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Experience Level
Manager
Qualifications
Proven experience in quality management or a related field. Strong understanding of quality assurance methodologies and tools. Excellent analytical and problem-solving skills. Effective communication and leadership abilities. Knowledge of industry standards and regulations.
About the job
Join Panelmatic Inc. as a Quality Manager where you will play a pivotal role in ensuring the highest standards of quality and excellence in our products and processes. Your expertise will help us enhance operational efficiencies while maintaining compliance with industry regulations.
In this role, you will lead quality assurance initiatives, oversee the quality team, and collaborate closely with various departments to foster a culture of quality throughout the organization. If you are passionate about quality management and seek to make a significant impact in a dynamic environment, we would love to hear from you!
About Panelmatic Inc.
Panelmatic Inc. is a leading provider of custom electrical enclosures and control systems, dedicated to delivering innovative solutions and superior service. With a commitment to quality and customer satisfaction, we strive to be at the forefront of our industry.
Join Panelmatic Inc. as a Quality Manager where you will play a pivotal role in ensuring the highest standards of quality and excellence in our products and processes. Your expertise will help us enhance operational efficiencies while maintaining compliance with industry regulations.In this role, you will lead quality assurance initiatives, oversee the quality team, and collaborate closely with various departments to foster a culture of quality throughout the organization. If you are passionate about quality management and seek to make a significant impact in a dynamic environment, we would love to hear from you!
Join ReviveRX, a leading licensed pharmacy dedicated to health, wellness, and restorative medicine. We prioritize addressing the root causes of health concerns through cutting-edge technology and personalized care. Our team consists of innovative pharmacists, healthcare providers, and pharmaceutical manufacturers, all working collaboratively to empower individuals to lead vibrant lives. We invite you to be part of our mission to transform healthcare and promote holistic wellness.POSITION OVERVIEWAs the Incoming QA (IQA) Associate, you will be on the front lines of ensuring that all materials and components entering ReviveRX are fit for use. This role is crucial in evaluating the quality of incoming components, including APIs, excipients, production materials, drug products, syringes, and other essential supplies. You will work closely with warehousing staff to ensure that compounding materials are accurately received, inspected, documented, and released in compliance with internal procedures and USP standards (e.g., USP <797>, <795>, <800>, <1163>). This position demands exceptional attention to detail, strong organizational skills, and the ability to assess component quality against specified standards. Your contributions will strengthen the IQA function and enhance patient safety.BACKGROUND & NEEDReviveRX is seeking an IQA Associate to further bolster our incoming quality processes. The ideal candidate will possess operational and/or quality experience, demonstrate exceptional organizational skills, and appreciate the critical nature of this role as ReviveRX's first line of defense. Supplier quality experience is essential to enhance and mature the IQA function.KEY RESPONSIBILITIES- Examine incoming materials and determine release status- Collaborate with warehousing and supply chain management to enhance the incoming quality function- Follow and improve established procedures for quality assurance- Document findings and maintain accurate records
Join the exceptional team at Optimal Field Services!We pride ourselves on our ability to compete with industry giants and consistently surpass expectations.Founded by experienced professionals who left traditional practices behind to create a company built on trust and teamwork, we believe every team member plays a pivotal role in achieving success.With a strong reputation and a growing client base, Optimal is not only making waves in the industry but also positively impacting the lives we touch. Our core values drive our commitment to delivering exceptional results for our clients and team members alike.As part of Crest Industries, we are seeking a skilled South West Regional Quality Control Manager to join our Pasadena, TX office. This role serves as the Quality Control representative for our Regional Corporate Office across multiple project sites, reporting directly to the Director of Quality Control. The ideal candidate will be responsible for overseeing daily construction activities, ensuring compliance with project specifications, engineering standards, and regulatory requirements. Our focus includes specialized services such as Specialty Welding, Mechanical Work, and Towers, along with the ability to manage various other services. The South West Regional QC Manager will play a crucial role in fostering a culture of quality within the organization and ensuring all site personnel receive necessary training to maintain our high standards.
Join our dynamic team at RR Donnelley as a Quality Inspector II, where your keen eye for detail will play a vital role in ensuring product excellence. You will be responsible for performing quality control checks and audits on our production processes, contributing to the continuous improvement of our manufacturing operations. The ideal candidate will possess a strong commitment to quality and a proactive approach to problem-solving.
