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 has been working to improve health and well-being around the world since 1909. We are leaders in plasma‑derived medicines and transfusion medicine, developing, producing and marketing innovative medicines, solutions and services in more than 110 countries and regions.
Help us lead one of the world’s largest pharmaceutical companies. Grifols is 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 Pharmacovigilance Specialist like you.
What Your Responsibilities Will Be
* Provide operational support for global pharmacovigilance activities of Grifols‑marketed products
* Ensure pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines
* Review, compile and analyse data, including management of the integrated safety database
* Manage adverse events, including processing adverse event case reports and conducting follow‑up
* Notify regulatory agencies and business partners as required and respond to regulatory agency requests
* Draft and review periodic safety update reports
* Participate in the evaluation of Grifols products’ safety profiles
* Contribute to ensuring compliance of pharmacovigilance activities
* Take part in self‑inspection visits, audits, inspections and in CAPAs management
* Provide training to concerned persons according to the training plan and manage training documentation
* Involve in specific countries’ local pharmacovigilance activities
* Support the creation and update of procedures for global pharmacovigilance operations such as SOPs, internal business practices and working instructions
* Serve in an advisory capacity, including activities such as product monograph review, drafting responses to regulatory agencies’ pharmacovigilance requests, participating in the drafting and implementation of pharmacovigilance contracts and agreements, and assisting management with ad hoc requests
Who You Are
* Have a bachelor’s degree in health sciences (pharmacy, nursing, medicine, veterinary) or bioscience (biochemistry, biotechnology, biology) or similar. If your degree is in bioscience, a master’s or a second degree is required.
* Have at least 4 years of pharmacovigilance experience, including knowledge of good pharmacovigilance practices, existing legislation, regulations and guidelines.
* Speak fluent Spanish and English.
* Have excellent communication skills with internal and external stakeholders.
* Be able to work on multiple projects simultaneously.
* Have good planning skills and organized work habits.
What We Offer
Grifols is committed to creating an atmosphere that encourages employees to develop their professional careers in an excellent working environment. We value diverse talent and aim to remove any barriers that may hinder participation. Adjustments to the selection process are available upon request.
We are an equal opportunity employer.
Flexible schedule: Monday‑Thursday 7:10 to 16:19 h and Friday 8:15 h (with the same flexible start time).
Contract of Employment: Permanent position.
Location: Sant Cugat del Vallès, Spain.
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