6,949 Quality Assurance Specialists jobs in the United States
Quality Assurance/Quality Control Manager
73521 Altus, Oklahoma
CyberCoders
Posted today
Job Viewed
Job Description
Project located in Altus, OK.
The Quality Assurance/Quality Control Manager is responsible for overseeing all aspects of quality assurance and control within the organization. This role aims to ensure that products meet the required quality standards and comply with regulatory requirements. The manager will implement quality management processes and foster a culture of continuous improvement throughout the organization.
Key Responsibilities
Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa.
This job was first posted by CyberCoders on 07/08/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.
CyberCoders is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at to make arrangements.
The Quality Assurance/Quality Control Manager is responsible for overseeing all aspects of quality assurance and control within the organization. This role aims to ensure that products meet the required quality standards and comply with regulatory requirements. The manager will implement quality management processes and foster a culture of continuous improvement throughout the organization.
Key Responsibilities
- Develop and implement quality assurance policies and procedures to ensure compliance with ISO standards and regulatory requirements.
- Manage and lead the quality assurance and quality control team to ensure effective testing and quality checks.
- Conduct regular audits of processes and products to identify areas for improvement and ensure adherence to quality standards.
- Oversee the development and execution of testing protocols, including manual and automation testing.
- Utilize root cause analysis to investigate quality issues and implement corrective actions to prevent recurrence.
- Collaborate with cross-functional teams to promote quality awareness and ensure quality practices are integrated into all aspects of production and development.
- Analyze quality data and metrics to identify trends, risks, and opportunities for process improvement.
- Facilitate training sessions for staff on quality standards, documentation, and best practices in quality control.
- Bachelor's degree in Quality Assurance, Engineering, or a related field.
- Minimum of 5 years of experience in quality assurance and quality control roles, with at least 2 years in a management position.
- Strong knowledge of ISO standards and regulatory compliance requirements.
- Proven experience in testing methodologies, including software testing, automation testing, and manual testing.
- Excellent analytical and problem-solving skills with a focus on continuous improvement.
- Strong documentation skills with the ability to create and maintain quality manuals and policies.
- Experience in risk management and root cause analysis.
- Ability to work collaboratively in a team environment and communicate effectively with all levels of the organization.
- Full Benefits
- 3 Weeks PTO
- Company vehicle
Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
- Please do NOT change the email subject line in any way. You must keep the JobID: linkedin : RC L784 -- in the email subject line for your application to be considered.***
For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa.
This job was first posted by CyberCoders on 07/08/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.
CyberCoders is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at to make arrangements.
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0
Quality Assurance/Quality Control Manager
73116 Oklahoma City, Oklahoma
CyberCoders
Posted today
Job Viewed
Job Description
Project located in Altus, OK.
The Quality Assurance/Quality Control Manager is responsible for overseeing all aspects of quality assurance and control within the organization. This role aims to ensure that products meet the required quality standards and comply with regulatory requirements. The manager will implement quality management processes and foster a culture of continuous improvement throughout the organization.
Key Responsibilities
Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa.
This job was first posted by CyberCoders on 07/08/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.
CyberCoders is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at to make arrangements.
The Quality Assurance/Quality Control Manager is responsible for overseeing all aspects of quality assurance and control within the organization. This role aims to ensure that products meet the required quality standards and comply with regulatory requirements. The manager will implement quality management processes and foster a culture of continuous improvement throughout the organization.
Key Responsibilities
- Develop and implement quality assurance policies and procedures to ensure compliance with ISO standards and regulatory requirements.
- Manage and lead the quality assurance and quality control team to ensure effective testing and quality checks.
- Conduct regular audits of processes and products to identify areas for improvement and ensure adherence to quality standards.
- Oversee the development and execution of testing protocols, including manual and automation testing.
- Utilize root cause analysis to investigate quality issues and implement corrective actions to prevent recurrence.
- Collaborate with cross-functional teams to promote quality awareness and ensure quality practices are integrated into all aspects of production and development.
- Analyze quality data and metrics to identify trends, risks, and opportunities for process improvement.
