What is Product Quality?
Product quality is the basic element of a business. It means to add features in a product or service in such a way that it meets the needs and wants of the customers. Enhancing the product quality also means improve the goods from any existing defects to ensure customer satisfaction.
How is Product Quality used?
Zippia reviewed thousands of resumes to understand how product quality is used in different jobs. Explore the list of common job responsibilities related to product quality below:
- Inspected product quality and updated information about setting up machines for maximum production.
- Inspected merchandise pre-production to ensure product quality.
- Enhanced product quality 10% reduction in field returns by developing and implementing the Divisional Manufacturing Process Verification Quality initiatives.
- Monitored production of operators, communicated with management regarding quotas, product quality, machinery functionality, staffing and safety concerns.
- Monitored product quality and measured thickness of electroplating to ensure compliance to standards and specifications.
- Implemented Advanced Product Quality Planning systems which ensured aggressive product launches and achieved customer expectations.
Are Product Quality skills in demand?
Yes, product quality skills are in demand today. Currently, 21,375 job openings list product quality skills as a requirement. The job descriptions that most frequently include product quality skills are engraver, machine group leader, and assistant quality control manager.
How hard is it to learn Product Quality?
Based on the average complexity level of the jobs that use product quality the most: engraver, machine group leader, and assistant quality control manager. The complexity level of these jobs is challenging.
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What jobs can you get with Product Quality skills?
You can get a job as a engraver, machine group leader, and assistant quality control manager with product quality skills. After analyzing resumes and job postings, we identified these as the most common job titles for candidates with product quality skills.
Engraver
- Quality Standards
- Product Quality
- Engraving
- Customer Service
- Jewelry
- Customer Orders
Machine Group Leader
- Machine Operators
- Product Quality
- GMP
- CNC
- Lean Manufacturing
- Safety Procedures
Assistant Quality Control Manager
- Product Quality
- Quality Standards
- Internal Audit
- R
- HACCP
- Quality Issues
Process/Product Engineer
Job description:
A Process/Product Engineer usually works at manufacturing facilities where they are in charge of designing and developing products and procedures. Working alongside development teams, a process/product engineer conducts extensive research and analysis, conceptualizes plans, develops prototypes and schematics, and establishes test structures to evaluate and ensure the quality and efficiency of products and procedures. They may also assess existing practices, identifying their strengths and weaknesses to optimize operations. Moreover, they set guidelines and specifications, overseeing staff's performance while implementing safety standards and policies for a smooth and efficient workflow.
- Product Quality
- R
- Process Engineering
- Technical Support
- Sigma
- Engineering Support
Quality Control And Production Manager
- Product Quality
- Safety Regulations
- QC
- Production Supervisors
- R
- Production Schedules
Produce Department Manager
- Sales Floor
- Product Quality
- Store Management
- Gross Profit
- Customer Service
- Leadership
Chemist Assistant
Job description:
Chemist assistants maintain laboratory readiness in supporting the production and contingency operations for instrument maintenance and personnel training. The assistants manage daily laboratory operations such as conducting and recording instrument maintenance. They develop minimum product property tolerances and production standards. It is their job to monitor the quality of products to ensure standard compliance. Also, they support capacity expansion projects, product quality projects, and process improvement initiatives.
- Laboratory Instruments
- Product Quality
- Chemical Analysis
- HPLC
- Analytical Instrumentation
- Lab Equipment
Quality Control Assistant
Job description:
Quality assurance technicians work as testers, samplers, and inspectors of quality control in the organizations. They are equipped with skills in visual inspection, written and verbal communication, and active listening. In carrying out their jobs, they are expected to work well and be detail-oriented. Working as a quality assurance technician involves problem-solving, decision making, and creative thinking. They see to it that products and services meet the quality standards for the entire organization.
- Product Quality
- Quality Checks
- Lab Equipment
- Safety Standards
- Data Entry
- GMP
Quality Control
Job description:
As the name entails, the job of a quality control inspector is to inspect, maintain, and improve the quality and standard of products. They are responsible for ensuring the company's reputation is not damaged due to defective products or inferior manufacturing processes. This can be done by detecting and resolving the problem early on, and returning the product for repair. A quality control inspector should also notify the supervisors immediately when issues arise and coordinate with them to address the problem.
