must be able to see to perform work and to see approaching vehicles, aircraft and machinery. **WORK ENVIRONMENT** _The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job._ + Work near moving mechanical parts, work with fumes or airborne particles over 50% of the time. + Work in high, precarious places up to 10% of the time. + Work around toxic or caustic chemicals up to 10% of the time. + Work in outdoor weather conditions within an open air hangar up to 20% of the time. + The work environment can be loud. + Able to work nights, evenings, weekends and holidays. **TRAVEL REQUIREMENTS** Travel up to 20% of the time, including overnight stays. **Equal Opportunity Employer, Disability and Veteran Accommodations** All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Founded in 1974 and headquartered in Indianapolis, Indiana, Republic Airways is one of the largest regional airlines in North America. Republic operates a fleet of 200+ Embraer 170/175 aircraft and offers scheduled passenger service with 900 daily flights to 80+ cities in the U.S. and Canada. Republic continues to lead the way in innovation and operational excellence for 50 years. The unrivaled work being done by our over 6,000 Associates sets us apart from the competition. We are in an era of growth and untapped potential across the aviation industry. It's an exciting time to be part of our Company, from corporate positions to the flight deck. No matter your role, your opportunities are elevated at Republic Airways. Republic Airways fosters a culture of trust, respect, care and fun. We believe our people and the passion they bring to their work is what distinguishes us. We work to encourage, support and invest in our Associates both professionally and personally. We live and breathe our Vision, Mission, Culture Statement and Guiding Principles - those words are put into action each and every day at Republic.

Huntsman is seeking a Sr. Quality Assurance Specialist supporting the Performance Products (PP) Division located in Conroe, Texas. This position will report to the Technical Manager. Job Scope With responsibility for supporting critical quality activities within the Conroe manufacturing site, we are seeking a highly experienced Sr. Quality Assurance Specialist with 10+ years of experience in chemical or process manufacturing-the Sr. level role is responsible for ensuring end-to-end quality and regulatory compliance across the facility, including ISO 9001, IATF 16949, FMEA, SAP QM. Our ideal candidate will be a process-driven, detail-oriented professional with deep knowledge of ISO 9001:2015, 14001, and 31000:2018 In summary, as the Sr. Quality Assurance Specialist, you will: With no supervision required and high decision-making: Quality Systems & Procedures: Reporting to Site Quality Leadership, Act as SME on site quality systems and procedures, driving standardization, compliance, and alignment with ISO 9001:2015, ISO 31000:2018, and IATF 16949 standards.. Develop & Implement SOPs, Work Instructions, Control Plans, and Audit Ready Documents. Maintain the quality management system for the site, review the quality manual and quality procedures as per the guidelines, and make recommendations for improvement as necessary. Facilitate the management review meetings and ensure all actions are closed within the accepted timeline. SAP Quality Management (QM): Responsible for maintaining and optimizing the use of the SAP QM module for quality planning, supporting NPI (SAP), traceability, and overall data integrity. Ensures SAP QM integration with other modules and external systems for seamless quality control workflow. Shared responsibilities with Analytical Chemistry Expert, act as SAP quality module SME for power-users, such as chemists, technical analysts, process engineers, and operators. Generate and analyze SAP data to drive improvements in process capability, SPC, SQC, Gage R&R, and material non-conformance. Generate and provide reports as directed by the QA/QC Team Lead/ Quality Management as needed. Provide SAP QM module technical support for other Huntman sites such as Freeport (EA), Pensacola (MA), and Ringwood (HPU). Maintain other Conroe critical shipping-related applications, such as CarProd, CarRaw, and NextDay, etc. Compliance, Audit & Continuous Improvement: Site representative for ISO 9001,17025,14001,31000 and customer audits: Responsible for: All audit preparedness & full compliance. CAPA (5-Whys, 8Ds. Fishbone, etc..) Monitoring trends and KPIs - generate & present data to Team Laed/ Quality Management as needed for quick decision making. Act as a QA analyst for site Quality (Bring the Data). FMEA & Risk Mangement: Facilitate FMEA across all portfolios - products, processes, equipment, and tools, be nimble and move quickly in identifying and mitigating risk. Be the “quarterback” for Site FMEA. Develop and implement risk management tools, training materials, and train new and existing staff. Training & Coaching: Train and coach engineers, technicians, and operators on FMEA methodology. Facilitate understanding of how risk-based thinking supports preventive quality and product reliability. Integration with Other Systems: As a Sr. Quality Assurance Specialist, you are responsible for ensuring alignment of Failure Mode and Effect Analysis (FMEA) with all other core quality tools, to achieve a comprehensive quality planning and process validation. Lead Cross-Functional FMEA Teams: Bring every stakeholder together to perform structured PFMEA and DFMEA for new process, product, and plant changes. FMEA Lifecycle Management: Ensure FMEAs are treated as living documents, regularly updated to reflect process changes, non-conformances, customer complaints, and lessons learned. Ensure traceability of revisions and integration with Control Plans. Continuous Improvement, Production & Laboratory Automation: Working with the Analytical Chemist Expert, Process Engineers, supporting the digitalization and automation of testing processes in production (line) and laboratory. Fostering Data-Driven Decision-Making, support laboratory efforts to digitize and automate the capturing of data from equipment to SAP, from production to SAP, and other supported systems, and make the process of capturing, analyzing, and interpreting lab data seamless. This includes Historical Data, Record-Keeping, Customer Investigation Records, In-process and Finished Product Data. Other general responsibilities: Follows instructions and performs other duties as may be assigned by the supervisor. Assists other employees in the accomplishment of the Huntsman Company's goals. Participates in and completes company-required training programs. Participates in Environmental, Health, & Safety initiatives as set forth by the company Document Control/ Manager Qualifications You must possess the below minimum qualifications to be initially considered for this position. Preferred qualifications are in addition to the minimum requirements and are considered a plus factor in identifying top candidates. The candidate must have an unrestricted right to work for Huntsman in the United States. Minimum Qualifications Bachelor of Science or Chemistry with 10+ years of auditing and root cause investigation experience. Or Master's degree with 8+ years of experience. Degrees in Chemistry, Materials Science, or Chemical Engineering are preferred. Other degrees will be considered based on experience. Education could be substituted for years of experience. FMEA, CAPA, RCA knowledge required. ISO 9001 experience required. Skills and knowledge Quality Management Systems Strong Mathematical Aptitude Data Analysis & Interpretation Troubleshooting & Root Cause Analysis Some Exposure to Lean Six Sigma or Continuous Improvement Methodology Knowledge in 8D Methodology Competencies Communicates tactfully and effectively both verbally and in writing. Maintains effective work relations with those encountered during the course of employment. Flexibility and adaptability to new instructions and/or dynamic organizational priorities are critical for job success. Huntsman is proud to be an equal opportunity workplace and is an affirmative action employer. We provide equal employment opportunities (EEO) to all qualified applicants for employment, without regard to race, color, religion, sex, national origin, disability status, protected veteran status, gender identification, sexual orientation and/or expression or any other characteristic protected by law in every location in which we have facilities national or local. Please refer to ****************************************************** for Company's Data Privacy and Protection information. All unsolicited resumes presented by recruitment agencies are treated as pro bono information or service. Huntsman is aware of a scam involving fraudulent job offers. Huntsman does not make job offers until after a candidate has submitted a job application and has participated in a face-to-face interview. Please be advised that emails from Huntsman always end in “@huntsman.com” , and that any job offer that requires payment or requires you to deposit a check is likely a scam. If you have questions about any open positions at Huntsman, please visit our Careers website at ******************************************** Additional Locations:

