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PHARMA JOBS POST > Walk In Interview > Be part of Pfizer’s Global Regulatory Affairs team |Walk-in drive at Bangalore on 21st and 22nd May 2022
Walk In Interview

Be part of Pfizer’s Global Regulatory Affairs team |Walk-in drive at Bangalore on 21st and 22nd May 2022

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Last updated: May 16, 2022 2:54 pm
ADMIN 3 years ago 252 Views
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Be part of Pfizer’s Global Regulatory Affairs team |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)

Also Read : Ajanta Pharma Walk In Interview @ Baddi for various positions in Manufacturing & Packing department on 22/05/2022

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.

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