- Quality Checks
- Product Quality
- Safety Standards
- Laboratory Equipment
- Quality Standards
- R
Quality Control Officer
- Safety Procedures
- Product Quality
- OSHA
- Corrective Action
- Laboratory Equipment
- Internal Audit
Product Quality Engineer
Job description:
A product quality engineer is responsible for conducting quality check procedures for outputs and manufacturing processes to ensure high-quality deliverables according to business requirements and client specifications. Product quality engineers implement quality assessment criteria with strict adherence to internal guidelines and regulatory policies. They inspect the tools and equipment used for the production and solve inconsistencies, recommending and writing process reports to prevent fault reoccurrence that may affect product standards and market quality and cause distribution delays.
- Product Quality
- Continuous Improvement
- Sigma
- Corrective Action
- ISO
- Data Analysis
Senior Process And Quality Engineer
- Product Quality
- ISO
- Sigma
- Failure Analysis
- Data Analysis
- FMEA
Lead Barista
Job description:
A Lead Barista provides quality customer service and demonstrates knowledge of coffee equipment, products, and menu products. Lead baristas serve all products with friendly and individualized attention towards each customer. They are responsible for making a difference to customers by educating them about our premium coffees. They establish relationships with customers and foster a positive and friendly store environment. They also assist new team members in the training program and provide technical guidance.
- Cleanliness
- Customer Service
- Product Quality
- Customer Satisfaction
- Culinary
- BARS
Meat Department Manager
Job description:
A meat department manager manages a store's meat department. Their responsibilities include performing department related training, developing procedures for the department employees, overseeing quality control in the department, consulting with the sales departments to develop strategies that increase sales, and operating the machinery used to prepare products.
- Sales Floor
- Product Quality
- Gross Profit
- Food Safety
- Slicers
- Customer Service
Lead Quality Control Technician
- Quality Control Procedures
- Product Quality
- Lab Equipment
- Quality Standards
- Test Procedures
- Food Safety
Mixing Machine Operator
- Quality Checks
- Basic Math
- Math
- Product Quality
- Safety Rules
- Production Data
Plant General Manager
- Continuous Improvement
- Product Quality
- Safety Program
- Plant Operations
- OSHA
- R
Batching Operator
Job description:
A batching operator conducts quality assurance tests to ensure products comply with industry standards and customer orders. They have the responsibility to oversee the batching plant's daily operations, delegate duties among employees, monitor processes and provide instructions as necessary, and resolve issues and concerns should any arise. There are also times when they must coordinate with clients and suppliers, sign documents and delivery slips, and conduct maintenance checks on machines. Moreover, as a batching operator, it is essential to supervise staff while implementing the company's safety policies and regulations.
- Customer Orders
- Basic Math
- GMP
- Lot Numbers
- Product Quality
- Math
Machine Adjuster
- Preventative Maintenance
- Safety Rules
- Dexterity
- Product Quality
- Production Machines
- Trial RUN
Quality Control Engineer
Job description:
A quality control engineer is responsible for conducting quality assessments for the company's products and services to ensure adherence to federal regulations and quality standards. Quality control engineers recommend strategic methods by analyzing processes and writing test results. They also identify opportunities for more services that meet public demands and market trends, helping the business generate more resources for revenues. A quality control engineer utilizes various software tools and applications to document findings, requiring them to have excellent communication and technical skills.
- Product Quality
- Quality Standards
- Corrective Action
- ISO
- Continuous Improvement
- R
How much can you earn with Product Quality skills?
You can earn up to $40,071 a year with product quality skills if you become a engraver, the highest-paying job that requires product quality skills. Machine group leaders can earn the second-highest salary among jobs that use Python, $111,580 a year.
Job Title | Average Salary | Hourly Rate |
---|---|---|
Engraver | $40,071 | $19 |
Machine Group Leader | $111,580 | $54 |
Assistant Quality Control Manager | $82,810 | $40 |
Process/Product Engineer | $84,709 | $41 |
Quality Control And Production Manager | $72,641 | $35 |
Companies using Product Quality in 2025
The top companies that look for employees with product quality skills are Walmart, Dunkin Brands, and Advance Auto Parts. In the millions of job postings we reviewed, these companies mention product quality skills most frequently.