SQA Services delivers managed supplier quality support to manufacturers across multiple industries. For nearly three decades, the company has worked with a broad network of quality assurance professionals in the United States and over 90 countries, providing clients with on-site and remote solutions tailored to their requirements. Role overview This contract-based Medical Device Supplier Quality Auditor role centers on performing supplier quality audits for medical device manufacturers. The position is based in Houston, TX, and includes travel to supplier sites throughout Texas and nearby states. Auditors can choose assignments based on their availability, with most audits lasting one to two days. Key responsibilities Carry out supplier quality audits at various locations in Texas and neighboring states Evaluate supplier compliance with applicable medical device quality standards Document audit results and share findings with SQA Services and clients Represent client interests professionally during site visits Requirements Background in quality assurance or auditing within the medical device industry Willingness and ability to travel to supplier sites as needed Clear communication and strong documentation skills Professionalism and adaptability when working in different supplier environments This is a flexible contract position. Assignments are offered as needed, and auditors may accept or decline work depending on their schedule.
Join our team at Panelmatic Inc. as a Quality Control Inspector, where you will play a crucial role in ensuring that our products meet the highest quality standards. You will be responsible for performing inspections, documenting findings, and collaborating with production teams to implement improvements. If you are detail-oriented and passionate about quality assurance, we want to hear from you!
Join our dynamic team at QIMA as a Quality Control Inspector, where you will play a crucial role in ensuring the highest standards of quality in our products. In this part-time position, you will conduct inspections and assessments to maintain compliance with industry standards.
Stratas Foods seeks a Bilingual Quality Assurance Supervisor for its Houston facility. This position plays a key role in maintaining product quality and safety throughout the operation. The supervisor will guide the QA team and support a diverse workforce, requiring fluency in both English and Spanish. Key Responsibilities Develop and oversee quality assurance protocols that meet company and regulatory requirements. Conduct regular audits to monitor compliance and identify opportunities for improvement. Lead, mentor, and communicate with the QA team in both English and Spanish. Collaborate with production, operations, and other departments to strengthen product quality and safety initiatives. Requirements Experience supervising or leading within a quality assurance setting. Fluency in English and Spanish. Keen attention to detail and dedication to high standards. Ability to work effectively with cross-functional teams.
Join AECOM as a Senior Ambient Air Quality Specialist in Houston, Texas, where you will play a crucial role in advancing environmental compliance and sustainability initiatives. You will be responsible for conducting air quality assessments, managing projects, and developing strategies to ensure compliance with local, state, and federal regulations.Your expertise will contribute to innovative solutions that promote clean air and environmental stewardship. You will collaborate with multidisciplinary teams to deliver high-quality results for our clients.
Join our dynamic team at Ramboll as a Managing Consultant specializing in Air Quality Compliance and Permitting within the Chemical and Pharmaceutical sectors. In this pivotal role, you will leverage your expertise to guide clients through complex environmental regulations and ensure adherence to compliance standards. Your insights will be essential in navigating permitting processes and delivering tailored solutions that meet the unique challenges of our clients.
At Xometry (NASDAQ: XMTR), we are at the forefront of innovation, bridging the gap between visionary ideas and manufacturing capabilities. Our digital marketplace empowers manufacturers with essential resources to thrive, while enabling Fortune 1000 companies to efficiently leverage global manufacturing capacity.We are on the lookout for dynamic Quality Assurance Engineers to support our rapid growth in customer demand. If you excel in high-pressure environments and have a passion for transforming industries, this position is tailored for you. Your strength in prioritization and effective communication will be key to navigating challenges successfully.In the role of Quality Assurance Engineer, you will join a dedicated team of engineering professionals focused on resolving quality assurance issues for custom parts. Collaborating closely with the Senior Director, you will help develop a quality system aligned with corporate policies, objectives, and AS9100 requirements.Responsibilities in Process and Quality Assurance:Lead or participate in process improvement initiatives to enhance supplier quality culture, setting our Global Partner Network up for success.Utilize quality tools (Lean and Six Sigma) to address issues related to non-conformances and Customer RMAs.Oversee supplier-related NCR/SCAR/CAR activities to ensure timely record-keeping and administration.Ensure compliance with company policies, practices, and procedures to maintain AS9100 standards.
