experience from Regulatory Affairs/QA in the pharmaceutical industry.
preparing & handling stringent country registrations, worked on CTD/ACTD formats.
- Understand and be oriented towards the ERP system as a tool and use it
efficiently within own area of work.
- Active and proactive in everyday issues as a solution oriented provider with
decision making capabilities.
- Understand the role of RA in the Project Life Cycle in Companyâs core business.
- Exposure in preparation of technical data for product information &
leaflets.
- Should be a team player/builder and coordinator to ensure an efficient process
and communication.
- Should be a strong coordinator with decision making capabilities.
oriented, efficient with ability to follow up conduct meetings and report.
- Ability to use current job-related computer software, with proficiency in
Microsoft office in particular Work, Excel, power point is required.
- Should follow core values.
Good English skills verbally and in writing. Monster IN - 1 day ago - save job - block |
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