- Facilitate training sessions for staff on quality standards, documentation, and best practices in quality control.
- Bachelor's degree in Quality Assurance, Engineering, or a related field.
- Minimum of 5 years of experience in quality assurance and quality control roles, with at least 2 years in a management position.
- Strong knowledge of ISO standards and regulatory compliance requirements.
- Proven experience in testing methodologies, including software testing, automation testing, and manual testing.
- Excellent analytical and problem-solving skills with a focus on continuous improvement.
- Strong documentation skills with the ability to create and maintain quality manuals and policies.
- Experience in risk management and root cause analysis.
- Ability to work collaboratively in a team environment and communicate effectively with all levels of the organization.
- Full Benefits
- 3 Weeks PTO
- Company vehicle
Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
- Please do NOT change the email subject line in any way. You must keep the JobID: linkedin : RC -- in the email subject line for your application to be considered.***
For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa.
This job was first posted by CyberCoders on 07/08/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.
CyberCoders is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at to make arrangements.
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1
Director Quality Assurance Quality Control
07004 Fairfield, New Jersey
ClinLab Staffing
Posted today
Job Viewed
Job Description
QA/QC Director – Fairfield, NJ
Summary:
The QA/QC Director is primarily responsible for the development and implementation of quality management systems. Establishing quality standards and procedures as well as monitor compliance and regulatory requirements.
Responsibilities
- To ensure that the production facility is operating at a high operational and compliance standard.
- Lead, coach and manage a team of chemists to ensure data integrity and performance to meet business objectives
- Monitor each department’s operations to ensure that all procedures are being adhered to and that only approved products or services are being delivered to the company’s clients.
- Oversee the entire department, ensuring that proper procedures are being followed when approving each product or service.
- Ensure that deadlines are met
- Train and develop colleagues
- Assist employees to solve problems, using quality management techniques
- Consult with the quality managers and other personnel to design quality strategies and goals for the department, which will be implemented by employees
- Help to promote the implementation of quality systems throughout the company
- Develop and implement policies relating to all operations in accordance with company objectives. Ensure these policies are adhered to by personnel under your supervision and that appropriate records are kept for future reference
- Keep management informed on product quality and any concerns that may influence this measure, such as complaints from customers or suppliers, etcetera
- Other duties assigned by Management
Education:
- Bachelor’s degree in a scientific discipline with a minimum of 10 years’ experience in quality management
Experience Requirements:
- Experienced with liquid manufacturing and packaging of Rx products.
- Experience with Empower 3
- Experience working in an FDA regulated environment
- Experience with ANDA and NDA submissions
- Experience with validations of processes, cleaning, analytical methods, facilities and equipment
- Knowledge of CFR & ICH Regulatory Guidelines
- Knowledge of cGMP processes and GDP.
Computer Skills:
- Microsoft Word
- Microsoft Excel
- Empower 3
Other Requirements:
- Has significant technical knowledge of quality management principles.
- In depth knowledge of all laboratory equipment, practices, and procedures
- Ability to think logically and independently
- Demonstrated managerial abilities
- Problem analysis, solving and resolution skills
- Has excellent oral and written skills
- Has excellent interpersonal skills
- Is self motivated
- Has a very high attention to detail
- Has a positive attitude
- Must speak, read, and write in English
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2
Quality Assurance/Quality Control Manager
43054 Fairfield, Ohio
BlackRock Resources LLC
Posted today
Job Viewed
Job Description
You must be able to work in the U.S. without sponsorship. No C2C or 3rd parties, please.
We're hiring an experienced QA/QC Manager to support a greenfield data center construction project in New Albany, OH. This is a high-impact role for someone who understands the complexity of electrical installations and thrives in a detail-driven, fast-paced construction environment.
This is an on-site role focused on maintaining and overseeing all aspects of the project's quality assurance and control plan. You’ll report directly to the Project Manager and coordinate with on-site and off-site teams, subcontractors, and stakeholders to ensure compliance, safety, and precision across the board.
