Personnel competence records under ISO/IEC 17025
Competence must be defined, achieved, authorised and monitored — with records for each step, for every activity that affects results.
Clause 6.2 requires all personnel who could influence laboratory activities to act impartially, be competent and work according to the management system. Competence requirements must be documented; personnel must be authorised for activities such as developing and validating methods, analysing results, reporting and authorising results.
A workable record set
- Job or role description with competence criteria.
- Training plan and evidence of completion, including supervised work.
- Authorisation record naming the activities, methods and equipment the person may operate independently.
- Periodic monitoring: witnessed calibrations, replicate measurements, proficiency results.
In ValiTrac's model, review and approval actions are tied to named, authorised users so that this evidence is produced as a by-product of the workflow.
Four steps, and the record each one leaves
Competence under clause 6.2 is a cycle rather than a certificate. Each step produces a record, and assessors follow the chain for one named person through one named activity — so a break anywhere in it is visible immediately.
| Step | The question | Record |
|---|---|---|
| Define | What does competence for this activity consist of? | Role description with criteria: qualifications, training, experience, demonstrated skills |
| Achieve | Has this person met those criteria? | Training records, supervised work with the supervisor named, evidence of the demonstration |
| Authorise | What may they now do unsupervised? | A dated authorisation naming the activities, methods and equipment, signed by someone empowered to grant it |
| Monitor | Are they still competent? | Witnessed calibrations, replicate or blind measurements, proficiency-test participation, review of their reports |
Authorisation is narrower than people assume
Clause 6.2.6 lists the activities requiring authorisation, and they are specific: developing, modifying, verifying and validating methods; analysing results including statements of conformity or opinions; reporting, reviewing and authorising results. Being authorised to perform a calibration is not the same as being authorised to sign the certificate, and it is not the same as being authorised to issue the conformity statement on it.
In practice that means an authorisation matrix, not a list of trained people: rows for individuals, columns for activities and methods, and a date in each cell that is filled. The common finding is an authorisation that says calibration technician with no scope attached, under which nobody can tell whether the person who signed a thermocouple certificate was authorised for thermocouples.
Monitoring, which is the step that lapses
- Witnessed calibration: a second authorised person observes the full procedure against the method and records what they saw, not merely that they attended.
- Replicate measurement: the same artefact measured independently by two people, with the difference compared against the claimed uncertainty. This is the single most informative check, and the one that catches a drifting technique.
- Proficiency testing and interlaboratory comparison results, traced back to the individuals who performed the work.
- Review of issued reports for the errors competence is supposed to prevent: missing decision rules, wrong coverage factors, uncertainties quoted to four figures.
- A defined frequency, with the rationale. Annual for everyone is a schedule, not a risk-based plan.
Monitoring has to be recorded even when it finds nothing. A file containing only the year a problem was found reads as though monitoring began that year.
Frequently asked questions
- Does every technician need a formal qualification?
- No. The standard requires demonstrated competence against the laboratory's own criteria, which may combine education, training and experience.
References
- [1]ISO/IEC 17025:2017 — General requirements for the competence of testing and calibration laboratories
General technical guidance written against the cited sources. It is not regulatory or legal advice and does not replace the applicable standard, guideline or a qualified reviewer's judgement.
Have a question on this topic?
Ask ValiTrac AI and see the evidence and calculation behind the answer.
Ask ValiTrac AIFree calculator: Certificate checker
Paste the text of a calibration certificate and screen it against ISO/IEC 17025:2017 clause 7.8: uncertainty with k, traceability, as-found and as-left, the decision rule behind a pass, and every other required element, with the matched text shown for each.
Open the calculatorCalibration on ValiTrac
Support calibration workflows, uncertainty budgets and certificate generation.
Open the calibration worksheetRelated articles
Impartiality and confidentiality under ISO/IEC 17025
The 2017 edition made impartiality a first-class requirement: laboratories must identify risks to it on an ongoing basis and show how they are managed.
Technical records: what to keep and for how long (clause 7.5)
Records must let the measurement be repeated under conditions as close as possible to the original, and every amendment must show who changed what, when.