Job Purpose The Quality Assurance/Quality Control Auditor will audit the processes to ensure the product is made/processed according to internal procedures/instructions. He/She will immediately notify discrepancies so appropriate personnel take actions accordingly. Duties & Responsibilities • Daily audit applicable processes and provide real time feedback on any issues that may occur. • Monitor processes and products to identify opportunities for continuous improvement. • Reporting and instigating Non-conformances and Corrective actions. • Helping problem solve any quality issues on line. • Provide technical and data retrieval support for site projects and investigations. • Taking steps to ensure that all laid down procedures and specifications. • Controls material disposition according to Quality Specification Sheet as well as placing QA Hold, removal of QA Hold, Reject, Release and Material Inspection process. Record data analysis from daily auditing reports. • Provide training to new and existing SeAH Steel USA, LLC employees if applicable. • Suggest changes to ensure that the work procedures and equipment's fall in line with the required specifications and requirements. • Ensure all equipment is in compliance with calibration frequency. • Conduct investigations for quality complaints, deviations, and product failures. • Monitor and support the audit and release of incoming/outgoing materials. • Third party auditing if applicable. • Ensures proper paperwork is being utilized in the different operative areas. • Other duties as assigned. Qualifications / Competencies Education : o Prefer undergraduate degree, technical/associate degree, and/or NDT experience. Years of Experience : o Must have at least 3-4 years' experience in ERW manufacturing process and/or heat treat and/or quality of an OCTG Threading Facility, API, Q1, ISO, 5CT, 5L, and ASTM. o Job Knowledge : o Current knowledge and understanding of all relevant SeAH Steel USA, LLC's SOP's, customer specs, and API specs. o Certification in NDT Disciplines - EMI. MP, UT, PT preferred. Personal Competencies: Excellent verbal and written communication skills. Safety: o Understands all applicable location safety rules and regulations and makes sure that all are being followed. Physical Requirements & Working Conditions • Working conditions are split between a professional office environment and a normal manufacturing environment. • Work involves delegated and operation detail. • Substantial movements (motion) of the wrist, hands, and/or fingers in a repetitive manner. • Sedentary physical activity performing non-strenuous daily activities of an administrative nature. • Manual dexterity sufficient to reach/handle items, works with the fingers, and perceives attributes of objects and materials. • Well-lighted, heated and/or air-conditioned indoor office setting with adequate ventilation. • The ability to work in loud, hot environments/extreme weather while wearing required PPE. • Ability to see 20-20 when corrected. • Ability to identify and distinguish colors. Pay Based On Experience.

Job Description Job Purpose The Quality Assurance/Quality Control Auditor will audit the processes to ensure the product is made/processed according to internal procedures/instructions. He/She will immediately notify discrepancies so appropriate personnel take actions accordingly. Duties & Responsibilities • Daily audit applicable processes and provide real time feedback on any issues that may occur. • Monitor processes and products to identify opportunities for continuous improvement. • Reporting and instigating Non-conformances and Corrective actions. • Helping problem solve any quality issues on line. • Provide technical and data retrieval support for site projects and investigations. • Taking steps to ensure that all laid down procedures and specifications. • Controls material disposition according to Quality Specification Sheet as well as placing QA Hold, removal of QA Hold, Reject, Release and Material Inspection process. Record data analysis from daily auditing reports. • Provide training to new and existing SeAH Steel USA, LLC employees if applicable. • Suggest changes to ensure that the work procedures and equipment's fall in line with the required specifications and requirements. • Ensure all equipment is in compliance with calibration frequency. • Conduct investigations for quality complaints, deviations, and product failures. • Monitor and support the audit and release of incoming/outgoing materials. • Third party auditing if applicable. • Ensures proper paperwork is being utilized in the different operative areas. • Other duties as assigned. Qualifications / Competencies Education: o Prefer undergraduate degree, technical/associate degree, and/or NDT experience. Years of Experience: o Must have at least 3-4 years' experience in ERW manufacturing process and/or heat treat and/or quality of an OCTG Threading Facility, API, Q1, ISO, 5CT, 5L, and ASTM. o Job Knowledge: o Current knowledge and understanding of all relevant SeAH Steel USA, LLC's SOP's, customer specs, and API specs. o Certification in NDT Disciplines - EMI. MP, UT, PT preferred. Personal Competencies: Excellent verbal and written communication skills. Safety: o Understands all applicable location safety rules and regulations and makes sure that all are being followed. Physical Requirements & Working Conditions • Working conditions are split between a professional office environment and a normal manufacturing environment. • Work involves delegated and operation detail. • Substantial movements (motion) of the wrist, hands, and/or fingers in a repetitive manner. • Sedentary physical activity performing non-strenuous daily activities of an administrative nature. • Manual dexterity sufficient to reach/handle items, works with the fingers, and perceives attributes of objects and materials. • Well-lighted, heated and/or air-conditioned indoor office setting with adequate ventilation. • The ability to work in loud, hot environments/extreme weather while wearing required PPE. • Ability to see 20-20 when corrected. • Ability to identify and distinguish colors. Pay Based On Experience.

