Pfizer’s hiring for Global Regulatory Affairs team at Chennai, Ahmedabad, Mumbai & Vishakhapatnam
Are you an experienced CMC Regulatory Professional? If yes, then this opportunity is for you!
We are inviting applications from Regulatory Affairs professionals
experienced in developing strategy and authoring of CMC packages
for Life Cycle Management (LCM) submissions with various Global
Health Authorities, for our current job openings across all job levels
(Associates, Associate Managers, Managers, Principal Managers, Group Managers and Group Leads).
Be part of Pfizer’s Global Regulatory Affairs team!
Work location: Chennai, Ahmedabad, Mumbai & Vishakhapatnam
We are inviting applications from Regulatory Affairs professionals experienced in developing strategy and authoring of CMC packages for Life Cycle Management (LCM) submissions with various Global Health Authorities, for our current job openings across all job levels (Associates, Associate Mangers, Mangers, Principal Managers, Group Managers and Group Leads).
Experience:
2-15 years in Pharmaceutical Industry. predominantly in Global Regulatory Affairs function
• Experienced in authoring and review of high-quality regulatory submissions for new & post-approval supplements / variations) in global markets (US, EU, Canada, AnZ & RoW) for Sterile Injectables, Oral Solid Dosages (OSDS) and other dosage forms.
Preferred Qualification:
• Minimum Postgraduate in Pharmacy / Life Sciences
Interested candidates can share their resumes with [email protected]
Suitable candidates will be contacted by our People Experience team for a virtual 1:1 interview.
