*URGENT HOT REQUIREMENT……. * *Please Send Resume to ja...@dtscinc.com <ja...@dtscinc.com>*
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. *Job Title Validation QA/Analyst* *Project Location Northridge /CA* *Duration 10+ Months* *Interview Mode: Phone and Skype* * Skills Required and Job Description: * *RESPONSIBILITIES: * · Establish and successfully execute our supplier management plans which will align to overall business objectives. · Communication of Medtronic expectations for continuous improvements and provide leadership for executing inspection at source program. · Improve material quality by ensuring proper inspection methods and drawing requirements are communicated, understood, and deliverable by our suppliers and perform sources inspections. · Perform thorough supplier audits and assessments of their processes and QMS and drive improvement. · Update supplier’s records, and supplier performance metrics, produce supplier reports and drive improvements. · Conduct MRB reviews (In-process-WIP and incoming) and initiate proper corrective action and effective supplier feedback. · Assist with supplier development by evaluating and developing supplier processes through process and product and/or tooling validations and provide assistance, conduct supplier review meetings and supplier training. · Assist with First Article evaluations and approval of parts, subsystems, and products. · Demonstrate knowledge of national and international requirements and standards such as FDA QSR Part 820, ISO 14971, ISO 13485, ISO 9001, CMDCAS/CMDR and others. · Statistical Analysis: The person should have a basic understanding of and ability to apply statistical concepts, SPC, Continuous Improvement, Trending, Process Capability, MSA’s and DRM concepts. · Metrology Concepts: Knowledge of Measurement methodology and understanding and trending the measurement data, to ensure proper actions are taken. · Individual will be involved with Process Validations and Test Method Validations. · Geometric Dimensioning & Tolerancing: Individual in role will be expected to have a basic understanding of GD&T. · Provide Manufacturing, Quality, and other departments with timely investigations into supplier quality issues, including coordinating material purges, participating in QITs/CITs, inspections, and corrective actions (SCAR, SCN). · Assist by writing and revising policies and procedures, and creating forms to support our supplier development processes. · Up to 25% travel possible. *QUALIFICATIONS:* · Experienced with Process Validations and Test Method Validations · Knowledge or experience with FDA QSR’s, GMP’s, or ISO-13485. · Med device industry experience or other regulated field · Effective verbal and written communication skills Regards Javed Ansari Sr. Technical Recruiter, Dominion Technology Services Corp. (DTSC Inc.) Email: ja...@dtscinc.com <nik...@dtscinc.com> , Ph. no. 804-410-0066 Extn. 116 *Gtalk: javed.rgtalent | YIM : javed.rgtalent* -- -- To unsubscribe from this group, send email to cbe-software-engineer-unsubscr...@googlegroups.com For more options, visit this group at http://groups.google.com/group/CBE-Software-Engineer?hl=en --- You received this message because you are subscribed to the Google Groups "CBE Software Engineer" group. To unsubscribe from this group and stop receiving emails from it, send an email to cbe-software-engineer+unsubscr...@googlegroups.com. For more options, visit https://groups.google.com/d/optout.