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 an Operational Quality Assurance Specialist II to join our Operational Quality Assurance team. In this role, the specialist will be responsible for conducting internal audits of manufacturing and CMC (Chemistry, Manufacturing, and Controls) procedures, ensuring compliance with regulatory and company standards. The position also involves tracking and maintaining critical documentation such as standard operating procedures, work instructions, lab notebooks, and manufacturing data. Additionally, the specialist will oversee and execute official batch and material release activities, supporting overall quality assurance operations. FLSA Classification: Hourly, Non-Exempt Schedule: 1230 - 2100; Monday to Friday; On-site This is a critical position and may require working overtime, after-hours, weekends, or holidays to ensure business continuity. Reports to: Operational Quality Assurance Associate Manager - 2nd Shift Location: 13203 Murphy Road Suite 100 Stafford, TX 77477 What You'll Do: As an Operational Quality Assurance Specialist II, you will play a key role in supporting our batch and material release: Maintaining equipment logs and files Tracking manufacturing numbers Performing internal audits of the manufacturing process Writing audit reports Creating and performing internal Quality Assurance trainings for Immatics personnel Writing new standard operating procedures and batch records Keeping track of lab notebooks Providing support for the investigation and recall of non-conforming materials Writing, reviewing, and tracking deviation reports, corrective and preventive actions (CAPA) reports, maintenance reports and Out of Specification (OOS) reports Issuance and reconciliation of final product labels Certificate of Analysis (CoA) review and release for completed batches Review of sterility, endotoxin, and mycoplasma results Reagent review and release Initiation and completion of Change Controls for all updates to processes or documents Maintains electronic log of all US equipment Secondary Functions: N/A Required Experience and Education: Bachelor's Degree in a Life Science Discipline is required. 3+ years of experience in QA, Auditing, or clinical manufacturing in a research environment. At least 3-5 years of Biotechnology and/or Pharmaceutical industry experience is required. Experience comprehending regulations and guidance documents. Preferred Experience and Education: N/A Competencies: Ability to make sound decisions and approach problems with curiosity and open-mindedness High degree of independent working, analytical reasoning, and the ability to communicate effectively Careful editing and documenting of results Ability to embrace rapidly changing requirements with an open mind and show a high degree of flexibility in an environment which is marked by a constant striving for excellence Ability to approach tasks in a structured, reliable, and foresighted manner; combined with a high level of individual responsibility, enthusiasm, and strong social skills Ability to effectively collaborate with members from other departments Work Environment: This is a sedentary position (at least 50% of time) in a typical office environment. There may be frequent interruptions with moderate noise levels and frequent use of printers, copiers, scanners, computers and other office equipment. Ability to sit, talk, walk, hear and communicate verbally and in writing is required. Occasional lifting of objects up to 25 lbs is expected. Travel required: N/A 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, up to 100K (club together) 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 coverage 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.

The QA/QC Manager is responsible for developing, implementing, and maintaining Envent's quality management system (QMS) across all service lines. This role ensures that field operations, engineering, fabrication, and maintenance activities consistently meet or exceed regulatory, client, and internal quality standards. The QA/QC Manager will play a critical role in driving a culture of quality, compliance, and continuous improvement throughout the organization. PRIMARY ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Essential duties may vary according to region, division, area, and/or assignment. Other duties may be assigned. · Develop, implement, and maintain ISO-aligned quality assurance and quality control procedures to ensure consistent performance across all projects and operations. · Establish inspection and testing protocols for equipment, field services, and fabrication work to verify compliance with specifications and industry standards. · Lead internal and external audits, manage corrective and preventive action records (CAPRs), and ensure all compliance documentation is accurate, current, and properly maintained. · Oversee the Management of Change (MOC) process for regional designs, builds, or modifications, and communicate findings from MOC and CPAR processes to all affected parties, including Engineering, Operations, Fabrication, and Maintenance groups across all regions. · Monitor EPA, OSHA, and applicable state and local environmental regulations to ensure that all Envent operations remain in full compliance. · Ensure proper documentation, retention, and reporting of QA/QC records for clients, regulators, and internal stakeholders. · Oversee adherence to client-specific quality standards and project specifications to maintain strong customer satisfaction and regulatory alignment. · Support field project teams by providing quality planning, inspection services, and technical guidance throughout the project lifecycle. · Conduct thorough root cause analyses for quality incidents or non-conformances and develop and implement corrective improvement plans. · Deliver QA/QC training programs to operations staff, engineers, and field technicians to strengthen quality awareness and competency. · Develop key performance indicators (KPIs) and quality dashboards to measure, track, and improve quality performance across all business lines. Collaborate with Operations, Engineering, HSE, and Fabrication teams to implement process improvement initiatives aimed at increasing efficiency and reducing waste. ADDITIONAL DUTIES AND RESPONSIBILITIES include the following (Duties may vary according to region, division, area, and/or assignment. Other duties may be assigned): 1. Adheres to all company policies, procedures, and business ethics codes and ensures that they are communicated and implemented within the team. 2. Work with the Purchasing Team to specify equipment for purchase; Cost effectively procures parts, materials equipment and supplies. 3. Ensure the optimal application of current technology, engineering resources, fabrication material and any outsourced services meet product development requirements. 4. Be fully responsible for managing the development of operational, maintenance and compliance procedures and be able to train and audit all personnel with a commitment to safety and compliance. 5. Shall understand and lead and participate in various forms of Process Hazard Analysis including what-if, fault tree, HAZOP checklist and other forms of risk assessment. 6. Must ensure all regulatory permits are maintained and current for the Region and shall work closely with the corporate Director of Health, Environment and Safety to ensure compliance with rules, regulations and laws. 7. Shall be intimately familiar with and understand engineering drawings, specifications and industry standards and be able to apply this information to all projects. 8. Should be able to read and develop Piping & Instrumentation Diagrams, Process Flow Diagrams, Schematics, Electrical Plans, Logic Diagrams, Ladder Diagrams, Wire and Mechanical Plans, Isometrics and vendor cut sheets. 9. Should have working knowledge of rotating equipment including pumps, blowers, compressors, etc. and be proficient in performance curves and design characteristics. 10. Shall understand instrumentation principles including failsafe design of safety and controls. 11. Shall have the ability to research suppliers and source materials and equipment for the highest level of value, quality and suitability for use. 12. Shall continually research new equipment, technologies, or methods that promote more efficient processes, increasing safety margins, and higher degree of reliability. 13. Understands that he or she is working in a twenty four hour, seven days a week (24/7) industry environment and as such, understands that he or she must be available on a 24/7 basis when required, which will include off hours, weekends, and holidays. 14. Ability to travel and stay overnight typically up to ten percent (10%) of the time. Travel will be by vehicle or airline to meet and work with customers. EDUCATION and/or EXPERIENCE The QA/ QC Manager position requires a four year engineering degree and a minimum five to seven years of experience in Envent's core service line. This position requires the ability to understand engineering concepts, theories and practices as applied to equipment fabrication and or repair work, be able to manage a project from start to finish, have experience in working with multiple discipline projects, read and interpret technical documents and or procedures, contractual language, safety procedures and requirements. ADDITIONAL TRAINING Company-specific and customer safety training is required. ADDITIONAL KNOWLEDGE, SKILLS, AND ABILITIES 1. Analytical, general management, people, and computer skills. 2. Excellent language and communication skills. Effective negotiating and listening skills. 3. Ability to be persistent, patient, creative, and flexible. Ability to maintain a high energy level. Ability and willingness to learn. Ability to work in a team environment and contribute positively. 4. Ability to adapt to changing priorities. Ability to assemble information from a variety of sources. 5. Will have intimate knowledge of refinery flare systems including flare gas recovery and flare management plans. 6. The incumbent must demonstrate a commitment to compliance with all applicable laws, regulations, company policies, customer policies and an unwavering commitment to safety. The position requires handling all business affairs with the highest ethical standards set forth by the company and its clients. 7. The QA/ QC Manager shall be able to obtain permits and work closely with environmental agencies in the course of our projects. 8. The QA/ QC Manager must understand and effectively manage fiscally when assigned projects and ensure that projects come within budget guidelines. The candidate must be able to manage his or her costs and keep them within company guidelines. 9. The QA/ QC Manager must be proficient in Microsoft Office, Excel, Outlook, Word and other data base software. AutoCAD is highly desirable. 10. The QA/ QC Manager must be proficient in the care and use of all site specific, facility and customer required Personal Protection Equipment (PPE). The candidate must be able to pass all site specific facility, company and industry tests. CERTIFICATES, LICENSES, REGISTRATIONS QA/ QC Manager must maintain a valid driver's license. The candidate or employee must provide his or her motor vehicle record from the state of residency and must be insurable by the Envent Corporation insurance provider. Professional Engineer's certification is preferred but not required. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by a QA/ QC Manager to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable a QA/ QC Manager with disabilities to perform the essential functions. Physical demands of this position are sitting, walking, climbing, stooping and bending. QA/ QC Managers may on occasion lift and or move up to fifty pounds (50lbs). QA/ QC Managers must be physically fit and pass the company physical in order to be qualified to work in this position. WORK ENVIRONMENT The work environment characteristics described here are representative of those a QA/ QC Manager encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable a QA/ QC Manager with disabilities to perform the essential functions. The noise level in the work environment is moderate but can be loud when working in the field. Work environment is a combination of office and field. The QA/ QC Manager will be exposed to various outdoor weather conditions. He or she will be in industrial plants which will expose them to potentially hazardous situations. You must have all necessary PPE and be prepared to use it as the situation dictates. The QA/ QC Manager can be subjected to extreme heights and moving mechanical parts. While performing the duties of this job, the QA/ QC Manager may work in outside weather conditions and is regularly exposed to fumes or airborne particles and toxic or caustic chemicals common to an active site - appropriate PPE is provided and required.

