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Abbott Regulatory Affairs Specialist in New Delhi, India

RESPONSIBLE FOR

  • Execute strategies developed for regulatory approvals as per annual registration plans

  • Technical Evaluation of the dossiers and files and compilation for submission in India

  • Working cohesively with Business Unit on the additional requirements for the product approval, response to queries

  • Work with Labeling team to be compliant to India Specific labels as per local regulation

  • Manage Product Release Approval (PRA)/GTS Release post approvals after India Specific labels are released

  • Support Sales team with regards to any regulatory documents required for tender approval

  • Coordinate with India Marketing team

  • Prepare and submit all PSURS, PMS reports, Adverse Event Reports and other safety reports to the regulators

  • Regularly gets updated and self-trained with the latest regulations on Medical devices in the country

  • Networking and Liasioning with the Regulatory agencies both at centre and state level

  • Creates / develops regular checklists based on overall business regulatory plans as assigned.

  • Support Evaluation of adequacy and compliance of systems, operations and practices against regulations and company documentation

  • Support in Tracking emerging issues and identify solutions

  • Support Field Safety Corrective Action / Recall, Corrective & Preventive Actions (CAPA)& Stop Shipment

  • Support Internal & External Quality & Compliance Audits

  • Provide feedback on the new procedures (SOP or DOP) being developed by International quality & compliance team

An Equal Opportunity Employer

Abbot welcomes and encourages diversity in our workforce.

We provide reasonable accommodation to qualified individuals with disabilities.

To request accommodation, please call 224-667-4913 or email corpjat@abbott.com

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