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| add to favorites | Quality Assoc I / Supplier Quality | No Picture |
| Supports the facility GMP activities for the Rceiving and InspectionsI department in the Quality organization. Provide continuous improvement to the group through Quality Systems. Conduct audits of GMP activities, documentation and reports for conformance to procedures, protocols and regulatory requirements, specifically those related to Supplier Quality Assurance. Strong interpersonal skills and great attention to detail are necessary. Must be a strong team player with good problem solving, and good verbal and written communication skills. Must be able to handle multiple projects concurrently, have computer experience. Knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices preferred. Working knowledge of statistics and production processes. Prefer Bachelor Degree in Engineering with 0-2 years related experience. Associate level degree holders with 1 - 3 years-related experience or High School graduates with 2-4 years directly related supplier quality experience. |
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| add to favorites | Experienced QA | No Picture |
| Adecco Medical & Science, a leading provider of contract and permanent staffing in the Pharmaceutical, Life Science Technology, Medical Device, and Health Care industry is seeking an experienced QA to work with in one of our leading pharmaceutical clients in San Diego County: - Reviews cGMP related documentation for compliance - Verify and maintain compliance with established regulatory requirements including: CFR Section 21 part 211 and SOPs through auditing of quality systems and processes, training, and implementation activities associated with a cGMP pharmaceutical manufacturing environment. - Provide inter-departmental guidance, support, and communication concerning internal compliance and regulations. - Complete audits of various departments/processes including planning of the audit, execution, and preparation and communication of the audit report with team members - Participate in Corrective Action/Preventive Action (CAPA) analysis including the investigation of failures - Write and revise SOPs and Controlled Forms and related documents to ensure best practices and current operations - Support compliance inspections including preparation and corrective actions as needed - Maintain paper archives (lot history records, reports, logbooks) and electronic databases - Maintain Document Creation/Change/Control System, Equipment Qualification/Maintenance/Calibration/Inventory System - BS Degree in Science or related degree with a at least two years relevant industry experience or equivalent combination of education and experience. - Must have working cGMP and 21 CFR Part 211 experience - Experience implementing quality assurance compliance within a manufacturing discipline - Ability to analyze data with demonstrated attention to detail This position is for 3rd shift and Direct Hire Please email your resume to mo.ouranos@adeccona.com and we will contact you if you are qualified for our position or contact you for any future positions. |
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