Department: Quality Assurance Reports to: Associate Director, Quality Ops, Quality Assurance CTMC is a pioneering biotech joint venture, formed by National Resilience and MD Anderson Cancer Center, located in the heart of the Texas Medical Center. Our mission is to accelerate cell therapies from bench to bedside. We offer a wide range of cell therapy modalities, including CAR-T, TIL, and TCR-T. Our expert team collaborates closely with MD Anderson's research and clinical faculty, bringing impactful cell therapies to cancer patients. Since inception in May 2022, our team has filed eight INDs and have received approval, without delay, demonstrating our commitment to delivering innovative treatments to patients with speed and precision. Our alliance with National Resilience enables us to remain at the forefront of biomanufacturing practices, leveraging advanced technology and processes to deliver exceptional results. Our growing, state-of-the-art, 60,000 sq. ft. industrial facility in the Texas Medical Center is staffed by an integrated team of industry veterans and academic scientists who are passionate about bringing life-saving cures to patients. Our unique joint venture structure, with two highly established partners, provides us with the financial stability and long-term horizon to achieve our organizational goals. At CTMC, we value our employees and offer a variety of development opportunities within our novel corporate structure to inspire professional growth and satisfaction. We foster a team-first culture and a balanced work-life environment to ensure our staff is energized and engaged in our mission to accelerate cell therapies from bench to bedside for patients who need them. If you share our passion for advancing the frontiers of medical science with innovative therapeutics and want to join a highly dedicated team committed to delivering novel cures to patients, we invite you to submit your application. We look forward to hearing from you and exploring how your skills and expertise can help us achieve our mission. Responsibilities: Review and approve QC test results, laboratory records, and batch analysis documentation. Investigate QC-related deviations, OOS/OOT results, and non-conformances. Participate in root-cause analysis and develop CAPA actions. Review, evaluate, and approve change control requests impacting QC processes or systems. Review and support method validation, method verification, and transfer documentation. Review equipment qualification records (IQ/OQ/PQ) and calibration documents. Conduct internal audits of QC laboratories and follow up on corrective actions. Assist with external audits by regulatory authorities and customers. Ensure data integrity and laboratory compliance with electronic systems (LIMS, ELN, etc.). Support disposition/ Hold/ Rejection of raw materials Partner with other departments to implement, optimize, review, and approve quality control records, practices, and procedures. Participate in audits when needed. Other duties as required. Qualifications/Skills Bachelor's degree in a scientific field required. 5+ yrs in Quality Assurance/Quality Control within the field or an equivalent combination of education and experience. Quality Control experience required Understanding of Cell and Gene Therapies. Understanding of cGMPs, GLPs and GXPs. Previous experience with LIMS systems (preferable LabVantage experience) Knowledge of local and global regulations. Verbal and written communication skills. Interpersonal and customer service skills. Organizational skills and attention to detail. Time management skills with a proven ability to meet deadlines. Analytical and problem-solving skills. Proficient with Microsoft Office Suite or related software. Working Conditions, Equipment, Physical Demands The incumbent in this position works in an office environment. The incumbent in this position will use the following equipment and shall have the following physical demands: Equipment- Computer, printer, fax, and telephone. Physical Demands- Prolonged periods of sitting at a desk and working on a computer and must be able to lift up to 15 pounds at times. In addition, ability to sterile-gown and perform activities in the manufacturing suite as well as raw material area when applicable. The physical demands and work environment that have been described are representative of those an employee encounters while performing the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions in accordance with the Americans with Disabilities Act. The above job description is an overview of the functions and requirements for this position. This document is not intended to be an exhaustive list encompassing every duty and requirement of this position; your supervisor may assign other duties as considered necessary.

