Pfizer Released Job Openings On 21/05/2022. 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 05+ Years Experience For Regulatory Affairs and Labeling (Multiple Roles).Complete Details for the Regulatory Affairs and Labeling (Multiple Roles)Â as follows.
Important Details :
- Location : Visakhapatnam, Ahmedabad, Chennai, Mumbai (All Areas)
- No of Vacancies:NA
- Details of Salary: NA
- Opening date for online Application: 21/05/2022
- Mode of application :Walk In
- Time And Venue :Â 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
Interested candidates are requested to apply and fill in the form by accessing following link: https://forms.office.com/r/WV9g1SN2Uy
We are inviting applications from Regulatory Affairs professionals experienced in New drug development (NDD) & Life-cycle Management (LCM) submissions with Global Health Authorities for openings described below –
Regulatory Strategy Position Description:
To function as Global Regulatory Strategists responsible for developing & executing robust regulatory strategies (including CMC authoring & 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 Position Description:
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:
- 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.
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