Hi ,
I hope you are doing great!! Please go through the job description mentioned below and let me know if you are interested in the position. Role :- *Project Manager With (QMS)* Location : Barrington IL Duration : 6+ Months Role Summary/Purpose: This role of Software Project Lead is for a multi-product software project within DGS and CVIT. The purpose of this role is to manage, coordinate and document project activities within the cross functional teams, facilitate tracking and identify project risks. Essential Responsibilities: • Provides additional control and communication within a project area or function. Collaborates with project team members to build project schedules and analyze impact to schedules in event of change to timing of deliverables. Facilitates definition and tracking of action plans for sub-team or key issues. • Follows up with team members to collect status or reinforce priority. • Identifies early and solves complex and ambiguous cross-functional integration problems leading the team to deliver per project commitments, including (but not limited to) completing functional goals, execution adjustments/iterations, process confusion, and cross functional teamwork Ensuring product designs are compliant to relevant FDA standards • Coordination and integration of cross-product development efforts and managing of systems integration strategy and execution throughout the program lifecycle • Creation, review and approval of *QMS-relevant documentation*, like risk reviews, design reviews, technical reviews, engineering documentation, verification and validation related documents, FMEA,… • Support and manage 510k related activities • Organize and lead core team meetings and follow up on action items • Oversight of Defect Management ensuring compliant DRB assessments and appropriate risk-based decisions on the resolution and classification of SPRs • Development of Usability File including, but not limited to, user profiles, use environment, usability requirements, formative testing, and summative testing Qualifications/Requirements: Basic Qualifications: · Bachelor’s Degree in Computer Science or in “STEM” Majors (Science, Technology, Engineering and Math) · A minimum of 5 years of professional experience in software development · A minimum of 3 years of program planning and execution · Experience in risk management of medical software · Experience in medical device standards and regulations · Experience with GE quality system and documentation practice *Eligibility Requirements*: o Legal authorization to work in the U.S. is required. GE may agree to sponsor an individual for an employment visa now or in the future if there is a shortage of individuals with particular skills. o Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen o Must be willing to work out of an office located in Milwaukee, Wisconsin Desired Characteristics • Master’s degree in a technical field ' • Excellent organizational skills • *Six Sigma Green Belt*, DMAIC and DFSS • Experience in design verification of complex systems • Experience in systems architecture and integration for complex systems *Thanks & regards * *Chalapathi Goud, * GSS Infotech Inc A SEI-CMMI Level 5 Company Direct:- *8606404324,* Phone: *860-640-4354* Ext *3016* Email:- *chalapathi.pal...@gssinfotech.com <chalapathi.pal...@gssinfotech.com>* Web site:- www.gssinfotech.com [image: Description: Description: Description: C:\Users\chalapathi.pallay\Desktop\gss_logo.png] -- You received this message because you are subscribed to the Google Groups "Oracle-Projects" group. To unsubscribe from this group and stop receiving emails from it, send an email to oracle-projects+unsubscr...@googlegroups.com. To post to this group, send email to oracle-projects@googlegroups.com. Visit this group at https://groups.google.com/group/oracle-projects. For more options, visit https://groups.google.com/d/optout.
