table>| Enable Skills-Based Hiring | No |
| Business case justification | |
| Increase in workload |
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| Fast paced environment, working in an open concept area (able to focus with possible multiple distractions), problem solver and be resourceful to find solutions on your own |
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| Office and Manufacturing environments. Must wear safety gear when on the manufacturing floor |
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| Are there any safety risks associated with the role? | |
| No |
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| Will the worker be working at a customer's facility? | |
| No |
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| Essential Requirements of the Role | |
| " 3 7 years of experience in quality assurance within manufacturing or industrial environments.Coordinate and document Management of Change (MOC) activities affecting processes, materials, or products. Identify opportunities for process improvement using tools such as Lean, Six Sigma, or root cause analysis. Review and approve GMP master documents and executed GMP documents from QC, manufacturing, material management, and any other department that supports lot production. If youre ready to help turn our customers breakthrough ideas into viable therapies, we look forward to welcoming you on board. Houston, Texas30+ days ago Demonstrated knowledge of Quality Management System tools, continuous improvement methodologies & in-depth understanding of site level products & related processes • Demonstrated expertise to effectively communicate within all levels of the organization around concepts of Repair/services controls, Repair/services verification and validation activities; production &process controls; Corrective & Preventive Action (CAPA), complaints & risk management; & product quality improvement using tools such as six sigma, DFR, etc. DMIAC, SPC, Lean SS, 5S, 8D) • Experience leading and implementing change • Experience performing internal and external audits • Exceptional analytical, problem solving & root-cause analysis skills • Ability to multi-task & handle tasks with competing priorities effectively • Strong technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures), global regulatory experience & demonstrated experience interfacing with regulators. This role will report to the Director of Quality and work closely with factory quality engineers (action owners), site quality stakeholders (observation submitters and field QA/QC), operations leads (execution), engineering (technical disposition), and project management (escalation and resourcing). We specialize in delivering optimized turnkey solutions that bring together speed, quality, and reliability - helping our clients build and operate the mission-critical infrastructure that powers today’s digital world. Houston, Texas30+ days ago If you have questions about any open positions at Huntsman or Rubicon, please visit our Careers website at http://www.huntsman.com/corporate/a/Careers. This role is responsible for supplier quality management, audit governance, supplier qualification, continuous improvement initiatives, and regional coordination across Americas manufacturing sites. li>Seven (7) years of progressively responsible and directly related work experience (five (5) years with a Master's degree) within a large acute care hospital or health care system in one or more of the following: data-driven performance improvement, quality assurance/quality improvement. A hospital in Houston, TX is seeking a mid-level Senior Quality Specialist to support data-driven performance improvement and quality assurance initiatives within a large acute care environment. p>The role requires strong healthcare quality expertise, stakeholder collaboration, project leadership, and the ability to translate data into actionable improvement strategies that enhance patient outcomes, operational efficiency, and regulatory compliance. This individual will leverage data analytics, process improvement methodologies, and project management principles to identify opportunities, drive sustainable improvements, and support organizational quality goals. Sugar Land, TX30+ days ago She/he maintains precise records of the findings, documenting any design or manufacturing issues which help to ensure that defects are quickly remedied and don’t recur in the future. · Skills/ Abilities: Ability to use microscope; Steady hands; Need to be able to handle very small components. Deer Park, TX30+ days ago Demonstrated history of understanding regulatory requirements (ASME, API, etc) Proficient in Microsoft Office Suite (Word, Excel, Outlook and TEAMS) Attentive to detail, good planning and time management skills Ability to maintain records, and documents and compile and organize reports accurately Ability to read and interpret manufacturers requirements and customer specifications Effectively listening and communicating tactfully, verbally and written Ability to establish and maintain effective working relationships internally and externally Must be able to lift, carry, push, and pull or otherwise move objects up to 49 pounds Work involves frequent periods of standing, walking, stooping, kneeling, crouching, twisting/turning, reaching, and bending at the waist. How We Win Together We are committed to solving customer problems and are looking for team members that want to be a trusted resource to those looking for a partner who out-knows, out-cares, and out-serves everyone else. p>The Quality Specialist is responsible for reviewing, monitoring, and analyzing data to drive quality improvement that improves delivery of safe patient care as measured by external reporting programs such as CMS, Vizient, Leapfrog, and USNEWS. This role shares best practices to allow for local as well as system-wide learning, collaborates with hospital councils to share knowledge