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Regulatory Publisher

3 months ago

Bengaluru, Karnataka, India Indegene Full time
Looking to jump-start your career?


We understand how important the first few years of your career are, which create the foundation of your entire professional journey.

At Indegene, we promise you a differentiated career experience.

You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry.

We are offering a global fast track career where you can grow along with Indegene's high-speed growth.

We are purpose-driven.

We enable healthcare organizations be future ready and our customer obsession is our driving force

. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work.

Job Description:

EDUCATION:
BPharm / MPharm/ Pharm D/ MSc

EXPERIENCE:
Required 2-4 years of experience in ASEAN markets

LOCATION:
Bangalore, Hyderabad (Office-based/Hybrid)

SKILLS:

  • Handson experience in Lorenz Docubridge & Trackwise
  • Hands on experience on RIMS preferably Veeva Vault
  • Good communication skills (Written and Oral)
  • MS Office (Excel and Power point), Adobe Professional, ISI Toolbox

PRINCIPAL RESPONSIBILITIES & ACCOUNTABILITIES:

  • Experience with global regulatory submission formats, including familiarity with submission publishing activities
  • Thorough knowledge of major HA global/regional/national country requirements/regulatory affairs procedures for initial submission, licensing, post approval submission management
  • Markets Handled: Australia, Cambodia, Hong Kong, Korea, Malaysia, Macao, Indonesia, Pakistan, Philippines, Singapore, Taiwan Thailand, Vietnam
  • Prepare and compile global regulatory dossiers in ACTD, eCTD and non eCTD format in accordance with ASEAN HA legislations and client specific requirements
  • Thorough understanding of all aspects of the publishing software, tools, process, and output requirements.
  • Performs eCTD readiness/prepublishing tasks (i.e., formatting and document navigation) and assist Medical Writers in the development and compilation of appendices and publishing of various regulatory documents
  • Perform publishing QC tasks within the electronic publishing system and QC of the published output to ensure high submission quality. Perform document quality control checks for others in the department, promptly communicating irregularities in documents and coordinating issue resolution.
  • Dispatch submissions to Regulatory Authorities via agency portal, through customers or directly.
  • Operates in compliance with regulations, company policies, procedures, and processes.
  • Analyse challenges/limitations in dossier publishing and provide logical, unbiased and rational recommendations for modifying quality standards or introducing newer ones
  • Coordinate with crossfunctional teams, including R&D, quality assurance, and manufacturing, to gather necessary information and documentation for dossier preparation
  • Regular tracking and maintaining the submission trackers
  • Stay updated with evolving regulatory requirements and industry trends and able to extract regulatory intelligence information (requirements for initial filing, drug/device/cosmetic/food registration etc.)
  • Participate in trainings and learn through handson experience on the job
  • Exhibit flexibility in moving across new projects and preparing multiple document types
  • Continuously enhance and maintain knowledge of various regulatory guidelines for different deliverables by doing various assignments
  • Volunteer in training programs to develop skills in areas relevant to the job in addition to the areas of interest

EQUAL OPPORTUNITY
We are an Equal Opportunity Employer.

All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.