Hi Partner, Greetings for the Day.
Please go through the below Requirement and please send me the updated resumes and contact details to my mail id: *[email protected]* *Job Title :* Sr Quality Engineer (Medical Devices) *Location :* Philadelphia, PA *Duration :* 6 Months ** *Primary Skills:** * · Some Manufacturing Design/development experience, Medical device industry, complaint investigations. · CAPA process, quality engineer activities for risk management, FDA regulations*:* * * *Description:** *Lead quality engineer activities for risk management, as it relates to design and development, complaint investigations, and non-conforming materials. Ensure high level of compliance to *FDA QSR* and *ISO 13485* in all assigned areas Work closely with internal departments (Operations, Advanced Operations and Research & Development) to provide risk assessments as required Participate in project teams with internal departs to support product and/or process design and development activities Perform literature review and analysis to support FDA submissions, utilizing medical knowledge and experience Support the *NC/CAPA* process with risk assessments *Thanks & Regards*** *Mohan **|| IT Recruiter * *MSR COSMOS LLC* *T:** 309-365-6526 | F: 925-219-0934 * *M:** **[email protected]* <[email protected]>** *GTalk:** mohankumar025* -- 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 [email protected]. To post to this group, send email to [email protected]. Visit this group at http://groups.google.com/group/oraapps. For more options, visit https://groups.google.com/groups/opt_out.