Join Ramboll as a Principal Air Quality Consultant, where you will lead air quality projects that help shape environmental policies and regulations. You will play a key role in developing innovative solutions to complex environmental challenges while ensuring compliance with local, state, and federal regulations.Your responsibilities will include managing project timelines, overseeing technical analyses, and collaborating with multidisciplinary teams to deliver high-quality outcomes. This is an exciting opportunity to make a significant impact on air quality and environmental sustainability.
Stratas Foods is looking for a Bilingual Quality Assurance Supervisor to oversee quality operations at the Houston facility. This position leads a team dedicated to upholding strict product standards and regulatory compliance. Role overview This supervisor manages quality assurance processes and ensures products consistently meet company and industry requirements. The role involves guiding a diverse team and using bilingual skills in English and Spanish to facilitate clear communication with staff and partners. Key responsibilities Lead the quality assurance team in daily operations Implement and monitor quality control procedures Ensure compliance with relevant industry regulations and standards Communicate effectively in both English and Spanish across teams Requirements Experience supervising quality assurance or related teams Fluency in English and Spanish Strong understanding of quality control processes and regulatory standards This role is central to maintaining Stratas Foods’ commitment to high-quality products and operational excellence in Houston.
About Giga EnergyAt Giga Energy, we are transforming the landscape of energy infrastructure with cutting-edge AI technology. Our mission is to revolutionize the energy sector and provide a seamless infrastructure experience. Based in Texas, we collaborate with AI hyperscalers and data center operators, ensuring rapid project delivery through our integrated approach encompassing site origination, manufacturing, and power market engagement.Why Join Our Team?Speed: Take ownership of projects that progress faster than any other in the industry.Impact: Be the pivotal player turning innovative ideas into tangible contracts and permits.Team Excellence: Collaborate with a top-tier team of engineers and builders shaping the future of AI infrastructure.Key ResponsibilitiesAs a Quality Control / Shipping and Receiving Technician, you will serve as the vital connection within our supply chain, ensuring the highest standards of quality and accuracy. Your role will involve:Inspecting incoming materials and components against specifications and purchase orders.Conducting outgoing quality checks on finished products to confirm compliance with documentation, labeling, and packaging standards.Accurately logging and staging incoming shipments using ERP and inventory management systems.Coordinating and processing outbound shipments to guarantee timely delivery.LocationThis position is based at our Houston MV Facility, requiring full-time in-office attendance to foster collaboration and speed in building infrastructure.
Fleetzero is building advanced hardware in Houston, TX, and seeks a Senior Quality Assurance and Manufacturing Engineer to help turn innovative designs into reliable, production-ready products. Role overview This position leads both quality assurance and manufacturing engineering for battery module and Battery Management System (BMS) assembly. The engineer will design and validate assembly processes, develop detailed work instructions, and set inspection criteria to support consistent quality across the production line. Defining quality standards for each step, from incoming part checks to final functional testing, will be central to the role. Key responsibilities Create and refine assembly processes for battery modules and BMS. Write clear work instructions and establish inspection requirements. Set quality benchmarks for all stages of assembly and testing. Work hands-on on the production floor, developing tooling and troubleshooting process issues. Collaborate with the assembly team on experiments and process improvements. Promote continuous improvement and systematize quality assurance practices. What success looks like Assembly processes are repeatable, transparent, and well-documented. Quality assurance tasks are initiated proactively, not just by directive. Production issues are addressed quickly and collaboratively.
As a Data Quality Control (QC) and Processing Specialist, you will play a crucial role in ensuring the integrity of raw data by thoroughly inspecting and analyzing observer logs generated by data acquisition teams. Utilizing our proprietary software tools, your technical expertise will be vital in testing, adapting, and debugging programs tailored to specific datasets. Collaboration is key, as you will often work within teams on multiple projects, leveraging your exceptional communication skills to discuss dataset processing requirements with colleagues and advisors. You will also oversee the progress of lengthy processing programs, prioritizing tasks based on runtime and project urgency. Please note that you must have the legal right to work in the region you are applying for and be open to occasional travel.
We are seeking a skilled and experienced Test Manager to join our dynamic team in Houston. In this pivotal role, you will be responsible for overseeing all testing activities within our projects, ensuring that all deliverables meet the highest quality standards. You will lead a team of testers, develop test strategies, and collaborate closely with various departments to deliver exceptional software solutions.
