Hello All,
Please share your consultant resume at ankit.sha...@tech-pro.com along with following details: *Hourly Rate on C2C: * *Visa Status: * *Phone: * *Email:* *Current location: * ______________________________________________________________ *Job Title: **Validation Engineer* *Location: Louisville, CO* *Duration: 6+ Months contract (High Possibility of Extension)* POSITION DESCRIPTION Collaborate with suppliers to ensure product specifications are met. Recommend, plan and lead corrective and preventive actions for continuous improvement with suppliers as appropriate. Work with Suppliers and MNAV purchasing to ensure that supplier management files are maintained according to established requirements to include the development and management of supplier control plans. Conduct supplier audits as required. POSITION RESPONSIBILITIES · Actively participate in the product development cycle to drive supplier selection process. · Engage suppliers to establish appropriate qualifications, validations, inspection plans and gauging for both new products and changes to released product. · Devise and implement methods and procedures for inspecting, testing, and evaluating the precision and accuracy of products and production equipment with respect to suppliers. Establish incoming inspection requirements and revise as necessary. · Lead problem solving efforts to identify and resolve difficult quality issues that may be a result of supplier processes to ensure production of safe and effective medical devices. Work independently to determine and develop solutions that are imaginative, thorough, practicable, and consistent with organizational objectives. · Mentor suppliers in the performance of machine and process capability and performance studies. Lead the implementation of changes and upgrades to systems, procedures, and processes to improve product quality. Provide well-written reports and supporting documentation. · Assist in the development and assessment of the supplier program. Address problems and recommend solutions to supplier quality. Disposition nonconforming product at the Material Review Board meetings. · Interface with suppliers to ensure product specifications are met and control plans are implemented. · Lead supplier audits and assessments, and ensure identified non-conformances are resolved in a timely manner. · Identify and implement supplier corrective and preventive actions to improve quality and reduce incoming quality NCR’s. · Promote continuous improvement through the use of such tools as Lean, Six Sigma and Kaizen. · Follow all Quality System Practices as defined by Medtronic Navigation’s practices, policies and Standard Operating Procedures to ensure that FDA, ISO and European Medical Device quality standards and regulations are met where applicable. · Foster good working relationship with co-workers and able to work collaboratively in a team environment with general supervision. · Able to prioritize assignments and manage time effectively, and maintain positive attitude when handling multiple project demands. *Education Required* •B.S./B.A. in Engineering or similar related field *Years Of Experience * •5+ years of previous experience in a supplier quality position in a regulated environment with B.S./B.A. •3+ years of previous experience in a supplier quality position in a regulated environment with M.S./M.A. Thanks and Regards Ankit Sharma Team Recruitment *tech**•**pro* 3000 Centre Pointe Drive Roseville, MN 55113 651.634.1480 Direct 651.634.1499 Fax 651.634.1400 Ext. 5009 ankit.sha...@tech-pro.com <an...@tech-pro.com> http://www.tech-pro.com *People Solutions Results* *Looking for a job:* *Tech-Pro Careers* <http://www.tech-pro.com/job-seeker> <http://www.linkedin.com/pub/ankit-sharma/43/115/947> <http://www.facebook.com/techproinc> <http://www.youtube.com/user/techpro1989> -- You received this message because you are subscribed to the Google Groups "it req" group. To unsubscribe from this group and stop receiving emails from it, send an email to it-req+unsubscr...@googlegroups.com. To post to this group, send email to it-req@googlegroups.com. Visit this group at http://groups.google.com/group/it-req. For more options, visit https://groups.google.com/d/optout.