Key Requirements:
- Hands-on experience with high voltage electrical projects
- Strong command of construction quality regulations
- Exceptional attention to detail and documentation
- Ability to communicate effectively with all levels – from tradespeople to leadership
- Previous experience in greenfield or data center construction strongly preferred
- Skilled in electrical inspections, walk-downs, and system testing
- Comfortable with tools like Excel, Word, and QA documentation systems
What You'll Be Doing:
- Implement and manage the project’s QA/QC plan
- Oversee subcontractor compliance and coordinate inspections
- Lead documentation processes – from submittals and logs to final as-builts
- Conduct walk-downs, material tracking, shop drawing reviews, and 4-phase inspections
- Maintain testing records, rework lists, and support third-party audits
- Actively ensure the project stays on track, safe, and within quality specs
Additional Info:
- Must be able to read and interpret blueprints, specs, and system documentation
- Prior work with systems like CSA, CX mapping, Bus Duct, Cable Bus, and MV/LV gear
- Physical ability to move around large construction sites and wear PPE daily
- 15+ years in QA/QC for heavy industrial construction preferred
If you're someone who takes pride in doing it right the first time, keeps quality at the forefront, and is ready for a major project, let’s talk.
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3
Manager, Quality Assurance & Quality Control
60071 Richmond, Illinois
Danaher Corporation
Posted 1 day ago
Job Viewed
Job Description
Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Leica Biosystems, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
At Leica Biosystems, we're not just shaping the future of cancer diagnostics - we're transforming lives. Our mission of "Advancing Cancer Diagnostics, Improving Lives" is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you're not just taking a job; you're becoming part of a passionate team that knows every moment matters when it comes to cancer. You'll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you'll be inspired each day to stretch, grow, and make an impact.
Learn about the Danaher Business System ( which makes everything possible.
The Manager, Quality Assurance and Quality Control for Leica Biosystems Richmond is responsible for providing leadership and support of daily quality operations including QC finished goods and raw material inspection program, QA product release, nonconformance workflows, CDT&R, and calibration.
This position reports to the Director, Quality Assurance and Regulatory Compliance responsible for ensuring that the business, product, and processes meet all Quality and Regulatory standards and requirements. This position is part of the Quality Assurance and Regulatory Compliance department located in Richmond, Illinois and will be onsite.
In this role, you will have the opportunity to:
+ Hire, develop, engage, and retain highly capable QA and QC team members, ensuring that each associate is meeting performance requirements and that each critical position has an identified successor with a targeted and robust development plan.
+ Oversee inspection and product release activities as well as CDT&R, and develop key strategies to support future business success.
+ Coach the team on how to effectively manage and anticipate changing needs for resources and how to flex resource allocation in the face of changing circumstances, including notifying stakeholders and recommending countermeasures to ensure that cross-functional teams and projects are staffed with qualified and skilled QA and QC associates and business needs are met.
+ Manage relationships with relevant cross-functional leaders including participating in Daily Management meetings and effectively communicating issues, risks, and needs to the Leadership team.
+ Plan, prioritize, and coordinate workflow and cross-site/function interactions to ensure on time delivery of product and projects and compliance with quality systems and standards, using advanced knowledge of Danaher Business System (DBS) tools.
+ Ensure site audit readiness at all times through monitoring and learning from past audits, training and preparation of staff and mitigation of risks.
+ Support team in formulating and testing effective data-based strategy for winning against the competition or exceeding expectations as a team.
The essential requirements of the job include:
+ Bachelor's degree or equivalent advanced degree in engineering, science, medical, or technical field and 5+ years' experience with increasing responsibility in medical device/IVD
+ Experience working within a medical device quality system in compliance with US FDA, ISO 13485 and EU MDR/IVDR regulations
+ Proven experience in developing and implementing mining tools to monitor product complaint trends including defined control and/or action limits to detect emerging field issues
+ Track record of collaborating with technical groups to identify product improvement opportunities
Travel, Motor Vehicle Record & Physical/Environment Requirements:
+ Travel requirements <5% of the time, domestic and international
+ Overnight travel may be required
+ Be able to occasionally lift and/or move up to 40 pounds.
+ Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
+ This position will occasionally require travel by car and flying in and out of airports with possible long wait times
It would be a plus if you also possess previous experience in:
+ Knowledge of lean tools such as 5S, Standard Work, KANBAN, Policy Deployment, Value Stream Management, Visual Management, SAP etc.
+ Demonstrated knowledge of Quality Management Systems, continuous improvement methodologies, and understanding of manufacturing processes with high mix low volume and high mix high volume environment.
+ Demonstrated ability to lead, develop, communicate, and implement a strategy to ensure compliance to company, regulatory and industry requirements.
+ Experience and/or knowledge of NCRs
The annual salary range for this role is $120,000 - $140,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
#LI-GC1
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here ( .
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Leica Biosystems, one of Danaher's ( 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
At Leica Biosystems, we're not just shaping the future of cancer diagnostics - we're transforming lives. Our mission of "Advancing Cancer Diagnostics, Improving Lives" is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you're not just taking a job; you're becoming part of a passionate team that knows every moment matters when it comes to cancer. You'll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you'll be inspired each day to stretch, grow, and make an impact.
Learn about the Danaher Business System ( which makes everything possible.
The Manager, Quality Assurance and Quality Control for Leica Biosystems Richmond is responsible for providing leadership and support of daily quality operations including QC finished goods and raw material inspection program, QA product release, nonconformance workflows, CDT&R, and calibration.
This position reports to the Director, Quality Assurance and Regulatory Compliance responsible for ensuring that the business, product, and processes meet all Quality and Regulatory standards and requirements. This position is part of the Quality Assurance and Regulatory Compliance department located in Richmond, Illinois and will be onsite.
In this role, you will have the opportunity to:
+ Hire, develop, engage, and retain highly capable QA and QC team members, ensuring that each associate is meeting performance requirements and that each critical position has an identified successor with a targeted and robust development plan.
+ Oversee inspection and product release activities as well as CDT&R, and develop key strategies to support future business success.
+ Coach the team on how to effectively manage and anticipate changing needs for resources and how to flex resource allocation in the face of changing circumstances, including notifying stakeholders and recommending countermeasures to ensure that cross-functional teams and projects are staffed with qualified and skilled QA and QC associates and business needs are met.
+ Manage relationships with relevant cross-functional leaders including participating in Daily Management meetings and effectively communicating issues, risks, and needs to the Leadership team.
+ Plan, prioritize, and coordinate workflow and cross-site/function interactions to ensure on time delivery of product and projects and compliance with quality systems and standards, using advanced knowledge of Danaher Business System (DBS) tools.
+ Ensure site audit readiness at all times through monitoring and learning from past audits, training and preparation of staff and mitigation of risks.
+ Support team in formulating and testing effective data-based strategy for winning against the competition or exceeding expectations as a team.
The essential requirements of the job include:
+ Bachelor's degree or equivalent advanced degree in engineering, science, medical, or technical field and 5+ years' experience with increasing responsibility in medical device/IVD
+ Experience working within a medical device quality system in compliance with US FDA, ISO 13485 and EU MDR/IVDR regulations
+ Proven experience in developing and implementing mining tools to monitor product complaint trends including defined control and/or action limits to detect emerging field issues
+ Track record of collaborating with technical groups to identify product improvement opportunities
Travel, Motor Vehicle Record & Physical/Environment Requirements:
+ Travel requirements <5% of the time, domestic and international
+ Overnight travel may be required
+ Be able to occasionally lift and/or move up to 40 pounds.
+ Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
+ This position will occasionally require travel by car and flying in and out of airports with possible long wait times
It would be a plus if you also possess previous experience in:
+ Knowledge of lean tools such as 5S, Standard Work, KANBAN, Policy Deployment, Value Stream Management, Visual Management, SAP etc.
+ Demonstrated knowledge of Quality Management Systems, continuous improvement methodologies, and understanding of manufacturing processes with high mix low volume and high mix high volume environment.