Rank | Company | % Of All Skills | Job Openings |
---|---|---|---|
1 | Walmart | 15% | 33,884 |
2 | Dunkin Brands | 14% | 7,575 |
3 | Advance Auto Parts | 14% | 1,738 |
4 | Kroger | 13% | 9,172 |
5 | Papa John's International | 9% | 2,888 |
Departments using Product Quality
Department | Average Salary |
---|---|
Plant/Manufacturing | $51,755 |
4 courses for Product Quality skills
1. Advanced Product Quality Planning (APQP)
Advanced Product Quality Planning (APQP) is a framework that helps manufacturing organizations develop and implement a structured approach to ensure that their products meet customer needs and expectations while also adhering to relevant industry standards and regulations. The APQP process involves a series of stages, including planning, design and development, process validation, and ongoing production monitoring, which are all designed to minimize the risks of product defects, reduce waste and rework, and ultimately improve the quality and reliability of the product. The benefits of APQP include: Improved quality and reliability: By following a structured approach to product development and validation, organizations can identify and mitigate potential quality issues before they arise, resulting in fewer defects and higher overall product reliability. Better collaboration and communication: APQP emphasizes collaboration and communication between different functional areas within an organization, including engineering, manufacturing, and quality control. This helps to ensure that everyone is aligned around the same goals and priorities and can work together more effectively to achieve them. Greater efficiency and cost savings: By identifying potential quality issues early in the development process, organizations can avoid costly rework and production delays. Additionally, by optimizing the manufacturing process and reducing waste, organizations can achieve cost savings and improve their bottom line. Compliance with industry standards and regulations: APQP helps organizations to ensure that their products meet relevant industry standards and regulations, reducing the risk of legal and reputational damage. In this course, students will learn: Standard practices and approaches to the APQP processThe connections between APQP and cost of qualityThe three levels of APQP. the major positions within the supply chain that use APQPWho is using APQP and whyThe personality attributes of a successful APQP leaderThe 6 stages of the APQP process and the major tools used at eachThe general launch progressionThe launch management levelsA comparison of APQP modelsAnd much more! APQP helps manufacturing organizations improve the quality and reliability of their products, reduce costs, and enhance customer satisfaction, positioning them for long-term success in a competitive marketplace. And manufacturing professionals who effectively use and understand the APQP process also position themselves for greater career growth, promotion and opportunity. This course is far more than an academic approach to APQP. But instead, this course is taught by seasoned manufacturing professionals who have used APQP to launch hundred of new products across multiple industries and processes. Plus, when you purchase this course, you get two major benefits in addition to the course material: Lifetime access to the course materials. No limits to when you start the course or how long you have access to it. Answers to your course-related questions through Udemy's messaging system by industry professionals. So if you are looking to gain critical skills to advance your career, THIS IS THE CLASS FOR YOU!! Sign up today!...
2. Design of Experiments for Product, Process & Quality Manager
Structured Experimentation or Design of Experiment (DOE) helps Product Engineers to develop and refine designs. It is simply not possible to develop optimal designs that deliver right product performance without understanding the relationship between dependent and independent factors (& within independent factors). Unstructured experimentation consumes indefinite resources and time, that no organizations have. This is true for both Engineering Product Managers and Service Product Managers. Similarly, both Engineering and Service Process Managers cannot optimize process parameters or design products without conducting structured experiments. Quality Managers have to constantly improve the quality of product, its reliability and that cannot happen without improvising design in a structured manner. As a part of DMAIC or DFSS improvement projects, Lean Six Sigma Black Belts & Lean Six Sigma Green Belts are expected to find ways to improve the process and optimize it and it would not be possible with knowledge of structured experimentation (Design of Experiments - DOE)This course is going to help Product and Process Engineering Managers from both Service & Engineering Sectors to learn DOE from scratch. Practical Knowledge of DOE is non-negotiable for any Product, Process, Quality Managers & Lean Six Sigma Black Belts. Target Audience: Product ManagersProcess ManagersQuality ManagersLean Six Sigma Black Belts What you will accomplish after completing this course: After completing the course you will be able to plan, set up, perform and analyze Full Factorial, Fractional Factorial and Taguchi DOEWhat is Covered: Structured ExperimentsTypes of ExperimentsPhases of ExperimentsTerms used in DOEFull Factorial Experiment (Performing & Analyzing)Fractional Factorial Experiment (Performing & Analyzing)Taguchi Designs (Performing & Analyzing)...
