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Sr Systems Specialist, Global Regulatory Operations

Req #: 1700675
Location: Summit, NJ US
Job Category: Regulatory Affairs
Work Location: 86 Morris Avenue CELSUM 07901
Organization: Celgene Corporation
Schedule: 40
Employee Status: Full time
Job Type: Regular
Job Level:
Other Locations:US- NJ- Summit East


Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health.  We value our passion for patients, ​quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries, and growing - we look for talented people to grow our business, advance our science and contribute to our unique culture.

Responsibilities will include, but are not limited to the following:

  • Support day to day management of the Global Regulatory Information systems including but not limited to:
    • eSub (Electronic Document Management System)
    • eCTDXPress (eCTD Submissions Publishing System)
    • GLTS (Labelling Tracking System)
    • eQRMS PR module (Submissions Tracking System)
    • Pre-Approval Access (SharePoint Workflows System)
  • Provides regulatory systems training and support to new users and current users.
  • Collaborate with users to develop an understanding of business needs and take those business needs to next level
  • Work collaboratively with multi-site team members and cross-functional departments
  • Maintains/updates user & training materials.
  • Ensures compliance with SOPs and WPs.  Supports development of new SOPs, WPs, or best practices documents for regulatory systems.
  • Support technology roadmap for Global Regulatory Affairs

    Skills/Knowledge Required:

  • 3-5 years of pharmaceutical industry experience required. Regulatory systems experience will be preferred.
  • Good written and oral communication skills.
  • At least 2 years of working experience on document management systems, such as Veeva, Documentum, SharePoint or OpenText Content Server
  • Good business documentation writing skills
  • At least 2 years of experience in creating training material and providing user training
  • Ability to work and contribute in a team environment.
  • Ability to perform tasks proactively with minimal supervision.
  • Experience with regulatory systems in a life sciences industry
  • Ability to effectively interface with business users and the technical team.

Strong attention to detail


BA/BS in a relevant discipline; 3-5 years in a Life Sciences industry experience


Celgene is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Celgene complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must have authorization to work for Celgene in the U.S.
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About Celgene

Celgene is a global biopharmaceutical company committed to improving the lives of patients worldwide. At Celgene, we seek to deliver truly innovative and life-changing treatments for our patients.

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