Georgia Quality Assurance & Control Job Listings

Quality Assurance Manager63846021235969120

Workable

Quality Assurance Manager

Who is CorDx？ CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare. Position: QA Manager Location: Alpharetta/Chamblee Position Type: 5 days Onsite Exempt Position Job Summary: We are seeking an experienced Quality Assurance Manager to lead our quality assurance team in the development, manufacturing, and distribution of Class II IVD devices. The ideal candidate will have at least 7 years of experience in the IVD industry, with a strong background in quality management systems, regulatory compliance, and team leadership. Key Responsibilities: Quality Systems & Compliance Develop, implement, and maintain Quality Management Systems (QMS) in accordance with, US FDA, ISO 13485, and applicable regulations. Lead internal and external audits, regulatory inspections, and corrective action plans (CAPAs). Oversee batch record reviews, deviations, non-conformance reports (NCRs), and change controls to maintain product quality and integrity. Process & Product Quality Assurance Develop and enforce Standard Operating Procedures (SOPs) and best practices to ensure consistent quality across manufacturing operations. Collaborate with R&D, production, and regulatory affairs teams to ensure new products and processes meet quality standards. Monitor and analyze quality metrics (KPIs) to drive continuous improvement initiatives. Ensure adherence to Good Documentation Practices (GDP) and data integrity policies. Leadership & Team Development Lead, mentor, and develop the QA team, fostering a culture of quality, compliance, and continuous improvement. Train manufacturing and quality teams on quality systems, and root cause analysis (RCA) methodologies. Serve as the primary point of contact for quality-related issues and escalations. Risk Management & Continuous Improvement Identify quality risks and implement proactive mitigation strategies. Lead investigations and root cause analyses for product defects, deviations, and non-conformances. Drive LEAN, Six Sigma, or other process improvement initiatives to enhance efficiency and reduce waste. Stay updated on industry trends, new regulations, and technological advancements in medical device IVD quality assurance. Requirements Bachelor’s or Master’s degree in Biotechnology, Microbiology, Chemistry, Biochemistry, Pharmaceutical Sciences, or related field. 7+ years of experience in quality assurance within biotech, pharmaceutical, or medical device manufacturing. 3+ years in a managerial or leadership role overseeing QA teams. Skills & Competencies Strong knowledge of US FDA, ISO 13485, and other regulatory standards. Experience with QA audits, inspections, CAPA investigations, and risk management. Proficiency in QMS software and documentation control systems. Strong analytical and problem-solving skills, with a data-driven approach to decision-making. Excellent leadership, communication, and cross-functional collaboration skills. Benefits Medical Insurance Plan Retirement Plan Paid Time Off Training & Development We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service.

Alpharetta, GA, USA

Negotiable Salary

Workable

Quality Manager

Who is CorDx？ CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare. Job Type: Full time Job Title: Quality Manager Location: Onsite - Atlanta Office We are seeking an experienced Quality Manager to join our team in the IVD (In Vitro Diagnostic) industry. The ideal candidate will have a minimum of 10 years of relevant experience in the medical device manufacturing sector, with a strong background in quality management systems, regulatory compliance, and ISO standards. The Quality Manager will play a critical role in implementing, managing, and improving our company's quality management system, with a focus on IVD products and equipment. Key Responsibilities: Implement, manage, and improve the company’s quality management system, with a primary focus on IVD products and equipment. Conduct internal audits, compile audit reports, perform problem analysis, propose improvement initiatives, and monitor the implementation of corrective and preventive actions (CAPA). Lead and participate in internal audits and management reviews of the company's quality system as a key member of the quality department. Manage the documentation of the company’s quality management system, ensuring compliance with relevant standards and regulations. Oversee the quality management system for IVD equipment, ensuring compliance with applicable regulations and standards. Perform statistical analysis of IVD equipment quality data, prepare reports, and develop corrective and preventive measures as needed. Update company documents in accordance with new or revised quality standards, laws, and regulations. Establish collaborative relationships with key opinion leaders and certification bodies to ensure alignment with industry best practices and regulatory requirements. Requirements Minimum Bachelor’s degree in Science or related field. ISO 13485:2016 lead auditor certification preferred. Thorough knowledge of US FDA 21 CFR 820 Quality System Regulation and ISO 13485:2016 standards. Strong understanding of quality management principles and practices in the medical device industry. Excellent communication and interpersonal skills. Ability to work collaboratively in a team environment. Demonstrated problem-solving and analytical skills. Attention to detail and strong organizational skills. Minimum 10 Years experience in Medical devices, Quality Management , Regulatory compliance and ISO standards Benefits Health Care Plan (Medical) 401K Paid Time Off Training & Development We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service.

Atlanta, GA, USA

Negotiable Salary

Landfill Gas Technician63499947818499122

Workable

Landfill Gas Technician

How you can make an impact as a Construction Quality Assurance Technician Conduct daily site inspections at landfills or construction sites. Oversight and inspection of landfill gas and landfill construction (cell and closure) to ensure compliance with design plans. Construction quality assurance (CQA) for compliance with drawings and technical specifications. Landfill gas or remedial system maintenance and monitoring. Coordinate with General Contractors and Subcontractors. Responsible for submitting a daily written and photo log reports. Preparation of construction documentation reports as requested. Assist in training engineering technicians, associate staff, and staff professionals in field activities. Assists in office operations when requested. Requirements 1 year of experience in active construction sites or engineering field work preferred. AA in engineering degree preferred. Valid driver’s license with a driving record in good standing required. Ability to use Microsoft Office and read maps and construction plans required. Strong oral presentation, and written communication skills. Geosynthetics and soils knowledge preferred. Must meet physical requirements for driving (pick-up truck), lifting and carrying equipment/mechanical components (up to 50 lbs. unassisted), hand excavation/digging (using shovels/picks), carrying and climbing ladders, operating and working from man lifts, operating electric tools, (drills, saws, etc.), using hand tools, (screwdrivers, wrenches, hammers, etc.), and providing services under various weather conditions. Benefits Medical, Dental, Vision, Life and Disability Insurance 100% employer- funded Employee Stock Ownership Plan (ESOP) and 401K including employer match Annual Bonus Program Student Debt Employer Contribution Program Paid holidays and PTO Company truck for certain Field Services positions

