*Dear Associate, Hope the day is treating you well! We have the following requirement currently open. Please review the requirement and send me the best matching resume.
Job Title: Quality Project Manager Location: Arlington Heights, IL 60004 Duration: 3 Months Contract and possibility of extension PLEASE SEND ME THE RESUME ON shiv.ku...@panzersolutions.com Job Description: The Program Leader is responsible for the execution & validation of assigned programs that support the GEHC Quality Management System. Responsibilities focused on the development and execution of policies and procedures compliant to the global regulators in the areas of CAPA, device and pharmaceutical complaint review boards, management review, and field corrective action assessment Key Resposibilities: Supports operational excellence of assigned program(s), including project reviews, feasibility analysis, cost benefit analysis, prioritization, resourcing, initiation, execution and closure for all project work related to the program. Developed CAPAs in response to FDA Led and facilitated the problem solving team which resolved site issues Communicates program status, issues, risks, plans, etc. to Quality Program Manager & business leadership. Provides direction to project team resources to support and deliver solutions relating to the program(s). Maintains effective working relationships with peers and vendors to seamlessly integrate the program area into the overall strategic objectives and activities of the organization. Coordinates program support activities, including the support of internal and external communications, establishing roadmaps and benchmarks, requirements gathering, development, implementation, testing and training plans, and supporting the successful transition to the functional owners. Quality Specific Goal: Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position. Complete all planned Quality & Compliance training within the defined deadlines. Identify and report any quality or compliance concerns and take immediate corrective action as required. Aware of and comply with the change management work instruction as applicable. Develop an open quality culture within the organization that fosters issue discussion and decision-making based on quality and compliance objectives. Qualification: Bachelor’s degree (or high school diploma/GED plus 4 years working experience and understanding of product development, manufacturing, quality control and servicing in a medical device environment). Demonstrated program/project management experience Experienced in compliance activities related to GMP and FDA inspections Experience developing and executing the strategy for remediation of CAPAs Excellent communication skills: able to clearly communicate complex information in an easy to understand manner; able to deliver message effectively verbally and in writing. Demonstrated effective interpersonal, teamwork, negotiation & conflict resolution skills. Strong analytic skills: able to clearly link results to operational performance drivers, and generate alternatives. Change agent with energy, passion & enthusiasm to drive change . Strong organizational skills. Prior experience using word processing, spreadsheet, and presentation software. Ability to communicate effectively in English (or local language). Prefered Qualification: Demonstrated knowledge with regulations in the medical device and/or pharmaceutical industries. Demonstrated knowledge of Quality Management System tools. Ability to multi-task & handle tasks with competing priorities effectively. Thanks, Shiv Kumar* -- You received this message because you are subscribed to the Google Groups "SAP BASIS" group. To post to this group, send email to sap-basis@googlegroups.com. To unsubscribe from this group, send email to sap-basis+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/sap-basis?hl=en.