+ Demonstrated ability to lead, develop, communicate, and implement a strategy to ensure compliance to company, regulatory and industry requirements.
+ Experience and/or knowledge of NCRs
The annual salary range for this role is $120,000 - $140,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.
#LI-GC1
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.
The U.S. EEO posters are available here ( .
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact: or .
View Now
4
Quality Assurance/ Quality Control Supervisor
Alma, Michigan
HiFyve
Posted today
Job Viewed
Job Description
Job Description
Job Description
HiFyve is working with a company in Alma, GA that is hiring for a Quality Assurance Supervisor in the Food and Beverage Industry.
$60k-$80k + bonus
Full Benefits Package
Day Shift
Key Responsibilities
- Maintain and update HACCP protocols in collaboration with the Food Safety Coordinator and management.
- Implement and monitor quality, sanitation, and SSOP programs to ensure food safety and regulatory compliance.
- Serve as the lead contact for third-party audits, preparing and managing all necessary QA and food safety documentation.
- Maintain records related to label approvals and ensure accurate documentation for products produced.
- Work with food safety, technical service, and QA teams to manage product specifications (including allergen, nutritional, and formulation data).
- Distribute new product information and specifications to relevant departments.
- Oversee quality review during initial production runs of new items.
- Manage quality incident reporting and follow up on product issues.
- Develop and maintain customer product specifications and conduct shelf life studies as needed.
- Promote and execute quality and food safety policies, procedures, and training programs across the facility.
- Assist with SSOP documentation and addressing USDA-related matters.
Qualifications
- Bachelor’s degree in Animal Science, Meat Science, or a related field is preferred.
- Minimum of two years’ experience in QA and/or Food Safety within meat processing.
- At least two years of management experience in QA and Food Safety.
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5
Quality Assurance/Quality Control Manager (Altus)
73521 Altus, Oklahoma
CyberCoders
Posted today
Job Viewed
Job Description
Project located in Altus, OK.
The Quality Assurance/Quality Control Manager is responsible for overseeing all aspects of quality assurance and control within the organization. This role aims to ensure that products meet the required quality standards and comply with regulatory requirements. The manager will implement quality management processes and foster a culture of continuous improvement throughout the organization.
Key Responsibilities
Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa.
This job was first posted by CyberCoders on 07/08/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.
CyberCoders is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at to make arrangements.
The Quality Assurance/Quality Control Manager is responsible for overseeing all aspects of quality assurance and control within the organization. This role aims to ensure that products meet the required quality standards and comply with regulatory requirements. The manager will implement quality management processes and foster a culture of continuous improvement throughout the organization.
Key Responsibilities
- Develop and implement quality assurance policies and procedures to ensure compliance with ISO standards and regulatory requirements.
- Manage and lead the quality assurance and quality control team to ensure effective testing and quality checks.
- Conduct regular audits of processes and products to identify areas for improvement and ensure adherence to quality standards.
- Oversee the development and execution of testing protocols, including manual and automation testing.
- Utilize root cause analysis to investigate quality issues and implement corrective actions to prevent recurrence.
- Collaborate with cross-functional teams to promote quality awareness and ensure quality practices are integrated into all aspects of production and development.
- Analyze quality data and metrics to identify trends, risks, and opportunities for process improvement.
- Facilitate training sessions for staff on quality standards, documentation, and best practices in quality control.
- Bachelor's degree in Quality Assurance, Engineering, or a related field.
- Minimum of 5 years of experience in quality assurance and quality control roles, with at least 2 years in a management position.
- Strong knowledge of ISO standards and regulatory compliance requirements.
- Proven experience in testing methodologies, including software testing, automation testing, and manual testing.
- Excellent analytical and problem-solving skills with a focus on continuous improvement.
- Strong documentation skills with the ability to create and maintain quality manuals and policies.
- Experience in risk management and root cause analysis.
- Ability to work collaboratively in a team environment and communicate effectively with all levels of the organization.
