Job Description
Job Title : Associate u2013 CSCC & RM
Job Description :
Description of required job responsibilities :
- Responsible for timely creation, compilation and distribution of Product Quality Report (PQR) as applicable from regulatory affairs system.
- Co-ordinate with affiliates and other stakeholders to gather required information to track certificates and sample status.
- Closely track the progress on the certificates and samples requests.
- Coordinate the Translation of documents required for submission with the registered vendor and timely deliver to the end user (country affiliates).
- Cordinate for sample request required for registration with affiliates.
- Task assignment to relevant stakeholders through accurate workflow management based on category of requests received.
- Timely update and archival of requests on Sharepoint for visibility of status to global affiliates.
- Bulk updates in regulatory affairs system, as applicable.
- Any other Operational activities based on business needs as and when requested.
- Exhibit good team player attributes and ownership to work closely with the team and actively coordinate with key stakeholders.
Specific Education / Competencies / qualifications required to perform the role :
Bachelor Degree in Biology, Chemistry, Pharmacy, Bio Science or equivalent.6 months to 2 years experience in regulatory affairs or related fields.Skills Required
Sharepoint, workflow management