Job Purpose:
The Regulatory Affairs Pharmacist is responsible for assisting the Regulatory Affairs Manager with the end to end cycle of product registration across the Sub Saharan Africa. The Regulatory Affairs Pharmacist is a self-driven individual to manage the therapeutic portfolios assigned to relevant countries, in every aspect of new product submission, product registration and life-cycle management by ensuring high quality, timeous submissions, responses and approvals. He/ she will conduct and complete technical and administrative duties on dossiers.
Key Accountabilities:
Provide Regulatory intelligence
Ensure pre-launch statge product submission and registration activities
Ensure dosier life cycle management registration activities
Support and enable delivery for the Cipla India SSA, CGA and CiplaQCiL team
Develop and manage stakeholder relationships
Ensure execution of all regulatory Activities
Cross functional integration support
Qualifications:
Bachelor in Pharmacy, Post graduate qualifications are an added advantage
Relevant experience:
5 years’ experience in the pharmaceutical industry. Experience in regulatory affairs, manufacturing and managing others desirable
Apply via :
www.linkedin.com
