• Gurugram
  • Save Job
  • 14 - 16 Years
  • Posted : above 1 month

Job Description:

Illustrative Responsibilities

Strategic Regulatory Affairs Quality Compliance (SRAQC) department is responsible for regulatory and quality compliance for the entire Johnson Johnson Medical franchise in India and IB Countries (SriLanka , Bangladesh , Maldives , Nepal Bhutan)

This role is responsible for managing all facets of regulatory and compliance support to JJ products including any new integration and divestiture project in IB market This includes development of regulatory strategies , submissions , reviewing labelling and promotional materials , providing guidance and consultation for local regulations , interacting with government authority , participating in industry working groups , leading compliance initiatives , managing a staff of regulatory professionals , and managing regulatory projects and budget An understanding of Johnson Johnson products and their use as well as an understanding of the regulations and their application is required

Shape the India BIS standards by working with authorities and source companies
Overall responsible for regulatory deliverables from initial product registration to EOL for IB Market
Works closely with Regional , Country , and Global teams to drive new registrations and maintain registrations
Lead responsible for all acquired business integration and divestiture project completion in the IB market , as per defined strategy
Support Transformation project team for timely fillings and remediation s in IB market
Defines , communicates , and implements regulatory strategies and plans
Directs to comply with QMS , procedures , and controls within Regulatory function
Acts as advisor to subordinate supervisors or staff to help meet established schedules or resolve technical or operational problems
Plans and manages IB Regulatory Affairs budget , resources , and projects Responsible for oversight and prioritization of departmental tasks and projects Directs and oversees the work of regulatory professionals , including training , mentoring , and professional development
Ensures People Development through internal external trainings
Ensuring coordination with QA , Medical Affairs and other stakeholders in managing field action/ adverse event reporting to meet local country regulatory requirements
Review promotional materials for regulatory compliance and act as regulatory expert to develop teams
Interface and coordinate with regulatory agencies/competent authorities on submissions , approvals , audits or other issues
Interpret existing and/or new regulatory requirements as they relate to company products and procedures Communicate this to appropriate personnel
Understands and influences local medical device regulatory environment by leveraging key relationships with regulatory authorities and industry groups Participates in working groups
Interprets and applies local regulations to business practices and provides regulatory input , advice , and guidance to the organization
Responsible for Regulatory Compliance , which includes
Oversees review of labelling , including relevant internet activities to comply with all relevant internal policies/procedures and local country regulations

Coordinates with Business Quality/ Regional QA/Regulatory Compliance Leader on Quality field actions PMS

Sound knowledge MOH set up , drugs act and registration Procedure
Good understanding of ISO/GHTF regulations
Implement QMS systems and generate SOPs
Completes other regulatory activities as assigned by Department Head

Qualifications
Minimum requirements
Postgraduate - Post Graduate- Life science/ Bio Medical/ Pharmacy

Minimum 14- 16 years Industry Experience in Regulatory Affairs , preferably in medical devices

Experience in People development and management

Experience in research/DD , manufacturing and regulatory affairs in medical devices

Experience of Submitting , Registering and maintaining Product registrations with Global Regulatory Authorities

Professional training a plus

Understanding of product development , protocols , research reports , and dossier preparation

Experience in assembling product dossiers for submission to Regulatory Authorities

Good understanding of ISO/GHTF regulations

Good technical writing and communication skills

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Profile Summary:

Employment Type : Full Time
Industry : FMCG / F&B
Salary : Not Disclosed
Deadline : 07th Jun 2020

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