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Open nowPosted 65 days ago

Quality Assurance Associate

EURES job mobility portal29,165 open roles

Where
Noordoost-Noord-Brabant, Netherlands
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Your applicationOpen nowQuality Assurance AssociateEURES job mobility portal · Noordoost-Noord-Brabant, Netherlands

  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

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The clock on this job

Early applications get read.

7.9% 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. 3.4%3 days
  3. 7.9%7 days
  4. 14.2%14 days
  5. 34.1%30 days
This job: posted 65 days ago

The posting

- Mobilisatie van personeel - Digitale transformatie Quality Assurance Associate - Locatie: Boxmeer, Nederland - Contactpersoon: Diana Braat - Contractsoorten: - Telefoon contactpersoon: +31 (0)20 406 97 50 - Bedrijfssectoren: - E-mail contactpersoon: [email protected] Wil jij jouw carrière in QA starten of verder ontwikkelen binnen een internationaal farmaceutisch bedrijf? Ben jij nauwkeurig, kwaliteitsbewust en wil je werken in een GMP-omgeving waar jouw werk direct bijdraagt aan de kwaliteit van geneesmiddelen? Dan is deze functie als Quality Assurance Associate iets voor jou. Functieomschrijving : Als Quality Assurance Associate kom je terecht bij een internationaal opererende farmaceutische organisatie waar kwaliteit, innovatie en samenwerking centraal staan. Binnen deze functie krijg je de kans om ervaring op te doen met GMP, kwaliteitssystemen en regulatory processen. In deze rol ben je verantwoordelijk voor het tijdig en correct verwerken van wijzigingen binnen de kwaliteitssystemen. Je zorgt ervoor dat processen en documentatie voldoen aan de geldende GMP-richtlijnen en ondersteunt verschillende afdelingen bij het beheren van kwaliteits- en masterdata. Hierbij werk je nauw samen met Qualified Persons en diverse productie- en kwaliteitsteams. Verantwoordelijkheden : - Verwerken van regulatoire wijzigingen binnen de kwaliteitssystemen - Beheren en onderhouden van masterdata en kwaliteitsdocumentatie - Werken met systemen zoals SAP, LIMS en MS Office - Ondersteunen bij het waarborgen van GMP- en GDocP-compliance - Samenwerken met Qualified Persons en verschillende IPT's om kwaliteitsprocessen optimaal te laten verlopen - Signaleren van verbetermogelijkheden binnen kwaliteitsprocessen en administratieve workflows Profiel : - Een afgeronde HBO-opleiding in Biochemie, Microbiologie of een vergelijkbare richting - Minimaal 1 jaar relevante werkervaring binnen een kwaliteits- of farmaceutische omgeving - Erv...

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