QA Operations Expert — Pharma Release & Compliance (Assoc)

Novartis

Puurs

Sur place

EUR 47 000 - 88 000

Plein temps

Il y a 4 jours
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Résumé du poste

Novartis in Puurs, Belgium, seeks a QA Release Specialist to ensure compliant and timely release of materials and finished products. You will apply QA expertise to assess quality, support investigations, and maintain processes across QA, production, QC, MS&T, and supply chain. Strong GMP knowledge and English/Dutch communication are essential.

The role emphasizes CAPAs, audits, and continuous improvement to uphold quality standards and supply reliability for medicines.

Qualifications

  • Master's degree in a scientific field (pharmacy, industrial pharmacy, bio-engineering, or related).
  • Experience in the pharmaceutical industry.
  • Strong understanding of GMP and relevant pharma legislation.
  • Proficiency with computerized systems and digital documentation.
  • Excellent English and Dutch communication; cross-functional collaboration.

Responsabilités

  • Ensure compliant and timely release of materials and products.
  • Maintain up-to-date expertise in production and release processes.
  • Review non-conformities, support investigations, define CAPAs.
  • Contribute to initiatives reducing deviations and improving robustness.
  • Monitor file/batch status and liaise with logistics and QA partners.
  • Explain QA release docs during audits.
  • Keep procedures accurate and aligned with requirements.

Connaissances

Excellent English & Dutch comm.
Pharma industry experience
GMP knowledge
Digital documentation proficiency

Formation

Master's degree in Pharmacy/related field

Description du poste

Novartis in Puurs, Belgium, seeks a QA Release Specialist to ensure compliant and timely release of materials and finished products. You will apply QA expertise to assess quality, support investigations, and maintain processes across QA, production, QC, MS&T, and supply chain. Strong GMP knowledge and English/Dutch communication are essential.

The role emphasizes CAPAs, audits, and continuous improvement to uphold quality standards and supply reliability for medicines.

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