LIMS Data Manager - Benchling
Description
Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
This role offers an exciting opportunity to support the deployment and validation of a new scientific data platform within a leading pharmaceutical R&D environment. You will work closely with Data Management, Product Owners, Business stakeholders, and technical teams to ensure the successful implementation and adoption of the VIVO ecosystem.
Key Responsibilities:
- Support the deployment, testing, and validation of the VIVO platform (Benchling) and its functionalities.
- Perform data consistency checks between Benchling, VIVO DB, LIMS, BI reports, and FederateS.
- Review and validate operational data imported from laboratory systems.
- Support Product Owners and Business Owners in prioritizing product enhancements and implementation activities.
- Execute UAT and sprint-related testing activities based on defined test plans.
- Analyze business requirements and contribute to process improvements.
- Document system changes, validation activities, and user guidance materials.
- Participate in Agile/SCRUM ceremonies and collaborate with multidisciplinary teams.
Requirements
Qualifications & Skills Required
- Master's degree or Engineering degree.
- Junior to experienced profile with exposure to business analysis, data management, or scientific information systems.
- Knowledge of biology, laboratory environments, preclinical research, or translational sciences.
- Understanding of pharmacology, toxicology, or PK studies is highly desirable.
- Familiarity with Master Data Management (MDM) and reference data concepts.
- Good knowledge of Excel and SQL.
- Experience with UAT testing or software validation is a plus.
- Good level in French and English.
Benefits
Why Join Us?
At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
Here's what makes us unique—
We are a young, ambitious health company representing 900 Excelyates, driven to become Europe's leading mid-size CRO with the best employee experience. Our one-stop provider service model—offering full-service, functional service provider, and consulting—enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.
Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.
Skills
As published by workable · 7 questions · 7 written answers
First name, Last name, Email, Headline, Phone, Address, Photo, Resume
- Do you have experience working with preclinical research environments?
- Have you participated in user acceptance testing (UAT), software validation, or system deployment projects?
- Are you comfortable working with SQL, EXCEL and performing data consistency or data quality checks?
- Do you have knowledge of biology, pharmacology, toxicology, PK studies, or laboratory workflows?
- This role requires being on‑site in Saclay (Paris‑Saclay) 2 days per week. Are you able to commit to this onsite requirement?
- When would you be available to start this mission? Do you currently have a notice period?
- What are your salary expectations for this position (annual gross)?