Expert Medical Writer

 

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 an Expert/Senior Expert Medical Writer, you will support medical writing efforts for molecules across therapeutic areas, both globally and at regional/local levels. You will independently prepare clinical and regulatory documents such as protocols, clinical study reports, investigator brochures, and summary documents. Additionally, you will be responsible for supporting submissions for market approval and line extensions with minimal supervision. Your proactive contributions will help develop and implement medical writing best practices and process improvements.

 

Who You Are:

 

Minimum Requirements:

 

• Experience: 6 to 10 years in regulatory medical writing.
• Education: Graduate or postgraduate degree in relevant fields (BPharm/MPharm, PhD, BDS, BSc/MSc).
• Comprehensive knowledge of medical writing theories, principles, and concepts.
• Familiarity with clinical and regulatory documents.

 

Maximum Requirements:

 

 

• Prepare clinical and regulatory documents independently.
• Support submissions for market approval and line extensions.
• Contribute to the development of medical writing best practices.
• Coordinate with other writers to ensure adherence to business objectives and company standards.
• Ensure timely production of documents in compliance with relevant SOPs and regulatory authority requirements.
• Participate in meetings related to key medical writing, quality control, and compliance activities.

 

 

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!