Pharma QA Compliance Expert (Hybrid)

Novartis AG

Torre Annunziata

Hybride

EUR 30 000 - 55 000

Plein temps

Il y a 3 jours
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Avantages offerts par ce poste

Hybrid working options
Insurance plans
Retirement plans
Wellbeing resources
Global recognition programs

Résumé du poste

Novartis AG is seeking a QA Compliance professional to oversee quality systems, data integrity, and regulatory adherence at our site in Italy. The role focuses on PQR/APQR activities, qualification and validation, supplier oversight, CAPA, change control, and audits.

You will ensure DI and eCompliance oversight, coordinate inspections, and promptly report technical complaints and adverse events. A university degree in a related field and 3–5 years of pharma QA experience are required, with

Qualifications

  • University degree in pharmacy or related field.
  • 3–5 years in QA compliance in the pharmaceutical industry.
  • Fluent in Italian and English; strong collaboration and stakeholder management skills.

Responsabilités

  • Plan and support PQR/APQR activities.
  • Support site qualification and validation activities (planning, advising, review).
  • Implement Quality Systems (documentation management).
  • Supplier management activities (agreements, oversight, audit).
  • Coordinate CAPA and follow-up.
  • Audit and inspection preparation and support.
  • Review change control.
  • Ensure DI and eCompliance oversight (training, inspections, plan, risk ID).
  • Report technical complaints/adverse events within 24 hours.

Connaissances

Quality compliance
Stakeholder management
Collaboration
Italian-English bilingual

Formation

University degree in Pharmacy or related field

Description du poste

Novartis AG is seeking a QA Compliance professional to oversee quality systems, data integrity, and regulatory adherence at our site in Italy. The role focuses on PQR/APQR activities, qualification and validation, supplier oversight, CAPA, change control, and audits.

You will ensure DI and eCompliance oversight, coordinate inspections, and promptly report technical complaints and adverse events. A university degree in a related field and 3–5 years of pharma QA experience are required, with

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