leading to optimal outcomes and continuous education of robust process improvement within the hospital. Houston, Texas30+ days ago IMPORTANT NOTICE: TAS has a tobacco-free workplace policy, under which individuals are not allowed to smoke or use tobacco or nicotine products on the TAS premises, while conducting TAS business off premises or take "smoking" breaks during working hours. When you join TAS, you join a Houston-headquartered company that is part of a large Houston-headquartered publicly traded company, Comfort Systems USA, with a solid reputation built on outstanding value, integrity, and customer focus. p>Our client is seeking a Quality Assurance Specialist to support quality systems, compliance, auditing, documentation, and continuous improvement initiatives within a manufacturing environment. Manage document control processes, including versioning, approvals, distribution, and employee access to current documentation. Houston, Texas30+ days ago IMPORTANT NOTICE: TAS has a tobacco-free workplace policy, under which individuals are not allowed to smoke or use tobacco or nicotine products on the TAS premises, while conducting TAS business off premises or take "smoking" breaks during working hours. When you join TAS, you join a Houston-headquartered company that is part of a large Houston-headquartered publicly traded company, Comfort Systems USA, with a solid reputation built on outstanding value, integrity, and customer focus. When you join TAS, you join a Houston-headquartered company that is part of a large Houston-headquartered publicly traded company, Comfort Systems USA, with a solid reputation built on outstanding value, integrity, and customer focus. "smoking" and "tobacco or nicotine products" includes, but is not limited to, product such as cigarettes, e-cigarettes, cigars, pipes, vaping, all forms of smokeless tobacco (chewing tobacco, snuff, dip) and clove cigarettes. The Air Quality Specialist supports corporate and local teams in achieving environmental compliance, focusing on emissions reduction, regulatory adherence, and sustainability initiatives. Lead environmental initiatives, utilizing emissions tracking software and online dashboards, OGI Leak Survey and Repair programs, and OGMP-aligned ESG efforts. The Air Quality Specialist supports corporate and local teams in achieving environmental compliance, focusing on emissions reduction, regulatory adherence, and sustainability initiatives. Lead environmental initiatives, utilizing emissions tracking software and online dashboards, OGI Leak Survey and Repair programs, and OGMP-aligned ESG efforts. p>The Air Quality Specialist supports corporate and local teams in achieving environmental compliance, focusing on emissions reduction, regulatory adherence, and sustainability initiatives. Lead environmental initiatives, utilizing emissions tracking software and online dashboards, OGI Leak Survey and Repair programs, and OGMP-aligned ESG efforts. Houston, Texas14 days ago p style="margin:0px">Astrion has an exciting opportunity for a Quality Assurance Specialist 2 to support NASA Safety and Mission Assurance (S&MA) by performing Quality Assurance inspections to ensure compliance with specifications. Knowledgeable of the assurance of quality for all phases of the mission life-cycle including design, procurement, manufacturing, auditing, assembly, testing, and operations. Job Overview: We're seeking a detail-oriented Manufacturing Quality Assurance Specialist to independently execute quality assurance processes, conduct audits, and ensure compliance with oil and gas industry regulations. • Excellent written and verbal communication skills with the ability to communicate effectively with internal & external stakeholders at all levels of the organization. Galveston, TX30+ days ago JOB SUMMARY: The Educator and Quality Assurance Specialist for the Sterile Processing Department works to promote the development of a motivated and cohesive team and supports educational strategies to enhance staff knowledge with respect to processing practices and service delivery. Monitors all Sterile Processing Department quality systems and performs necessary audits for compliance practices, instrument sets in the Decontamination area, Assembly, Sterilization, Storage, and Case Cart preparation. p>JOB SUMMARY: The Educator and Quality Assurance Specialist for the Sterile Processing Department works to promote the development of a motivated and cohesive team and supports educational strategies to enhance staff knowledge with respect to processing practices and service delivery. Monitors all Sterile Processing Department quality systems and performs necessary audits for compliance practices, instrument sets in the Decontamination area, Assembly, Sterilization, Storage, and Case Cart preparation. li>Coordinate and document Management of Change (MOC) activities affecting processes, materials, or products. Identify opportunities for process improvement using tools such as Lean, Six Sigma, or root cause analysis. li>Supervisors are expected to actively engaging their employees to support talent management through Weatherford's performance management process, including but not limited to talent assessments, succession planning & regular coaching opportunities. Seeks continual improvement in Health, Safety, Security & protection of the Environment, taking into account responsible care, process vulnerabilities, public, customer and employee inputs, knowledge and technology and best business practices to exceed customer expectations. Houston, Texas30+ days ago p style="text-align:inherit"/>The Air Quality Specialist supports corporate and local teams in achieving environmental compliance, focusing on emissions reduction, regulatory adherence, and sustainability initiatives. Crescent is a differentiated U.S. energy company committed to delivering value through a disciplined, returns-driven growth through acquisition strategy and consistent