Pfizer Limited Walk-in Interview 2023.Pfizer Limited Notification full details below. Interested and eligible candidates can attend interview on scheduled time and venue.Life, it is the underlying purpose of everything we do at Pfizer. A purpose that defines our R & D strategy of discovering and developing innovative products that improve the quality of life. The worlds number one healthcare company, we have an annual turnover exceeding US $ 54 Billion and an annual global R & D spend of over US $ 7 Billion. 

Vacancy details:

• Post Name: Associate – Validation
• Qualification: B.Pharm/ M.Pharm/M.S (Pharmacy)/M.Sc/BE
• Experienced:2+ years of experience in quality assurance and /or validation function of sterile dosage form facility.

Job Description: Greeting from Pfizer Limited !!!!

Important Details :

• Location: Vishakhapatnam
  
• Post of date:28/03/2023
• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

How You Will Achieve It

• 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.

Qualifications

B.Pharm/ M.Pharm/M.S (Pharmacy)/M.Sc/BE

2+ years of experience in quality assurance and /or validation function of sterile dosage form facility.

Must-Have

• Knowledge on the Qualification lifecycle for the batch manufacturing and process equipment.
• Knowledge on the Qualification lifecycle for the manufacturing, Lab and packing equipment.
• Knowledge on the preparation and Review of qualification protocols.
• Knowledge on sampling techniques.
• Adherence to Safety Procedures/GMP & Good Documentation Practices.
• Execute validation of manufacturing equipment, visual inspection equipment, packing equipment, Utilities, LAB equipment, Cleaning Validation and Process Validation in accordance with regulatory requirements, cGMPs, corporate policies and procedures and as per schedule.
• Operation and Calibration of KAYE Validators and validation Accessories.
• Coordinate and plan validation activities with Manufacturing, QC, Microbiology and Projects.
• Performs Data analysis, Investigation of validation deviations for the root cause identification. 
• Compile validation documents and results.
• Execution/ oversite of executions and reporting of deviations.
• Assisting to Reporting during Validation planning and execution.
• Perform Risk assessment to establish the scope and extent of validation activities.
•  Assist reporting manager in performing the Risk assessment to establish the scopeand extent of validation activities.
• Understanding of pharmaceutical manufacturing, packaging, quality assurance, and quality control operations.
• Knowledge of validation principles and practices related to the following areas: manufacturing process, analytical method, cleaning methods, facility, equipment, instrument, utility system, and CSV systems.
• Conversant with design & working principles of key equipment used in sterile manufacturing –autoclave, tunnel, lyophilizers, homogenisers, filling machine, filter integrity testing devices.
• Well versed with Terminal process – design, execution and review.
• Experience in plant and QC lab operations
• Good document written skills, with ability to identify issues and recommend actions.

Nice-to-Have

• Knowledge of current validation regulations in the industry.
• cGMPs and FDA , MHRA, TGA, MCC etc. regulatory guidelines and validation principles.

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Quality Assurance and Control

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