- Full Benefits
- 3 Weeks PTO
- Company vehicle
Looking forward to receiving your resume through our website and going over the position with you. Clicking apply is the best way to apply, but you may also:
- Please do NOT change the email subject line in any way. You must keep the JobID: linkedin : RC L784 -- in the email subject line for your application to be considered.***
For this position, you must be currently authorized to work in the United States without the need for sponsorship for a non-immigrant visa.
This job was first posted by CyberCoders on 07/08/2025 and applications will be accepted on an ongoing basis until the position is filled or closed.
CyberCoders is proud to be an Equal Opportunity Employer
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity or expression, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, status as a crime victim, disability, protected veteran status, or any other characteristic protected by law. CyberCoders will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable state and local law, including but not limited to the Los Angeles County Fair Chance Ordinance, the San Francisco Fair Chance Ordinance, and the California Fair Chance Act. CyberCoders is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. Individuals needing special assistance or an accommodation while seeking employment can contact a member of our Human Resources team at to make arrangements.
View Now
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6
Director Quality Assurance Quality Control (Fairfield)
07004 Fairfield, New Jersey
ClinLab Staffing
Posted 1 day ago
Job Viewed
Job Description
QA/QC Director Fairfield, NJ
Summary:
The QA/QC Director is primarily responsible for the development and implementation of quality management systems. Establishing quality standards and procedures as well as monitor compliance and regulatory requirements.
Responsibilities
- To ensure that the production facility is operating at a high operational and compliance standard.
- Lead, coach and manage a team of chemists to ensure data integrity and performance to meet business objectives
- Monitor each departments operations to ensure that all procedures are being adhered to and that only approved products or services are being delivered to the companys clients.
- Oversee the entire department, ensuring that proper procedures are being followed when approving each product or service.
- Ensure that deadlines are met
- Train and develop colleagues
- Assist employees to solve problems, using quality management techniques
- Consult with the quality managers and other personnel to design quality strategies and goals for the department, which will be implemented by employees
- Help to promote the implementation of quality systems throughout the company
- Develop and implement policies relating to all operations in accordance with company objectives. Ensure these policies are adhered to by personnel under your supervision and that appropriate records are kept for future reference
- Keep management informed on product quality and any concerns that may influence this measure, such as complaints from customers or suppliers, etcetera
- Other duties assigned by Management
Education:
- Bachelors degree in a scientific discipline with a minimum of 10 years experience in quality management
Experience Requirements:
- Experienced with liquid manufacturing and packaging of Rx products.
- Experience with Empower 3
- Experience working in an FDA regulated environment
- Experience with ANDA and NDA submissions
- Experience with validations of processes, cleaning, analytical methods, facilities and equipment
- Knowledge of CFR & ICH Regulatory Guidelines
- Knowledge of cGMP processes and GDP.
Computer Skills:
- Microsoft Word
- Microsoft Excel
- Empower 3
Other Requirements:
- Has significant technical knowledge of quality management principles.
- In depth knowledge of all laboratory equipment, practices, and procedures
- Ability to think logically and independently
- Demonstrated managerial abilities
- Problem analysis, solving and resolution skills
- Has excellent oral and written skills
- Has excellent interpersonal skills
- Is self motivated
- Has a very high attention to detail
- Has a positive attitude
- Must speak, read, and write in English
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7
Quality Control/Quality Assurance Inspector - Manufacturing
65806 Fairview, Missouri
Adecco US, Inc.
Posted 15 days ago
Job Viewed
Job Description
**Quality Control / Quality Assurance (QC/QA) Inspector - Modular Construction**
**Location: Springfield, MO**
**Job Type: Full-Time**
**Schedule: 7:00am to 4:00pm - Monday thru Friday**
**Remote: On-site**
**Salary: $44,000.00 to $5,000.00 based on experience and certifications**
**Benefits: Medical, Dental, Life Insurance, 401K and PTO**
**Relocation: Not available**
**Required: You must have previous Quality Control/Quality Assurance experience in manufacturing, construction, or municipal inspection to be considered for this position.**
**The Role:**
We are seeking a detail-oriented and proactive QC/QA Inspector to join our growing team in a dynamic modular construction manufacturing environment. This role focuses on ensuring the quality, compliance, and performance of modular panel enclosures used in the commercial construction of restaurants, coffee shops, and convenience stores.
