Pfizer QA & Control Validation Job Openings in both Fresher & Experienced Candidates. interested & Eligible Candidates apply. Application Link Mentioned below

Job Responsibilities :

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 Pharmacy / M Pharmacy /M.S (Pharmacy)/MSc/BE

Experience : Fresher to 03 years.

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.
Knowledge of current validation regulations in the industry.
cGMPs and FDA , MHRA, TGA, MCC etc. regulatory guidelines and validation principles.
Excellent attention to detail and working knowledge of Food and Drug Administration Regulations/Guidance, and Good Manufacturing Practices
Excellent organizational skills, and ability to handle changing deadlines
Strong communication with written and verbal skills
Working knowledge of Microsoft Office, especially Excel for evaluation of data

Nice-to-Have

Technical writing experience
Pharmaceutical Industry with laboratory process validation experience
Working knowledge of equipment qualification and calibration specifically for laboratory equipment

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.

Pfizer Job Opening – Apply Here

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