Quality assurance manager jobs in Stafford, TX

Project Description: We're seeking a seasoned Test Lead to own test execution, coordination and data staging across the full Workday E2E implementation (HR, Payroll, Integrations, Reporting & Analytics). This is a high-visibility role partnering with internal and external to drive quality and readiness. Responsible for leading all test data staging activities for the Workday implementation, ensuring the correct data is in place for E2E, integration, and reporting testing. Responsibilities: • Lead setup and validation of test data across environments (development, QA, UAT) • Coordinate data loads with HRIT and integration teams; ensure prerequisite data is ready for test cycles • Manage and validate data loads, cleanses, transformations and error remediation • Develop and maintain the test data staging plan and schedule • Monitor data readiness metrics and support test teams with pre-load and post-load validations Mandatory Skills Description: • 5+ years' experience in data staging/data migration in enterprise Workday implementations • Familiarity with Workday data loads (EIBs, Studio), data validation, and troubleshooting • Strong Excel and data validation skills preferred • Excellent coordination and leadership in a cross-functional environment Nice-to-Have Skills Description: Airline experience Languages: English: C1 Advanced

Job Title: Workday Testing Data Staging Lead Tenure: 6+ months About the Role: We're seeking a seasoned Test Lead to own test execution, coordination and data staging across the full Workday E2E implementation (HR, Payroll, Integrations, Reporting & Analytics). This is a high-visibility role partnering with internal and external to drive quality and readiness. Responsible for leading all test data staging activities for the Workday implementation, ensuring the correct data is in place for E2E, integration, and reporting testing. Key Responsibilities: Lead setup and validation of test data across environments (development, QA, UAT) Coordinate data loads with HRIT and integration teams; ensure prerequisite data is ready for test cycles Manage and validate data loads, cleanses, transformations and error remediation Develop and maintain the test data staging plan and schedule Monitor data readiness metrics and support test teams with pre-load and post-load validations Required Skills & Experience: 5+ years' experience in data staging/data migration in enterprise Workday implementations Familiarity with Workday data loads (EIBs, Studio), data validation, and troubleshooting Strong Excel and data validation skills preferred Excellent coordination and leadership in a cross-functional environment

Job purpose The Laboratory Manager will work in coordination with Stone Clinical Laboratories/Gulf South Diagnostics leadership and in alignment with established Stone Clinical Laboratories/Gulf South Diagnostics strategies and policies to provide, maintain, control, and improve laboratory testing services. The Laboratory Manager is responsible for day-to-day supervision of testing personnel, reporting of test results, and proper performance of all laboratory procedures while working closely with the Technical and General Supervisors and Laboratory Director. The Laboratory Manager shall conduct job responsibilities in accordance with the standards set forth by Stone Clinical Laboratories policies and procedures, applicable federal and state laws, and applicable professional standards. Duties and responsibilities Included, but not limited to: · Participate in the establishment and maintenance of laboratory policies and procedures · Participate in the establishment of ranges, specimen requirements for tests, and acceptance criteria · Perform QC testing and recognize deviation from acceptable values · Follow established protocol for remedial action for QC variances · Ensure proper maintenance is completed · Ensure calibration period is adequate to cover testing · Oversee and direct proficiency survey testing · Assure remedial or corrective actions take place when test systems deviate from the laboratory's specified performance specifications · Ensure testing and recording of results in all lab areas are managed by the technical team · Understand reference laboratory workflow · Provide resolution for technical and non-technical variances occurring in the laboratory · Verify the Lab Director's review of monthly QC, maintenance, patient records, and QA monitors · Ensure test analysis and specimen examination meets all acceptable performance criteria · Evaluate and/or implement new procedures, tests, or methodologies · Ensure that patient test results are reported & all criteria for test performance characteristics are acceptable · Organize workflow and ensure that employees understand their duties · Provide orientation to testing personnel ensuring lab users are trained on the correct use of the lab equipment · Ensure all users of the lab are wearing the appropriate PPE · Ensure all CAP, CLIA, OSHA, HIPAA, and any other appropriate regulatory standards are adhered to while performing related duties · Identify and resolve workplace problems, including tardiness or absenteeism · Ensure that the laboratory is cleaned/sanitized and maintain inventory in a neat and acceptable manner · Familiarity with LC-MS/MS instruments · Perform other similar or related duties as requested or assigned The preceding functions have been provided as examples of the types of work performed by employees assigned to this job classification. Management reserves the right to add, modify, change or rescind the work assignments of different positions and to make reasonable accommodations so that qualified employees can perform the essential functions of the job. Qualifications Required · Bachelor of Science or higher in medical technology, chemistry, toxicology, or related science plus 4+ years of high-complexity toxicology testing experience Preferred · Previous experience working autonomously in a clinical chemistry environment preferred · Prior experience in general blood testing preferred · Method development/validation experience considered a plus but not required · Previous lab management/supervisory experience preferred Working conditions · May be exposed to noise, dirt, dust, fumes, loud noises and blood borne pathogens. · Must be able to work under stress and in fast-paced environment. · Emergent situations could extend working hours or require infrequent week-end work. Physical requirements Must be able to work under conditions that require sitting, standing, walking, lifting, bending, reaching, pulling, grasping, talking, hearing and seeing. Reasonable accommodation may be made to accommodate a qualified individual with a disability.

