Pharmacovigilance IT Systems Specialist

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

Your Role:

As a Pharmacovigilance IT Systems Specialist, you will be tasked with supporting, maintaining, and enhancing the pharmacovigilance system to ensure adherence to regulatory standards. You will take the lead in implementing and continuously improving safety databases, ensuring data integrity and compliance with regulations. Collaboration with cross-functional teams will be essential as you integrate new technologies and processes. Additionally, you will act as a primary point of contact for system users and technical teams, overseeing the entire lifecycle of safety system operations. This role is vital for supporting high-priority safety data migration and E2B Gateway exchange projects, contributing to strategic Global Patient Safety initiatives, and managing numerous LSMT platform releases and operational activities.

The role will be based in Bangalore, India, and reporting to Team Lead, Pharmacovigilance Services.

Who You Are:

• A university degree (Master's or Bachelor’s) or equivalent in information technology or life sciences, with a strong interest in IT systems.
• Over 10 years of experience with drug safety database systems in the pharmaceutical industry, healthcare organizations, or software application vendors.
• In-depth knowledge of

  LSMV

  and

  pharmacovigilance systems

  , along with drug safety regulatory requirements (ICH, GVP, FDA CFR Part 11, GxP).
• Strong understanding of software validation processes and methodologies (

  GAMP

  ).
• Proven experience in IT project management, service delivery, or vendor management is advantageous.
• Exceptional organizational skills with the ability to prioritize tasks and quickly adapt to shifting priorities.
• A collaborative team player who considers the broader goals beyond individual targets.
• Excellent written and verbal communication skills in English.
• Strong interpersonal skills in an international setting.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!