3. Qbd: Quality by Design in Pharmaceutical Product Development
Become Certified Professional in Quality by Design (QbD)The certification covers all the statistical tools for QbD framework. The certification features with industry specialists and experts facilitating quality implementation in various industries. QBD implementation can give manufacturers much more confidence in the robustness of their product, potentially increases the efficiency and quality of their development and manufacturing process as well as reduces profit leakages. QbD elements include the following: (QbD elements include the following: (1) a quality target product profile (QTPP) that identifies the critical quality attributes (CQAs) of the drug product; (2) product design and understanding including identification of critical material attributes (CMAs); (3) process design and understanding including identification of critical process parameters (CPPs), linking CMAs and CPPs to CQAs; (4) a control strategy that includes specifications for the drug substance(s), excipient(s), and drug product as well as controls for each step of the manufacturing process; and (5) process capability and continual improvement. QbD tools and studies include prior knowledge, risk assessment, mechanistic models, design of experiments (DoE) and data analysis, and process analytical technology (PAT). This certification will provide insight into the key principles of QbD covering quality risk management and formal experimental design. The certification is intended as continuing professional development (CPD) for professionals in the pharmaceutical industry, particularly in production, regulatory affairs and quality functions. The certification will offer an excellent introduction for those less familiar with QbD and provide those with more experience with QbD, new ideas on how to further implement the QbD programme. The case study based approach in certification programme is designed for working professionals in full time employment who want to update their knowledge and gain required skills and attitude in the area in order to become a certified GMP professional in the domain. This certification is also beneficial for professionals from different streams to help them intensify their knowledge. This is an advanced certification having rigorous case studies based methodology throughout the duration. While quality by design principles have been used to advance product and process quality in industry, and particularly the automotive industry, they have also been adopted by the U. S. Food and Drug Administration (FDA) for the discovery, development, and manufacture of drugs. QbD Overview - a US FDA initiative and its advantagesSince the introduction of Quality-by-Design (QbD) concepts, it has been accepted that quality of pharmaceutical products should be designed and built during the manufacturing process. Most of quality problems are related to the way in which a pharmaceutical product was designed. A poor-designed pharmaceutical product will show poor safety and efficacy, no matter how many tests or analyses have been done to verified its quality. Thus, QbD begins with the recognition that quality will not be improved by merely increasing testing of pharmaceutical products. In other words, quality must be built into the product. Quality by Design (QbD) is one of the most important initiative by US FDA. "Pharmaceutical Quality for the 21st Century: A Risk-Based Approach in 2002 by FDA was the first step towards this goal of QbD compliance. Same period FDA issued another guideline on "Process Analytical Technology" (PAT) to guide the Generic Industry about the advantages of PAT in Real Time Release. This was the beginning of the journey towards implementing QbD. The concept is based on enhancement of Process & Product understanding with the help of Risk assessments, identifying Critical Quality Attributes & Critical Process Parameters to be monitored thru right control strategy. Customers are benefitted thru consistency in commercial manufacturing. FDA recommended the implementation since 2013. US FDA initiative on QbDQbD principles have been adopted by the US Food and Drug Administration (FDA) for the discovery, development, and manufacture of drugs. The FDA initiative is outlined in its report "Pharmaceutical Quality for the 21st Century: A Risk-Based Approach (1). FDA has taken this initiative to guide the Pharmaceutical Industry on how to implement the concepts of QbD into its processes. The focus is on quality should be built into a product with an understanding of the product and process by which it is developed and manufactured with understanding risks involved in manufacturing the product and how best to manage those risks. This is improvement is over "Quality by Testing" (QbT), traditional approach, by the Industry. QbD facilitates design of products and processes that enhances the product's Qurity, Efficacy and Safety in the interest of Patients. While QbD will provide design space (DS), the scale-up and commercial manufacturing experience provides knowledge about the process and the interactions of raw materials used therein with excipients. FDA's Process Validation (2) guidance in January 2011 is for companies to continue benefiting from knowledge gained, and continually improve throughout the process lifecycle by making adaptations to assure root causes of manufacturing problems are addressed. International Conference on Harmonization (ICH) Guidelines Working with regulators in the European Union (the European Medicines Agency) and Japan, the US FDA has improved Quality by Design objectives through the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. ICH introduced the guidelines: ICH Q8 (Pharmaceutical Development), ICH Q9 (Quality Risk Management), and ICH Q10 (Pharmaceutical Quality System). These ICH guidelines improve understanding to build "Quality by Design" into Formulation development. This will ensure that "Quality Risk Management and Knowledge Management" are used to monitor the lifecycle management that maintain process control and product quality. The difference between QbD for New Drug Application (NDA) and Abbreviated New Drug Application (ANDA) products is most apparent at the first step of the process(4). US FDA defines QbD as "Systematic approach to development that begins with predefined