| Hyderabad Jobs |
| Banglore Jobs |
| Chennai Jobs |
| Delhi Jobs |
| Ahmedabad Jobs |
| Mumbai Jobs |
| Pune Jobs |
| Vijayawada Jobs |
| Gurgaon Jobs |
| Noida Jobs |
| Hyderabad Jobs |
| Banglore Jobs |
| Chennai Jobs |
| Delhi Jobs |
| Ahmedabad Jobs |
| Mumbai Jobs |
| Pune Jobs |
| Vijayawada Jobs |
| Gurgaon Jobs |
| Noida Jobs |
| Oil & Gas Jobs |
| Banking Jobs |
| Construction Jobs |
| Top Management Jobs |
| IT - Software Jobs |
| Medical Healthcare Jobs |
| Purchase / Logistics Jobs |
| Sales |
| Ajax Jobs |
| Designing Jobs |
| ASP .NET Jobs |
| Java Jobs |
| MySQL Jobs |
| Sap hr Jobs |
| Software Testing Jobs |
| Html Jobs |
| Job Location | Pune |
| Education | Not Mentioned |
| Salary | Not Disclosed |
| Industry | IT - Software |
| Functional Area | IT Operations / EDP / MIS |
| EmploymentType | Full-time |
Exp: 8+ Job TitleCoNQ Project ManagerImplement and drive a company-wide program to ensure products meet Cost-of-Non-Quality meets targets in close collaboration with cross functional teams. Moreover; the CONQ Project Manager establishes dashboards to supervise overall progress and ensures availability of data to help businesses identify required improvements. Key areas of focus would be to drive the CoNQ targets established for Field Change Orders & sustained improvements in the Manufacturing line.You are responsible foro Ensure that project is adequately executed and help getting it to the right level of standard.o Define and manage a activities to provide adequate data allow businesses to identify areas for improvement.o Provide means (dashboards) for periodic overview and review overview on the status of activities.o Consolidate results of activities for review and reporting.o Frequently interact with functional peers and senior management.To succeed in this role; you should have the following skills and experienceo BS or MS in relevant field including Quality Management; Manufacturing; or another related MBA. o Preferred experience in a medical device or regulated industry.o Solid understanding of Design; Production and Process Controls; and Supplier Quality activities.o DMAIC; 8D; PRIDE and other problem solving and analytical skills.o Excellent writing & communication skills; as well as interpersonal relationship skills including negotiating and relationship management.o Preferred working knowledge of appropriate global medical device regulations; requirements; and standards; such as 21 CFR Parts 803; 806; and 820; ISO13485; ISO14971; European Medical Device Directive (93/42/EEC); Canadian Medical Devices Regulation (SOR/98-282); Japanese MHLW Ordinance 169; and ISO 9001. Furthermore:o Strong leadership skills; identifies gaps and takes action to address and resolve them.o Prior experience quality continuous improvement programs and projects; with demonstrated success and impact on quality KPI s.o Data-driven decision-making and the ability to move teams through vague and complex situations to develop clearly defined programs.o Thrives as a Project Manager in a challenging and multidisciplinary environment and is motivated to manage and resolve competing priorities in a fast-paced environment.,
Keyskills :
continuous improvement facilitationiso 13485problem solvingmedical device directivemedical devicesleadership skillssupplier quality21 cfrchange orders