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Validation & CQV jobs in Eindhoven

Validation & CQV jobs in Eindhoven at pharma, biotech and CDMO sites, technically screened by a GMP consultant. There is currently 1 open role in Eindhoven and the surrounding area. Validation Engineers, CQV Engineers, CSV Specialists and Validation Leads for equipment qualification, process validation, cleaning validation and computerised systems. GMP, ISO 13485 and MDR jobs in Eindhoven: Brainport's health-tech and medical device industry, combination products, sterile devices and the engineering firms that build pharma automation. Salaries for Validation & CQV roles run from €55–85k gross per year across medior to senior profiles; interim day rates and regional differences are in our salary guide. Every vacancy states the client type, contract form, salary band and whether Dutch is required. Not seeing the right role? Register and we will call you when one opens; most Validation & CQV roles in this market are never advertised.

(Example vacancies. These show how a role is presented; they are not live searches.)

  • ValidationInterim / secondmentDutch not required

    Validation Engineer – CSV / Automation

    Engineering firm serving pharma, Brainport

    Secondment via Pharma Recruit: GAMP 5 validation of MES and DeltaV projects at Benelux pharma sites.

    €70–82k
    Hybrid · Eindhoven

Consultant for this discipline

Gregory Sivo

Founder · Practising GMP quality professional

  • · Founder, Truex Consultancy: GMP and GDP compliance
  • · 10+ years in regulated pharmaceutical quality
  • · Personally conducts every technical conversation

Frequently asked questions

What is the difference between validation, qualification and CQV?

Qualification proves equipment and systems are fit for purpose (IQ/OQ/PQ). Validation proves a process or method reliably produces the intended result. CQV adds commissioning: the project-phase work of getting a new facility from construction to qualified state.

Do I need CSV experience for a validation role?

Not for most equipment and process roles, but computerised-system validation is increasingly requested alongside them. Candidates with both are placed faster.

Is validation work mostly permanent or project-based?

Both. Capital projects create interim and freelance demand; established sites keep a permanent team for requalification, cleaning validation and change control. We tell you which fits the vacancy.

Are there pharma GMP jobs in Eindhoven?

Mostly device, combination product and automation-related: ISO 13485 QA, MDR RA, process and computerised systems validation. Classical drug manufacturing is in Oss, Leiden and Bilthoven.

Is English enough in Eindhoven?

Yes at most Brainport companies, the region is one of the most international in the Netherlands.