*Please send me the profiles at [email protected] <[email protected]>*
Hi, I have an urgent requirement with one of my clients, details given below. If you find your self suitable for the position, please send me your latest updated resume along with contact details. Please include your employer details as well. *Job Title* SW Quality Engineer *Project Location* Louisville, CO *Duration* 6 months /Contract *Skills Required and Job Description:* *MOI Telephonic + Skype* "This person's primary responsibility will be DHF remediation for a recently acquired product. B.S/B.A in Engineering or similar field Works with minimal guidance to support the design, development, test, and market release of software used in both surgical navigation applications and other medical devices. Contribute to the processes and tools used to create and test software applications. Develop and assess the quality programs and systems of the client to applicable standards. •Actively participate in product development cycle by reviewing software project documentation, participating in product risk assessments, and working closely with Product Development to develop appropriate verification and validation testing requirements. •Work cross-functionally to implement improvements to the software life cycle, including the establishment of risk management as an integral part of the quality management system as an overall framework for the application of appropriate software engineering methods and techniques. •Create and revise Standard Operating Procedures (SOPs) and other documentation to support the Quality System in regards to software and system design. •Identify and implement software process metrics for the software product development life cycle. Develop, analyze and monitor metrics pertaining to software defects uncovered during development, testing and post-release. •Recommend and lead corrective and preventive actions to improve software product quality. Ensure documentation and findings are completed on time and in a timely manner in accordance with FDA and European Regulatory agency standards and procedures. •Provide solutions to a wide range of difficult challenges. Work independently to determine and develop solutions that are imaginative, thorough, practicable, and consistent with organizational objectives. •Provide QA oversight to assigned suppliers. Disposition nonconforming product at the Material Review Board meetings. Interface as necessary with suppliers to ensure product specifications are met. Lead supplier audits and assessments. •Promote continuous improvement through the use of such tools as Lean, Six Sigma and Kaizen. •Follow all Quality System Practices as defined by the client's practices, policies and Standard Operating Procedures (SOPs) to ensure that FDA, ISO and European Medical Device quality standards and regulations are met where applicable." Thanks & Regards, *Deepak Gulia* *Technical Resource Specialist* *RG Talent Inc* *39120 Argonaut way* * Suite # 157, Fremont CA 94538* Phone : 510-443-0758 Ext - 139 Email : [email protected] <[email protected]> URL : www.rgtalent.com -- You received this message because you are subscribed to the Google Groups "SAP Resource Center" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/sap-resource-center. For more options, visit https://groups.google.com/d/optout.
