4,980 Quality Assurance jobs in the United States

Job Title: Quality InspectorJob Description

We are seeking a skilled Quality Inspector to perform First Article Inspections (AS9102) and Final Inspections as specified in customer purchase orders and internal procedures. The role requires working from engineering blueprints on returns, new parts, and customer specifications.

Responsibilities

• Perform First Article and Final Inspections in accordance with AS9102 standards.

• Assist quality engineering with root cause analysis and corrective actions.

• Inspect products and articles with a proficient understanding of ANSI Y14.5 Dimensioning and Tolerancing.

• Report the status of assignments, including completion dates.

• Conduct training for quality and production personnel to maintain product quality and system requirements.

• Support corrective and preventative actions, including follow-up to verify closure.

• Perform receiving and in-process inspections to provide dimensional reports.

• Verify external party material certifications, process certifications, inspection reports, and first article reports against purchase order and specification requirements.

• Support the Quality Policy and Quality Management System, including participation in internal audits.

• Create accurate and detailed discrepancy reports for nonconforming features in support of engineering dispositions.

• Communicate effectively with internal and external parties.

• Assist other quality personnel in completing assigned tasks.

Essential Skills

• AS or BS in engineering or technical field.

• Minimum 5 years of experience in a machine shop environment, preferably precision-focused.

• Experience in inspection processes, audits, CAPA, root cause analysis, and First Article Inspections.

• Preferred experience with CMM (PCDIMS is a plus).

• Ability to read and understand detailed, complex engineering drawings for machined parts.

• Strong understanding of Geometric Dimensioning and Tolerancing (GD&T).

• Excellent communication, reading, and computer skills, particularly in MS Office (Word, Excel, Outlook).

• Good record-keeping skills and organizational abilities.

Additional Skills & Qualifications

• Experience in aerospace quality assurance standards.

• Capability in quality assurance, quality control, and quality systems.

Work Environment

The position is within the Quality Engineering department, reporting to the Quality Manager. The work is conducted in a clean shop environment, spending 50% of the time on the floor with machinists. Collaboration will be with engineering, machinists, quality personnel, and other departments. The work schedule is Monday to Thursday from 7:00 AM to 4:30 PM, and Friday from 7:00 AM to 11:00 AM.

Pay and Benefits

The pay range for this position is $35.00 - $45.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Sun Valley,CA.

Application Deadline

This position is anticipated to close on Aug 11, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

• Use manual and programmable measurement tools to gather mechanical and dimensional data
• Read and interpret technical drawings to verify product compliance
• Operate and program automated testing systems
• Apply geometric principles to calculate inferred specifications
• Maintain high accuracy when using precision measuring tools
• Prepare documentation such as compliance reports, data sheets, and quality analysis
• Follow ISO 9001 quality standards and participate in internal audits
• Investigate defects and contribute to continuous improvement initiatives
• Maintain a clean, safe, and organized work area

• Mechanical aptitude and a strong attention to detail
• Ability to read and understand technical drawings
• Experience using precision dimensional measurement tools
• Willingness to learn and operate automated inspection equipment
• Knowledge of geometric dimensioning and tolerancing (GD&T) principles
• Familiarity with quality standards in industries such as aerospace, defense, or medical preferred
• Ability to create accurate, well-organized documentation and reports
• Commitment to safety, quality, and continuous improvement within ISO 9001 standards
• Eagerness to learn and grow within a quality-focused role

• Full Time
• Pay Rate is $ 17-21per hour
• Shift 1st 8a-430p
• Weekly pay while employed through Career Concepts
• Benefits available while employed through Career Concepts
• Temp-To-Hire
• Benefits after Probation period

• McKees Rocks, PA

• Competitive Compensation Package!
• Complete Benefits Package!
• Excellent Work/Life Balance!
• Accelerated Career Growth!
• Fun Company Activities!
• Many More!