Adroit Advanced Technologies, Inc. Responsibilities: ● Responsible for monitoring and evaluating staff members on the quality and process of work performed as measured against standards. ● Assist with the development, analysis and distribution of recaps, findings and summaries. ● Assist with training new agents and re-training on policies and procedures. ● Remain proficient and up-to-date on policies and procedures for all operations. ● If needed, assist in developing new procedures, and update existing procedures when changes occur. ● Conduct agent monitoring activities, while providing live in the moment coaching for quality assurance purposes. ● Monitor and report on agent activity, schedule adherence, and productivity while reporting daily, weekly and monthly findings. ● Research, analyze, identify, and evaluate data from assigned tasks to evaluate existing and potential trends and issues while recapping for leadership. ● Perform other duties as may be assigned by leadership. Beacon Mobility is a growing family of companies committed to serving the diverse needs of our customers. Experienced, compassionate, and inspired, we take pride in our ability to create customized, mobility-based solutions that empower people to get where they need to go. Our purpose is simple - MOBILITY WITHOUT LIMITS: Transporting people to live, learn, and achieve. We are dedicated to providing those we serve with the opportunities, resources, and support to confidently move ahead. We support safe, compassionate, and inclusive environments that provide our communities with the mobility solutions they need to flourish and succeed. Backed by nearly 70 years of experience, Beacon Mobility operations can be found in Massachusetts, New York, Pennsylvania, Illinois and Minnesota providing support to over 10,000 employees in over 1,300 communities through the delivery of Paratransit and School Bus services leveraging a fleet of over 6,500 vehicles.

Reagent Chemical & Research, LLC. has been a leading US marketer of Hydrochloric Acid for over 65 years with terminals across the US, as well as truck and rail fleets. Employment with Reagent Chemical offers a competitive salary package, 401K with matching, profit sharing, 15 days PTO, 10 paid holidays, and a comprehensive health benefits package. Reagent is seeking to fill the position of Railcar Shop Quality Assurance Specialist at our AAR certified Tank Car Repair Shop located in the Channelview area of Houston, TX. This role will report directly to the Facility Manager. The Railcar Shop Quality Assurance Specialist is responsible for ensuring adherence to Reagent's Quality Assurance Program and work is performed in compliance with company, industry, and regulatory requirements which includes verifying that all repair and maintenance activities are conducted in strict compliance with company procedures, industry best practices, and all applicable regulatory requirements, including those set by the AAR and FRA. The specialist will play a key role in supporting audit readiness and promoting continuous improvement in quality and compliance across the facility. The position will be on 1st shift, working 8-12 hour days, and requires 40 hours with possible overtime. Principal Duties and Responsibilities Implement and oversee the Quality Assurance Program at the site level. Perform inbound, in-process and final inspections and audits of work performed on tank cars to ensure compliance with the quality assurance program, company procedures and regulatory requirements. Prepare work instructions for shop personnel. Oversee tank car inspections and repairs to ensure they are performed and documented correctly. Assist with tank car service equipment modifications to ensure they are performed and documented correctly. Review completed tank car inspection documents, photos and qualification dates stenciled on tank cars to ensure the requested work was performed and reported accurately. Compile and submit forms and documents to car owners and accounting. Perform incoming material inspections and place parts and material into designated areas. Maintain calibrated measuring and test equipment. Train employees on safety and quality procedures, forms and requirements. Oversee employee NDT certifications, safety training and other training and certification records. Monitor training and certification expiration dates to ensure there is no lapse and schedule or perform training and recertification as needed. Lead internal/external audits and prepare responses to audit findings. Initiate and complete nonconformance reports consisting of root cause, corrective action, and preventive action and process improvement plans. Lead and participates in continuous improvement opportunities. Assist with annual QA Manual review and updates and Management Review as required by AAAR MSRP M-1003 Section J. Ensure adherence to company safety policies, company procedures, and regulatory requirements. Performs other duties as required. Required Skills / Abilities Knowledge of the Association of American Railroads (AAR) AAR's Manual of Standards and Recommended Practices (MSRP) for tank cars specifications M-1002 and M-1003. Ability to navigate within the Federal Register and the AAR Circular Library to stay current with publication for rules, proposed rules, and notices from Federal agencies and organizations and the AAR. In-depth understanding of root cause analysis and corrective action plans. Proficient in computer software applications, including Word, Excel, Outlook, and other applications. Strong written and oral communication skills. Able to read and comprehend basic drawings and scopes of work. Strong attention for detail in identifying potential issues or safety hazards. Ability to operate effectively when faced with changing circumstances or uncertainty. Ability to clearly report findings and collaborate with team members to address them. AAR Basic and Lead Auditor Certification recommended. AAR Root Cause Analysis Certification recommended. Excellent communication skills (verbal and written). Must speak fluent English, bilingual in Spanish a plus. NDT Level II in BT, VT, PT, UTT a plus. Knowledge of rubber linings, rubber lining inspection, application, and repair experience a plus. Education and Experience: A minimum educational requirement is a high school diploma or equivalent. Minimum 5 years' experience in tank car repair quality assurance or tank car regulatory compliance. Previously held a tank car quality assurance position Hazardous Material (HAZMAT) training complying with Title 49 CFR Part 172 Subpart H in the last three years. Knowledge of regulations as they apply to Qualification and Maintenance of Tank Cars, specifically Title 49 CFR Part 180 Subpart F Physical Requirements: Must be able to lift 50 pounds at a time. Must be able to work in various elements indoors/outdoors. Must be able to pass a physical, drug screen, and background check Travel Requirements: Must be able to travel 1 - 15 days per year to attend training to enhance existing knowledge and skills. Placement agencies should not reach out regarding candidates. We will not reach out via text or make any offers before an in-person interview is completed. Please do not respond to any spam or fraudulent texts.

