Regulatory Affairs Part-Time

Pfizer Türkiye

QUALIFICATIONS

What we expect from you:

• Scientific degree from Pharmacy, Biology, Chemistry or Chemical Engineering departments
• Have a good command of written and spoken English 
• Have good Planning and coordination skills
• Have good communication-influencing skills
• Be familiar with legislation governing the activities of the pharmaceutical industry
• Be computer literate (Word, Excel, PowerPoint, etc.)

JOB DESCRIPTION

• Complete assigned tasks for preparation of the New Drug Application (NDA), GMP submissions, lifecycle maintainance activities (label updates, variations, renewals, etc.) for registered products and correspondences with the authority 
• Archive all registration relevant documents
• Update the electronic global and local databases according to the current SOPs
• Check package & leaflets to ensure complaince
• Completion and follow-up of assigned tasks for ongoing projects