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MR-MRI-North Naples

QA / RA Contractor - Medical Device

Post Date:Nov 14, 2017Type:Full-Time
Start Date:11/14/2017Salary:
Location:US-FL-St. Petersburg, Fl area Job Reference:2365
Skills:

Requirements:

* Experienced working in an ISO 13485 and 21 CFR 820 environment
* Proficient in Excel, Word, PowerPoint and Access
* BS/BA
* Minimum 5 years experience working in QMS compliance

Three simple steps for consideration:

1. Connect with Micah Di Sabato on LinkedIn http://www.linkedin.com/in/micahdisabato
2. Submit your resume to [Click Here to Email Your Resumé]
3. Enjoy the benefits of joining my LinkedIn group: Medical Device Premiere Talent http://www.linkedin.com/groupRegistration?gid=3698983 to network with the movers & shakers of the industry!



Job Description:


Job 2365

Location: St. Petersburg, FL 33701


QA / RA Contractor - Medical Device - St. Petersburg, FL

Our growing international medical device client is seeking a QA / RA Contractor to work on an 8-10 month contract with our key client.
  
Qualified individuals that would be willing to relocate after the contract expires would be considered for full-time permanent employment (but not required.)

Our client is a Class I and II International Medical Device Manufacturer.

Challenges:

* Oversee and maintain the QMS document and change control system
* Manage various QMS activities such as: audits, CAPA, supplier assessments, post-market surveillance, complaint handling and MRB Reports
* Perform batch record reviews for product releases
* Support global regulatory compliance to our distribution networks
* Produce QMS reports
* Maintain and support UDI compliance program as well as our barcode databases
* Support QA maintenance of product design project files





Contact Information
MR-MRI-North Naples



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