Job Details Experienced Houston, TX Individual Contributor 4 Year Degree None Full Time Health CareDescription Sagis Diagnostics is an entirely physician-led sub-specialty pathology group supported by a CAP-accredited histology lab located in the heart of Houston, Texas. Led by a team of board-certified pathologists, our lab is at the forefront of diagnostic science. We offer the highest quality services to physicians, physician groups, ambulatory surgery centers, and hospitals. One of our many strengths is we develop strong collaborative relationships with each of our referring physicians by offering accurate, prompt, and clear diagnoses in a personal and customized manner. A Quality Assurance (QA) Specialist in Anatomic Pathology ensures the lab adheres to regulatory standards and quality protocols by monitoring quality assurance activities, managing documentation, training staff, and facilitating process improvements. Key responsibilities include assisting with CAP, CLIA, and NY state licensing compliance, conducting internal audits, and to support and assist the Director of Quality & Compliance. Key Responsibilities Regulatory Compliance: Support the laboratory's quality assurance programs to ensure alignment with federal, state, and accrediting body regulations (CLIA, CAP). Process Improvement: Help Identify and resolve quality-related issues through data analysis, process improvement initiatives, and collaboration with laboratory staff. Documentation & Audits: Assist in the preparation and review of quality reports, regulatory compliance checklists, and other relevant laboratory documentation. Reporting & Communication: Provide updates to Director of Quality & Compliance quality improvement opportunities. Accreditation Readiness: Help the department maintain an inspection-ready environment to support accreditation readiness. Required Skills & Knowledge: Technical Expertise - Some knowledge of Anatomic Pathology principles, techniques, procedures, and instrumentation. Regulatory Knowledge: Strong understanding of laboratory quality regulations and accreditation standards (e.g., CLIA, CAP). Communication: Excellent communication and interpersonal skills to work effectively with multidisciplinary teams and provide clear guidance in a professional manner. Data Analysis: Skill in analyzing data to identify trends, resolve issues, and support process improvements. Collaboration: Ability to work collaboratively with other teams. Schedule: Full-Time, Monday-Friday, 100% On-Site Salary: $54,000 - $60,000 /year Qualifications Education: Bachelor's degree in science discipline Minimum ONE year of laboratory experience Excellent professional verbal and written communication skills Ability to work exceptionally well with others Highly detail-oriented and organized At Sagis, we offer: Medical, Dental, and Vision Insurance Company-Paid Short-term and Long-term Disability, Basic Life, EAP Voluntary Accident/Critical Illness/Life insurance Fair Wages 401(k) Contribution Vacation Paid Parental Leave Floating Holidays Scheduled Holidays Comfortable work environment Wellness Initiatives Tuition Assistance Job Training/Career Development Great Team Leaders

Job Description Quality Assurance Specialist Department: Sugar Duties / Responsibilities: The Quality Assurance (QA) Specialist will ensure the raw materials and finished product meets the quality, integrity and efficiency standards set by the organization. Responsible for ensuring that all the products packaged in the plant are safe to consume and have the highest standards of quality. Ensure that each bag of sugar packaged fulfills the customer's specifications. Responsible for monitoring of the Critical Control Points in the facility. Responsible for identifying deviations from the CCPs and once detected is responsible for stopping the line and following the established corrective actions. Enforce policies and process as it relates to proper hygiene, safety, GMP's and guidelines ensuring they are followed by employees. Check all work areas pre start up and provide authorization for production work to initiate. Perform the daily scale verification and the first metal detector test before production starts. Responsible for checking products against the specifications and confirming that it fulfills all the requirements so regular production can start. Perform the metal detection verifications at the frequencies dictated by the HACCP plan, as indicated in the PQTF and ensuring the checks are within the established limits. Performs other duties as assigned. Required Skills/Abilities: Excellent verbal and written communication skills with the ability to train staff. Understanding of quality control standards and methodologies. Understanding of manufacturing and production in the industry is a plus. Excellent organizational skills and attention to detail. Strong analytical and problem-solving skills. Proficient with Microsoft Office Suite or related software. Education and Experience: High school degree or GED preferred At least one year quality assurance experience preferred Physical Requirements: Must be able to stand and walk for long periods of time. Ability to work while standing, pushing, pulling, bending, twisting, kneeling and lifting for the entire duration of the shift Ability to work in multi-temperature environments, hot or cool Must be able to lift up to 25 pounds at times.

Job DescriptionSalary: 18-25 hour TRELS Home For Children is seeking an organized, reliable, and task-oriented Quality Assurance Specialist. The Quality Assurance (QA) Specialist will be responsible for developing and implementing QA policies and procedures, conducting regular audits and assessments, and ensuring that all organizational activities meet or exceed internal and external standards. This role requires a detail-oriented individual with a strong understanding of quality assurance methodologies and the ability to work collaboratively across departments to promote a culture of quality. Key Responsibilities: -Quality Assurance Planning: Develop and maintain the organization's quality assurance policies and procedures, ensuring they are aligned with industry standards and best practices. -Audits and Assessments: Conduct regular internal audits and assessments to identify areas for improvement and ensure compliance with legal, regulatory, and organizational standards. -Reporting and Documentation: Prepare and maintain detailed reports on QA activities, findings, and outcomes. Document all quality assurance activities and ensure that records are accurate and up to date. -Training and Support: Provide training and support to staff on quality assurance processes and best practices. Work closely with teams to implement quality improvement initiatives. -Human Resources: Help with the orientation, onboarding, and ensuring that all employees adhere to training compliance, regulations, and policies. -Stakeholder Engagement: Liaise with external stakeholders, including funders, partners, and regulatory bodies, to ensure that quality standards are met and maintained. -Continuous Improvement: Lead continuous improvement efforts, using data and feedback to drive enhancements in quality across all aspects of the organization. Work week: Monday - Thursday (8:30-4:30) Qualifications: -Bachelor's degree in a related field (e.g., Quality Management, Business Administration) or equivalent experience. -Proven experience in a quality assurance role, preferably within a nonprofit or similar setting. -Strong knowledge of quality assurance methodologies, tools, and standards. -Excellent analytical, problem-solving, and decision-making skills. -Proficient in the use of Microsoft Office Suite and QA software tools. -Exceptional attention to detail and the ability to manage multiple tasks simultaneously. -Strong communication and interpersonal skills, with the ability to work effectively in a team environment. -A passion for the mission of the nonprofit sector and a commitment to quality and excellence. What We Offer: - A supportive and mission-driven work environment. - Opportunities for professional development and growth. - Competitive salary and benefits package, commensurate with experience. Competencies: 1. Professionalism and strong work ethic. 2. Problem-solving capabilities. 3. Proactive attitude and ability to take initiative. 4. Ability to adapt to changing priorities. If you have previous experience as a Quality Assurance Specialist and familiarity within our industry, wed like to meet you. Prefer someone with a strong background in residential foster care (not required) and someone who is extremely organized, extreme attention to detail, self-starter, excellent communicator, and multi-tasker. Requirements: 3 Day Web Based Training TB Test Results Cleared Background Check Clear Driving History For Your Application To Be Considered Please provide the following: Two Professional References Resume Download & Complete The State Of Texas Application ******************************************************************************* Applicants who do not submit the above listed items will not be considered. Job Type: Full-time Benefits: Dental insurance Health insurance Vision insurance Work Location: In person