Job: Quality Control & Operational Excellence Manager Reports to: Operations Director About Us National Wire LLC is a leading welded wire manufacturer based in Conroe, Texas. With a commitment to product quality, customer satisfaction, and operational efficiency, we are seeking a Quality Control & Operational Excellence Manager to lead our efforts in driving continuous improvement and maintaining compliance with industry standards. Position Summary To lead and sustain a culture of quality and continuous improvement by ensuring consistent product excellence and driving operational efficiency through innovative methodologies, in alignment with the company's strategic objectives and industry best practices. Key Accountabilities Quality Management System: Lead the development, implementation, and continuous improvement of the QMS. ISO 9001: Ensure annual certification. Compliance: Ensure appropriate customer and government compliance (regulatory). Strategic Aligning: Responsible for supporting CEOs' efforts to develop and execute the implementation of the strategic alignment process. Company Values: Responsible for conducting his/her day-to-day actions by using National Wire's Values. Continuous Improvement: Lead and implement methodologies, techniques, and systems to enable the company's continuous improvement capabilities, including training and coaching Leadership: Build and lead a high-performing team of QC and Operational Excellence professionals, ensuring effective resource allocation, performance management, and professional development. Knowledge and Skills Required Education: Bachelor's degree in Engineering, Industrial Engineering, or a related technical field (MUST). Master's degree or certifications in Quality Management, Lean, or Six Sigma (Preferred) Experience: 7+ years of progressive experience in quality control, operations, or continuous improvement, with a strong background in manufacturing or industrial environments. Leadership: 5 years in a managerial or leadership position, leading quality assurance teams and operational excellence initiatives across multiple departments. Experience training and coaching personnel at all levels on quality and operational standards. Technology: Working knowledge of Microsoft Office and ERP applications. Languages: Bilingual English Spanish (MUST) Physical requirements: Able to stand long periods of time and travel occasionally within US. Why Join Us At National Wire, you won't just be filling a role-you'll be shaping the future of our operations. We're a fast-growing company where your ideas and leadership will directly impact performance, quality, and long-term success. You'll have the opportunity to work alongside senior leadership, lead strategic initiatives, and be part of a company culture that values innovation, ownership, and excellence in execution. We offer a stable, growth-oriented work environment where continuous improvement isn't just encouraged-it's expected. If you're looking to lead with purpose and drive real results, this is the place for you.

Type: Contract Domain: Retail / Supply Chain / OMS / Personalization We are seeking a Manager - Quality Engineering (QE) with strong Retail/Supply Chain domain expertise and hands-on OMS experience. This role will lead the test automation strategy for a large-scale Retail Personalization initiative while also supporting OMS quality needs. The ideal candidate must have deep understanding of OMS workflows and be able to clearly articulate their specific responsibilities and contributions on prior OMS projects. This position requires a combination of technical leadership, automation expertise, data validation skills, and the ability to work closely with cross-functional and offshore teams. Key Responsibilities Lead end-to-end QE strategy for personalization and OMS-related workflows. Manage and coordinate with both client stakeholders and offshore QE teams. Build and maintain automated test suites for API, UI, and data validation. Ensure data integrity and validation across personalization models and high-volume datasets. Partner with developers, data engineers, and product teams to define and enforce quality standards. Support performance and scalability testing for personalization and OMS scenarios. Integrate continuous testing practices into CI/CD pipelines. Provide detailed documentation and clearly communicate test results, coverage, and risks. Must-Have Qualifications Domain Expertise Strong Retail and/or Supply Chain domain knowledge. In-depth Order Management System (OMS) experience: Must be able to detail systems worked on (e.g., Manhattan, IBM Sterling, custom OMS, etc.) Must articulate specific roles, modules handled, integrations tested, and contributions. QE & Automation Expertise 7+ years in Quality Engineering with strong hands-on automation experience. Automation expertise using Selenium, Cypress, or equivalent frameworks. Strong API testing skills using Postman, Rest Assured, or similar. Solid scripting knowledge in Python, Java, or JavaScript. Strong SQL skills with experience validating large datasets. Experience working with datasets tied to personalization or recommendation engines. Data + Cloud Exposure to Big Data ecosystems-Spark, Hive, or large-scale data validation. Cloud experience with AWS, GCP, or Azure (at least one required). Nice-to-Have Experience with A/B testing, experimentation platforms, or ML model validation. Understanding of data governance and privacy compliance in retail environments. Prior QE leadership experience on personalization or customer experience programs. Additional Expectations Must be able to work onsite in Katy, TX at the client location (5 days/week preferred). Strong communication skills and ability to present OMS experience clearly and confidently. Ability to work in a fast-paced environment with evolving business requirements.

We are seeking an experienced QE Developer with strong automation expertise and a technical background suited for a fast-paced environment. This role will focus on designing, developing, and maintaining automated test frameworks and validations for the GasQuest application. The ideal candidate will have hands-on experience with Java-based automation, CI/CD execution pipelines, and modern QA tooling, along with the ability to work both independently and in cross-functional teams. Responsibilities Develop, maintain, and enhance automated test scripts using Java and Playwright. Implement hybrid test automation frameworks leveraging Page Object Model (POM) principles. Integrate automation scripts with CI/CD pipelines to support continuous testing and deployment. Conduct API testing and validation using Rest Assured and related test utilities. Execute automated test suites across containerized environments using Docker and Selenium Grid. Validate database operations leveraging MySQL JDBC for test data verification and backend checks. Monitor execution dashboards, analyze failures, and deliver actionable defect reporting through Extent Reports and CircleCI. Collaborate with developers, QA analysts, and product teams to align automation efforts with release cycles and business expectations. Participate in code reviews, source control workflows, and best practices using GitHub. Assist in on-call support rotations and after-hours deployment testing when required. Required Technical Skills Proficiency in automation testing using Playwright Java API. Strong Java programming experience for script development. Hands-on experience with: Extent Reports (HTML-based reporting) Maven (build and dependency management) TestNG (execution framework) Experience with CI/CD execution pipelines, especially CircleCI, Docker, and Selenium Grid. Familiarity with debugging tools, Chrome DevTools, and repository workflows (branching, PRs, merging). Additional Preferred Skills SQL experience (Aurora and/or Redshift). Basic AWS familiarity (S3 navigation, Lambda log review, CLI usage). API testing with Postman. JSON data format understanding. PowerBI, Excel, and PowerShell or Git Bash for scripting. Experience using Snag-It or similar screenshot/documentation tools. Knowledge of Oil & Gas industry applications is a plus.

