Pharmacovigilance (PV) Subject Matter Expert

We are seeking an experienced Pharmacovigilance (PV) Subject Matter Expert to join our team in Barcelona on a permanent basis.

You’ll join our Life Sciences & Healthcare Regulatory team, playing a key role in shaping pharmacovigilance intelligence and solutions that support regulatory compliance and help pharmaceutical companies navigate an evolving global regulatory landscape. Working alongside experts across product, technology, consulting, and content teams, you will have the opportunity to make a meaningful impact for customers worldwide.

About You – experience, education, skills, and accomplishments

• Degree in Life Sciences (Pharmacy, Pharmacology, Biology, Chemistry, Biomedical Sciences, etc.) or equivalent experience
• At least 5 years of experience within a global corporation (pharma, CRO or consulting) with strong knowledge of Pharmacovigilance regulatory landscape and country-specific requirements.
• Demonstrated expertise in pharmacovigilance regulations, compliance processes, and pre-/post-marketing safety reporting requirements across multiple regions and jurisdictions.
• Excellent written and oral communication skills in English.

It would be great if you also had . . .

• Proven ability to interpret and assess the impact of evolving pharmacovigilance regulations and translate regulatory changes into actionable business insights.
• Strong analytical and problem-solving skills, with the ability to manage complex regulatory information and deliver practical recommendations.
• Experience working in cross-functional and international environments, collaborating effectively with product, technology, consulting, and customer-facing teams.
• Strong customer focus, stakeholder management, and relationship-building skills.
• Ability to work independently, manage multiple priorities, and thrive in a dynamic, fast-paced environment.

What will you be doing in this role?

• Serve as the primary Pharmacovigilance Subject Matter Expert, providing expert guidance on global and local PV regulations, requirements, and best practices.
• Ensure the accuracy, quality, and consistency of pharmacovigilance content across multiple countries and regions.
• Monitor, analyze, and interpret pharmacovigilance regulatory changes and assess their impact on pharmaceutical industry compliance obligations.
• Drive the achievement of key performance indicators related to quality, timeliness, and completeness, while promoting a culture of continuous improvement.
• Partner closely with Product, Technology, Consulting, and Content teams to support pharmacovigilance-related projects and product development initiatives.
• Validate pharmacovigilance-related content, recommendations, and decision-support outputs to ensure alignment with regulatory requirements, industry practice, and customer expectations
• Contribute to the design and enhancement of innovative pharmacovigilance solutions by bringing a strong customer-focused perspective.
• Provide expert insights and regulatory intelligence to support customer needs, business decisions, and strategic initiatives.
• Respond to internal and external customer inquiries, delivering clear, accurate, and actionable guidance.
• Conduct independent reviews of pharmacovigilance content and processes, identifying improvement opportunities and supporting corrective and preventive actions where needed
• Support knowledge sharing, training, and awareness activities to strengthen pharmacovigilance expertise across the organization.

About the Team

· You’ll be reporting to the Director, Content Editing, based in France and join an international team

• The team culture is dynamic, creative, and supportive – excellence, integrity, and care are in our DNA.

Hours of Work

This is a permanent full-time position at 40 hours a week (35 hours during July and August). The working schedule is flexible, mostly centered on CET time zone with occasional need to accommodate late or early meetings with US or East Asia time zones.

The position is hybrid going to the office in Barcelona 2-3 times per week.

What We Can Offer You

• A modern culture environment combined with all the financial and stability advantages of working for a large business.

• Active volunteering community, with annual paid hours of volunteering time.

• Private Health and Life & Disability insurances.

• Tax-free benefits (Ticket Restaurant scheme, kindergarten and transport cards).

• Global and dynamic employee base (more than 20 nationalities).

• 30 working days of vacation.