Genpact Vacancy for Technical Associate - Regulatory Affairs ,
Pharmacy/Science
The Role demands a self-driven Individual contributor who
will be responsible for all the activities related to –
Publishing of Renewals, Baseline Renewals for EMEA, ASIAPAC,
LATAM etc.
Publishing submissions using liquent insight publisher,
Extend and validating submissions using insight validator, Global summit,
Lorenz validator.
Ensure Documents provided in the submission content plan are
accurate through RCAM application.
Annual Report Submission publishing, Quality checks and
dispatch it through FDA ESG Gateway.
Preparation of work instruction guide.
Conducting training of new onboarded team members.
Maintain the record of the country profile sheet of Renewal
publishing.
Supervising updates of a new regulatory requirement for
publishing.
Ensure adherence to the specific project specifications or
standards throughout the lifecycle of submissions.
Conducts performance appraisals. Provides measurable feedback
to assigned personnel and suggestions for improved performance. Formulates and
implements employee corrective actions as needed. Should be able to coach,
mentor and help all his/her direct reports to be motivated and engaged to grow
their career with Genpact. Assists in interviewing and assigning new personnel
as vital
Qualifications
Minimum qualifications
Any graduate/Post graduate degree or equivalent with a good
academic record
Preferred Qualifications / Skills
Pharmacy/Science
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