Pfizer Released Job Openings On 29/11/2022.Pfizer Inc. is an American multinational pharmaceutical and biotechnology corporation headquartered on 42nd Street in Manhattan, New York City
Pfizer Recruiting Bachelors/Master or Ph.D in Biotechnology/Pharmacy/Science/Engineering/Biological Sciences with 04-06+years experience for Regulatory Affairs, Medical Devices position.Complete Details for the Regulatory Affairs, Medical Devices as follows.
Important Details :
- Location : Chennai
- No of Vacancies:Not Disclosed
- Details of Salary: Not Disclosed
- Opening date for online Application: 29/11/2022
- 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
Job Description/Skills Required
Maintenance of the expansive combination of CMC product information, market registration details, component level dossier content and compliance of an integrated regulatory change management process to provide a comprehensive and compliant view of the CMC registered details of all products in all markets, in support of Global Devices Team.
Assuring product compliance through timely and accurate maintenance of CMC submission documentation and product knowledge in Regulatory systems in collaboration with Global Devices.
Contribute to GCMC projects, initiatives & actions along with prioritizing assigned workload appropriately.
Mentors team(s) of regulatory strategists responsible for device related submissions; coordinates and presents regulatory data needs and negotiates with and/or influences management, cross functional teams and external partners to ensure regulatory data requirement and the deliverables are met.
Serving as CMC representative on a core project(s) demonstrating ability to manage project activities, assess regulatory risks & development plans to develop global regulatory strategies for programs in accordance with regulatory, scientific & technical criteria. Manage regulatory issues, maintain submission information in relevant GCMC systems, tracks regulatory commitments & timelines for specific projects/products/markets with minimal supervision.