BACHELORS DEGREE IN A TECHNICAL OR SCIENTIFIC SKILL OR A HIGH SCHOOL DIPLOMA WITH 0-3 YEARS OF EXPERIENCE UNDERSTANDING OF GLOBAL PHARMACEUTICAL PRODUCT REGULATIONS WITH EXPERIENCE WITH ISO 9001 AND OR 13485 2003 AND 21 CFR PARTS 210 AND 211 WITH PART 820. DEMONSTRATE THE ABILITY TO PERFORM GMP OPERATIONS FOLLOWING DETAILED SOPS, MAINTAINING TRAINING DOCUMENTS AND OR GOOD DOCUMENTATION PRACTICES. 0-3 YEAR TECHNICAL DOCUMENTATION FOR QUALITY ACTIVITIES. SPECIFIC TO MANUFACTURING. SOLID ORGANIZATIONAL SKILLS ABILITY TO COMMUNICATE EFFECTIVELY, VERBALLY AND IN WRITING WITH DETAILED REPORT WRITING AND TECHNICAL WRITING SKILLS. THE ABILITY TO INTERDEPARTMENTALLY WORK WITH VENDORS AND CONTRACTORS. TEAM ENVIRONMENT. RESPONSIBLE FOR ALL ACTIVITIES INVOLVING QUALITY ASSURANCE AND COMPLIANCE WITH APPLICABLE REGULATORY REQUIREMENTS. INITIATE, INVESTIGATE AND COMPLETE NONCONFORMANCE REPORTS SUPPORTS THE GENERATION OF PRODUCT CERTIFICATE OF COMPLIANCE RESPONSIBLE FOR THE LABEL CONTROL AND PRINTING PROVIDE HELP AND SUPPORT FOR ALL ASPECTS OF TESTING RELATED TO MANUFACTURING FIRST ARTICLE INSPECTIONS IN PROCESS RELEASE INSPECTION FINAL QC RELEASE OF FINISHED GOODS DOCUMENT REVIEW ENSURES THAT ALL INSPECTIONS AND PROCEDURES ARE PROPERLY COMPLETED AND DOCUMENTED. ENSURES DOCUMENTS ARE ENTERED IN THE QUALITY DATABASES, SCANNING, INDEXING AND FILING WHILE ARCHIVING OLD DOCUMENTS.
Posted on: Mon, 22 Dec 2014 20:35:39 +0000
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