Pfizer Deputy Manager in Chennai, India

Validation

Ensures that quality control procedures adequately evaluate an organization's products. Determines if current methods and techniques result in meeting reliability standards or require modification. (More concerned with standards, methods and procedures than with testing devices and equipment used to check products). Devises equipment to assure reliability of product in conjunction with product design and specifications. Performs laboratory equipment qualification used in testing of finished products, raw materials, and in-process material in support of the company's quality control program. Prepares reports and/or exercises administrative control in support of the company's quality control program.

Accountable for activities involved in the evaluation, review and approval of the validation master plan, validation protocols and reports and typically includes developing and evaluating quality process and system standards to ensure compliance with company standards and governmental regulatory requirements, investigating/troubleshooting validation problems for equipment and/or performance processes, conducting statistical analyses of testing results and process anomalies, and writing, reviewing, approving and/or implementing documentation for new and current validation procedures and technical reports related to equipment, products and/or processes.

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