Roche
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.
The Opportunity
As a Regional Center Partner (PV, Pharmacovigilance), you will be at the heart of our Pharmacovigilance (PV) operations, ensuring that safety information is collected, reported, and handled with the highest level of integrity. You will join a mission-driven team dedicated to delivering compliant, high-quality outcomes that directly impact patients' lives worldwide.
In this role, you will act as a guardian of our PV system, driving continuous improvement and simplification of processes. You will collaborate with a diverse network of global experts and external vendors, navigating a complex matrix environment to maintain an inspection-ready state. This is an opportunity to apply your "systems thinking" and entrepreneurial mindset to a function that is critical to Roche’s success and reputation.
You will ensure the end-to-end collection and reporting of safety information in strict compliance with Roche and local regulatory requirements.
You will maintain robust oversight of safety risk management activities, including those executed by our external partners and vendors.
You will lead the preparation of safety-related documents, serving as Lead Author for Local Aggregate Reports (LAR) and Periodic Benefit-Risk Evaluation Reports (PBRER).
You will drive continuous improvement initiatives to enhance efficiency and effectiveness within the Patient Safety Operations.
You will identify and escalate potential risks or deviations, ensuring appropriate follow-up actions are taken to maintain compliance.
You will collaborate closely with Country Champions and Affiliate Patient Safety teams to ensure seamless execution of safety activities.
Who you are
You are a detail-oriented professional with a strong quality mindset and the ability to navigate complex regulatory landscapes with sound judgement. You thrive in collaborative environments and are passionate about continuous learning and process optimization. We offer a positive work environment where your contributions to patient safety are valued, and you are empowered to grow your expertise in a global pharmaceutical leader.
You hold a Health Care Professional degree (e.g., Medicine, Pharmacy) or a Life Science degree (e.g., Biology, Neuroscience).
You bring at least 2-3 years of experience in Drug Safety or Pharmacovigilance.
You have a solid understanding of global Pharmacovigilance and Medical Device regulatory requirements.
You possess a deep knowledge of end-to-end PV processes and Quality Management Systems (QMS).
You have the ability to independently evaluate, analyze, and interpret complex data to draw meaningful conclusions.
You are a proactive problem-solver with excellent communication skills in fluent English.
Location: This position is based in Budapest.
Relocation Assistance is not available
A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
Let’s build a healthier future, together.
Roche is an Equal Opportunity Employer.