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.
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 is responsible for supplier quality management, audit governance, supplier qualification, continuous improvement initiatives, and regional coordination across Americas manufacturing sites. Maintain and continuously improve the Regional Quality Management System (QMS) to meet supplier certification requirements, evolving business needs, and divisional alignment.
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.
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.
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.
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.
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.
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.
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.
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.
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.
Success in this position requires exceptional organizational discipline, a proactive and results-driven mindset, and the ability to influence and hold both internal stakeholders and external suppliers accountable to commitments, ensuring consistent execution and delivery of high-quality outcomes. The Process Specialist is responsible for driving disciplined execution of supplier quality processes, including Preproduction Kickoff Meetings (PPKOM) and Supplier Nonconformance (MSN) management, to ensure alignment, defect prevention, and timely resolution of quality issues.
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.
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.
Reports To: QA/QC ManagerWork Location: 6401 North Eldridge Pkwy, Houston, TX 77041 Position ResponsibilitiesAssist with all necessary requirements to meet or exceed ISO certification, as well as represent GTM as the ISO compliance specialist / liaison. In Houston, Texas, our 500,000 sq ft Center for Excellence in Lifecycle Care features a Level-IV depot and aero repair facility, which executes comprehensive services for aeroderivative engines under one roof.
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.
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.
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 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.
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.
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.
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>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.
Responsible for developing, reviewing, and refining quality control procedures and processes; conducting audits and inspections; analyzing performance data; and implementing effective solutions to enhance overall quality and operational efficiency. Work closely with the Quality Supervisor / Manager to execute monitoring and measuring critical aspects of the Quality Management System such as: Deviation/Concession System.
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.
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.
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>A successful candidate will possess these skills:
p>A successful candidate will possess these skills:
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