Company Name: Actavis, Inc. Import
Min Education: Not Specified
Job Type: Full Time
Min Experience: Not Specified
- USA - Ft. Lauderdale Florida, 33301
* Carries out responsibilities in accordance with the organization's policies, procedures, and state, federal and local laws. * Write Raw Material, Finished Product and Microbiological Test Methods based on Analytical R&D Validation Reports, Laboratory Technical Services Validation Reports, Microbiological Validation Reports, USP/NF or BP Compendial Monographs, Pharmacopeial Forum (PF) Articles, CFR Methods and/or any other suitable method source. * Write general test methods based on USP or BP compendial monographs, CFR methods and/or any other suitable method source. * Update and implement changes in laboratory testing documentation as required. * Maintain and control all original, signed documents * Maintain all test method and change control files. * Maintain test method database and distribute copies/updates on a regular basis. * Participates in training programs, which result in the development of successful working understanding of the material presented and become proficient in assigned duties and tasks. * Performs duties in a timely manner and complies with all Company policies and procedures including safety rules and regulations. * Performs other related duties as assigned. Current cGMPs, SOPs and FDA, and other regulatory compliance regulations and Business, scientific and personal computer hardware and software applications. Business English usage, spelling grammar and punctuation. Principles of mathematical computations. Establishing and maintaining cooperative working relationships with others. Maintaining complete, accurate and organized records. Reading, understanding and complying with current Company policies and procedures Communicating clearly and concisely, both orally and in writing. Operating personal computer and spreadsheet/database software. Handling multiple projects, duties and assignments. Incumbents in this class are subject to extended periods of sitting, standing and walking, vision to monitor, moderate noise levels, and occasional lifting. Work is performed in office and manufacturing environments. Current cGMPs, SOPs and FDA, and other regulatory compliance regulations and standards. * Business, scientific and personal computer hardware and software applications. * Business English usage, spelling grammar and punctuation. * Principles of mathematical computations. * standards. * * * Skill in: * * * including safety rules and regulations. * * * Bachelor of Science degree in a related scientific discipline from an accredited college or university, and two (2) years Quality Assurance and/or quality control experience in pharmaceutical industry, or equivalent combination of education and experience.