Regulatory Affairs Specialist II Role at Teva Pharmaceuticals | M. Pharm Freshers Job Opportunity

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M.Pharm Freshers Job at Teva Pharmaceuticals | Apply Now
M.Pharm Freshers Job at Teva Pharmaceuticals | Apply Now

M. Pharm Freshers Job at Teva Pharmaceuticals | Regulatory Affairs Role | Apply Now

Are you looking for an exciting M.Pharm Freshers Job in the pharmaceutical industry? Explore Teva Pharmaceuticals Careers with this excellent opportunity for a Regulatory Affairs Specialist II role. If you are passionate about Regulatory Affairs Jobs and want to build a global career, this position in Navi Mumbai could be your perfect start. Notably, this is a great M.Pharm Freshers Job for candidates seeking regulatory affairs roles.

About the Company

Teva Pharmaceuticals is a leading innovative biopharmaceutical company, enabled by a world-class generics business. The company focuses on advancing treatments in neuroscience and immunology while delivering high-quality medicines worldwide. With a strong emphasis on collaboration, innovation, and employee growth, Teva offers a dynamic environment for professionals pursuing Regulatory Affairs Jobs and M. Pharm Freshers Job opportunities. In fact, securing an M.Pharm Freshers Job here can be a significant advantage for your career.

Job Details 

  • Position: Regulatory Affairs Specialist II
  • Location: Navi Mumbai, India
  • Job ID: 67021

Key Responsibilities 

  • Publish and dispatch major and complex routine/lifecycle management eCTD submission projects for EU, US, and Canada.
  • Exposure in handling post approval submissions, publishing, and transmitting quality submissions to the agency.
  • Perform document-level publishing activities, troubleshoot document issues, and perform quality control checks for submission-ready documents as per the agency guidance.
  • Collaborate with scientific personnel for planning, preparation, and publishing.
  • Maintain working knowledge of internal and external publishing standards.
  • Basic knowledge of ICH and eCTD-related specifications/guidelines governing regulatory submissions (eCTD, NeeS, paper).
  • Must be aware of technical systems like Global Insight, Veeva Vault, ISI Toolbox, Adobe Acrobat, and Lorenz Validator.

Qualifications 

  • B. Pharm: Minimum 2 years of experience in Regulatory Affairs
  • M. Pharm/ Master of Life Sciences: 0-1 year of experience in Regulatory Affairs

Experience 

  • 0–1 year (M. Pharm candidates). Ideal for freshers seeking an M.Pharm Freshers Job in this profile.
  • Minimum 2 years (B. Pharm candidates)

Skills Needed 

  • Command over spoken and written English
  • Sensitivity to the cultural diversity of a global organization
  • Good understanding of regulatory IT systems

Start your journey with Teva Pharmaceuticals Careers today and secure a promising M. Pharm Freshers Job in Regulatory Affairs Jobs with global exposure and career growth.

APPLY ONLINE HERE

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