Regulatory Affairs Data Manager

Galderma; Barcelona; Hybrid; EUR 40,000 - 80,000; Full time

Benefits offered by this job

Competitive compensation

Hybrid work environment

Personalized career development

Inclusive organization valuing diversity

Job summary

An established industry player is seeking a Regulatory Affairs Data Manager to enhance data management practices within their new Global Capability Centre in Barcelona. This role involves analyzing and reporting regulatory data, transitioning to a unified platform, and ensuring data consistency across departments. The company values diversity and offers a hybrid work environment, competitive compensation, and opportunities for professional growth. Join a forward-thinking team where your contributions will significantly impact the organization and your career trajectory.

Qualifications

• 2-3 years of experience in Regulatory Affairs within a pharmaceutical setting.
• Strong proficiency in data management and reporting tools.

Responsibilities

• Manage and analyze regulatory data to ensure consistency across systems.
• Identify discrepancies and propose improvements for data utilization.

Skills

Regulatory Affairs experience

Data analysis

Excel proficiency

Knowledge of RIMS

Database management

Tools

Business Object

EDMS

Job description

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At Galderma, we embrace diversity and difference

Our unique offerings span Aesthetics, Consumer, and Prescription products, and we are committed to recognizing and rewarding our employees. Working here offers the chance to gain challenging experiences and make a significant impact.

We are establishing a new Global Capability Centre in Barcelona, supporting our global teams. Located in the Eixample District, it provides opportunities for professional growth through international projects and career advancement.

Job Title: Regulatory Affairs Data Manager

Location: Barcelona, Spain (hybrid)

Job Description

As the Regulatory Affairs Data Manager, you will support regulatory operations by managing, analyzing, and reporting regulatory data. This role involves transitioning from siloed applications to a unified platform, ensuring consistent data management across departments, and executing reporting activities.

Key Responsibilities

1. Inventory data and establish metadata dictionaries for Regulatory Affairs systems (e.g., RIMS, EDMS, Publishing tools)
2. Identify discrepancies and alignments between systems
3. Propose process and system improvements for better data utilization
4. Perform routine data analysis to ensure consistency
5. Maintain reports on business activities and system usage
6. Assist in IT projects involving data analysis or migration
7. Act as Data Steward and participate in Data Governance

Skills & Qualifications

• Experience in Pharmaceutical companies in similar roles
• 2-3 years in Regulatory Affairs
• Proficiency with IT systems, Excel, data mapping, databases
• Knowledge of RIMS and reporting tools (e.g., Business Object) preferred

What We Offer

• An inclusive organization valuing diversity
• Competitive compensation and benefits
• Hybrid work environment
• Personalized career development
• Ownership and accountability in a growing company

Next Steps

1. Initial virtual interview with the recruiter
2. Interview with the hiring manager
3. Panel interview with the team

Our People Make a Difference

At Galderma, we value professionalism, collaboration, and diversity, fostering an environment where everyone can thrive.