Genpact Great Opportunity For B.Sc,M.Sc,B. Pharmacy,M. Pharmacy Graduates

Genpact Released Job Openings On 23/04/2022.Genpact (NYSE: G) is a global professional services firm focused on delivering digital transformation for our clients, putting digital and data to work to create competitive advantage. We do this by integrating lean principles, design thinking, analytics and digital technologies with our domain and industry expertise to deliver disruptive business outcomes – an approach we call Lean DigitalSM…Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Genpact Recruitment 2021 are provided below. Interested and eligible candidates can  submit application along with resume. 

Vacancy Details:

Genpact Recruiting B.Sc,M.Sc,B. Pharmacy,M. Pharmacy Graduates with 01+ Years of Experience for Lead Consultant – Regulatory Affairs Position.Complete Details for the Lead Consultant – Regulatory Affairs as follows.

Important Details :

• Location :Mumbai 
• No of Vacancies: Not Disclosed by Recruiter
• Details of Salary: Not Disclosed by Recruiter
• Opening date for online Application:23/04/2022
• 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

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Job Description/Skills Required

• Responsible for implementing CMC regulatory strategies for assigned consumer products in accordance with global regulations, guidances and defined regulatory strategies.
• Responsible for the writing of CMC quality documents for the dossier and/or the entire module 3 from raw data.
• Review and evaluation of existing quality documentation and assessment of required updates during Project Renewals.
• Preparation of Quality Overall Summaries (QOS);
• Compilation of dossiers for launch applications for marketing authorization and new drug applications in Global markets.
• Submission of relevant sections in Annual Reports for US Market.
• Preparing RA expert response for deficiency letters from various regulatory authorities;
• Assessment of registration documentation for consumer products as per the current Health Authority requirements.
• Knowledge of review and assessment of manufacturing, analytical, validation and stability documents.
• Post-approval submission knowledge for EU markets

Click here for Official notification and Apply