ppYour role mission: Provides operational support for global pharmacovigilance activities for Grifols investigational and marketed products. Ensures pharmacovigilance deliverables are of the highest quality and meet general regulatory reporting timelines. Responsible for data reviews and management of the integrated database utilized by worldwide Grifols pharmacovigilance personnel. /p h3What your responsibilities will be /h3 ul liParticipate in safety data collection, review, processing, evaluation, analysis and compilation. /li liProcess adverse event case reports for marketed products, define required submissions, and conduct follow‑up with reporters. /li liCompile and reconcile information to prepare documentation required by pharmacovigilance legislation. /li liReview weekly literature and updates in pharmacovigilance legislation, ensure compliance with archiving tasks, and compile information for periodic safety update reports. /li liEnsure quality and compliance with legal requirements, support staff in audits and inspections,



provide training, and support review and update of SOPs. /li liPerform PV database operating activities: query data extraction, ensure data consistency and integrity, and support updates in database configuration. /li /ul h3Who you are /h3 ul liBachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry). A Master's or Postgraduate degree in the pharmaceutical sector and/or in Pharmacovigilance is valuable. /li li1–2 years of experience in a similar position within the pharma industry (CRO or pharmaceutical company), highly valued. /li liKnowledge of MS Office and SAP. /li liAdvanced level of English. /li /ul h3Benefits package /h3 pSchedule: Monday‑Thursday 7‑10 to 16‑19h and Friday 8‑15h (with the same flexible start time). /p pContract of Employment: Permanent position. /p pGrifols is an equal opportunity employer. /p /p #J-18808-Ljbffr

📌 Drug Safety Officer (San Cugat del Vallés)
🏢 Grifols
📍 San Cugat del Vallés