Postgraduate DiplomaElectronics, Embedded Systems & Telecom Applications open

Postgraduate Diploma in Laboratories, Dossiers and Audits

Online 800-hour Postgraduate Diploma in Laboratories, Dossiers and Audits. 8 modules covering ISO/IEC 17025, ISO 19011 and LabWare LIMS. Dedicated tutor and open enrolment.

Duration800 h
ModeOnline
AwardSEIUM Institute diploma
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Learning outcomes

What you will be able to do

01

Understand quality infrastructure and accreditation.

02

Apply the requirements of ISO/IEC 17025 in a laboratory.

03

Calculate measurement uncertainty and apply decision rules.

04

Prepare complete and traceable technical dossiers.

05

Plan and conduct audits in accordance with ISO 19011.

06

Prepare product certification inspections.

07

Manage corrective actions and continuous improvement.

Profile

Who it's for

  • Laboratory quality manager looking to specialise in Laboratories, Dossiers and Audits.
  • Management systems auditor looking to specialise in Laboratories, Dossiers and Audits.
  • Testing laboratory technician looking to specialise in Laboratories, Dossiers and Audits.
  • Certification engineer looking to specialise in Laboratories, Dossiers and Audits.
  • Technical dossier manager looking to specialise in Laboratories, Dossiers and Audits.
  • Metrologist looking to specialise in Laboratories, Dossiers and Audits.
  • Engineering or science graduates seeking to enter testing laboratories.
Standards & tools

What you'll work with

  • ISO/IEC 17025
  • ISO 19011
  • ISO/IEC 17065
  • ISO/IEC 17020
  • ISO/IEC 17011
  • JCGM 100 (GUM)
  • ILAC-G8
  • ISO/IEC 17067
Syllabus

8 modules · 800 h

  1. 1.1Standardisation, metrology and accreditation
  2. 1.2Conformity assessment according to ISO/IEC 17000
  3. 1.3Laboratories, inspection and certification bodies
  4. 1.4Accreditation under ISO/IEC 17011 and ENAC
  5. 1.5ILAC and IAF mutual recognition arrangements
  6. 1.6Notified bodies in the EU
  7. 1.7Certification schemes under ISO/IEC 17067
  8. 1.8Role of third-party laboratories
  9. 1.9Trust and traceability across the chain
  10. 1.10Case study: mapping the actors in a certification
  1. 2.1General requirements: impartiality and confidentiality
  2. 2.2Structural and resource requirements
  3. 2.3Staff competence
  4. 2.4Equipment and metrological traceability
  5. 2.5Method validation and verification
  6. 2.6Sampling and handling of items
  7. 2.7Ensuring the validity of results
  8. 2.8Test and calibration reports
  9. 2.9Laboratory management system
  10. 2.10Workshop: method validation procedure
  1. 3.1GUM guide and measurement uncertainty
  2. 3.2Type A and type B evaluation
  3. 3.3Combined and expanded uncertainty
  4. 3.4Uncertainty budgets
  5. 3.5Decision rules under ILAC-G8
  6. 3.6Guard bands and risk
  7. 3.7Proficiency testing and interlaboratory comparisons
  8. 3.8Control charts in the laboratory
  9. 3.9Communicating uncertainty
  10. 3.10Practice: uncertainty budget for a test
  1. 4.1Structure of a technical dossier
  2. 4.2Documentary requirements by sector
  3. 4.3Test reports and their validity
  4. 4.4Design evidence and risk analysis
  5. 4.5Controlled document management
  6. 4.6Versions, signatures and approval
  7. 4.7Dossiers for notified bodies
  8. 4.8Electronic formats and presentation
  9. 4.9Common errors that delay certification
  10. 4.10Workshop: dossier index for an electronic device
  1. 5.1Audit principles
  2. 5.2Audit programme
  3. 5.3Audit planning
  4. 5.4Interview and sampling techniques
  5. 5.5Gathering and verifying evidence
  6. 5.6Findings, nonconformities and observations
  7. 5.7Audit report
  8. 5.8Auditor competence
  9. 5.9Remote audits
  10. 5.10Case study: internal audit of a laboratory
  1. 6.1Certification under ISO/IEC 17065
  2. 6.2Initial factory inspection
  3. 6.3Production control in the factory
  4. 6.4Surveillance audits
  5. 6.5Product sampling on the market
  6. 6.6Managing manufacturer nonconformities
  7. 6.7Suspension and withdrawal of certificates
  8. 6.8Audits of critical suppliers
  9. 6.9Relationship with ISO 9001 system audits
  10. 6.10Practice: factory inspection checklist
  1. 7.1LIMS systems and data management
  2. 7.2Data integrity in the laboratory
  3. 7.3Corrective actions and root cause analysis
  4. 7.4Laboratory performance indicators
  5. 7.5Complaint management
  6. 7.6Management review
  7. 7.7Risk and opportunity management
  8. 7.8Digitalisation of audits
  9. 7.9Preparation for accreditation
  10. 7.10Case study: action plan following an audit
  1. 8.1Selecting the laboratory or product
  2. 8.2Diagnosis against ISO/IEC 17025
  3. 8.3Selected technical procedure
  4. 8.4Uncertainty budget
  5. 8.5Model technical dossier
  6. 8.6Audit programme and plan
  7. 8.7Simulated audit report
  8. 8.8Improvement plan
  9. 8.9Report and presentation
  10. 8.10Final review with the tutor
Methodology, software & labs