- Core Specialty's Data Environment is the organizational data ecosystem that supports enterprise requirements for data management, consolidation, insights, and reporting. The Data & Analytics organization ingests and manages data from over 200 distinct sources and growing, which serves business intelligence, AI/ML models, and enterprise decision-making. Maintaining the integrity, accuracy, and completeness of this extensive data environment requires a scalable and automated quality assurance strategy. The Director of Engineering - QA Automation will be responsible for designing and implementing this strategy, integrating quality processes throughout the data platform-including ingestion pipelines, semantic models, and machine learning workflows. This role will require 40% hands on involvement to start in order to build out the architecture, blueprints, and coding standards required for QA Engineers to adhere to. It may also include development efforts as needed. Key Accountabilities/Deliverables: Define and lead the QA automation strategy for data engineering, analytics, and machine learning initiatives. Architect and implement scalable, reusable automation frameworks for data pipelines, ingestion models, semantic layers, and ML workflows. Collaborate with Data Engineering, Data Science, and DevOps teams to integrate automated testing into CI/CD pipelines. Establish coding standards, architectural patterns, and best practices for test automation across the organization. Develop automated validation for data quality, schema enforcement, lineage tracking, and model performance. Mentor and grow a high-performing QA team with deep domain knowledge in data and analytics. Drive continuous improvement in testing tools, processes, and observability. In addition to the above key responsibilities, you may be required to undertake other duties from time to time as the Company may reasonably require. Technical Knowledge and Understanding: Programming Languages: Python (preferred), SQL, Java/Scala (for Spark-based pipelines) Automation Frameworks: PyTest, Great Expectations, dbt tests, Selenium, Airflow test suites Data Technologies: Spark, Kafka, Airflow, dbt, Delta Lake, Parquet, Avro Cloud Platforms: AWS (Glue, S3, Redshift), Azure, GCP (BigQuery, Dataflow), Databricks Data Warehouses: Snowflake, BigQuery, Redshift CI/CD & DevOps: GitHub Actions, Jenkins, Docker, Kubernetes ML Testing: MLflow, TensorFlow Model Analysis, custom validation pipelines Observability & Monitoring: Monte Carlo, Databand, OpenLineage SDLC: Agile/SCRUM Frameworks, Kanban, JIRA Data Quality Management: MS Purview Preferred Skills Experience with synthetic data generation and data fuzzing tools Experience with Data Contracts and the Producer vs. Consumer model Familiarity with data governance and compliance frameworks (e.g., GDPR, HIPAA) Exposure to AI-assisted testing platforms Experience: Bachelor's degree in computer science, data engineering, or related field required Master's degree in computer science, data engineering, or related field preferred Minimum of 15 years of experience in Data Engineering (hands-on roles) Minimum of 5 years of experience in a leadership position Prior QA and automation experience within data engineering space required Proven experience in testing large-scale data systems and ML workflows Strong architectural thinking and ability to define scalable testing patterns Excellent leadership, communication, and cross-functional collaboration skills Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa for this position. #LI-Hybrid - At Core Specialty, you will receive a competitive salary and opportunities for professional development and advancement. We offer medical, dental, vision, and life insurances; short and long-term disability; a Company-match of 100% of a 6% contribution 401(k) plan; an Employee Assistance Plan; Health Savings Account, Flexible Spending Account, Health Reimbursement Account, and a wellness program

Inspects accepts and/or rejects work performed in compliance with applicable codes and specifications. RESPONSIBILITIES - Understanding and working knowledge of the company quality control program, company standards, procedures and codes. - Performs audits to ensure compliance - Completes records, maintains tools and equipment, and performs various clean-up and housekeeping activities. - Responsible for observing and complying with all safety and project rules, including wearing required personal safety equipment. Performs other duties as required.

