Regulatory Affairs Part-Time

Pfizer Türkiye

At Pfizer, we are working to “deliver breakthroughs that change patients’ lives”!

As active supporters of diversity and inclusion, we work to achieve our mission with our values of “Courage, Excellence, Equity, and Joy”. We declare, “There are no limits here when it comes to touching lives”, and we believe that “science will win”. In the Pfizer world we fell “the joy of working for life,” have a career path” full of opportunities,” and enjoy  a “flexible and pleasant working environment.”

We look forward to having you join us to challenge the status quo with breakthroughs, to change patients’ lives by always doing the best, to always do the right thing, to act responsibly towards each other and patients, and to be happy and proud of your job!

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