Join Our Trailblazing Team:At Venus Aerospace, we are at the forefront of innovation in rocket engine propulsion. Our cutting-edge Rotating Detonation Rocket Engine and Venus Detonation Ramjets mark a significant advancement in aerospace technology, delivering unparalleled efficiency and performance for a variety of applications. We are dedicated to creating the next generation of propulsion platforms that will unlock transformative capabilities in space exploration, defense, and commercial high-speed travel. Our dynamic team is passionate about tackling the most challenging engineering problems and pushing the limits of aerospace possibilities. We invite daring engineers and visionary thinkers to help us forge the future of propulsion. Your Role:The Quality Engineer will play a crucial role in maintaining the integrity and precision of machined and manufactured components. This position merges engineering knowledge with practical manufacturing and inspection skills to establish, execute, and uphold quality systems, processes, and tools that drive ongoing improvements in production operations.
Join WGC Constructors, LLC as a Regional Construction Safety, Compliance and Quality Assurance Coordinator. In this pivotal role, you will ensure that safety standards and compliance protocols are adhered to across our construction sites in the region. Your expertise will help foster a culture of safety, quality assurance, and regulatory compliance, contributing to the successful delivery of our projects.
ReviveRX stands at the forefront of health, wellness, and restorative medicine as a premier licensed pharmacy. Our innovative approach emphasizes treating the root causes of health issues rather than merely alleviating symptoms, leveraging cutting-edge technology to deliver exceptional care. We partner with forward-thinking pharmacists, healthcare professionals, and pharmaceutical manufacturers to provide personalized treatment plans. Join us in our mission to transform healthcare and empower individuals to lead healthier, more vibrant lives.POSITION OVERVIEWThe Document Control and Record Management Lead is an essential role at ReviveRX, responsible for overseeing the comprehensive Quality Management System (QMS) documentation and records management system. This position ensures adherence to regulatory standards, compounding quality protocols, and internal policies. You'll play a pivotal role in maintaining precise and updated documentation, facilitating efficient processes, and enhancing overall product quality.Serving as the central resource for managing all QMS 503A documentation, including SOPs, forms, work instructions, batch records, and testing records, this position manages a high volume of documents generated daily across various functions such as operations, quality, and facilities. The ideal candidate will possess 5-10 years of experience in a regulated industry, showcasing exceptional organizational abilities and skills for effective collaboration across diverse departments.KEY RESPONSIBILITIESDocument Management & Control:• Oversee the daily influx of documents, including SOPs, forms, work instructions, and other controlled documentation.• Maintain and update the master document control system to ensure accurate numbering, versioning, and tracking of all documents.• Facilitate document creation, revision, approval, and distribution workflows according to established protocols.• Ensure that only current, controlled, and approved document versions are utilized while effectively retiring obsolete versions.
Join Panelmatic Inc. as a Quality Manager where you will play a pivotal role in ensuring the highest standards of quality and excellence in our products and processes. Your expertise will help us enhance operational efficiencies while maintaining compliance with industry regulations.In this role, you will lead quality assurance initiatives, oversee the quality team, and collaborate closely with various departments to foster a culture of quality throughout the organization. If you are passionate about quality management and seek to make a significant impact in a dynamic environment, we would love to hear from you!
