Validation consultant

☞ Trevalco BV

Aussicht: 135

Update Tag: 11-11-2025

Ort: Willebroek Antwerp

Kategorie: Qualitätssicherung / Qualitätskontrolle

Industrie:

Position: Associate

Jobtyp: Full-time

Loading ...

Jobinhalt

Job position: validation consultant

Location: Belgium

A job as validation consultant in the pharmaceutical industry has a lot of variation. It includes technical analysis, document writing, execution of tests in production or laboratory environments, as well as a lot of interaction with different departments in the company where you work.

As validation consultant you execute validation projects on location at clients in the pharmaceutical industry. This can be production equipment validation, lab equipment validation but it can also concern the validation of facilities and utilities, processes and computer systems. Depending on your background and interests you will be active in one or more of these areas.

For this position we are looking at all levels of experience, from starter to senior level.

Your Responsibilities As Validation Consultant Include
  • write validation plan and report
  • write URS
  • write IQ, OQ and PQ protocol
  • plan and execute or oversee execution of qualification tests
  • manage quality records such as deviations, CAPA’s and change controls
  • participate to risk assessments and quality investigations
  • participate to internal and external audits
  • advise on pharmaceutical regulatory requirements such as GMP, GLP and GDP
Validation consultant executing a filter integrity test, as part of cleanroom validation.

Qualifications

Must have
  • fluent in English, at least intermediate in Dutch
  • strong analytical skills, well organized, studious and precise
  • you can explain, you can convince, you can correct... you have perfect communication skills
  • you enjoy managing documentation: creating documents, reviewing and updating, getting approval on documents
  • master degree in science or engineering, or equivalent through experience
Nice to have
  • experience working in a GxP environment
  • experience as tester or technical writer
  • knowledge of pharmaceutical regulations
Our offer

Attractive salary package

including CAO90 bonus, hospitalization and dental care insurance, meal vouchers and much more

Company car or mobility budget

you choose what works best for you: company car, (e)bike, public transportation or a cash bonus

Training and development

coaching, classroom and digital online training, professional memberships, or whatever way is working best for you

Interesting projects

we don’t decide this for you, we decide with you what your next project or assignment will be

A fair, respectful employer

the right company culture is important to us: fair, respectful, transparent, being there for our employees

Work / life balance

because we have a family to take care of or non-professional commitments after working hours
Loading ...
Loading ...

Frist: 26-12-2025

Klicken Sie hier, um sich für einen kostenlosen Kandidaten zu bewerben

Anwenden

Job melden
Loading ...

ÄHNLICHE ARBEITEN

Loading ...
Loading ...