Genpact Released Job Openings On 26/05/2022.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 2022 are provided below. Interested and eligible candidates can submit application along with resume.
Vacancy Details:
Genpact Recruiting B. Pham,M.Pharm,Science Graduates with at least 9 to 14 year(s) of relevant experience for Head – Regulatory Affairs Position.Complete Details for the Head – Regulatory Affairs as follows.
Important Details :
- Location :Hyderabad/Secunderabad, Bangalore/Bengaluru, Delhi / NCR, Mumbai (All Areas)
- No of Vacancies:Not Disclosed
- Details of Salary:Not Disclosed
- Opening date for online Application: 26/05/2022
- 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
The Role demands for an experienced Submission Manager with demonstrated ability to execute responsibility in a highly regulated & process driven environment, the Person will be responsible for all the activities related to
• Managing the operations and team
• Taking care of administrative responsibilities of team
• Project & resource management
• Team management and team engagement
• Should be technical expert in eCTD/CTD submissions of US/EU/Canada and Row market
• Hands on experience on submissions
• Capability to trouble shoot technical validation errors
• Good client communication skills
• Publishing and performing technical validation (eCTD/CTD/NeeS/Paper) for Asia pacific, Europe Submissions and US submissions
• Performing final technical quality review.
• Dispatching submission to the relevant authority ((eCTD/CTD/NeeS/Paper) or affiliate so that affiliate can dispatch to authority;
• Performing post-submission processing activities such as receiving acknowledgement from authority of submission receipt; capturing and the electronic receipt and metadata in RIM; communicating submission receipt to key stakeholders;
• Capturing submissions-related correspondence from health authorities, such as uploading documentation, commitments and metadata.
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