Pharma QA Release Specialist - Hybrid Barcelona

ES06 (FCRS = ES006) Novartis Farmacéutica, S.A.; Sabadell; Hybride; EUR 35 000 - 64 000; Plein temps

Avantages offerts par ce poste

Hybrid working options

Paid parental leave (14 weeks)

Résumé du poste

Novartis Farmacéutica, S.A. is seeking a QA Release Officer to ensure compliant release of commercial medicinal products in Barcelona, hybrid work option.

You will review batch documentation and support GMP compliance across manufacturing, testing and distribution processes. Responsibilities include managing quality aspects, initiating EU batch certificates, and coordinating with Supply, DRA and related teams.

Qualifications

• Degree in Health Sciences.
• 1+ years of experience in Quality Assurance and/or Quality Control.
• Strong knowledge of GMPs and pharmaceutical manufacturing processes.
• Native Spanish and good level of English.

Responsabilités

• Managing Quality aspects and projects within the area of responsibility.
• Ensuring and supporting overall GxP compliance and compliance with Novartis Quality Management Systems.
• Performing batch documentation review prior to release by the QP.
• Initiating and obtaining the EU Batch Certificate for centrally authorized products.
• Assessing the transport of commercial medicinal products and evaluating cases involving temperature excursions.
• Managing and prioritizing urgent requests and releases.
• Managing the reconditioning of commercial batches in compliance with GMPs.
• Ensuring the implementation of SLC in collaboration with Supply, DRA, and other related departments.
• Reporting and following up on monthly indicators, as well as managing the documentation archive and sample archive.

Connaissances

Quality Assurance

Quality Control

GMP

Pharmaceutical Manufacturing

Formation

Health sciences degree

Description du poste

Novartis Farmacéutica, S.A. is seeking a QA Release Officer to ensure compliant release of commercial medicinal products in Barcelona, hybrid work option.

You will review batch documentation and support GMP compliance across manufacturing, testing and distribution processes. Responsibilities include managing quality aspects, initiating EU batch certificates, and coordinating with Supply, DRA and related teams.