Pfizer Released Excellent Job Opportunity

Pfizer Released Job Openings On 09/05/2022. 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 Postgraduate in Pharmacy / Science with 9+ years of experience For Manager – Reg CMC Strategy, Brands CMC Position.Complete Details for the Manager – Reg CMC Strategy, Brands CMC as follows.

Important Details :

• Location :Chennai
• No of Vacancies:NA
• Details of Salary: Not Disclosed by Recruiter
• Opening date for online Application: 09/05/2022
• Mode of application :Online
• How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps

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Job Description/Skills Required

• Provide guidance, lead/co-lead projects, manage own time to meet objectives and plan resource requirements for projects across the division.
• Provide strategic regulatory input into WRS global regulatory strategies, thus providing optimal support for meeting local business objectives under Country Regulatory Head lead.
• Train Pfizer Consumer Healthcare Worldwide Strategy and Regulatory team on Pfizer systems and ensure integration into regional work processes.
• Responsible for the co-ordination of translations for core documents required for submission.
• Manage regulatory aspects of projects/products, including the preparation and submission of correspondence and applications to regulatory agencies.
• Support regulatory compliance activities with monitoring and reporting compliance in all critical points required of Worldwide Strategy and Regulatory systems.
• Maintain licenses in compliance with local regulations by ensuring that corporate regulatory processes, Standard Operating Procedures (SOPs) and systems are in place.
• Collaborate with HUB colleagues to ensure support is appropriately aligned with local High Availability requirements, maintain constructive relationship with HUB and proactively seek continuous improvement in HUB processes.
• Manages the compilation for core package build, contributing to (Clinical Trial Application) CTA and authoring documentation.
• Update and check recorded/newly entered data regularly and in timely manner according to the standard operation procedures/guidelines.

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