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers . If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Dover Precision Components is hiring a Quality Manager for our FW Murphy Production Controls brand, located at our Rosenberg, TX facility. We offer competitive pay and benefits and the ability to be part of the market leader at a stable, growing, and innovative company. We design and manufacture electrical controls supporting the oil and gas industry, primarily on an engineered-to-order basis. We are part of $7.5 billion Dover Corporation. WHAT YOU'LL DO In this role, you will own delivering sustainable performance through an effective Quality Management System (QMS) and continuous improvement goals. You will work cross- functionally to ensure quality in a Lean Manufacturing technical components' environment. You will supervise a Customer Quality Manager, 3 Quality Technicians, a Quality Engineer, and a Documentation Control Specialist. You will plan and direct activities to develop, apply, sustain, and improve the QMS to ensure external and internal requirements are met. Specific responsibilities include: Provide supervision, coaching, training, career progression opportunities, and mentoring for a Quality Team. Hire and supervise employees. Oversee internal and external quality, customer complaints, and all customer communication related to quality issues. Lead execution of corporate and specific site quality goals. Promote a proactive Built in Quality (BIQ) approach to quality and partners/collaborates with internal stakeholders to achieve site's performance goals. Manage activities related to the ISO Certification. Lead and serve as the subject matter expert for advanced problem-solving methodologies. Collaborate with internal stakeholders to modify and continuously improve processes to enhance quality, and stability of processes. Develop and promote Built in Quality concepts into the quality system using methodologies such as Poke Yoke, Quality Gates, and Upstream Certification process. Design and implement policies and procedures to ensure that quality standards are met during production. Ensure testing of processes and products are conducted per documented standards. Develop training programs and materials and conduct training sessions on quality concepts. Work closely with Team Leaders and production personnel on all shifts to provide guidance and instruction on proper inspection and reporting procedures. Confer with customers on changes in quality standards and communicate requirements to internal stakeholders. Establish and use programs to evaluate precision and accuracy of production and testing/measurement equipment. Develop and devise standards and methods for inspection, testing and evaluation of materials, in process and finished products. Develop process control methodologies to ensure quality requirements. Audit and qualify suppliers to ensure compliance with standards. Collaborate with suppliers on problems or necessary corrective actions to be taken. Investigate deviations from standards and completes necessary analysis. Coordinate government or customer visits for source inspection or quality system audits. Conduct visits to obtain required customer acceptance of products and maintain all associated records and documentation as needed. Review materials, components or products returned under warranty claims. Analyze reason(s) for failure and advise customers of action to be taken. Report and monitor Quality performance metrics. Conduct/coordinate analysis to determine failure root cause and ensure necessary actions are taken to improve quality performance metrics. Additional Qualifications/Responsibilities WHAT YOU'LL BRING Bachelor's degree required; preference for Engineering field, other degrees considered depending on work experience. 7+ years' work experience in an engineered product environment with specific experience in product and/or material quality and compliance. Supervisory experience, to include mentoring, performance reviews, and hiring. Lean Six Sigma manufacturing experience. Project Management experience or training. Experienced in quality audits and working collaboratively with internal and external partners to ensure quality standards are set and achieved. Excellent problem- solving skills and demonstrated success in root cause analysis and troubleshooting. Excellent collaboration and communication skills. Strong computer skills, including ERP, MS Office, and data visualization. Ability to travel (overnight 10-15%) to meet customers, internal partners, and/or attend conferences. ALSO GREAT IF YOU BRING/ PREFERENCES Electrical components, control panels, and/or automation product expertise preferred. Master's degree in engineering or related technical field. Lean Six Sigma Certification. Certification in Quality (i.e. Six Sigma, CQE, etc.) is preferred. Must be willing to obtain certifications if not already accredited. Strong understanding and application of engineering principles and design practices. Experience with Quality Management Systems. DOVER PRECISION COMPONENTS Dover Precision Components 'DPC' ('the Company') is part of Dover Corporation's ('the Parent Company') Pumps and Process solutions segment. DPC holds market leading positions globally and delivers performance-critical solutions across the oil & gas, power generation, marine, industrial, chemical and general processing markets. We design and manufacture mission-critical equipment components to deliver more affordable, cleaner energy solutions and enable manufacturers to operate more efficiently. WE DELIVER CUSTOMER SUCCESS Dover Precision Components delivers products and services that enhance performance, improve safety, reduce carbon emissions, and accelerate clean energy adoption, through collaborative Customer relationships, expert engineering, and an innovative culture. Our strong Company portfolio is comprised of long products and services offered under Cook Compression, Cook Mechanical Field Services, Waukesha Bearings, Waukesha Magnetic Bearings, Inpro/Seal, Bearings Plus, and FW Murphy Production Controls. Our global footprint reaches more than twelve locations in the Americas and more than six locations in Europe and China.

