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Open nowPosted 3 days ago

C&Q Engineer

EURES job mobility portal131,388 open roles

Where
Antwerpen, Belgium
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Your applicationOpen nowC&Q EngineerEURES job mobility portal · Antwerpen, Belgium

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on EURES job mobility portal's own form.

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The clock on this job

Early applications get read.

7.7% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.6%1 day
  2. 3.3%3 days
  3. 7.7%7 days
  4. 14.0%14 days
  5. 33.7%30 days
This job: posted 3 days ago

The posting

Ben jij gepassioneerd door commissioning, qualification en validatie binnen een GMP-omgeving? Wil je meewerken aan uitdagende projecten binnen de farmaceutische sector waar kwaliteit, compliance en techniek centraal staan? Dan is deze opportuniteit iets voor jou.

Als C&Q Engineer – Facilities & Utilities ben je verantwoordelijk voor het coördineren en uitvoeren van commissioning-, qualification- en change control activiteiten. Je werkt nauw samen met engineering-, productie- en kwaliteitsteams om installaties en systemen conform de geldende regelgeving en kwaliteitsnormen op te leveren.

Je krijgt de kans om betrokken te zijn bij volledige projecttrajecten, van ontwerp en documentatie tot testing, kwalificatie en overdracht.

Wat ga je doen?

  • Coördineren en documenteren van change controls binnen verschillende projecten.
  • Verzamelen en analyseren van technische informatie met betrekking tot wijzigingsaanvragen.
  • Bijwonen van constructie- en projectmeetings en uitvoeren van technische walkdowns en P&ID-verificaties.
  • Opstellen, reviewen en actualiseren van essentiële projectdocumentatie zoals URS, IA en FS.
  • Uitwerken van kwalificatieprotocollen, testmatrices, testrapporten en testformulieren.
  • Uitvoeren en opvolgen van commissioning-, FAT-, SAT- en kwalificatietesten.
  • Verzamelen en beheren van testbewijzen en kwaliteitsdocumentatie.
  • Opstellen van commissioningplannen, green/blue tag rapporten en eindrapportages.
  • Bewaken van de voortgang en rapporteren van de status van kwalificatie- en commissioningactiviteiten.
  • Afronden, documenteren en archiveren van change controls volgens GMP-richtlijnen.

Wie ben jij?

  • Je beschikt over een bachelor- of masterdiploma in een technische, wetenschappelijke of Life Sciences richting.
  • Je hebt minimaal 3 jaar ervaring als C&Q Engineer binnen de farmaceutische industrie.
  • Je bent vertrouwd met GMP-richtlijnen en relevante regelgeving binnen een gereguleerde omgeving.
  • Je hebt ervaring met technische documentatie zoals P&ID’s, specificaties en kwalificatieprotocollen.
  • Je werkt gestructureerd, nauwkeurig en hebt een sterk analytisch inzicht.
  • Je neemt eigenaarschap over je projecten en hanteert een proactieve aanpak.
  • Je communiceert vlot in het Nederlands en Engels.
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    An application in CV Rocket: every answer filled in on the employer's form.

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