*Please share Resume to [email protected] <[email protected]>*



*Rate: $52/hr. on C2C*



*Client: Depuy*

*VISA: USC, GC, H1B Only*

*BE Mechanical* with *7+ years of exp. In Medical device domain in MDR
projects*



*Job: MDR Quality Lead*

*Location: Raynham, MA*

*Duration: 12 months*



   -            *BE Mechanical* with *7+ years of exp. In Medical device
   domain in MDR projects*
   -             Provide support for review of existing documents,
   assessing gaps, revising documents, creating design engineering rationales
   to meet EU MDR requirements
   -             Review and approve design documentation including
   Verification & Validation rationales, risk documents (design and process),
   standards evaluations, mechanical test protocols and reports.
   -             Support risk management activities including planning,
   design & clinical risk management DFMEA, production risk management PFMEA,
   and overall risk summary reporting
   -             Revise, review and approve verification and validation
   activities as required
   -             Review and approve any required drawing updates, including
   design impact assessments
   -             Review and approve any labeling updates, including design
   impact assessments
   -             Deliverables to be quarterly based on assigned files
   -             Apply statistical methods and design/process excellence
   tools to support design engineering rationales/memos as required
   -             Provide leadership in all areas of the Quality System,
   including, but not limited to corrective and preventive actions, product
   complaints, post market surveillance, nonconforming materials, risk
   management, and audit support functions
   -             Provide leadership in the understanding of medical device
   regulations to other disciplines.
   -             Ability to work in a team setting within Design Quality
   and cross-functionally is required
   -             Communicate effectively at all levels within Quality, as
   well as cross functionally with departments such as Product Development,
   Regulatory, Medical Affairs, Manufacturing, and Marketing
   -             Know and follow all laws and policies that apply to one's
   job, and maintain the highest levels of professionalism, ethics and
   compliance at all times.
   -             Report task progress and status on a weekly basis







*VINEET SHARMA*
<https://em-ui.constantcontact.com/em-ui/em/page/em-ui/email>* | Sr
Recruiter | 1Point System LLC  *

*Mobile: (315) 514-3320 *• [email protected]

*Desk:    (803) 818-3474 Ext: 112*

*Gtalk/Skype:* [email protected]

*LinkedIn:* linkedin.com/in/vineet-sharma-11043aa4
<https://www.linkedin.com/in/vineet-sharma-11043aa4>

• Fax: 803-832-7973

115 Stone Village Drive • Suite C • Fort Mill, SC • 29708

*An E-Verified company | An Equal Opportunity Employer*

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