Join ReviveRX, a leading licensed pharmacy dedicated to health, wellness, and restorative medicine. We prioritize addressing the root causes of health concerns through cutting-edge technology and personalized care. Our team consists of innovative pharmacists, healthcare providers, and pharmaceutical manufacturers, all working collaboratively to empower individuals to lead vibrant lives. We invite you to be part of our mission to transform healthcare and promote holistic wellness.POSITION OVERVIEWAs the Incoming QA (IQA) Associate, you will be on the front lines of ensuring that all materials and components entering ReviveRX are fit for use. This role is crucial in evaluating the quality of incoming components, including APIs, excipients, production materials, drug products, syringes, and other essential supplies. You will work closely with warehousing staff to ensure that compounding materials are accurately received, inspected, documented, and released in compliance with internal procedures and USP standards (e.g., USP <797>, <795>, <800>, <1163>). This position demands exceptional attention to detail, strong organizational skills, and the ability to assess component quality against specified standards. Your contributions will strengthen the IQA function and enhance patient safety.BACKGROUND & NEEDReviveRX is seeking an IQA Associate to further bolster our incoming quality processes. The ideal candidate will possess operational and/or quality experience, demonstrate exceptional organizational skills, and appreciate the critical nature of this role as ReviveRX's first line of defense. Supplier quality experience is essential to enhance and mature the IQA function.KEY RESPONSIBILITIES- Examine incoming materials and determine release status- Collaborate with warehousing and supply chain management to enhance the incoming quality function- Follow and improve established procedures for quality assurance- Document findings and maintain accurate records
Join the exceptional team at Optimal Field Services!We pride ourselves on our ability to compete with industry giants and consistently surpass expectations.Founded by experienced professionals who left traditional practices behind to create a company built on trust and teamwork, we believe every team member plays a pivotal role in achieving success.With a strong reputation and a growing client base, Optimal is not only making waves in the industry but also positively impacting the lives we touch. Our core values drive our commitment to delivering exceptional results for our clients and team members alike.As part of Crest Industries, we are seeking a skilled South West Regional Quality Control Manager to join our Pasadena, TX office. This role serves as the Quality Control representative for our Regional Corporate Office across multiple project sites, reporting directly to the Director of Quality Control. The ideal candidate will be responsible for overseeing daily construction activities, ensuring compliance with project specifications, engineering standards, and regulatory requirements. Our focus includes specialized services such as Specialty Welding, Mechanical Work, and Towers, along with the ability to manage various other services. The South West Regional QC Manager will play a crucial role in fostering a culture of quality within the organization and ensuring all site personnel receive necessary training to maintain our high standards.
Join our dynamic team at RR Donnelley as a Quality Inspector II, where your keen eye for detail will play a vital role in ensuring product excellence. You will be responsible for performing quality control checks and audits on our production processes, contributing to the continuous improvement of our manufacturing operations. The ideal candidate will possess a strong commitment to quality and a proactive approach to problem-solving.
SQA Services delivers managed supplier quality support to manufacturers across multiple industries. For nearly three decades, the company has worked with a broad network of quality assurance professionals in the United States and over 90 countries, providing clients with on-site and remote solutions tailored to their requirements. Role overview This contract-based Medical Device Supplier Quality Auditor role centers on performing supplier quality audits for medical device manufacturers. The position is based in Houston, TX, and includes travel to supplier sites throughout Texas and nearby states. Auditors can choose assignments based on their availability, with most audits lasting one to two days. Key responsibilities Carry out supplier quality audits at various locations in Texas and neighboring states Evaluate supplier compliance with applicable medical device quality standards Document audit results and share findings with SQA Services and clients Represent client interests professionally during site visits Requirements Background in quality assurance or auditing within the medical device industry Willingness and ability to travel to supplier sites as needed Clear communication and strong documentation skills Professionalism and adaptability when working in different supplier environments This is a flexible contract position. Assignments are offered as needed, and auditors may accept or decline work depending on their schedule.
Join our team at Panelmatic Inc. as a Quality Control Inspector, where you will play a crucial role in ensuring that our products meet the highest quality standards. You will be responsible for performing inspections, documenting findings, and collaborating with production teams to implement improvements. If you are detail-oriented and passionate about quality assurance, we want to hear from you!
Join our dynamic team at QIMA as a Quality Control Inspector, where you will play a crucial role in ensuring the highest standards of quality in our products. In this part-time position, you will conduct inspections and assessments to maintain compliance with industry standards.
Stratas Foods seeks a Bilingual Quality Assurance Supervisor for its Houston facility. This position plays a key role in maintaining product quality and safety throughout the operation. The supervisor will guide the QA team and support a diverse workforce, requiring fluency in both English and Spanish. Key Responsibilities Develop and oversee quality assurance protocols that meet company and regulatory requirements. Conduct regular audits to monitor compliance and identify opportunities for improvement. Lead, mentor, and communicate with the QA team in both English and Spanish. Collaborate with production, operations, and other departments to strengthen product quality and safety initiatives. Requirements Experience supervising or leading within a quality assurance setting. Fluency in English and Spanish. Keen attention to detail and dedication to high standards. Ability to work effectively with cross-functional teams.
Join AECOM as a Senior Ambient Air Quality Specialist in Houston, Texas, where you will play a crucial role in advancing environmental compliance and sustainability initiatives. You will be responsible for conducting air quality assessments, managing projects, and developing strategies to ensure compliance with local, state, and federal regulations.Your expertise will contribute to innovative solutions that promote clean air and environmental stewardship. You will collaborate with multidisciplinary teams to deliver high-quality results for our clients.
