ppWould you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a integral healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. /ppbWe believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities, fostering an inclusive environment where diversity makes us outstanding. /b /ppHelp us lead one of the world’s largest pharmaceutical companies. We are a world leader in plasma-derived medicines with a presence in more than 100 countries, and a growing global team of over 20.000 people. That’s why we need a Technical Drug Safety Officer like you. /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 global regulatory reporting timelines. Responsible for data reviews and management of the integrated database utilized by worldwide Grifols pharmacovigilance personnel. /ph3What your responsibilities will be /h3ulliTo participate in the safety data collection, review, processing, evaluation, analysis and compilation: /liliProcessing Grifols marketed products adverse event case reports (including definition of submissions required and conducting follow-up with reporters). /liliCompilation and reconciliation of information in order to prepare documentation required by pharmacovigilance legislation: /li /ulolliReview of the weekly literature review. /liliReview of the updates in pharmacovigilance legislation.



/liliCompliance with archiving tasks for deliverables and relevant documents. /liliCompilation of information for and participation in preparation of periodic safety update reports. /li /olulliEnsure quality and compliance with the legal requirements for pharmacovigilance tasks and responsibilities: /li /ulolliSupport to the pharmacovigilance staff involved in audits and inspections /liliProvide training to concerned personnel based on the training plan and managing training documentation and deliverables within relevant company departments /liliSupport to the review and update of the SOPs, working practices or conventions /li /olh3Who you are /h3pTo perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills, education, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions). /pulliBachelor's degree in Health Sciences (Pharmacy, Biology, Chemistry), being valuable to have a Master or Postgraduate degree in the pharmaceutical sector and/or in Pharmacovigilance. /liliYou have 1-2 experience in a similar position within pharma industry (CRO or pharmaceutical company), being high valuable. /liliYou have knowledge of MS Office and SAP program. /liliYou have advanced level of English. /li /ulh3What we offer /h3pIt is a brilliant opportunity for you, Grifols is fully aware that its employees are one of its major assets. We are committed to maintaining an atmosphere that encourages all our employees to develop their professional careers in an excellent working environment. /ppWe believe in diverse talent and want to remove any barriers that may hinder your participation. If you require any adjustments in our selection process, please do not hesitate to inform us when applying. We are here to help. /p /p #J-18808-Ljbffr

📌 Drug Safety Officer (Barcelona)
🏢 Grifols
📍 Barcelona