return of capital. Houston, Texas14 days ago p style="text-align:inherit"/>The Air Quality Specialist supports corporate and local teams in achieving environmental compliance, focusing on emissions reduction, regulatory adherence, and sustainability initiatives. Lead environmental initiatives, utilizing emissions tracking software and online dashboards, OGI Leak Survey and Repair programs, and OGMP-aligned ESG efforts. JOB SUMMARY: The Educator and Quality Assurance Specialist for the Sterile Processing Department works to promote the development of a motivated and cohesive team and supports educational strategies to enhance staff knowledge with respect to processing practices and service delivery. Monitors all Sterile Processing Department quality systems and performs necessary audits for compliance practices, instrument sets in the Decontamination area, Assembly, Sterilization, Storage, and Case Cart preparation. p>The Quality Operations Specialist ensures consistent delivery of safe, sterile, and compliant pharmaceutical products, directly impacting patient outcomes and regulatory standing. The employee is often required to remain in a stationary position for a significant amount of the workday and frequently use their hands and fingers to handle or feel in order to access, input, and retrieve information from the computer and other office productivity devices. p>The Quality Operations Specialist ensures consistent delivery of safe, sterile, and compliant pharmaceutical products, directly impacting patient outcomes and regulatory standing. The employee is often required to remain in a stationary position for a significant amount of the workday and frequently use their hands and fingers to handle or feel in order to access, input, and retrieve information from the computer and other office productivity devices. p>A successful candidate will possess these skills: - Demonstrated project management and organizational skills, including the ability to manage multiple priorities, maintain accurate follow-through, identify issues or risks that may affect timelines or outcomes, and escalate appropriately in a fast-paced environment. This role works closely with Quality and Risk leaders, Finance Risk Leaders, and other stakeholders to maintain visibility into engagement health, support risk-related discussions, and help ensure quality issues are tracked, communicated, and addressed.
p>A successful candidate will possess these skills: - Demonstrated project management and organizational skills, including the ability to manage multiple priorities, maintain accurate follow-through, identify issues or risks that may affect timelines or outcomes, and escalate appropriately in a fast-paced environment. This role works closely with Quality and Risk leaders, Finance Risk Leaders, and other stakeholders to maintain visibility into engagement health, support risk-related discussions, and help ensure quality issues are tracked, communicated, and addressed.
li>Coordinate and document Management of Change (MOC) activities affecting processes, materials, or products. Identify opportunities for process improvement using tools such as Lean, Six Sigma, or root cause analysis. This role provides QA oversight on the production floor, supports batch disposition activities, and collaborates with cross-functional teams to maintain cGMP compliance. The position also supports investigations, deviations, and change controls while ensuring timely and accurate review of GMP documentation in a fast-paced manufacturing environment. This role provides QA oversight on the production floor, supports batch disposition activities, and collaborates with cross-functional teams to maintain cGMP compliance. The position also supports investigations, deviations, and change controls while ensuring timely and accurate review of GMP documentation in a fast-paced manufacturing environment. Galveston, TX30+ days ago Function: To serve as a facilitator of quality assessment activities for Laboratory Services to include patient safety initiatives, regulatory and accreditation compliance, risk management, laboratory safety, and performance improvement in all clinical and anatomic pathology laboratory departments. Participates in the monitoring, reporting, and improvement activities related to clinical guidelines, healthcare quality/safety initiatives, accreditation and regulatory requirements, in collaboration with clinical staff and leadership. p>JOB SUMMARY: The Patient Services Specialist II has advanced Patient Services Specialist skills and is proficient in independently maintaining a positive patient experience by consistently exceeding expectations in customer service and patient care, by coordinating clerical and medical activities of a healthcare team, patient registration activities and facilitating access to UTMB services for new and returning patients. LICENSES, REGISTRATIONS OR CERTIFICATIONS: Required: For departments reporting under Health System Ambulatory Operations, a valid Basic Life Support (BLS) certification must be obtained within 90 days of hire. Trusted by industries such as heavy oil and refining, petrochemical, power generation, energy transmission, and agriculture, Blackstone is shaping the future of compressor maintenance and operation, striving to set new benchmarks. Validate Quality and Safety processes by establishing control specifications, measuring production, documenting evidence, determining operational performance qualification, and developing and updating assurance procedures. This role focuses on proactively leading issue resolution with efficiency and precision while driving accurate defect analysis to support continuous quality improvement initiatives. You will serve as the key point of accountability for NC management within a defined region or area, collaborating cross-functionally and providing regular updates to management. |
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