Pfizer Released Job Openings On 10/05/2022. 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 Candidates with 01+ 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: 10/05/2022
- Mode of application :Walk In
- Time And Venue :  14th and 15th May 2022,9:00 am to 7:00 pm IST,Lemon Tree Premier – Hyderabad
Plot No.2, Survey No.64, Hi-Tech City, Madhapur, Hyderabad 500081
Related Job : Syngene International Ltd Walk-In Interviews On 15th May 2022 for Multiple PositionsÂ
For more Latest pharma jobs https://pharmajobscooin.wordpress.com/
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 inÂ
Regulatory Strategy:
To function as Global Regulatory Strategist responsible for developing and executing robust regulatory strategist (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/ NDAs/ ANDAs/ MAAs/ 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, USPI, SPC for products registered in EU and their associated Patient Labeling Documents.
Experience:Â 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:Â Minimum Postgraduate in Pharmacy / Life Sciences



No Responses