Associate – CSCC & RM role at Abbott | Apply now for Regulatory Affairs Jobs in Mumbai | Pharma Sector
Looking for Regulatory Affairs Jobs in a leading global healthcare company? This Associate – CSCC & RM opportunity at Abbott Laboratories in Mumbai is an excellent option for professionals seeking growth in Pharma Jobs within the Regulatory Affairs domain. This role offers hands-on exposure to regulatory affairs systems, Product Quality Report (PQR) management, documentation coordination, and collaboration with global affiliates. If you have a background in Biology, Chemistry, Pharmacy, or Bio Science, this position provides strong career progression in Regulatory Affairs Jobs and Pharma Jobs.
- Job Title: Associate – CSCC & RM
- Location: India – Mumbai
About the Company
Abbott Laboratories is a global healthcare company devoted to helping people live more fully at all stages of life. With a broad portfolio of science-based products in diagnostics, medical devices, nutrition, and branded generic pharmaceuticals, Abbott operates in more than 160 countries and is recognized for innovation, quality, and regulatory excellence in the Pharma sector.
Job Description
- Responsible for the timely creation, compilation, and distribution of Product Quality Report (PQR) as applicable from the regulatory affairs system.
- Coordinate with affiliates and other stakeholders to gather required information to track certificates and sample status.
- Closely track the progress of the certificates and sample requests.
- Coordinate the Translation of documents required for submission with the registered vendor and timely delivery to the end-user (country affiliates).
- Coordinate for sample requests required for registration with affiliates.
- Task assignment to relevant stakeholders through accurate workflow management based on the category of requests received.
- Timely update and archival of requests on SharePoint for visibility of status to global affiliates.
- Bulk updates in the 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.
Key Responsibilities
- Product Quality Report (PQR) creation and distribution
- Certificate and sample tracking coordination
- Regulatory documentation translation coordination
- Workflow management and stakeholder task assignment
- SharePoint updates and request archival
- Regulatory affairs system bulk updates
- Cross-functional coordination with affiliates
Qualifications
- Bachelor’s Degree in Biology, Chemistry, Pharmacy, Bio Science, or equivalent.
- 6 months to 2 years of experience in regulatory affairs or related fields.
