Pfizer Walk-In Drive on 21st & 22nd May 2022 Multiple Locations

Pfizer Released Job Openings On 17/05/2022. Pfizer Inc. is an American multinational pharmaceutical corporation. Pfizer is one of the world’s largest pharmaceutical companies, and was ranked 64th on the 2020 Fortune 500 list of the largest U.S. corporations by total revenue, at $47.644 billion as of December 31, 2020 .

Vacancy Details:

Pfizer Recruiting Minimum Postgraduate in Pharmacy/Life Sciences Candidates with 02+ Years Experience For Regulatory Affairs professionals.Complete Details for the Regulatory Affairs professionals department as follows.

Important Details :

• No of Vacancies:NA
• Details of Salary: NA
• Opening date for online Application: 17/05/2022
• Mode of application :Walk In
• Time And Venue :  21st and 22nd May 2022,(9:00 am to 7:00 pm IST)The Oterra Hotel, # 43, Electronic City Phase 1, Hosur Road, Bengaluru-560100, India.

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Job Description/Skills Required

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.