Job title: User Acceptance Testing Specialist

• Location: Budapest
• 60% Remote working and 40% office
• Job type: Permanent, Full time

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 the User Acceptance Testing group and be part of its mission to perform User Acceptance Test script writing and execution for the Global Regulatory Affairs owned technology projects, support internal audits and regulatory inspections by providing appropriate user acceptance documentation.

Main responsibilities:

• Being the primary point of contact for User Acceptance Testing script writing and execution
• Ensuring UAT strategy aligns with Global Regulatory Affairs (GRA) system capabilities, Business Continuity Plan, and user experience
• Partnering with the Business Process & Innovation group and the ITS Validation Lead to assess the EMA and FDA regulations and ensures the UAT function is in sync with regulations and guidelines
• Establishing quality compliance to script writing with tests aligned with role, functionality, architecture, and testing
• Ensuring documentation to support these processes is in place and current
• Ensuring UAT scripts are written and executed in a controlled state and follow good validation methodology and documentation practices
• Leading the vendor UAT team. Ensuring that the team operates in a harmonized and efficient manner
• Providing operational strategy and direction to the vendor team
• Collaborating with external personnel to provide UAT support for Veeva and integrated platform
• Supporting records management and user support activity

About you

Experience:

• Ability to interface with upper-level management of support and client organizations
• Process oriented with knowledge in Operational excellence
• Experience in problem-solving techniques
• Knowledge and experience in implementing operational metrics, process improvements
• Knowledge of Regulatory Affairs and Operations domain and regulatory requirements a plus but not required
• Prior experience with UAT, testing, scripting, validation would be a plus

Technical skills:

• Knowledge of JIRA, Confluence or Application Lifecycle Management
• Working knowledge in Microsoft Office and Windows (Outlook, Word, Excel, PowerPoint)
• Knowledge of Validation methodology, strategy, testing, documentation requirements and CFR (Code of Federal Regulation) Part 11 to support the validation of computer systems
• Experience with Veeva VAULT RIM and Business Objects Universe design, creation, testing, and technical skills is a plus but not required
• Regulatory Information Management knowledge is a plus but not required

Soft skills proposal:

• Willingness to learn and embrace new activities
• Strong interpersonal and collaboration skills in multifunctional and multicultural teams
• Team player focused on building relationships, with strong cultural awareness
• Excellent attention to detail and customer-focused approach
• Self-motivation with the ability to manage shifting priorities efficiently
• Solutions-driven with a continuous improvement mindset
• Ability to maintain discretion and confidentiality with sensitive data, while demonstrating a persuasive “can-do” attitude
• Strong problem-solving skills, with the ability to ensure database accuracy

Education:

• Minimum of a BS degree in scientific, IT, computer science, engineering or related field

Languages:

• Excellent written and verbal communication skills in English

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)

Pursue Progress. 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.

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Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But 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. So, let’s be those people.

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

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