• Lead incoming, in-process, and final inspections, ensuring parts meet exacting standards
• Own the ISO 9001 and AS9100 quality systems-handle audits, documentation, and compliance
• Perform and document 1st Article Inspections (FAIs)
• Operate and program CMMs
• Manage calibrations, track quality metrics, and complete all associated paperwork
• Work closely with production on the floor-this is a hands on role
• Interface with engineering, operations, and leadership to drive continuous improvement

• A self-starter who thrives with minimal direction
• Comfortable navigating blueprints and technical drawings, with basic GD&T familiarity (20-30% of prints include it)
• Hands-on with machine shop or fabrication experience (sheet metal experience a plus, but not required)
• Experienced in CMM programming/operation
• Experience with in-process and final inspections and related documentation

• Prepare and execute test plans for system, integration, and user acceptance validations.
• Review and validate software requirements and design specifications from a technical standpoint.
• Perform automated and manual functional testing efforts across all product platforms.
• Estimate, track, and review all QA testing efforts prepared and completed by QA Engineers.
• Ensure all deliverables are of high quality, on time, and accurately time reported.
• Identify and document opportunities for improving current processes and/or procedures.
• Assess future project requirements and provide detailed documentation for test implementation.
• Escalate issues that affect the company's product, quality, or delivery which are beyond the team's product / project base.
• Ensure all company and department processes and procedures are implemented appropriately by QA Engineers.
• Pro-actively seek clarification on Acceptance criteria for all stories submitted for review.
• Develop and implement test strategies that will increase productivity and quality output.
• Report, track, and uphold all software defects discovered by the team regardless of severity.
• Maintain, expand, and supplement existing test scripts and standards.
• Assign, monitor, and be responsible for all testing related components / resources including hardware, software, departmental team collaboration, and training.
• Actively participate in all grooming, planning and design meetings.
• Possess excellent interpersonal and communication skills and must be a team player.
• Be flexible to work on different projects based on the project and company needs.
• Mortgage lending experience and demonstrated knowledge within the mortgage industry experience is recommended.
• Experience with Ellie Mae's Encompass 360 Mortgage system is a plus.
• May require overtime or off-peak hours to meet commitments.

• Bachelors or Masters in Computer Science or equivalent from a fully-accredited college or university.
• 3+ years of experience as Senior or Lead QA Engineer within in a quality assurance team environment.
  Must possess a willingness and aptitude to embrace new ideas and master concepts rapidly.
• Demonstrated knowledge of the Software Development Lifecycle (SDLC).
• Familiarity and experience working with various testing stages such as unit testing, integration testing, and system testing enterprises.
• Knowledge of and some experience with automated testing tools, applications and languages such as QTP, UFT, Selenium, SoapUI, C#, and JAVA.
• Relational Database knowledge including SQL programming: understanding of queries and stored procedures.
• Experience or demonstrated knowledge of Loan Origination Systems within the mortgage industry.
• Working knowledge of Agile Test Methodology is essential.
• Experience with Microsoft Office, especially Microsoft Word, Microsoft Excel, and Microsoft PowerPoint
• Must be a responsive, flexible team player that is self-motivated, self-starting, and enthusiastic.
• Must have excellent verbal and written communication skills and have the ability to effectively communicate ideas, problems and solutions with all members of the organization.

We are currently hiring a Quality Assurance Associate for a well-established facility located in the Humboldt Industrial Park in Hazleton, PA. The ideal candidate will have a strong eye for detail and a commitment to ensuring product quality and comp Quality Assurance, Staffing, Assurance, Manufacturing, Quality

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Job Description

The

Job Description

The Quality Assurance (QA) Specialist will support laboratory quality and compliance efforts across a diverse range of CDC scientific and research laboratories. This position involves developing, implementing, and sustaining Quality Management Systems (QMS) in alignment with federal regulations and international standards. The QA Specialist will act as a consultant, educator, and technical advisor to CDC laboratory and program staff, and will play a critical role in strategic planning, risk management, audit readiness, and continuous quality improvement initiatives.

Requires a NACI Public Trust or the ability to obtain one.

Compensation & Benefits

Estimated Starting Salary Range for Quality Assurance (QA) Specialist : Pay commensurate with experience.

Full time benefits include Medical, Dental, Vision, 401K, and other possible benefits as provided.Benefits are subject to change with or without notice.

