• Job title: Senior Data Quality Analyst
• Location: Budapest, Hungary
• Job type: Permanent, full-time
• Hybrid working according to local policy
  

About the job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Join our Global Regulatory Operations (GRO) team in charge of Vault RIM Data Quality Control and Continuous Improvement as a Senior Data Quality Analyst and you will be a key member of a highly productive team, a collaborative team player, and an important driver of continuous improvement through analysing and monitoring the quality of Regulatory data.

 You will be responsible for developing new and updating existing data QC reports, including all documentation needed to support QC execution, implementing, and transferring developed data QC reports via training and supporting documentation to data QC team members responsible for execution.

Main responsibilities:

• Vault RIM Data QC Procedural document creation and coordination
• Support inquiries regarding data QC process/Vault RIM tool questions
• Analyze and determine root cause for data quality errors and makes recommendations for long term solutions
• Research and determine scope and complexity of issue to identify steps to resolve issues
• Support capability process lead with new requests as needed (e.g., process definition, documentation, presentations to stakeholders, support for ongoing projects)
• Leads small project teams focusing on data quality
• Serve as Lead Developer for Data QC checks
• Drive Continuous Improvement by updating and/or creating Data QC checks to address identified gaps in the existing Data QC monitoring system
• Assist in coordination of Data Quality Audit/Inspections activities (e.g., development of data QC report as part of CAPA)

About you

Experience:

• 3+ years’ experience in the bio/pharmaceutical industry with experience in Regulatory Affairs preferred
• Working knowledge of regulatory affairs/regulatory operations domain, regulatory requirements including Pharmacovigilance, and quality management systems preferred. Knowledge of drug product life cycle (i.e., research and development, variations, extensions, launches, pharmacovigilance, compliance, licensing) and relating to data lifecycle management within Vault RIM desired
• Previous experience with leading small projects is advantageous

Soft Skills:

• Strong verbal and written communication with the ability to present and convey business challenges, solutions, and improvements efficiently across varying functions and levels of management
• Good organizational and problem-solving skills, critical thinking and the ability to troubleshoot detected data issues and manage multiple priorities effectively
• Demonstrate a quality centred, continuous improvement mindset
• Demonstrates an agile mindset by fostering respect, building, and maintaining effective
• Ability to coordinate a group of people and work cross-functionally

Technical skills: 

• MS Office Suite, with proficiency in working with data in Excel spreadsheets (e.g., creating pivot tables)
• Power BI experience preferred
• Working knowledge of regulatory information management systems (Veeva Vault RIM) preferred
• Ability to understand complex data models
• Understanding of global regulatory/regulatory operations data, focusing on Regulatory Information Systems (Vault RIM Registration Tracking preferred)

Education: 

• Bachelor’s (University) degree required, preferred degree in life sciences, technology or information management

Language(s):

• Fluency in English in written and speaking, able to use in a global environment

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team in an international work environment
• Work from an "Office of the Year 2023" award winner with flexible home office policy
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave
• An individual and well-structured introduction and training of new employees and we will dedicate a Buddy for you to better navigate in your first weeks
• Join a great community & special events (Monthly Board Game Nights, Summer Events, Well-Being Lectures & Sport Clubs)

PursueProgress. Discover Extraordinary.

Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.

At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Discover our Code of Conduct, that serves as the moral compass that guides us when chasing the miracles of science to improve people’s lives. Please ensure to have read this document before applying.

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