Join our dynamic team at Ramboll as a Managing Consultant specializing in Air Quality Compliance and Permitting within the Chemical and Pharmaceutical sectors. In this pivotal role, you will leverage your expertise to guide clients through complex environmental regulations and ensure adherence to compliance standards. Your insights will be essential in navigating permitting processes and delivering tailored solutions that meet the unique challenges of our clients.
At Xometry (NASDAQ: XMTR), we are at the forefront of innovation, bridging the gap between visionary ideas and manufacturing capabilities. Our digital marketplace empowers manufacturers with essential resources to thrive, while enabling Fortune 1000 companies to efficiently leverage global manufacturing capacity.We are on the lookout for dynamic Quality Assurance Engineers to support our rapid growth in customer demand. If you excel in high-pressure environments and have a passion for transforming industries, this position is tailored for you. Your strength in prioritization and effective communication will be key to navigating challenges successfully.In the role of Quality Assurance Engineer, you will join a dedicated team of engineering professionals focused on resolving quality assurance issues for custom parts. Collaborating closely with the Senior Director, you will help develop a quality system aligned with corporate policies, objectives, and AS9100 requirements.Responsibilities in Process and Quality Assurance:Lead or participate in process improvement initiatives to enhance supplier quality culture, setting our Global Partner Network up for success.Utilize quality tools (Lean and Six Sigma) to address issues related to non-conformances and Customer RMAs.Oversee supplier-related NCR/SCAR/CAR activities to ensure timely record-keeping and administration.Ensure compliance with company policies, practices, and procedures to maintain AS9100 standards.
Join Ramboll as a Principal Air Quality Consultant, where you will lead air quality projects that help shape environmental policies and regulations. You will play a key role in developing innovative solutions to complex environmental challenges while ensuring compliance with local, state, and federal regulations.Your responsibilities will include managing project timelines, overseeing technical analyses, and collaborating with multidisciplinary teams to deliver high-quality outcomes. This is an exciting opportunity to make a significant impact on air quality and environmental sustainability.
Stratas Foods is looking for a Bilingual Quality Assurance Supervisor to oversee quality operations at the Houston facility. This position leads a team dedicated to upholding strict product standards and regulatory compliance. Role overview This supervisor manages quality assurance processes and ensures products consistently meet company and industry requirements. The role involves guiding a diverse team and using bilingual skills in English and Spanish to facilitate clear communication with staff and partners. Key responsibilities Lead the quality assurance team in daily operations Implement and monitor quality control procedures Ensure compliance with relevant industry regulations and standards Communicate effectively in both English and Spanish across teams Requirements Experience supervising quality assurance or related teams Fluency in English and Spanish Strong understanding of quality control processes and regulatory standards This role is central to maintaining Stratas Foods’ commitment to high-quality products and operational excellence in Houston.
About Giga EnergyAt Giga Energy, we are transforming the landscape of energy infrastructure with cutting-edge AI technology. Our mission is to revolutionize the energy sector and provide a seamless infrastructure experience. Based in Texas, we collaborate with AI hyperscalers and data center operators, ensuring rapid project delivery through our integrated approach encompassing site origination, manufacturing, and power market engagement.Why Join Our Team?Speed: Take ownership of projects that progress faster than any other in the industry.Impact: Be the pivotal player turning innovative ideas into tangible contracts and permits.Team Excellence: Collaborate with a top-tier team of engineers and builders shaping the future of AI infrastructure.Key ResponsibilitiesAs a Quality Control / Shipping and Receiving Technician, you will serve as the vital connection within our supply chain, ensuring the highest standards of quality and accuracy. Your role will involve:Inspecting incoming materials and components against specifications and purchase orders.Conducting outgoing quality checks on finished products to confirm compliance with documentation, labeling, and packaging standards.Accurately logging and staging incoming shipments using ERP and inventory management systems.Coordinating and processing outbound shipments to guarantee timely delivery.LocationThis position is based at our Houston MV Facility, requiring full-time in-office attendance to foster collaboration and speed in building infrastructure.
