Regulatory Affairs Specialist at Cipla

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