Quality Assurance Training

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TRAINING ON QUALITY ASSURANCE (QA)

Quality assurance (QA) is any systematic process of determining whether a product or service meets specified requirements. QA establishes and maintains set requirements for developing or manufacturing reliable products. A quality assurance process is meant to increase customer confidence and a company’s credibility while improving work processes and efficiency. It also helps a company compete in its market.  The International Organization for Standardization (ISO) is a driving force behind QA practices and mapping the processes used to implement QA.  

FARE Labs capped with a number of Quality Management Systems such as ISO 9001, ISO 14001, ISO 22000, ISO 45000, ISO 17025, ISO 17043, ISO 17020 is dedicated to upholding the highest quality standards in Organizations.  FARE Labs is not only implementing the Quality Assurance but also offers Quality Assurance (QA) Courses. This training program aims to enhance the competency of personnel, ensuring compliance with international best practices.

Objectives

  1. Provide a comprehensive understanding of Quality Assurance System.
  2. Provide detailed training ISO/IEC 17025:2017-Requirements for Testing & Calibration Laboratories.
  3. Equip participants with practical skills for laboratory operations and quality assurance.
  4. Develop a systematic approach to method validation, verification, and implementation.
  5. Strengthen data analysis, interpretation, and problem-solving capabilities.

Understanding ISO/IEC 17025:2017

ISO/IEC 17025:2017 is the international standard that specifies general requirements for the competence of testing and calibration laboratories. Compliance ensures consistency, reliability, and accuracy in laboratory operations.  The Quality Assurance (QA) Course will help in understanding clause wise various requirements of this International Standard.

What is to learn?

Training will be provided on selected Clauses from the list below:

Clause 1: Scope

Clause 2: Normative Reference

Clause 3: Terms & Definitions

Clause 4: General Requirements

  • Ensuring impartiality in laboratory activities.
  • Managing confidentiality of client data and test results.
  • Upholding ethical responsibilities of laboratory personnel.

 

Clause 5: Structural Requirements

  • Defining roles and responsibilities within the laboratory.
  • Establishing an effective organizational structure.
  • Maintaining independence in laboratory operations.

 

Clause 6: Resource Requirements

6.1 Personnel

  • Competency assessment and continuous professional development.
  • Training, qualification, and performance evaluation.

 

6.2 Facilities and Environmental Conditions

  • Providing a controlled testing environment.
  • Managing laboratory infrastructure and environmental influences.

 

6.3 Equipment

  • Selection, validation, and maintenance of laboratory equipment.
  • Calibration schedules, traceability, and record-keeping.

 

6.4 Metrological Traceability

  • Establishing traceability through reference materials and calibration standards.
  • Documenting measurement uncertainty.

 

6.5 Externally Provided Products and Services

  • Selection and evaluation of external providers.
  • Ensuring quality and compliance of outsourced services.

 

Clause 7: Process Requirements

7.1 Review of Requests, Tenders, and Contracts

  • Ensuring clear communication of customer requirements.
  • Evaluating laboratory capability before accepting work.

 

7.2 Selection, Verification, and Validation of Methods

  • Choosing appropriate testing methods.
  • Validating standard and in-house developed methods.

 

7.3 Sampling

  • Implementing standardized sampling procedures.
  • Maintaining sample integrity and traceability.

 

7.4 Handling of Test and Calibration Items

  • Proper storage and identification of test samples.
  • Preventing contamination and degradation.

 

7.5 Technical Records

  • Ensuring complete and accurate documentation of test data.
  • Managing laboratory records systematically.

 

7.6 Evaluation of Measurement Uncertainty

  • Identifying sources of uncertainty.
  • Calculating and documenting uncertainty budgets.

 

7.7 Ensuring the Validity of Results

  • Conducting proficiency testing and interlaboratory comparisons.
  • Monitoring data trends and identifying deviations.

 

7.8 Reporting of Results

  • Standardizing test reports and certificates.
  • Ensuring clarity, accuracy, and compliance in reporting.

 

7.9 Complaints Handling

  • Establishing a structured complaint resolution process.
  • Documenting all complaint handling procedures.

 

7.10 Management of Nonconforming Work

  • Identifying, documenting, and addressing nonconforming results.
  • Implementing corrective actions and preventive measures.

 

7.11 Control of Data and Information Management

  • Securing laboratory information systems.
  • Maintaining data integrity and backup records.

 

Clause 8: Management System Requirements

8.1 Options for Management System

  • Establishing a quality management system aligned with ISO 17025.
  • Documenting policies and quality objectives.

 

8.2 Management System Documentation

  • Defining the scope and applicability of the management system.
  • Ensuring document control and accessibility.

 

8.3 Control of Management System Documents

  • Reviewing and updating documents periodically.
  • Controlling document distribution and versioning.

 

8.4 Control of Records

  • Retaining and securing laboratory records.
  • Preventing unauthorized modification of records.

 

8.5 Actions to Address Risks and Opportunities

  • Identifying potential risks and mitigation strategies.
  • Implementing continuous improvement initiatives.

 

8.6 Improvement

  • Conducting periodic reviews of laboratory processes.
  • Encouraging process optimization and efficiency.

 

8.7 Corrective Actions

  • Identifying root causes of issues and implementing corrective measures.
  • Preventing recurrence through systematic interventions.

 

8.8 Internal Audits

  • Conducting regular internal audits of the management system.
  • Identifying non-conformities and areas for improvement.

 

8.9 Management Reviews

  • Holding periodic management review meetings.
  • Evaluating the effectiveness of the quality system.
  1. Basic testing & calibration and quality checks
  2. Internal and External quality control measures
  3. Understanding quality control charts and measurement trends
  4. Identifying and resolving quality control problems
  5. Strategies for maintaining instrument performance
  6. Preventive maintenance tips
  1. Adherence to Safety Protocols: Follow all laboratory safety guidelines and protocols to prevent accidents and ensure compliance.
  2. Active Participation: Engage in all training sessions, discussions, and practical exercises. Complete all assigned tasks on time.
  3. Collaboration and Teamwork: Work collaboratively with fellow participants, sharing knowledge and supporting each other’s learning.
  4. Integrity and Accuracy: Maintain a high standard of integrity in all testing procedures and documentation. Ensure that all results are accurate and reliable.

Commitment to the Program: Participants must demonstrate a commitment to the training program by attending all scheduled sessions, completing assignments, and actively participating in practical exercises.

Health and Safety Compliance: Participants must comply with health and safety regulations, including wearing appropriate personal protective equipment (PPE) and adhering to all safety protocols.

Designation: Quality Assurance Trainee
Section: Training
Qualification: Ph.D./ M.Tech./ M.Sc./ B.Tech./ B.Sc.
Fees: As Per Industry Standards
Experience: Freshers / Professionals
Employment Type: Short Term / Long Term
Location: Gurugram, Haryana

Note:

Limited Spots Available! Don’t Miss This Opportunity to Advance Your Quality Assurance Skills!

For any further inquiries or additional information, please reach out. We look forward to supporting your journey in Quality Assurance!

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