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Open nowPosted 15 hours ago

Batch Record Reviewer | Pharma | Geel

EURES job mobility portal437,260 open roles

Where
Turnhout, Belgium
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Your applicationOpen nowBatch Record Reviewer | Pharma | GeelEURES job mobility portal · Turnhout, 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.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

15.1% of postings close within 7 days. Measured by our own scanner across the market. EURES job mobility portal postings stay open a median of 6 days.

Share of postings closed within
  1. 2.4%1 day
  2. 6.5%3 days
  3. 15.1%7 days
This job: posted 15 hours ago

EURES job mobility portal median: 6 days open

The posting

Jouw baan als Batch Record Reviewer

Voor een uitdagend project bij een vooraanstaand farmaceutisch bedrijf in Geel zijn we op zoek naar een Batch Record Reviewer. In deze rol ben je een belangrijke schakel tussen productie en kwaliteit. Je zorgt ervoor dat batchdocumentatie volledig, correct en conform de geldende GMP-richtlijnen wordt verwerkt. Dankzij jouw kritische blik worden afwijkingen tijdig opgespoord en correct afgehandeld. Je werkt nauw samen met QA, procesingenieurs, operators en productieverantwoordelijken om de productkwaliteit te garanderen. Zo draag je dagelijks bij aan veilige en betrouwbare geneesmiddelenproductie.

Gelukkig kunnen we op jou rekenen bij het:

  • Reviewen van batchdocumentatie na productie en reiniging
  • Analyseren en documenteren van afwijkingen volgens GMP-procedures
  • Controleren en vervolledigen van batchrecords en bijlagen
  • Goedkeuren van kritische en niet-kritische productieverslagen
  • Organiseren en archiveren van batch- en reinigingsdocumentatie
  • Ondersteunen van productiezones en beheren van plantstock
  • Afstemmen met QA, productie en engineering rond documentatie

Je werkt nauwkeurig en behoudt het overzicht, ook wanneer verschillende dossiers tegelijk opgevolgd moeten worden. Dankzij je analytisch denkvermogen leg je snel verbanden en ga je gestructureerd te werk bij het onderzoeken van afwijkingen. Daarnaast communiceer je vlot met verschillende stakeholders en neem je verantwoordelijkheid voor de kwaliteit van je werk.

Je brengt bovendien mee:

  • Professionele bachelor in een wetenschappelijke richting (chemie, biochemie, farmaceutische of biologische laboratoriumtechnologie, ...)
  • Minstens 2 jaar ervaring binnen QA of kwaliteitscontrole in pharma of life sciences
  • Kennis van productieprocessen, validatie en afwijkingsbeheer
  • Goede beheersing van Nederlands en Engels, mondeling en schriftelijk
  • Ervaring met MS Office; kennis van SAP, MES of vergelijkbare systemen is een plus
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  1. A CV for this posting

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  2. 25 readers review it

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    The review screen in CV Rocket: how each CV was read, round by round.

  3. We apply on EURES job mobility portal's form

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    An application in CV Rocket: every answer filled in on the employer's form.

  4. Every reply, sorted

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  5. Reply with AI

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