The QA Document Specialist will be responsible for maintaining proper documentation practices to ensure compliance to FDA, ISO, and other regulatory requirements as applicable, including drafting new documents and review of records. Duties and responsibilities Work with a cross-functional team to ensure all documents are properly stored and archived Facilitate the periodic review of documents to comply with internal QMS requirements Ensure completed documentation meets internal quality standards Draft documentation for batch records and raw material specifications Draft procedures for technical processes Data entry and basic statistical analysis Support the Internal Quality Audit program Inspection of raw material and in-process and finished products Assist manufacturing with batch release and other relevant documentation Assist with post-market monitoring of the company's products Assist with training and provide technical expertise as required Assist with supplier quality checks Assist with maintaining proper documentation of incoming and outgoing product Assist in other duties as assigned by the QA Manager Qualifications Have at least 2 years of relevant experience and a relevant bachelor's degree OR at least 5 years of relevant experience without a degree, preferably in the Medical Device industry Be able to work with a cross-functional team on an international stage Be able to communicate effectively in written and spoken English Be able to troubleshoot as necessary Be able to prioritize tasks effectively Show initiative and be proactive in their day-to-day tasks Preference for bilingual individuals that can speak and write Chinese, Spanish, French or German. Please note that this position is 100% in the office.

Houston, TX Exp 3-5 yrs Deg Bach Relo Bonus Job Description Sign on Bonus available for candidates with at least one year current Clinical Documentation Specialist experience. Provide clinically based concurrent and retrospective review of inpatient medical records to evaluate the documentation and utilization of acute care services. Includes facilitation of appropriate physician documentation of care to accurately reflect patient severity of illness and risk of mortality. Will play a significant role in obtaining accurate and compliant reimbursement for acute care services and in reporting quality of care outcomes. Qualifications: Clinical Documentation Specialist experience required Minimum of 3 years clinical or inpatient coding experience in an acute care setting required; 5 years experience strongly preferred. Familiarity with coding concepts and coding software desired. Knowledge of care delivery documentation systems and related medical record documents. Knowledge of age-specific needs and the elements of disease processes and related procedures. Strong broad-based clinical knowledge and understanding of pathology/physiology of disease processes. Excellent written and verbal communication skills. Excellent critical thinking skills. Excellent interpersonal skills to build effective partnering relationships with physicians, nurse staff, hospital management staff, and health information systems coding staff. Ability to work independently in a time-sensitive environment. Computer literacy and familiarity with the operation of basic office equipment. Assertive personality traits to facilitate ongoing physician communication. Ability to stand and walk for periods of time is required in the performance of job responsibilities. • Working knowledge of Medicare reimbursement system and coding structures/national coding guidelines. • Graduate of an accredited school of nursing, AHIMA accredited school, international medical school Must possess a current RN or LPN license or an RHIA, RHIT, or CCS credential. Additional Information All your information will be kept confidential according to EEO guidelines. Direct Staffing Inc

Job Description Gray Hawk Land Solutions is currently hiring for the position of a Document Specialist to work in office in Houston, Texas. The individual we are looking for must have a complete understanding of all phases of a right-of-way project, be a self-starter, and able to perform the below tasks with little or no supervision. This position would be on site in the Galleria area of Houston, Texas. Responsibilities & Qualifications: Must be highly organized and have good time management skills, must have a complete understanding of all phases of a pipeline right-of-way project from line list development to construction, and is expected to maintain accurate and current information on the overall status of the project Must have working knowledge and experience with all necessary right-of-way documents such as, but not limited to, land acquisition easements including courthouse recording requirements, temporary workspace documents, damages and compensation documents, excel spreadsheet tracking sheets etc. Maintain hard files, including easements, lease documents, real estate deeds, and various other documents relating to ownership and rights Create system line lists as requested Conduct in-house ROW and title searches as requested Scan documents into client system(s) of record Add specific metadata to documents in client system(s) of record Must have a proven history of reviewing and understanding land acquisition agreements Must be fluent in Microsoft Office software, including MS Excel and MS Word, and have an excellent understanding of database entry Must have the ability to learn new systems quickly Experience with geo AMPS or Pandell Projects and ESRI GIS software is preferred Understands general access reporting functions and the uses of formula/equation statements to optimize reports and reporting functions Must be able to multi-task and work efficiently during high-peak times Must be highly organized with the ability to prioritize work based on project timelines and ensure that timelines are not jeopardized Must have the ability to proof-read and have a keen eye for details to ensure the accuracy and completeness of reports and data Be proficient at typing and use a calculator, copier, postage machine, and other large and small equipment common to a project Excellent written and verbal communication skills Experience providing administrative support to a wide variety of users Represents self with professionalism. Can relate to people from various backgrounds and work well with others Able to work well in a team environment or an individual role Education/Experience: Minimum of Five (5) years of preparing and processing ROW acquisition easement documents on ROW projects. This position offers full health, vision & dental benefits. Powered by JazzHR y9x1gunHdv

