Would 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 global 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.
We believe that diversity adds value to our business, our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment. Help 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.
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.
What your responsibilities will be Participate in the safety data collection, review, processing, evaluation, analysis, and compilation. Process Grifols marketed products adverse event case reports (including definition of submissions required and conducting follow-up with reporters). Review the weekly literature search. Review the updates in pharmacovigilance legislation. Compliance with archiving tasks for deliverables and relevant documents. Compile information for and participate in preparation of periodic safety update reports. Support the pharmacovigilance staff involved in audits and inspections. Provide training to concerned personnel based on the training plan and manage training documentation and deliverables within relevant company departments. Support the review and update of the SOPs, working practices, or conventions. Use queries for data extraction for different PV documents. Ensure data consistency and integrity within the safety database. Support updates in the database configuration. Who you are To 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 accommodations may be made to enable individuals with disabilities to perform the essential functions.
Bachelor's degree in life science. Fluent written and spoken English (C1 Advanced) and Spanish. Proficiency in additional languages such as Chinese, Italian, French, or others will be highly valued. 1 year of experience as a trainee, or similar, in the pharmaceutical industry or CRO working on quality, data entry, or pharmacovigilance. Flexible and adaptable to changing situations/projects within the company/industry. Organization, planning, and detail-oriented. Multitasking. What we offer It's a brilliant opportunity for someone with the right talents. Grifols understands you want a challenging and rewarding career in a critical function. Technical Drug Safety Officer helps you grow professionally.
Information about Grifols is available at www.grifols.com. If you're interested in joining our company and you have what it takes, then don't hesitate to apply. We look forward to receiving your application.
Grifols is an equal opportunity employer.
Flexible schedule: Monday-Thursday 7-10 to 16-19h and Friday 8-15h.
Benefits package Contract of Employment: Permanent position.
Flexibility for U Program: 2 days remote working.
Location: Sant Cugat del Vallès.
www.grifols.com
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Location: SPAIN: España: Sant Cugat del Valles: SC3
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