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Quality and Regulatory Specialist
Location:
Minnetonka, MN
Description:
Two (2) years of experience as an Engineer or related occupation with experience in advancing and maintaining medical device Quality Management Systems. Experience must include: Two (2) years of experience in the following (experience may be gained concurrently): - ISO 13485 and 21 CFR820 Quality Management Systems in a quality role- Good Documentation Practices (GDP)- Supplier Corrective Action Reports and CAPAs - Investigation and root cause analysis problem solving of quality issues and complaints.Requires a Bachelors degree (or foreign equivalent) in Engineering, Chemistry, Biology, Industrial Management or a directly related field Please send us your resume via email at candidates(at) placementservicesusa.com with reference #2703391 in the subject line. Do not copy and paste your resume in the body email. Please attach it as a Word document. Thank you.
Posted:
May 9 on Jobvertise
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More About this Listing: Quality and Regulatory Specialist
Quality and Regulatory Specialist is a Quality Assurance Regulatory Affairs Specialist Job located in Minnetonka MN. Find other listings like Quality and Regulatory Specialist by searching Oodle for Quality Assurance Regulatory Affairs Specialist Jobs.
Quality and Regulatory Specialist is a Quality Assurance Regulatory Affairs Specialist Job located in Minnetonka MN. Find other listings like Quality and Regulatory Specialist by searching Oodle for Quality Assurance Regulatory Affairs Specialist Jobs.