Apply now »

We are experiencing a technical issue with the Careers Website. At the moment, applications are not possible. We are working on resolving the issue as soon as possible. Thank you for your patience. 

Manager - Submission Management

 

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:

 

In this pivotal role, you will lead and shape the Submission Management sub-team within Global Regulatory Affairs, ensuring that every regulatory submission meets the highest standards of quality, compliance, and timeliness. You will be accountable for the day-to-day performance of your team — setting priorities, coaching team members, and driving continuous improvement across submission processes. As the primary expert for electronic Common Technical Document (eCTD) and submission management, you will guide your team through complex regulatory challenges, harmonize activities across functional areas, and serve as a key point of contact for submission-related expertise.

You will collaborate closely with cross-functional stakeholders to establish and monitor key performance indicators, support onboarding and capability development, and ensure the long-term sustainability of your team’s knowledge and capacity. Operating in a dynamic matrix environment, you will play a central role in streamlining regulatory operations and aligning submission activities with the broader strategic objectives of the organization.

 

Who You Are:

 

  • You bring 9 to 11 years of professional experience in regulatory publishing and submission management within the pharmaceutical industry, with at least 2 years in a team leadership or supervisory capacity.
  • You hold a degree in Pharmacy, Life Sciences, or a related scientific discipline, or equivalent professional experience.
  • You have deep expertise in electronic Common Technical Document (eCTD) standards and submission processes, and are recognized as a subject-matter authority in this area.
  • You are proficient with regulatory information management platforms and electronic document management systems used in submission workflows.
  • You have a proven track record of monitoring and improving compliance with submission standards, Health Authority requirements, and standard operating procedures.
  • You communicate with clarity and confidence, and are skilled at building effective relationships with stakeholders across functions and geographies in a matrix organization.
  • You demonstrate strong people leadership capabilities, including performance management, coaching, talent development, and fostering an inclusive and engaging team culture.
  • You bring familiarity with electronic submission management tools and an interest in continuously improving submission quality and process efficiency.

 

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!

Job Requisition ID:  303367
Location:  Bangalore
Career Level:  E - Professional (10+ years)
Working time model:  Full-time

North America Disclosure
The Company is committed to accessibility in its workplaces, including during the job application process. Applicants who may require accommodation during the application process should speak with our Candidate Services team at 844-655-6466 from 8:00am to 5:30pm ET Monday through Friday. If you are a resident of a Connecticut or Colorado, you are eligible to receive additional information about the compensation and benefits, which we will provide upon request.  You may contact 855 444 5678 from 8:00am to 5:30pm ET Monday through Friday, for assistance.

Notice on Fraudulent Job Offers
Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information.


Job Segment: R&D, Pharmaceutical, Document Management, Pharmacy, Oncology, Research, Science, Technology, Healthcare

Apply now »