Fleetzero is building advanced hardware in Houston, TX, and seeks a Senior Quality Assurance and Manufacturing Engineer to help turn innovative designs into reliable, production-ready products. Role overview This position leads both quality assurance and manufacturing engineering for battery module and Battery Management System (BMS) assembly. The engineer will design and validate assembly processes, develop detailed work instructions, and set inspection criteria to support consistent quality across the production line. Defining quality standards for each step, from incoming part checks to final functional testing, will be central to the role. Key responsibilities Create and refine assembly processes for battery modules and BMS. Write clear work instructions and establish inspection requirements. Set quality benchmarks for all stages of assembly and testing. Work hands-on on the production floor, developing tooling and troubleshooting process issues. Collaborate with the assembly team on experiments and process improvements. Promote continuous improvement and systematize quality assurance practices. What success looks like Assembly processes are repeatable, transparent, and well-documented. Quality assurance tasks are initiated proactively, not just by directive. Production issues are addressed quickly and collaboratively.
As a Data Quality Control (QC) and Processing Specialist, you will play a crucial role in ensuring the integrity of raw data by thoroughly inspecting and analyzing observer logs generated by data acquisition teams. Utilizing our proprietary software tools, your technical expertise will be vital in testing, adapting, and debugging programs tailored to specific datasets. Collaboration is key, as you will often work within teams on multiple projects, leveraging your exceptional communication skills to discuss dataset processing requirements with colleagues and advisors. You will also oversee the progress of lengthy processing programs, prioritizing tasks based on runtime and project urgency. Please note that you must have the legal right to work in the region you are applying for and be open to occasional travel.
We are seeking a skilled and experienced Test Manager to join our dynamic team in Houston. In this pivotal role, you will be responsible for overseeing all testing activities within our projects, ensuring that all deliverables meet the highest quality standards. You will lead a team of testers, develop test strategies, and collaborate closely with various departments to deliver exceptional software solutions.
Join Our Trailblazing Team:At Venus Aerospace, we are at the forefront of innovation in rocket engine propulsion. Our cutting-edge Rotating Detonation Rocket Engine and Venus Detonation Ramjets mark a significant advancement in aerospace technology, delivering unparalleled efficiency and performance for a variety of applications. We are dedicated to creating the next generation of propulsion platforms that will unlock transformative capabilities in space exploration, defense, and commercial high-speed travel. Our dynamic team is passionate about tackling the most challenging engineering problems and pushing the limits of aerospace possibilities. We invite daring engineers and visionary thinkers to help us forge the future of propulsion. Your Role:The Quality Engineer will play a crucial role in maintaining the integrity and precision of machined and manufactured components. This position merges engineering knowledge with practical manufacturing and inspection skills to establish, execute, and uphold quality systems, processes, and tools that drive ongoing improvements in production operations.
Join WGC Constructors, LLC as a Regional Construction Safety, Compliance and Quality Assurance Coordinator. In this pivotal role, you will ensure that safety standards and compliance protocols are adhered to across our construction sites in the region. Your expertise will help foster a culture of safety, quality assurance, and regulatory compliance, contributing to the successful delivery of our projects.
ReviveRX stands at the forefront of health, wellness, and restorative medicine as a premier licensed pharmacy. Our innovative approach emphasizes treating the root causes of health issues rather than merely alleviating symptoms, leveraging cutting-edge technology to deliver exceptional care. We partner with forward-thinking pharmacists, healthcare professionals, and pharmaceutical manufacturers to provide personalized treatment plans. Join us in our mission to transform healthcare and empower individuals to lead healthier, more vibrant lives.POSITION OVERVIEWThe Document Control and Record Management Lead is an essential role at ReviveRX, responsible for overseeing the comprehensive Quality Management System (QMS) documentation and records management system. This position ensures adherence to regulatory standards, compounding quality protocols, and internal policies. You'll play a pivotal role in maintaining precise and updated documentation, facilitating efficient processes, and enhancing overall product quality.Serving as the central resource for managing all QMS 503A documentation, including SOPs, forms, work instructions, batch records, and testing records, this position manages a high volume of documents generated daily across various functions such as operations, quality, and facilities. The ideal candidate will possess 5-10 years of experience in a regulated industry, showcasing exceptional organizational abilities and skills for effective collaboration across diverse departments.KEY RESPONSIBILITIESDocument Management & Control:• Oversee the daily influx of documents, including SOPs, forms, work instructions, and other controlled documentation.• Maintain and update the master document control system to ensure accurate numbering, versioning, and tracking of all documents.• Facilitate document creation, revision, approval, and distribution workflows according to established protocols.• Ensure that only current, controlled, and approved document versions are utilized while effectively retiring obsolete versions.
Feb 17, 2026
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