Great Lakes Dredge & Dock is seeking a Construction Quality Control Manaer. Candidates with prior Bechtel project experience are strongly encouraged to apply. Role Overview: The CQC Supervisor will be responsible for the overall management of construction quality control and will have the authority to act on all CQC matters for Great Lakes Dredge & Dock. This position is dedicated solely to quality control for a specific project and will serve as the primary liaison between Great Lakes and the U.S. Army Corps of Engineers (USACE). Skills: -Prior experience working on Bechtel projects or with Bechtel clients -Strong attention to detail and documentation skills -Oversee and manage all aspects of construction quality control for the project -Be onsite at all times during construction activities -Communicate regularly with the GLDD Project Manager and Site Managers to keep all parties informed of project status and quality issues Skills USACE, CQC, CQM, DREDGING, excavation, bridge, levy, wateway, excavation, levy, marine construction, Qcm, Quality control, Construction, Cqm, Osha 30, Federal construction, Qc, Construction management Top Skills Details USACE, CQC, CQM, DREDGING, excavation, bridge, levy, wateway, excavation, levy, marine construction,Qcm Additional Skills & Qualifications Minimum Qualifications: -USACE Construction Quality Management for Contractors certification, held for at least five years (certification must have been obtained five or more years ago; certifications earned within the last five years will not meet this requirement) -Minimum of five years' experience as Quality Control Manager -Proficiency with Primavera P6 scheduling software and Microsoft Office Suite -Physical capability to perform onsite inspections and fieldwork as required Experience Level Intermediate Level Job Type & Location This is a Contract to Hire position based out of Houston, TX. Pay and Benefits The pay range for this position is $50.00 - $55.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Houston,TX. Application Deadline This position is anticipated to close on Dec 24, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Quality Control Manager About PROENERGY PROENERGY is a global and vertically integrated energy transition platform. Focused exclusively on fast-start, dispatchable power, our company supports both energy security and renewable growth with complete turbine services, project development, equipment manufacturing, turnkey generation facilities, operations, and maintenance. Our Footprint We are primed for the energy transition with permanent service locations in Missouri, Texas, and Argentina. Our world-class Missouri headquarters is purpose-built to meet dispatchable power needs. It sits on 90 acres in Sedalia and features more than 600,000 sq. ft of service capacity under roof, which includes the only independent Level-IV aeroderivative depot and string-test facility in the world. Our Houston, Texas, office is a strategic satellite positioned near our own dispatchable power installations. Our Philosophy We take care of our people and strive to make a positive difference for the world. We offer competitive pay, excellent benefits that include Medical, Dental, Vision, and Life/Disability Insurance at minimal cost to the employee, 10 paid holidays, paid time off, and a 401K plan. If you are looking for a rewarding career and possess specialized knowledge and quality-oriented problem-solving skills, we encourage you to apply today. We are seeking a highly skilled and driven Quality Control Manager to lead and oversee all aspects of quality control within our Packaging and Gas Turbine Manufacturing operations. This role is critical to ensuring our products meet the highest standards of performance, safety, and compliance. The ideal candidate will bring expertise in manufacturing processes, quality systems, and team leadership to drive continuous improvement across the production lifecycle. Reports To: Director Quality Work Location: 6401 North Eldridge Pkwy., Houston, TX 77041 Position Responsibilities Quality Strategy & Leadership Develop and implement quality control strategies aligned with company goals and industry standards. Lead cross-functional quality initiatives across Packaging and Gas Turbine teams. Process Oversight Monitor and improve quality control processes for welding, machining, assembly, and testing of turbine components. Ensure compliance with ISO 9001, ASME, AWS, and other relevant standards. Inspection & Testing Oversee incoming material inspections, in-process checks / activities, calibrated equipment. Manage nonconforming materials. Root Cause Analysis & Corrective Action Lead investigations into quality issues. Implement corrective and preventive actions (CAPA) using tools like 8D, Fishbone, and FMEA. Supplier Quality Management Ensure supplier materials meet specifications and quality requirements. Provide quality oversight into Warehouse activities. Documentation & Reporting Maintain accurate records of inspections, audits, and quality metrics. Present quality performance data to leadership and recommend improvements. Team Development Train and mentor quality inspectors and technicians. Foster a culture of accountability, precision, and continuous improvement. Required Qualifications Excellent communication and leadership skills. Demonstrated attention to detail and analytical skills ASME/AWS Certified Welding Inspector qualification (preferred). 5+ Years' Experience in Quality Management in the manufacturing industry. Strong knowledge of fabrication, welding techniques and gas turbine components. Proficiency in quality tools: Six Sigma, Lean, SPC, Minitab, etc. Familiarity with ISO 9001. Ability to competently read and analyze engineering drawings, schematics, Piping and Instrumentation Diagrams (P&ID) and Flow and Instrumentation Diagrams (F&ID). US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa. Successful candidate will need to satisfactorily complete pre-employment drug screen and background check Desired Qualifications Proficient use of ProWrite software is preferred. Knowledge of communication principles and practices. Ability to work under pressure in a fast-paced environment. Ability to establish and maintain effective relationships with the public and co-workers. Ability to analyze and resolve problems in a logical and effective manner. Ability to perform research, compile and analyze data, and write clear, concise and accurate reports on complex subjects. Ability to simultaneously manage multiple job assignments. Ability to communicate clearly and concisely, both orally and in writing. While performing the duties of this position, the employee is frequently required to sit, stand, walk, communicate, reach and manipulate objects. Specific vision abilities required by the job include close vision and the ability to adjust focus. It is PROENERGY's policy to provide equal opportunity in employment to all its employees and applicants for employment without regard to race, color, religion, sex, pregnancy, age, disability, national origin, marital status, ancestry, medical condition, military status, or any other characteristic protected by State or Federal law.

located in Pearland, TX. The purpose of this role is to lead a team of associates and oversee all aspects of the Microbiology and Environmental Monitoring Program, helping to assure compliant, effective, and modern contamination control strategy at the Lonza Houston Site. This position will be a key member of the Quality Leadership team. What you will get: A competitive compensation. In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus. Medical, dental and vision insurance. 401(k) matching plan. Life insurance, as well as short-term and long-term disability insurance. Employee assistance programs. Paid time off (PTO). Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge. What you will do: Lead the QC Microbiology and Environmental Monitoring Program, ensuring detailed execution and compliance. Supervise and mentor the QC Microbiology and Environmental Monitoring teams, encouraging a problem-solving approach. Be responsible for the site environmental monitoring and utility trend program, sharing insights with the Quality Council and advancing adverse trends appropriately. Lead environmental excursion and microbial investigations, implementing timely corrective actions. Prepare audit responses, deviations, and CAPA, ensuring detailed and timely resolutions. Prepare responses to audits and deviations, out of specification/lab investigations, customer complaints, and corrective/preventative actions (CAPA). Lead strategic projects in line with site and global quality strategy, supporting the Site Quality Plan and deliverables. What we are looking for: 10+ years' QC Microbiology experience. 5+ years' people management/leadership experience. A plus for shift structured team management. Commercial experience in environmental monitoring, in a sterile (aseptic) manufacturing plant, and with MODA system. Bachelor`s degree in science or related field, MS or Ph.D. is preferred. About Lonza: At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now.

