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Location:
Conyers
Category:
Quality Assurance & Control

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

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
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

Workable
Quality Inspector - 1st Shift (Same Day Pay) $16-18hr Atlanta
***********PLEASE READ BELOW*****************
The Immediate Pay, Quality Inspector position offers individuals the opportunity to receive payment for their work on the same day they perform their duties. This position is designed to provide a quick and fair compensation system for workers who are seeking immediate income.
Upon starting the job, workers will be paid for their first day of work (ONLY) at the end of that day. However, it is important to note that if a worker does not show up for their second day of work without prior notice or valid reason, they will be terminated from the position. This is a W2 position. You will not be considered if you do not perform video screen.
Overall Purpose of the Quality Inspector
Provide Quality services and support for all missions assigned to a manufacturing or warehouse site while ensuring a healthy and safe work environment.
Reports to Site Supervisor/Site Leaders
Responsibilities
(To include but not limited to the following)
Client Relationship & Business Development
Act as an impartial third party between the production source and the customer facility to ensure the product meets set criteria
Operations
Check/inspect manufactured parts or products for defects
Read and follow work instructions and general processes
Use measuring or testing equipment as needed
Ensure products meet quality standards
Display excellent customer service
Must comply with local and company Health & Safety legislation, laws, and policies
Organization & Management
Collect and record data
Technical
Utilize company portal for time recording and policy acknowledgements
Other
Any other duties as assigned
Knowledge, skills, abilities
Hard skills
Requirements
Must be able to speak and read in the English language
Good communications skills
Must be able to multi-task
Ability to work in a fast-paced environment
Ability to handle sensitive and confidential material
Ability lift /move 50 pounds
Must have reliable transportation

Atlanta, GA, USA
Negotiable Salary