The Quality Assurance Associate Manager / Quality Assurance Manager is responsible for overseeing and directing quality assurance activities for RadioMedix's Contract Manufacturing Facility, SPICA Center located 19705 Aldine Westfield Rd Humble, Texas 77338. This includes establishment of Quality processes for our internal manufacturing capabilities, oversight of external partners and management of ongoing manufacturing and lot release. Duties and responsibilities Duties and responsibilities Supports and/or lead onsite FDA Inspections and client audits Identifies and works with functional areas as appropriate to facilitate operational improvements. Reviews and approves product complaints and Annual Product Quality Reviews; tracks and trends product and line performance to drive quality improvements. Interacts and communicates with clients to assure expectations are established, agreed to, and achieved. Works to establish Quality Assurance processes/documents/systems for manufacturing operations. Builds impactful relationships and collaborations across the organization to achieve corporate goals. Performs Quality Assurance activities including, but are not necessarily limited to, review/approval of: Critical compliance documents in support of GMP Executed batch records for compliance Certificate of Analyses against raw data and/or specifications for compliance Stability report against protocol and raw data Release of RadioMedix owned raw materials, packaging components and products as needed Review of project-specific procedures, protocols, and reports as needed Support Quality Assurance Audits Support and/or lead RadioMedix Inspection Readiness Program, including mitigation plans Coaches and develops direct reports Works on continuous improvement projects, knowledge management, and strive for operational excellence Promotes and integrates quality into every aspect of our business Establishes quality on the floor to assist and support the manufacturing team in detecting and solving compliance errors in real time Quality review of regulatory filings in support of projects Other duties as assigned. Qualifications A bachelor's degree in a science discipline or related field is preferred Minimum of 6-10 years' experience in a quality assurance role of increasing responsibility, CQA a plus Higher level understanding of industry regulation 21CFR 211 Experience in Radioligand therapy preferred Experience in supporting Quality Control partnerships Advanced knowledge of manufacturing and analytical services in the pharma industry, radiotheranostic therapeutic knowledge preferred Working knowledge of GMP international regulations and ICH guidelines Strong problem-solving skills Ability to work independently and effectively as a team member with a multidisciplinary project Attention to detail with the ability to perform a critical review of various types of documents Strong organizational and time management skills

Job Description The Quality Assurance Associate Manager / Quality Assurance Manager is responsible for overseeing and directing quality assurance activities for RadioMedix's Contract Manufacturing Facility, SPICA Center located 19705 Aldine Westfield Rd Humble, Texas 77338. This includes establishment of Quality processes for our internal manufacturing capabilities, oversight of external partners and management of ongoing manufacturing and lot release. Duties and responsibilities Duties and responsibilities Supports and/or lead onsite FDA Inspections and client audits Identifies and works with functional areas as appropriate to facilitate operational improvements. Reviews and approves product complaints and Annual Product Quality Reviews; tracks and trends product and line performance to drive quality improvements. Interacts and communicates with clients to assure expectations are established, agreed to, and achieved. Works to establish Quality Assurance processes/documents/systems for manufacturing operations. Builds impactful relationships and collaborations across the organization to achieve corporate goals. Performs Quality Assurance activities including, but are not necessarily limited to, review/approval of: Critical compliance documents in support of GMP Executed batch records for compliance Certificate of Analyses against raw data and/or specifications for compliance Stability report against protocol and raw data Release of RadioMedix owned raw materials, packaging components and products as needed Review of project-specific procedures, protocols, and reports as needed Support Quality Assurance Audits Support and/or lead RadioMedix Inspection Readiness Program, including mitigation plans Coaches and develops direct reports Works on continuous improvement projects, knowledge management, and strive for operational excellence Promotes and integrates quality into every aspect of our business Establishes quality on the floor to assist and support the manufacturing team in detecting and solving compliance errors in real time Quality review of regulatory filings in support of projects Other duties as assigned. Qualifications A bachelor's degree in a science discipline or related field is preferred Minimum of 6-10 years' experience in a quality assurance role of increasing responsibility, CQA a plus Higher level understanding of industry regulation 21CFR 211 Experience in Radioligand therapy preferred Experience in supporting Quality Control partnerships Advanced knowledge of manufacturing and analytical services in the pharma industry, radiotheranostic therapeutic knowledge preferred Working knowledge of GMP international regulations and ICH guidelines Strong problem-solving skills Ability to work independently and effectively as a team member with a multidisciplinary project Attention to detail with the ability to perform a critical review of various types of documents Strong organizational and time management skills Powered by JazzHR 71EFn5lZfe

Engineered Air Balance is looking for a Construction Document Specialist I to join our dynamic team in Spring. Our ideal candidate will be someone reliable with a high mechanical aptitude that is tech savvy. If you've had experience in any of these job titles, Project Engineer, Construction Data Specialist, Document Control Specialist, you might be a good fit for this position! This is a great opportunity to get your career started with an established, reputable company that is staffed by people who are passionate about their work! The Company Since 1956, Engineered Air Balance has led the industry as North America's largest and most respected independent provider of Testing & Balancing (TAB), Commissioning (Cx), and Critical Environment Certification (CEC) services. At EAB, our people are our greatest asset. Guided by our core values-Integrity, Quality, Consistency, and Teamwork-we deliver excellence across healthcare, education, research, industrial, and commercial projects. Join us and be part of a team that defines industry standards and drives meaningful impact. To learn more about our company and our industry please visit us at ************************** The Position The Construction Document Specialist I will work in our Spring, Texas office and be responsible for preparing a field takeoff prior to project startup by utilizing Bluebeam PDF editing software to markup plans, gathering relevant design data from plans and submittals for populating field equipment data forms, and compiling reports consisting of data collected by field technicians. This role requires an individual who possesses a high mechanical aptitude, analytical skills and is detail oriented. Exceptional on the job training will be provided to teach technical requirements, applications and job specific procedures. Job responsibilities include: Obtaining all necessary project documentation such as plans, specs and submittals in preparation for completing a takeoff prior to a project start up. Evaluating plans and submittal for the purpose of identifying deficiencies and determining the relevant design data needed for field technicians. Preparing mechanical drawings for field technician use. Organizing and managing project documents. Populating field forms. Assisting field project leaders and managers with development of conditions of operation and other technical writing tasks. Following a schedule of work that will ensure that project field data is completed in a timely manner and that the final reports are completed and processed without delay. Required Qualifications: Up to 2 years of related skill, knowledge, or experience Or a Associates degree or Technical Certification in related field. Experience with Bluebeam, Autodesk, PlanGrid Construction, Procore, and/OR Fieldwire. Experience with HVAC, drafting, submittals, understanding blueprints, and other related responsibilities. Strong mechanical aptitude required. Construction industry experience preferred. Required Skills: Strong computer competency with knowledge in Microsoft Office Strong mechanical aptitude. Exhibits strengths in spelling, grammar, document structure and detail. Exceptional oral and written communication skills to effectively interact with all levels of an organization. Highly organized and detail-oriented with ability to work with a high volume of documents in a fast-paced environment. Team player who can effectively handle frustrations encountered in completing multiple tasks or in conflict-laden situations while maintaining quality and consistency. Previous experience in Bluebeam, Autodesk Construction Cloud, BIM360, PlanGrid, Procore Software, and a general understanding of construction plans, specs or submittals is a plus! Interested? Apply today and let us know why you would be a great fit! Engineered Air Balance is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, national origin, age, disability, genetics, status as a protected veteran, or any other protected status established by federal, state, or local laws.