TCS Regulatory affairs jobs for B pharm & M pharma Candidates

Tata Consultancy Services(TCS) Released Job Openings On 06-11-2021.Tata Consultancy Services is the largest IT company in India. It is the sole subsidiary of the Tata Group. It is headquartered in Mumbai, India. TCS operates in 149 locations, including 46 countries..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Tata Consultancy Services(TCS) s Group Recruitment 2021 are provided below. 

Vacancy Details:

Tata Consultancy Services(TCS) Recruiting B pharm & M pharma candidates with 5 to 10 years. A maximum of 10 years of Regulatory Affairs pharmaceutical or related experience is required. US/EU experience will be preferred for  Regulatory Technical Services Professionals.

Important Details :

• Location :  Mumbai / Bangalore / Delhi / Gurgaon
• No of Vacancies:Not Disclosed
• Details of Salary:Not Disclosed
• Opening date for online Application: 06-11-2021
• Mode of application :Online
  
• How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

Job Description/Skills Required

• Be responsible for leading the operational management and delivery of regulatory submissions to support the development, registration, and compliance of products.
• Collaborate on the coordination of the preparation and maintenance of regulatory submissions and filings. Lead Submission Team meetings and influence stakeholders, as applicable.
• Create and manage the Dossier Plan(s)/Submission Packages in line with the regulatory strategy. Seek input from regulatory therapeutic areas, functional area representatives, and key stakeholders. Provide guidance to project team members.
• Assess, prepare and compile regulatory submissions (e.g. safety labeling changes, CMC, administrative, safety etc), ad hoc reports and maintain the life cycle of currently marketed products. Assist in the preparation and submission of larger submissions including new applications, variations, line extension etc
• Assist in the preparation and review of responses to and Notice of Deficiency [NOD]), RFPs in a timely manner.
• Participate in interactions and assist in negotiations with Health Authority Negotiations if any
• Work with global regulatory teams and the Global Regulatory Affairs (GRA) function/teams to facilitate regulatory activities.
• Support the resolution of emerging issues (e.g. new safety or quality finding) and the associated risk communications to stakeholders.

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