Quality Assurance (QA) Specialist Responsibilities Include

• Quality Systems Implementation & Support
• Provide consultation and technical support to CDC laboratory staff, quality managers, and senior scientists in implementing and maintaining Quality Management Systems (QMS).
• Translate complex quality and regulatory requirements (e.g., Code of Federal Regulations, ISO 17025/15189, CLIA, GxP standards) into actionable practices for laboratory personnel.
• Develop and implement strategic QMS plans, tailored to laboratory functions including diagnostic testing, surveillance, research, product development, and manufacturing.
• Audit Readiness & Regulatory Compliance
• Guide laboratories in preparing for internal and external audits, ensuring readiness for inspections from accrediting or regulatory agencies (e.g., CAP, CMS, FDA).
• Conduct GAP analyses to identify areas for improvement and ensure alignment with quality and regulatory expectations.
• Generate and review Nonconformance Events (NCEs) and assist in drafting and tracking Corrective and Preventive Action Plans (CAPAs).
• Risk Management & Safety
• Draft, review, and support the clearance process for risk assessments related to laboratory processes, equipment, and personnel safety.
• Communicate and promote agency-wide quality and safety initiatives to laboratory staff and stakeholders, ensuring alignment with CDC policies.
• Training & Communication
• Provide training and mentorship on QMS principles to quality managers, laboratory technicians, research scientists, and support staff.
• Assist with developing training materials, SOPs, job aids, and other QMS documentation.
• Serve as a liaison between laboratory personnel and agency leadership to ensure consistent quality practices across laboratory branches.
• Performs other job-related duties as assigned
  

• Bachelors degree in Biology, Laboratory Science, Public Health, Quality Assurance, or a related field.
• 35+ years of experience in quality assurance within a laboratory, healthcare, or public health environment.
• Deep understanding of QMS principles, regulatory requirements, and accreditation standards (e.g., CLIA, CAP, ISO, FDA).
• Experience conducting audits, risk assessments, and GAP analyses.
• Excellent communication, facilitation, and project management skills.
• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
• Preferred Qualifications:
• Advanced degree (e.g., MPH, MS, or MBA) in a relevant discipline.
• Certification in quality management or auditing (e.g., ASQ CQA, RAC, ISO Lead Auditor).
• Prior experience supporting CDC or federal laboratory quality programs.
• Familiarity with Good Laboratory Practices (GLP), Good Clinical Practices (GCP), or Good Manufacturing Practices (GMP).
• Must pass pre-employment qualifications of Cherokee Federal
  

• Quality Management Systems (QMS)
• Regulatory Compliance
• Laboratory Accreditation
• Audit Readiness
• Risk Assessment
  
  

• Laboratory Quality Specialist
• QA/QC Analyst
• Quality Systems Coordinator
• Compliance and Quality Assurance Officer
• Clinical Laboratory Quality Manager
  
  

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Business Consulting and Services

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Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.

We are seeking a detail-oriented and motivated Quality Assurance (QA) Technician. The QA Technician will support quality systems and compliance activities to ensure that our products and processes meet regulatory and internal quality standards. This role plays a key part in driving continuous improvement and maintaining a strong culture of quality throughout the organization.Responsibilities:Perform batch record reviews for accuracy, completeness, and compliance with Good Manufacturing Practices (GMP).Conduct quality inspections and audits of incoming materials, in-process operations, and final products.Support the documentation and investigation of deviations, non-conformances, CAPAs, and change controls.Assist in the maintenance and archiving of QA documentation and controlled records.Monitor and ensure compliance with internal SOPs, regulatory guidelines (FDA, EMA), and industry best practices.Participate in internal audits and prepare for external inspections by regulatory authorities and llaborate with manufacturing, QC, and engineering teams to ensure quality objectives are met.Support training initiatives and ensure QA-related training records are ntribute to the continuous improvement of QA processes and systems.Working hours: 8:00 AM - 5:00 PMSkills:Experience with quality management systems (QMS), electronic documentation systems, and LIMS.Prior involvement with regulatory inspections or client audits.Familiarity with viral vector or cell and gene therapy cation:High SchoolExperience:1-4 yearsQualifications:Minimum of 1?2 years of experience in a GMP-regulated environment, preferably in pharmaceuticals, biotechnology, or biologics manufacturing.Working knowledge of cGMP, FDA regulations (21 CFR Parts 210, 211), and ICH guidelines.Excellent attention to detail and strong documentation skills.Proficient in Microsoft Office Suite (Word, Excel, Outlook).Strong verbal and written communication skills.Ability to work independently and collaboratively in a fast-paced, regulated environment.Apply today!Spherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion. Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Spherion offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).key responsibilitiesPerform batch record reviews for accuracy, completeness, and compliance with Good Manufacturing Practices (GMP).Conduct quality inspections and audits of incoming materials, in-process operations, and final products.Support the documentation and investigation of deviations, non-conformances, CAPAs, and change controls.Assist in the maintenance and archiving of QA documentation and controlled records.Monitor and ensure compliance with internal SOPs, regulatory guidelines (FDA, EMA), and industry best practices.Participate in internal audits and prepare for external inspections by regulatory authorities and llaborate with manufacturing, QC, and engineering teams to ensure quality objectives are met.Support training initiatives and ensure QA-related training records are ntribute to the continuous improvement of QA processes and systems.experience1-4 yearsskillsExperience with quality management systems (QMS), electronic documentation systems, and LIMS.Prior involvement with regulatory inspections or client audits.Familiarity with viral vector or cell and gene therapy manufacturing.qualificationsMinimum of 1?2 years of experience in a GMP-regulated environment, preferably in pharmaceuticals, biotechnology, or biologics manufacturing.Working knowledge of cGMP, FDA regulations (21 CFR Parts 210, 211), and ICH guidelines.Excellent attention to detail and strong documentation skills.Proficient in Microsoft Office Suite (Word, Excel, Outlook).Strong verbal and written communication skills.Ability to work independently and collaboratively in a fast-paced, regulated cationHigh School

At Real, we're always seeking new and ambitious individuals to help us deliver exceptional service levels, positively impact the lives of the candidates we represent, and collaborate with some of the world's leading pharmaceutical, biotechnology, and medical companies.

As specialists in recognizing talent, we pride ourselves on not only finding the best people for our client partners but also on our ability to identify top talent to join our team. We are committed to providing training and long-term career opportunities to help our employees excel and maintain the high standards of expertise that Real is known for.

Building strong relationships is central to everything we do, ensuring that our clients and candidates choose to work with us repeatedly. This ethos influences our business culture. We promote knowledge sharing through support networks and international forums, enabling our employees to stay current with industry changes and share local insights to offer global perspectives.

This Quality role is a global position reporting to the supplier management team within PharmSci QA, supporting the Pharmaceutical Sciences R&D organization. The colleague will assist in managing supply chain security and the performance of external vendors providing materials for GMP manufacturing.

Responsibilities:

• Oversee and support the supplier program within the Pharm Sci QA group, including external vendor inventory management support
• Contribute to improvements in the supplier program
• Communicate quality status regularly and escalate supplier-related quality issues, maintaining close collaboration with Inventory Management, PharmSci QA, and other Pfizer sites

• Bachelors Degree or equivalent in a scientific discipline; knowledge of cGMP regulations related to supplier management is preferred
• Experience supporting supplier quality assurance is desirable
• Familiarity with SMS, M3, QTS, PDOCS, and GDMS systems is a plus
• Solid understanding of cGMPs related to the role
• Professional communication skills via email and phone
• Ability to adapt priorities and tasks throughout the workday to meet business needs

All your information will be kept confidential according to EEO guidelines.

If this opportunity interests you, please contact me at as soon as possible. I look forward to discussing your preferences.

If you know someone who might be interested, feel free to pass this along. I look forward to hearing from you!

A bit about us:With over 40 years of experience we are a leader in sheet metal fabrication. We provide quality pre-production prototypes for our clients, working from blueprints, drawings, or even completed parts which you wish to replicate precisely or with specified modifications.Why join us?Do you want to work with some of the nation's best Clients AND enjoy time at home w/ family? We do too! Competitive Compensation Package! Complete Benefits Package! Excellent Work/Life Balance! Accelerated Career Growth! Fun Company Activities! Many More!Job DetailsResponsibilities: Lead incoming, in-process, and final inspections, ensuring parts meet exacting standards Own the ISO 9001 and AS9100 quality systems-handle audits, documentation, and compliance Perform and document 1st Article Inspections (FAIs) Operate and program CMMs Manage calibrations, track quality metrics, and complete all associated paperwork Work closely with production on the floor-this is a hands on role Interface with engineering, operations, and leadership to drive continuous improvementQualifications: A self-starter who thrives with minimal direction Comfortable navigating blueprints and technical drawings, with basic GD&T familiarity (20-30% of prints include it) Hands-on with machine shop or fabrication experience (sheet metal experience a plus, but not required) Experienced in CMM programming/operation Experience with in-process and final inspections and related documentationJobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates diversity and all qualified candidates receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.