Atlanta, GA, USA

Negotiable Salary

Workable

Estimator

We are looking for a thorough estimator to calculate possible costs and gains of Disaster Restoration projects. You will collect and analyze data according to a series of useful variables. The ideal candidate will be very comfortable with numbers and analytical. You must have great attention to detail and excellent communication skills. The goal is to provide the company with accurate information that will help in operations and strategic planning. RESPONSIBILITIES Acquire understanding of the requirements of the project/program at hand Select metrics to produce valid estimates Review documents or consult experts to collect all necessary data Analyze data and produce forecasts Prepare detailed reports or bids for submission to appropriate parties Requirements Proven experience as estimator Basic understanding of accounting and project management concepts Deep understanding of research methodology, data analysis and estimation metrics Comfortable with numbers and technology Excellent knowledge of software like Restore365, Xactimate, or MICA Great attention to detail Excellent communication and negotiation abilities Well-organized and reliable Certified Professional Estimator (CPE) or other qualification will be a plus Benefits In addition to hourly wages, for full-time employees We offer a match on part of your pay for a simple-IRA for retirement savings. Our company provides a stable, pleasant work environment, friendly staff, and a thorough feedback process both up and down the chain of command.

Cartersville, GA, USA

Negotiable Salary

Quality & Health and Safety Specialist63392021430659124

Workable

Quality & Health and Safety Specialist

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare. Job Type: Full time Job Title: Quality & Health and Safety Specialist Location: Onsite - Atlanta Office Role Summary : The Quality & Health and Safety Specialist is responsible for ensuring that the company’s quality management systems and health and safety programs comply with regulatory standards and internal policies. This role involves implementing and monitoring quality assurance processes, conducting safety audits, and promoting a culture of safety and quality throughout the organization Key Responsibilities Quality Management: Maintain the Quality Management System (QMS) in accordance with ISO standards and other regulatory requirements. Conduct internal audits to ensure compliance with QMS procedures and regulatory standards. Manage nonconformance reports and corrective and preventive action (CAPA) processes. Coordinate with cross-functional teams to ensure quality standards are met in production, supply chain, and product development. Prepare and present quality performance metrics to management. Facilitate management reviews of the QMS and drive continuous improvement initiatives. Health and Safety: Implement and maintain health and safety programs and policies in compliance with OSHA regulations and other relevant standards. Conduct regular safety inspections and audits to identify and mitigate risks. Investigate accidents, incidents, and near-misses; document findings and implement corrective actions. Provide safety training and education to employees, including new hire orientation and ongoing safety awareness programs. Maintain accurate records of safety incidents, training, and compliance activities. Coordinate emergency response plans and drills. Regulatory Compliance: Stay up to date with local and industry regulations and standards related to quality and health and safety. Ensure all company activities and operations comply with applicable laws and regulations. Assist in preparing for regulatory inspections and audits and ensure timely resolution of any findings. Continuous Improvement: Identify opportunities for process improvements in both quality and safety areas. Lead or participate in cross-functional teams to implement improvement projects. Promote a culture of continuous improvement and proactive risk management within the organization. Requirements Bachelor’s degree in Quality Management, Occupational Health and Safety, Engineering, or a related field. Minimum of 3-5 years of experience in quality assurance and health and safety roles, preferably in a manufacturing or industrial environment. Certified Quality Auditor (CQA), Certified Safety Professional (CSP), or similar certifications are preferred. Skills and Competencies: Strong knowledge of ISO 9001, ISO 45001, OSHA regulations, and other relevant standards. Experience with quality management systems and health and safety programs. Excellent analytical and problem-solving skills. Effective communication and interpersonal skills. Ability to conduct training and presentations. Benefits Health Care Plan (Medical) 401K Paid Time Off Training & Development We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service.

Atlanta, GA, USA

Negotiable Salary

Workable

Quality Coordinator

CorDx is a successful biotechnology company that is expanding its operations and is seeking a Quality Coordinator to join our team. The successful candidate will be responsible for ensuring that our products meet the quality standards we have set, and will play a key role in ensuring the safety and effectiveness of our products. Working closely with senior management, the Quality Coordinator will develop and implement quality control measures, monitor performance of our products, and identify opportunities for improvement. The successful candidate will have a strong background in quality assurance in the biotechnology industry, and will have a meticulous attention to detail. Responsibilities Develop and implement quality control measures Establish and maintain quality standards for products Monitor and maintain the performance of our products Facilitate investigations into quality issues Coordinate with other departments to ensure quality standards are being met Manage documentation related to quality control Develop and maintain training programs related to quality control Requirements Bachelor's degree in a related field Strong understanding of quality assurance principles At least 3 years of experience in quality assurance in biotechnology or related industry Strong communication and organizational skills Demonstrated ability to create and manage documentation related to quality control Experience with developing and implementing training programs related to quality control Attention to detail and ability to identify areas for improvement. Mandarin speaking preferred Benefits Health Care Plan (Medical) Retirement Plan Paid Time Off Training & Development Company Sponsored Meals Individual and Team Bonding Spending

Atlanta, GA, USA

Negotiable Salary