*Dear Partners,* Hope your day is going well. I saw your profile online and tried reaching you a minute ago and left a voicemail. I hope you can call me back as soon as possible on 703-349-2825 so I can explain to you a bit more about the below role and our client. Please send me your updated resume. Looking forward to speaking to you.
*Need H1b Copy, DL copy along with linked in if you have* *Please fill the below details * *Candidate’s Full Name:* *Last 5 of SSN:* *Availability:* *Current Location:* *Work Authorization:* *Planned Absence Dates:* *LinkedIn Profile URL:* *Candidate Phone #:* *Candidate Skype ID:* *Candidate Email Address:* *Attach Any id copy :* *Job Description :* Position Title: Quality Engineer – USC or GC Only No. of opening: 1 *Duration: 4 Months* *Location:** Batesville , Indiana 47006 * *Job Description:* Description The QA Engineer, part of the QA team located in Batesville, IN, will work to provide the necessary data to make effective quality and business decisions, and will implement sound, data-driven quality and business solutions that emphasize quality system compliance. *Essential Duties and Responsibilities:* • The primary accountability of the QA Engineer is to support all initiatives to build product DHF, DMR • Identify and mitigate quality risks • Root cause investigations • Process and Test System validation • Develops and implements test methods and procedures for inspecting, testing and evaluating product and processes. • Conduct part qualification (FAI, FMEA, GRR, Capability Study etc.) for both internal and external parts • Conduct supplier audits and manage audit corrections meet deadlines • Review and disposition product design and manufacturing process changes orders • Other tasks as assigned *Qualifications* • BS in Engineering or closely related Bachelor’s degree required • 1-2 years of Quality/Regulatory experience is required • Experience in the Medical Device industry is required • Strong leadership skills, strong interpersonal skills, and the ability to deal effectively with system users are required. • Knowledge of Quality Systems and Process Improvement is preferred. • CQA, CQE or RAC preferred. • Experience in Design Controls is desirable. • Communication – displays developed interpersonal skills: leadership, team orientation, ability to communicate at all levels • Flexibility and Adaptability – make effective decisions and maintain effectiveness under changing circumstances and priorities • Teamwork, communication, positive attitude required to support the manufacturing environment • Ability to read and analyze technical prints and drawings • Problem Solving – able to perform root cause analysis and implement effective corrective actions • Project Management – able to effectively manage and complete multiple projects simultaneously • Computer Skills – Excellent computer skills including but not limited to Microsoft Office Suite • Establish, implement, and maintain the quality system in accordance to FDA Quality System Regulation, ISO 13485, European Union Medical Device Directives, and Canadian Medical Device Regulations *Thanks and Regards,* Vinay Kumar Sr.Talent Acquisition Specialist *Osair Technologies LLC* Phone 703-349-2825, FAX : 732-289-6076 vinayku...@osairtech.com <vi...@osairtech.com> gmail-vinay.os...@gmail.com <osairtech.vi...@gmail.com> www.osairtech.com Suite # 16D, Clifton, Chapel road VA 12642. -- You received this message because you are subscribed to the Google Groups "oraapps" group. To unsubscribe from this group and stop receiving emails from it, send an email to oraapps+unsubscr...@googlegroups.com. To post to this group, send email to oraapps@googlegroups.com. Visit this group at https://groups.google.com/group/oraapps. For more options, visit https://groups.google.com/d/optout.
