Pfizer Released Job Openings On 09/08/2022. 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 B.Pharm,M.Pharm,M.S (Pharmacy),M.Sc/BE with 01+ years of experience For Associate -Validation Position.Complete Details for the Associate -Validation as follows.
Important Details :
- Location : Pendurthi
- No of Vacancies:NA
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 09/08/2022
- 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
Related Job: IQVIA Looking For B.Pharma,B.Sc,M.Pharma,M.Sc FRESHERS
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Job Description/Skills Required
- Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.
- Determine process capability of new equipment through execution of approved protocols and assure defined parameters are incorporated into respective operating procedures and batch records.
- Assists with development of validation protocols and manage Regulatory queries and responses.
- Participate in deviation investigations to identify root causes and define corrective and/or preventative actions.
- Adhere to all company and Good Manufacturing Practices {also cGMP} procedures, along with safety regulations within the plant and participates in developments of validation programs as needed to remain current with cGMPs and industry.
- Work effectively as a member of the Quality Operations (QO) Good Manufacturing Practices {also cGMP} training team as well as directly with Business Area Training Leads / Coordinators and SMEs within Quality to support Good Manufacturing Practices {also cGMP} and site training initiatives.
- Report to the Validation Section Manager, the Validation Engineer will assure that equipment, facilities, and utilities are validated in accordance with {Current} Good Manufacturing Practices {part of GxP} principles, regulatory requirements, and company policies and standards.
- Work on summarization of data into concise reports that is reviewed by the QO product professional and approved by production and quality management.
- Define problems, collect data, establish facts, and draw valid conclusion.
- Work in a team environment to meet all team objectives and communicate progress on scheduled projects.
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