Hi Friends, Hope you are doing great,
I have an urgent requirement from one of my esteem client, I will appreciate if you can have an eye on the below requirement and send me your consultant updated profile ASAP. *Job Title: Sr. Quality Engineer* *Location: Chelmsford, MA / Morrisville, NC / Wyomissing, PA* *Duration: Long Term Contract* *Job Description: * · Good experience in performing Installation Qualification (IQ), Operation Qualification (OQ), and Process Qualification (PQ) validation protocols. Provides statistacally valid sampling plans when required. • Good experience in closure of both the CAPA and Non-Conformance quality systems. Track internal quality issues and report on corrective action progress, including performaing failure investigation and making recommendations for corrective actions. • Support and evaluate current test and inspection methods to identify areas for improvement, efficiency and cost reductions. • Partners with affiliated disciplines, (ie Regulatory Affairs, Quality Engineering, New Product Development, Operations, Supplier Management) through the Product Design and Development Process to assure that adequate design controls and/or procedures are complied with and met. • Works closely with purchasing and product development with onboarding and maintaining supplier files during the development process as well as routine maintenance of all supplier files. • Implements yearly objectives that support overall strategic plan. • Ensure full compliance with quality and regulatory requirements. • Proficient with Microsoft Office, including Word, Excel, Powerpoint and Outlook (ie database development, statistical software and analysis, simulation, word processing for report generation, etc) • Outstanding written and verbal communication skills including the ability to effectively communicate with a broad spectrum of people with varying backgrounds, education and experience. • Ability to use and apply statistical skills, such as DOE, SPC, Reliability, Gage R&R. *Education / Experience Requirements:* • Bachelors Degree required. Prefer focus in engineering, life science or related discipline. • 5 years minimum related quality experience in a manufacturing environment. Experience in the medical device industry preferred. Experience in the Design and Development process preferred. • Broad experience in manufacturing operations, including new product development and implementation, process qualification, cost reduction and quality engineering. • Prefessional Certification, ie 6 Sigma black belt, ASQ – CQA, CQE and/or CRE; RAB preferred. • Strong regulatory, cGMP, QSR, ISO knowledge base.. Thanks & Regards, Sai Kiran Nandrolu Sr. Recruiter W: (972) 393-2255 E: saikiran.nandr...@w3global.com A: 1701 Legacy Dr, Suite#1000, Frisco, Texas - 75034 -- You received this message because you are subscribed to the Google Groups "Android Developers" group. To unsubscribe from this group and stop receiving emails from it, send an email to android-developers+unsubscr...@googlegroups.com. To view this discussion on the web visit https://groups.google.com/d/msgid/android-developers/CAGquW%2BLvBVRSp92KB1y8p6mqC8H_At5T305N24oe%3D%2BiTzqrShw%40mail.gmail.com.
