Senior RQS Data Specialist (all genders)

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 the Associate Director of Regulatory Quality Systems (RQS) Information Management, your primary responsibility is to oversee the management of regulatory and quality data. This includes defining a clear framework for effective information management in regulatory collaborations, establishing standards and principles for data governance, and ensuring the quality of data content to support the organization's strategic goals. You will coordinate people, processes, and technology to create cohesive operational models, define data entry and maintenance rules, and ensure compliance with health authority requirements. Additionally, you will mentor junior team members and oversee external service providers to ensure the effective delivery of tasks.

Who You Are:

-a highly skilled professional with a Master degree in a scientific discipline or equivalent experience in the chemical-pharmaceutical industry especially in the Regulatory Affairs area.

- You possess at least five years of experience in the pharmaceutical or IT industry, with a minimum of three years in regulatory affairs.

- Your background includes excellent regulatory management and data governance experience, along with a strong command of current regulatory data standards.

- You are fluent in spoken and written English and have demonstrated experience collaborating with health authorities.

- Your strong communication skills, attention to detail, and ability to work with uncertainties make you a valuable asset to the organization.

Preffered location Poland, Croatia, India

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!

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