CQCM is responsible for establishing and maintaining the quality of work and control of the construction activities, and of implementing the Quality Control Plan for the project. The CQCM will assist in developing work plans and is responsible to verify that all features of work are in compliance with the contract requirements. Quality Control System (QCS) Manager - QC will input and/or track that all pertinent information is being included in the QCS daily. This includes but is not limited to Contract Administration, Finances, Quality Control (Daily Reports, Deficiency Reports, Requests for Information (RFIs) Work Plans, Accident Hazard Analysis (AHA), etc.), Submittals, Scheduling, Data Import/Export Sets up field filing system and maintains during the life of the project Drafts, maintains, and files daily reports (including safety reports) Performs Quality Control for all elements of work (planning, performance, compliance, and inspection) Submittal Register Owner - new submittals, resubmittals, verification of compliance, deviations, justifications, waivers, etc. Field Material Receiver (check for compliance and of all delivered and stored material and equipment and implementation of manufacturer's recommendations and file paperwork in field) Conducts Preparatory and Initial Meetings All permits received All equipment that will be on site Laydown plan Material storage Construction procedures Contingencies Compliance to specifications (how we are addressing the specifications for the particular feature of work) Access (ingress and egress) Utilities (interferences, outages, etc.) Design Changes (RFIs & RFPs) Outline of Subcontractor Coordination (subcontractors involved need to attend, but not present) Public Notices and Permits Facilitates for the schedule to move forward - Feedback for Next Day and Three Week Lookaheads, submittals in place, work plans reviewed, preparatory meetings scheduled and/or completed, issues or conflicts addressed. Skills and Qualifications Ability to address issues with all features of work at the site Knowledge of all the necessary coordination to complete project scope Good decision maker - desire to make decisions based on compliance, practicality, sound fact and for the benefit of the company Ability to work and communicate in a team atmosphere Computer Literate including Microsoft Office (a plus for knowledge in USACE RMS, CMIC) Knowledge in reading plans and interpreting specifications Training in the 3-Phase Quality Control Programs (USACE CQCM) General knowledge in First Aid/CPR, OSHA regulations Knowledge and/or Training in Confined Spaces, Rigging, Scaffolding Inspection, Benching and Shoring, Fall Protection and other safety procedures needed to complete the scope of the project. Innate desire to bring the client a quality based, fully compliant project. General knowledge of the Electrical Code, the International Mechanical Code, Plumbing Code, other Building and Industry Codes and Standards, LEED and Sustainability, etc. Experience Construction Quality Control: 3 years (Preferred) Construction industry with vertical building experience: 5 years You can also apply here: *************************************************************************

is contingent upon contract award. Maintains and implements the Quality program on a medical facility operations task order and ensures that the products and services rendered meet the specifications of the customer. Assists with the organization's quality improvement efforts, such as developing and administrating the program, training and coaching employees and facilitating change throughout the organization. Assists the PM/CA in establishing plans, policies and procedures, and quality improvement efforts to meet or exceed customers' needs and expectations. Located at Brooke Army Medical Center Joint Base San Antonio/Ft. Sam Houston, TX. The Quality Control Manager will understand and be knowledgeable with NFPA and OSHA codes and standards along with knowledge of the National Electric Code (NEC), Environmental Protection Agency (EPA), The Joint Commission (TJC), American Association for Ambulatory Health Care (AAAHC), and Occupational Safety and Health Administration (OSHA). RESPONSIBILITIES AND DUTIES: Develop, Maintain, and Implement the Quality Control Plan, • Perform Internal Quality Audits and Inspections, Identify Corrective and Preventive Actions, and perform Follow-up Activities, • Participate and Assist in External and 2nd Party Audits (government), • Prepare and update Quality Plans, Procedures and Processes, • Prepare minutes of meetings as needed, • Liaison for the quality director and regional operations management with project site and customer agencies, • Perform quality orientation, training programs, quality audits and inspections, • Document and record control, • Subcontractor Pre-qualification and Evaluation • Independently inspects standardized procedures, items, operations and/or contract requirements for compliance, • Independent record keeping and preparation of reports, inspection and testing, • Interpretation of plans, contracts and specifications and observation of activities to check adherence to quality and contract practices and requirements, • Prepare, coordinate, submit, and document Performance, Management Reviews, and Quality related summary reports to the government and corporate office. • Collect and input data from various sources into electronic spreadsheets or data bases for graphing and trending, • Update Quality SharePoint site with quality related documentation, including but not limited to, Project Data Report, monthly reports to government, corrective/preventive actions, customer satisfaction, performance reviews, etc. • Assist other areas in meeting contract or quality requirements, as required, • Attend meetings as required or requested by the government and project management, • Maintain the confidentiality of sensitive quality and company proprietary information, • Promote quality awareness throughout the organization QUALIFICATIONS: • Minimum five (5) years' experience of QC experience in a healthcare setting • Direct engagement of minimum of one (1) full TJC or equivalent survey in a major hospital facility • Must have working experience with NFPA, OSHA codes and standards, TJC accreditation and EOC. • High school diploma or equivalent Certification required. • Must have a valid State Vehicle Operators Permit. • Ability to read, write, speak, and understand English. • Competence with Microsoft Office products to include Word and Excel. • Meet all training requirements within 60 days of contract award EDUCATION REQUIREMENTS: • High school diploma or equivalent Certification required. PHYSICAL REQUIREMENTS: • Must be able to travel to job locations by automobile and commercial airline. • Must be able to lift up to 10 pounds on a regular basis and up to 50 pounds as needed. • Must be able to work in the sitting position for 8 or more hours per day. • Must be able to walk/travel to various locations within the facility and satellite locations to perform inspections. • Must be able to work at a computer station for extended periods of time.

DOD Site Safety Health Officer/Quality Control Manager (SSHO QCM) - Texas We are a large growing general contractor that specializes in working on Department of Defense construction projects in many of the department of defense's construction projects (this includes the Army, Navy, Army Corps of Engineers, Marines, Air Force, among others). This is a full-time position with great benefits. We are looking to hire the best and brightest DOD SSHO/QCM to grow with our great company. Responsibilities: Make sure all military, state and federal safety and quality control requirements are being met and exceeded Make sure all the crews are following and adhering to safety requirements Work closely with the superintendents and project managers as well as the owners Attend Site Safety meetings Meet with OSHA and submit required safety paperwork Manage all safety claims Requirements: Local Ability to travel. Stable work history. OSHA and USACE QC Certifications. 6+ years: SSHO, QCM, DOD Construction. Prior Apprentice, Journeyman, Foreman, or Superintendent field experience highly preferred. Knowledge in construction i.e prints, procedures, plans, scheduling, safety, and testing.

