Global Quality Documentation Specialist

About the job

Our Team:

Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions.

As a company with a global vision of drug development and a highly regarded corporate culture, Sanofi is recognized as one of the best pharmaceutical companies in the world and is pioneering the application of Artificial Intelligence (AI) with strong commitment to develop advanced data standards to increase reusability & interoperability and thus accelerate impact on global health.

The Global M&S Services acts as a cornerstone to this effort. Our team is responsible for delivering and supporting Global M&S teams by acting as a crucial link between our R&D and Manufacturing facilities, playing a vital role in securing the present portfolio and delivering future launches of high-quality and innovative drugs and vaccines.

Be part of something exceptional. Our Budapest Hub has been recognized for workplace excellence, innovation, and our commitment to putting people first. See the full list of our awards at the end of this posting.

Main responsibilities:

• Execute administration and governance related tasks: Mapping (per doc package) & process navigator update
• Update QualiPSO parameters related to CMS process: stakeholders review list, picklists.
• Support the coordination of gap assessment process for global documents.
• Management of definition of global glossary in the tool.
• With a focus on initiation of quality documents (QD) deliverables.
• Create DocID in QualiPSO and metadata: manage the creation & update of metadata.
• Coordinate transversal Content Management System (CMS) QualiPSO administration .
• Check global documents created by error (in the owning entity) – only global documents.
• Check user access and privilege (care request management), training assignment and annual review access.
• Support document change request (DCR) process – Monitoring of DCR process including KPI, DCR sharing for decision (to author and GQ Doc expert).
• Support periodic review by monitoring periodic revision process with KPI.
• Support the weekly communication on Global Quality Document approval, and generate QualiPSO extraction on demand.

About you

Experience:

• Professional experience in documentation.
• Experience in GxP environment is an advantage

Soft skills:

• Proficient in problem-solving.
• Attention to detail, and good organizational skills.
• Ability to work collaboratively with cross-functional teams in a flexible and proactive manner.
• Strong analytical skills.

Technical skills:

• Microsoft Office
• Strong analytical skills.
• Knowledge of Quality DMS, is an advantage.

Education:

• Bachelor’s or Master’s Degree in life sciences

Languages:

• Excellent English communication and writing

Why choose us?

• Bring the miracles of science to life alongside a supportive, future-focused team in an international work environment
• 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, Well-Being Lectures & Sport Clubs)