Pfizer Healthcare India careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place. We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place. It was Charles Pfizer’s vision at the beginning and it holds true today.
Pfizer’s | Walk-In Drive at Bangalore on 21st and 22nd May 2022
Be part of Pfizer’s Global Regulatory Affairs team!
Work location: Chennai, Ahmedabad, Mumbai & Vishakhapatnam
Walk-in drive at Bangalore on 21st and 22nd May 2022 (9:00 am to 7:00 pm IST)
Venue: The Oterra Hotel, # 43, Electronic City Phase 1, Hosur Road, Bengaluru-560100, India.
Inviting applications from Regulatory Affairs professionals experienced in New Drug Development and Life-cycle Management (LCM) submissions with various Global Health Authorities, for openings in
Regulatory Strategy:
- To function as Global Regulatory Strategist responsible for developing and executing robust regulatory strategies (including CMC authoring and review) for the assigned products/projects.
- Experience: 2-15 Years in Pharmaceutical Regulatory Affairs function experienced in authoring & review of high quality regulatory submissions (INDs/ IMPDS/ NDAU ANDA MAA Post-approval variations) in Global markets (US, EU, Canada, Anz & Row) for Sterile injectables, OSDs & other dosage forms for small and large molecules (Biologics/ Biosimilars)
Labeling:
- To function as Global Labeling Lead (GLL) with overall accountability for the initial creation and relevant updates to labeling documents, and driving the labeling strategy for the assigned products. This includes, ensuring development and maintenance of CDS, USPL SPC for products registered in EU and their associated Patient Labeling Documents
- Experience: 8-12 years of pharmaceutical labeling experience in content development and maintenance (CDS, USPI, SPC and other country labels, etc. Perspective from HQ Country office and/or Regional Regulatory Strategy (at a global/multi-national pharmaceutical environment) necessary. Experience at the country level important and advantageous
- Qualification: Minimum Postgraduate in Pharmacy/Life Sciences
Are you an experienced Regulatory Affairs professional aspiring for an exciting opportunity?
Then walk-in for a discussion with our technical and Candidate Experience team on 21 and 22 May in Bangalore, The Oterra Hotel.
Also Read: Ajanta Pharma Limited – Walk-In Interview for Manufacturing / Packing on 22nd May’ 2022 @ Baddi
Also Read: Syngene International Ltd – Virtual Recruitment Drive for Multiple Positions on 22nd May’ 2022
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