Title: Supplier Quality Manager Summary: The Supplier Quality Manager plays a critical role in supporting Everllence's supply chain strategy by driving supplier development and ensuring compliance with quality standards. This role serves as a key liaison between Everllence USA and the global supplier quality team, particularly with European headquarters, to ensure supplier performance aligns with corporate guidelines and expectations. Key Job Responsibilities: Lead supplier qualification, inspection, and product-related development activities. Define, implement, and monitor corrective and preventive actions to drive continuous supplier improvement. Plan, coordinate, and oversee quality assurance for complex engineering and manufacturing projects. Review construction and production drawings, as well as customer specifications, for compliance. Collaborate with regulatory authorities, inspection agencies, and notified bodies. Work cross-functionally with procurement, engineering, manufacturing, materials technology, and global teams. Maintain and manage quality documentation and ensure its proper application. Provide training and support to local teams on supplier quality processes and standards. Required Education: Bachelor's degree in Mechanical Engineering or a related technical field. Master's degree in Mechanical Engineering or a related technical discipline. Required Experience: Minimum 5 years of experience in machinery or plant engineering, preferably in turbomachinery and welding technology. Minimum 5 years of experience applying quality methods in industrial environments Experience leading audits and third-party examinations as a Lead Auditor. NDT certification (RT, VT, PT, UT, MT) to at least Level 2 per ISO 9712, ASME V, or ASNT Required 3rd party Certifications/Qualifications: None. Physical Requirements: Willingness and ability to travel internationally to industrial production plants, construction sites, and manufacturing facilities, including those in challenging environments. Competencies: Knowledge of welding technology and relevant standards (ASME IV, VIII, IX, B31.1, B31.3, ISO 3834, ISO 14731). Strong understanding of quality management systems and methods (ISO 9001, 14001, 45001). Proficiency in Microsoft Office and SAP. Excellent organizational, verbal, and written communication skills. Strong interpersonal skills and ability to work in cross-functional, international teams.

Be Part of an Extraordinary Team A proud member of the Elevance Health family of companies, Paragon Healthcare brings over 20 years in providing life-saving and life-giving infusible and injectable drug therapies through our specialty pharmacies, our infusion centers, and the home setting. Title: Quality of Life Program Manager- Paragon Ideal candidates will be comfortable traveling 60-70% of the time to local Hemophilia chapters across the U.S. The ability to attend Programs scheduled on nights and weekends will be required. Field: This field-based role enables associates to primarily operate in the field, traveling to client sites or designated locations as their role requires, with occasional office attendance for meetings or training. This approach ensures flexibility, responsiveness to client needs, and direct, hands-on engagement. Please note that per our policy on hybrid/virtual work, candidates not within a reasonable commuting distance from the posting location(s) will not be considered for employment, unless an accommodation is granted as required by law. Build the Possibilities. Make an Extraordinary Impact. The Quality of Life Program Manager- Paragon is responsible for developing and implementing innovative ""Quality of Life"" (QOL) programs for individuals with bleeding disorders to drive health outcomes and improve therapy adherence. How you will make an impact: Primary duties may include, but are not limited to: * Collaborate with territory representatives to leading the increased business generation and customer retention. * Develops and maintain business relationships with local chapters, clinics, and healthcare providers to enhance the business unit presence and impact in respective territories. * Utilize lifestyle tools and resources within the QOL program to empower patients in managing their health, thus fostering a sense of control over their condition. * Strategically integrate QOL initiatives into sales efforts to shorten the sales cycle and promote seamless health management solutions for patients. * Leverage the QOL program as a significant referral source, contributing to business growth while maintaining cost-effectiveness compared to traditional event sponsorships. * Monitor and evaluate the effectiveness of QOL programs regularly, making data-driven adjustments to ensure optimal patient engagement and satisfaction. * Collaborate with cross-functional teams to align QOL initiatives with overall company objectives and marketing strategies. Minimum Requirements: * Requires a BA/BS degree and a minimum of 10 years of related experience in Specialty Pharmacy; and experience in marketing software (Aperture and Photoshop); or any combination of education and experience which would provide an equivalent background. * Joint Health, Health and Nutrition and CPR certification are required. Preferred Skills, Capabilities and Experiences: * Prior experience as a professional Public Speaker is strongly preferred. For candidates working in person or virtually in the below location(s), the salary* range for this specific position is $71,544 to $112,194 Locations: Colorado, Washington State In addition to your salary, Elevance Health offers benefits such as, a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements). The salary offered for this specific position is based on a number of legitimate, non-discriminatory factors set by the Company. The Company is fully committed to ensuring equal pay opportunities for equal work regardless of gender, race, or any other category protected by federal, state, and local pay equity laws. * The salary range is the range Elevance Health in good faith believes is the range of possible compensation for this role at the time of this posting. This range may be modified in the future and actual compensation may vary from posting based on geographic location, work experience, education and/or skill level. Even within the range, the actual compensation will vary depending on the above factors as well as market/business considerations. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health. Who We Are Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve. How We Work At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business. We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few. Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process. The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws. Elevance Health is an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.

