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Global Computer Validation QA L'Arbresle France,  


Posted on : 22 March 2017

Project Description

Charles River Laboratories is a global provider of solutions that advance the drug discovery and development process. Our leading-edge products and services are designed to enable our clients to bring drugs to market faster and more efficiently. These products and services are organized into three categories spanning every step of the drug development pipeline: Research Models and Services, Preclinical Services, and Clinical Services. Our customers include all of the global pharmaceutical and biotech companies, as well as government agencies, leading hospitals and academic institutions. Charles River s 8,000 employees serve clients in more than 50 countries.To support our business development group we offer following permanent position: Specialist, Global Computer Validation Quality Assurance BASIC SUMMARY:Provide quality assurance monitoring and audits of all Charles River computer validation projects globally to assure compliance with applicable regulations, corporate policies, and procedures. Assist in periodic assessments of globally controlled IT regulated activities.ESSENTIAL DUTIES AND RESPONSIBILITIES: Communicate all identified compliance and quality risks to his/her supervisor. Provide quality assurance monitoring of projects to assure regulatory compliance of complex and critical computer systems at designated sites, assisting with the development and/or review of validation deliverables. Provide compliance support to Computer Validation QA managers on multisite and global computer systems, assisting with the development and/or review of validation deliverables. Assist in the development and maintenance of the computer validation training programs and present training in regulatory requirements for validation, maintenance, and operation of computer technologies. Assist with operational components, to develop and maintain an inventory of computerized systems used in regulated operations and their status relative to the Master Validation Plan (MVP). Review validation plans, test results, and summary reports for regulatory compliance. Prepare audit reports for validation projects describing regulatory and procedural deficiencies and deviations. Review audit responses and assure deficiencies are addressed before systems are commissioned for use. Assist in periodic assessments of globally controlled IT regulated activities. Maintain an up-to-date knowledge of computer validation requirements, practices and procedures, and inform other company staff of those requirements. Provide compliance guidance to operational personnel on regulatory requirements for computerized system validation, development of user requirements specifications, testing strategies, and documentation requirements. Perform all other related duties as assigned.QUALIFICATIONS:Education: Bachelor's degree (B.A./B.S.) or equivalent in a scientific discipline and/or computer related field.Experience: 2-4 years related experience in a pharmaceutical, biotechnology and/or biomedical industry. Working knowledge of computer validation requirements in government regulations including FDA 21 CFR parts 11, 58, 211, and 820, OECDs and related multinational industry standards and requirements. An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.Certification/License: None.Other: Must be able to communicate with essential personnel from all business sectors, i.e., manufacturing and research models services, clinical services, preclinical services. Demonstrated leadership skills required. Proficiency in computer-based word processing, spreadsheet and presentation applications required. Active membership of a professional organization specific to quality assurance and federal regulations (e.g. GLP, GMP, etc.)PHYSICAL DEMANDS: Must regularly operate a computer and occasionally operate other office productivity machinery such as a calculator, copy machine, and computer printer. Must regularly communicate with employees/customers; must be able to exchange accurate information. Must occasionally move about inside the office to access file cabinets, office machinery, etc.WORK ENVIRONMENT: General office working conditions; the noise level in the work environment is usually quiet.Comments: Requires occasional domestic and international travel.

Locations

LArbresle France

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