Job Description

Senior Analyst - Regulatory Affairs

========================================


Chennai
2.5-5 Years
INDIA

Job Family

Development (Development)

(Posting).

Experience with proofreading tools and version comparison techniques Proficiency in Adobe Illustrator and Adobe InDesign Strong understanding of medical device labeling standards and print production Familiarity with regulatory symbols, UDI, IFU formatting, and compliance documentation Excellent attention to detail and organizational skills (1.) To interact with the customer and internal teams to gather requirements for development purposes. (2.) To perform activities related to enhancement creation of documents for CMMi and client requirements (3.) To provide technical guidance to junior developers (4.) To maintain existing features, troubleshoot bugs , resolve ad-hoc requests and provide support for enhancement (major and minor) /new developments based on business/ client requirements as well as from the functional and technical team of HCL on the project. (5.) To provide client support by presenting data, information, ticket resolution and day to day support activities like monitoring client requirements as well as keeping track of schedule for on time delivery of assigned tasks as per the defined quality standards.

Qualification

B-Tech

No. of Positions

1

Skill (Primary)

Domain Competencies (ERS)-Labeling-Labeling Requirements

Auto req ID

1590991BR