Where You'll Work St. Luke's Health-The Vintage Hospital provides high-quality, compassionate care for residents of the Willowbrook, Champions, and Tomball areas of Northwest Houston. With the resources of the St. Luke's Health system, we are able to deliver the most advanced care available to our Northwest Houston community. The Vintage Hospital offers the latest in diagnostic and surgical expertise, including heart care, women's health, and orthopedics. Job Summary and Responsibilities The Quality/Patient Safety Program Manager supports, coordinates, and facilitates quality management (QM), patient safety (PS), and regulatory performance improvement (PI) activities for the hospital and medical staff. This role serves as a key resource to employees, leadership, nursing directors, senior management, councils, physicians, and interdisciplinary teams on quality management initiatives. The position requires handling sensitive and confidential patient and hospital information with discretion. Support the design, planning, implementation, and coordination of Quality Management, Patient Safety, and Performance Improvement activities across assigned hospital and medical staff departments, committees, service lines, and functions Proactively coordinate and facilitate performance improvement teams to support key initiatives, including but not limited to: Clinical quality improvement Patient safety and risk reduction Patient experience Operational efficiency Failure Mode and Effects Analyses (FMEAs) Root cause analyses Medical staff performance improvement activities such as peer review, OPPE, and FPPE Serve as a subject matter resource for quality management activities to staff, leadership, physicians, and interdisciplinary teams Ensure compliance with regulatory and quality reporting requirements, including CMS HIQRP/HOQRP, The Joint Commission (TJC), Leapfrog, and other applicable programs Play an integral role in the collection, abstraction, validation, and reporting of process and outcome quality measures Job Requirements Required Education and Experience Licensed Registered Nurse, Licensed Clinical Pharmacist, or other licensed clinical staff with three (3) years of clinical experience in an acute care setting Ability to perform case reviews for medical staff peer review and medical and/or surgical registry abstraction One (1) year of healthcare-related quality management or performance improvement experience (e.g., chart audits, PI team member participation) Required Licensure and Certifications Current, unrestricted state license in a clinical field in the state of practice Certified Professional in Healthcare Quality (CPHQ), Healthcare Quality and Management Certification (HCQM), or Certificate of Professional Healthcare Quality and Patient Safety (CPQPS) required within two (2) years of employment.

Ensure a high level of vendor performance in collaboration with internal auxiliary services staff and external vendors. Responsible for overseeing the efficient and effective delivery of high-quality food services, tenant services, and other support services that directly enhance the college's primary educational mission. ESSENTIAL FUNCTIONS Research and identify potential service vendors based on quality, reliability, pricing, and alignment with the institution's needs. In collaboration with procurement, manage and negotiate vendor contracts, focusing on cost-effectiveness, quality, and adherence to service level agreements (SLAs), invoice accuracy, timely payments, and budgetary guidelines. Serve as the primary point of contact for vendors, foster positive and productive relationships, assess vendor qualifications, conduct background checks. Identify vendor-related issues, analyze and recommend solutions, track and follow-up on corrective and preventive actions efficiently and professionally. Maintain accurate records and documentation related to vendor contracts, performance, and compliance to support continuous improvement. Conduct regular reviews of vendor performance and contracts, against established KPIs, including food quality, timeliness, health and safety compliance, and customer feedback, implementing renewals or changes as necessary. Conduct regular inspections of food preparation areas, dining facilities, and storage areas to ensure adherence to sanitation and safety regulations. Implement and monitor corrective action plans to address any non-compliance or underperformance issues promptly. Collaborate with internal stakeholders (students, staff, administration) to understand their needs and expectations. Ensure all service operations comply with federal, state, and local regulations. Perform other duties, tasks and assignments as required. QUALIFICATIONS Education & Experience * Bachelor's degree in Business Administration, hospitality management or related field required * 3 years experience in vendor management, hospitality, or supply chain management required Licensing & Certification * Valid Texas Driver License Special Skills * MS Office Programs * Budget Management * Project Management * Negotiation & Contract Management Competencies * Delivering High Quality Work * Accepting Responsibility * Serving Customers * Supporting Organizational Goals * Driving Continuous Improvement * Acting with Integrity * Thinking Critically * Managing Change * Communicating Effectively Working Conditions General Office. Must be able to perform all job requirements with or without reasonable accommodations; remain in a stationary position during shift; move items weighing up to 25 pounds; position self to operate job equipment; apply established protocols in a timely manner. Must access, input and retrieve information from technology devices; communicate with others to accomplish job requirements. May be required to work after hours to include weekends and holidays. SECURITY SENSITIVE: This job class may contain positions that are security sensitive and thereby subject to the provisions of Texas Education Code § 51.215 The Organization Houston City College (HCC) is composed of 14 Centers of Excellence and numerous satellite centers that serve the diverse communities in the Greater Houston area by preparing individuals to live and work in an increasingly international and technological society. HCC is one of the country's largest single-accredited, open-admission, community colleges offering associate degrees, certificates, workforce training, and lifelong learning opportunities. The Team Play a central role at HCC as you keep our everyday operations running like clockwork. You'll get the chance to make things happen and work closely with inspiring leaders across different parts of the institution. Whether your role is supportive, administrative, financial or something else, you'll be part of a dynamic team that not only provides HCC students with cutting-edge academic and career tools, it also takes care of its people. Location Houston is a city with limitless possibilities: * Fourth-largest city in the U.S. and home to 54 Fortune 500 companies, second only to New York City's 55. * Approximately 145 languages are spoken here. * Overall after-taxes living costs are 5.6 percent below the average for all 308 urban areas recently surveyed. * Houston is a major-league sports town, and don't forget the annual Houston Livestock Show & Rodeo. * The weather is great! Mild winters ensure that outdoor activities can be enjoyed year-round. * World-renowned medical care. The Houston metro area has long been known for its first-rate healthcare system, with many Houston area hospitals consistently ranking among the nation's top institutions. * With over 150 museums and cultural institutions in the Greater Houston area, museums are a large part of Houston's cultural scene. * Houston is the Culture & Culinary Capital of Texas with more than 7,500 restaurants and eating establishments covering 60+ cuisines. If this sounds like the role for you and you're ready to join an amazing team, please apply right away. EEO Statement Houston City College does not discriminate on the bases of race, color, religion, sex, gender identity and expression, national origin, age, disability, sexual orientation or veteran's status. The following person has been designated to handle inquiries regarding the non-discrimination policies: Sandra B. Jacobson, J.D., M.Ed., SHRM-SCP, Interim Director of EEO and Compliance & Title IX Coordinator Office of Equal Opportunity and Title IX PO Box 667517 Houston TX, 77266 ************ or ******************* HCC values its employees and their contributions, promotes opportunities for their professional growth and development, and provides a positive working and learning environment that encourages involvement, innovation, and creativity. Individuals with disabilities, who require special accommodations to interview, should contact **************.