As a QC/QA Inspector, you will be responsible for conducting inspections, verifying material conformance, performing system tests, testing documentation, and ensuring compliance with both project specifications and applicable state modular building codes.
We are a company guided by our core values: _Creative, Honorable, Respectful, Innovative, Synergistic, and Total Ownership (C.H.R.I.S.T)._
**Key Responsibilities:**
**Quality Control Execution -**
+ Implement and maintain the Quality Assurance / Quality Control (QA/QC) plan for modular manufacturing projects.
+ Conduct regular inspections of materials, fabricated components, and assembled modules.
+ Ensure all processes comply with project-specific quality standards and company protocols.
**Testing and Inspections -**
+ Perform structural, electrical, mechanical, and plumbing system tests to validate compliance and performance.
+ Conduct inspections both in-factory and on-site prior to shipping or final assembly.
+ Identify and document any non-conformances or deviations from specifications.
**Documentation and Compliance -**
+ Maintain detailed records of all inspections, test results, corrective actions, and compliance checks.
+ Prepare quality reports and inspection logs for internal use and for external regulatory review.
+ Ensure traceability and accountability for all quality-related records.
**Defect (Construction) Resolution -**
+ Conduct root cause analysis when defects or non-compliant items are discovered.
+ Collaborate with engineering and production teams to implement corrective and preventive actions.
**Regulatory Compliance -**
+ Ensure all modular units comply with state-specific modular construction regulations, including the International Building Code (IBC) and any state-adopted amendments.
+ Verify that manufactured modules meet the certification standards for each target installation state, including anchoring and foundation requirements.
+ Assist in ensuring units meet conditions for receiving modular compliance seals and final occupancy certificates.
**Cross-Functional Collaboration -**
+ Work closely with design, production, installation, and project management teams to ensure quality is maintained throughout the lifecycle of each project.
+ Support communication between internal teams and third-party inspectors, state regulatory agencies, and clients.
**Qualifications:**
**Required -**
+ 3+ years of experience in a QC/QA role, ideally within construction, manufacturing, or modular building sectors.
+ Knowledge of building codes and standards (e.g., IBC, NEC, IPC, state modular codes).
+ Experience performing inspections and quality tests in a manufacturing or construction environment.
+ Strong attention to detail and the ability to interpret technical drawings, plans, and specifications.
+ Proficiency in quality documentation, checklists, and reporting systems.
+ Ability to read and understand regulatory requirements across different U.S. states.
**Additional Preferred Skills -**
+ Familiarity with state-specific modular construction certification programs.
+ Experience with commercial construction projects (restaurants, retail, food service).
+ Certification in quality control (e.g., ASQ Certified Quality Inspector, ICC Certifications) is a plus.
**Why Join Us?**
+ Be part of a fast-growing company revolutionizing commercial construction through modular innovation.
+ Work in a controlled factory environment that prioritizes precision and quality.
+ Contribute to high-impact projects with nationally recognized brands.
+ Grow your career in an environment that values quality, safety, and continuous improvement.
**Work Environment -**
+ Factory-based with occasional travel to project installation sites.
+ Fast-paced manufacturing setting with an emphasis on safety and workflow efficiency.
+ Occasional lifting, bending, and exposure to standard construction materials and tools.
**Pay Details:** 44,000.00 to 65,000.00 per year
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
+ The California Fair Chance Act
+ Los Angeles City Fair Chance Ordinance
+ Los Angeles County Fair Chance Ordinance for Employers
+ San Francisco Fair Chance Ordinance
**Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
**Location: Springfield, MO**
**Job Type: Full-Time**
**Schedule: 7:00am to 4:00pm - Monday thru Friday**
**Remote: On-site**
**Salary: $44,000.00 to $5,000.00 based on experience and certifications**
**Benefits: Medical, Dental, Life Insurance, 401K and PTO**
**Relocation: Not available**
**Required: You must have previous Quality Control/Quality Assurance experience in manufacturing, construction, or municipal inspection to be considered for this position.**
**The Role:**
We are seeking a detail-oriented and proactive QC/QA Inspector to join our growing team in a dynamic modular construction manufacturing environment. This role focuses on ensuring the quality, compliance, and performance of modular panel enclosures used in the commercial construction of restaurants, coffee shops, and convenience stores.
