Standard (Mon-Fri) Environmental Conditions Office

Job Description
At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a integral scale. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on
- now and in the future.

We offer
continued career advancement opportunities, award-winning training and benefits focused on the health and wellbeing of our employees. A Day in the Life: Fulfills the role of European Union (EU) and/or UK Qualified Person for Pharmacovigilance, or Deputy EU/UK QPPV, for selected clients. Contributes to scientific safety services, such as safety writing, signal detection and/or literature surveillance. Promotes good practices within the department, including through engagement in process improvement activities and delivery of training. Manages scope of work,



budget oversight and resourcing for both new and existing QPPV services clients Works on complex issues where analysis of situations or data requires an in-depth evaluation of variable factors. Education and

Experience:
Master’s degree in Pharmacy, Medicine or equivalent Previous experience as EU/UK QPPV Extensive experience in pharmacovigilance (inclusive of at least 5 years of EU-specific PV experience) PV Regulatory Inspection experience Knowledge, Skills and Abilities: Proven ability to establish processes and build expertise in drug safety Ability to manage internal and external stakeholders and to exercise creativity and judgement Excellent oral and written communication Excellent interpersonal skills Ability to work independently, analyze and work with attention to detail, process and prioritize complex information, and problem solve Expert knowledge of the regulations governing pharmacovigilance Working knowledge of pharmacovigilance databases Good overall knowledge of the drug development process Understanding of medical/coding dictionaries and ontologies and data interoperability Expertise in budgeting, forecasting and fiscal management Ability to present safety services to potential clients Our Mission is to enable our customers to make the world healthier, cleaner and safer. As one team of 100,000+ colleagues, we share a common set of values
- Integrity, Intensity, Innovation and Involvement
- working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #

📌 Qualified Person (España)
🏢 ThermoFisher Scientific
📍 España