objectives and emphasizes product and process understanding and process control, based on sound science and quality risk management". QbD is a systematic process to generate Robust processes with the help of Quality Risk Management (ICH Q9). It is important to control the "Variability" of Raw materials as well as in Manufacturing process by identifying Critical Quality Attributes (CQA) / Critical Material Attributes (CMA) and Critical Process Attributes (CPP) through Risk Management process. It helps to have better understanding of Process & Product thus helping Life Cycle Management of the product (LCM) as explained in diagram no.1Elements of QbD1. Quality Target Product Profile (QTPP) that identifies CQAs of the drug product.2. Product design and understanding including the identification of Critical Material Attributes (CMAs).3. Process design and understanding including the identification of Critical Process Parameters (CPPs) and a thorough understanding of scale-up principles, linking CMAs and CPPs to CQAs.4. A control strategy that includes specifications forthe drug substance(s), excipient(s), and drug product as well as controls for each step of the manufacturing process.5. Process capability and continual improvement. Regulatory agencies objectives (7) for QbD initiatives are to:"Encourage early adoption of new technological advances by the pharmaceutical industry. Facilitate industry application of modern quality management techniques, including implementation of quality systems approaches, to all aspects of pharmaceutical production and quality assurance. Encourage implementation of risk-based approaches that focus both industry and the agency attention on critical areas. Ensure regulatory review and inspection policies are based on state-of-the-art pharmaceutical science. Enhance consistency and coordination of the FDA's drug quality regulatory programs, in part, by integrating enhanced quality systems approaches into the agency's business processes and regulatory policies concerning review and inspection activities". By obtaining increased process & product understanding in order to identify and monitor critical sources of variability helps to achieve Right First Time Performance. Therefore it is essential we shift from Compliance to improved Process & product understanding , which will allow QbD of effective and efficient manufacturing process as well as Real Time Quality Assurance. One of the important goals of QbD is to ensure that all Sources of Variability affecting a process are identified, explained and managed by appropriate measures. This enables the finished medicine to consistently meet its predefined characteristics from the start to achieve "Right first time". QbD focuses on the use of multivariate analysis, often in combination with modern process-analytical chemistry (PAT) methods and knowledge-management tools to enhance the identification and understanding of critical attributes of materials and critical parameters of the manufacturing process. This enhanced understanding of product and process is used to build quality into manufacturing and provide the basis for continuous improvement of products and processes. Knowledge gained through such process and product understanding helps to monitor Life Cycle Management of the product. process & product understanding to support Continual Improvement. Advantages of QbD to the Generic IndustryBetter understanding of the process and the product. Minimum batch failures. Better understanding of risks involved & mitigation. Minimising variations to achieve consistency in manufacturing quality. An enhance QbD approach to pharmaceutical development provides opportunities for more flexible regulatory approaches for example: Manufacturing changes within the approved design space can be without regulatory review or approval. Reduction of post-approval submissions. Greater regulator confidence of robust products. Innovative Process Validation approaches. More drug availability and less recalls from market. Improved yields, lower cost, less investigations, reduced testing, etc. Timely launch of products. Right first time & every time concept. Continuous improvement over the total product life cycle. Real time Release thru PAT implementation. Return on investment / cost savings. More efficient technology transfers. QbD Applications Scope: It can be applied to Drug substance development (ICH Q11); Drug Product (ICH Q8 R2) , Analytical method development. FDA strongly recommends to include QbD elements in ANDA submissions since JanuaryBenefits: Robust product and processesReduce Production lossesReduce deviations and recalls...
4. Quality and Regulatory: EU Product Legislation & CE Marking
The European Union is one of the wealthiest market in the world. and one of the most regulated! Selling a product in this market, whether you are a manufacturer bases within or outside the European Union, an importer o a simple reseller/distributor, implies that you takes responsibilities, wether you like it or not. This course introduce you to the most important concept of the European product legislation. After a short introduction on the European Union, it will explain the concept of the free movement of products, the main pillar on which the huge European market relies on. Then the course will go into details, explaining the product legislation framework, starting with its types of legal acts, and explaining two of the most common directives: - the General Product Safety Directive - the Directive on Product Liability Then we will explain when and how the legislation applies, introducing, among others, the concepts of - selling techniques and types of products - making available - placing on the market - intended use and misuse Finally, we will examine in details responsibilities and obligations of the main economic actors: - Manufacturer (within or outside European Union) - Authorised Representative - Importer - Distributor - End user (even though not an economic operator strictly speaking) At the end of the course you will gain a comprehensive knowledge of the European Union legislative framework, and you will have the vocabulary and the autonomy to further deepen your knowledge in a specific field like for instance in the Toys industry, in the Medical Device field, and so on. Do not lose valuable time and enroll today!...