Regulatory Affairs

Job Summary

Company
Cognizant Technology Solutions Asia Pacific Pte. Ltd
Industry
• IT/Computers - Software • Pharmaceutical
Location
Singapore
Years of Experience
1 - 5 years
Function
Pharmaceutical/Biotechnology
Posted On
30th Dec 2020
Skills
Regulatory Affairs, regulatory documentation, quality control

Job Description:

Job Description:

Primary Skills:

  • Required Degree in Science, Computer science or Pharma
  • Should have 1-5 year of experience in pharmaceutical industry / Medical Device / any related industry is must
  • Should have minimum 1+ years of experience in regulatory affairs is mandatory
Roles and Responsibilities:
  • Responsible for global regulatory submission / dossier publishing day-to-day activities and deliverables.
  • Compilation and maintenance of regulatory documentation as per the procedure in client repository.
  • Performing high level of files’ formatting using the client provided software (creating bookmarks, hyperlinks, file optimization etc.).
  • Performing peer-review of work and providing support to other regulatory related activities as per the business requirements.
  • Interacting with relevant stakeholders during preparation and quality control of reports and regulatory documentation
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About Us:

Cognizant is a global leader in business and technology services that helps Clients bring the future of work to life – today – in a business environment that is being transformed by accelerating globalization, virtualization, and the shift toward cloud technologies.

We continuously seek the “best and the brightest” when we recruit new employees, and we’re consistently an “employer of choice” at leading engineering and business schools around the world. Our domain industry specialists have well-established backgrounds working with companies in the industries we serve.

Our teams and their talent are a principle reason that we consistently outperform the competition.


Disclaimer: