#LI-Hybrid

Location: Barcelona, Gran Via

Key Responsibilities:

• Oversee and provide strategic inputs to process improvements (incl. standardization, simplification) across therapeutic areas in Medical Safety.
• Ensure compliance with global safety regulations and internal standards.
• Drive audit and inspection readiness through process enhancements.
• Represent Medical Safety in cross-functional initiatives and projects.
• Guide transition of process changes into successful project execution.
• Set and monitor quality metrics for medical safety activities.
• Provide expertise and support for process updates and issue management.
• Build & lead a high-performing team to meet process excellence objectives and maintain a sustainable compliance culture.

Essential Requirements:

• Advanced degree in Life Sciences or Healthcare; MD, MBBS, PharmD, or PhD preferred.
• Fluent in spoken and written English.
• Minimum 12 years’ experience in drug development within a major pharmaceutical company.
• At least 5 years in a global role providing strategic inputs for  global drug safety, clinical, or medical affairs position.
• Strong leadership and people management skills.
• Excellent negotiation, conflict resolution, and decision-making abilities.
• Strong critical and strategic thinking skills, with proven ability in business proposal development Solid knowledge of drug safety-related processes.

Desirable Skills:

• Results driven, self-starter with proactive working style; committed and accountable, transparent even under pressure.
• Quality oriented.