As a QC/QA Inspector, you will be responsible for conducting inspections, verifying material conformance, performing system tests, testing documentation, and ensuring compliance with both project specifications and applicable state modular building codes.
We are a company guided by our core values: _Creative, Honorable, Respectful, Innovative, Synergistic, and Total Ownership (C.H.R.I.S.T)._
**Key Responsibilities:**
**Quality Control Execution -**
+ Implement and maintain the Quality Assurance / Quality Control (QA/QC) plan for modular manufacturing projects.
+ Conduct regular inspections of materials, fabricated components, and assembled modules.
+ Ensure all processes comply with project-specific quality standards and company protocols.
**Testing and Inspections -**
+ Perform structural, electrical, mechanical, and plumbing system tests to validate compliance and performance.
+ Conduct inspections both in-factory and on-site prior to shipping or final assembly.
+ Identify and document any non-conformances or deviations from specifications.
**Documentation and Compliance -**
+ Maintain detailed records of all inspections, test results, corrective actions, and compliance checks.
+ Prepare quality reports and inspection logs for internal use and for external regulatory review.
+ Ensure traceability and accountability for all quality-related records.
**Defect (Construction) Resolution -**
+ Conduct root cause analysis when defects or non-compliant items are discovered.
+ Collaborate with engineering and production teams to implement corrective and preventive actions.
**Regulatory Compliance -**
+ Ensure all modular units comply with state-specific modular construction regulations, including the International Building Code (IBC) and any state-adopted amendments.
+ Verify that manufactured modules meet the certification standards for each target installation state, including anchoring and foundation requirements.
+ Assist in ensuring units meet conditions for receiving modular compliance seals and final occupancy certificates.
**Cross-Functional Collaboration -**
+ Work closely with design, production, installation, and project management teams to ensure quality is maintained throughout the lifecycle of each project.
+ Support communication between internal teams and third-party inspectors, state regulatory agencies, and clients.
**Qualifications:**
**Required -**
+ 3+ years of experience in a QC/QA role, ideally within construction, manufacturing, or modular building sectors.
+ Knowledge of building codes and standards (e.g., IBC, NEC, IPC, state modular codes).
+ Experience performing inspections and quality tests in a manufacturing or construction environment.
+ Strong attention to detail and the ability to interpret technical drawings, plans, and specifications.
+ Proficiency in quality documentation, checklists, and reporting systems.
+ Ability to read and understand regulatory requirements across different U.S. states.
**Additional Preferred Skills -**
+ Familiarity with state-specific modular construction certification programs.
+ Experience with commercial construction projects (restaurants, retail, food service).
+ Certification in quality control (e.g., ASQ Certified Quality Inspector, ICC Certifications) is a plus.
**Why Join Us?**
+ Be part of a fast-growing company revolutionizing commercial construction through modular innovation.
+ Work in a controlled factory environment that prioritizes precision and quality.
+ Contribute to high-impact projects with nationally recognized brands.
+ Grow your career in an environment that values quality, safety, and continuous improvement.
**Work Environment -**
+ Factory-based with occasional travel to project installation sites.
+ Fast-paced manufacturing setting with an emphasis on safety and workflow efficiency.
+ Occasional lifting, bending, and exposure to standard construction materials and tools.
**Pay Details:** 44,000.00 to 65,000.00 per year
Equal Opportunity Employer/Veterans/Disabled
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
+ The California Fair Chance Act
+ Los Angeles City Fair Chance Ordinance
+ Los Angeles County Fair Chance Ordinance for Employers
+ San Francisco Fair Chance Ordinance
**Massachusetts Candidates Only:** It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
View Now
8