How you'll learn

100% online training on the SEIUM Institute campus, with downloadable material, recorded classes and a dedicated technical tutor. There are no fixed timetables: students progress at their own pace within the intake, which makes it possible to combine study with work.

Each module combines theory, guided reading of the original standard and applied exercises. The working software is LabWare LIMS, Minitab, Siemens Polarion ALM, Microsoft Excel with GUM templates, in free, academic or evaluation versions. Cases are studied using real procedures for internal laboratory audit, proficiency testing and initial factory inspection. Assessment is continuous, module by module, plus the final integrative project.

Accreditable laboratories(EN ISO/IEC 17025) with a rotor test rig, EMC/Lightning pre-compliance, HIL/SIL and vibration/acoustics.
Evidence-driven final project:safety case, test plan, compliance dossier and operational limits.
Industry mentoring:lecturers with experience in training, , eVTOL/UAM and flight test.
Flexible format:(hybrid/online), international cohorts and support from SEIUM Career Services.
Ethics and safety:a safety-by-design approach, OT cybersecurity, DIH and compliance as its pillars.
Capstone project

Build it end to end

Your final project follows the real engineering workflow, step by step, reviewed by your tutor.

Selecting the laboratory or product

Understand quality infrastructure and accreditation.

Diagnosis against ISO/IEC 17025

Apply the requirements of ISO/IEC 17025 in a laboratory.

Selected technical procedure

Calculate measurement uncertainty and apply decision rules.

Uncertainty budget

Prepare complete and traceable technical dossiers.

Model technical dossier

Plan and conduct audits in accordance with ISO 19011.

Career opportunities

Where this takes you

Laboratory quality managerManagement systems auditorTesting laboratory technicianCertification engineerTechnical dossier managerMetrologist
Admissions & scholarships

Requirements

  • Prior technical training or professional experience in the sector. No university degree is required.
  • Internet connection and a computer capable of running the programme's software.
  • Sufficient level of Spanish to follow technical standards.

Ready to start?

Send your application today. Our admissions team replies within 72 hours with your study plan and funding options.

FAQ

Frequently asked questions

The programme comprises 800 hours in total, spread over 6 to 8 months. That is between 10 and 15 hours a week on average, compatible with a full-time job.

You will work with LabWare LIMS, Minitab, Siemens Polarion ALM and Microsoft Excel with GUM templates. Free, academic or evaluation versions are used, and the tutor indicates the free alternative where one exists.

An own-award diploma from SEIUM Institute upon passing continuous assessment and the integrative project. It is in-house training, not an official qualification from the Ministry.

Yes. Modules passed in a course or diploma in the same area are recognised in the advanced programme. Check the recognition policy when you enrol.

Postgraduate Diploma in Laboratories, Dossiers and AuditsEnrol
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