RCRI - Medical Device CRO    
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RCRI Services:

 
Regulatory Affairs Regulatory Affairs
Clinical Trial Design & Management Clinical Trial Design & Management
Database Development & Compliance Database Development & Compliance
Reimbursement Strategy and Implementation Reimbursement Strategy and Implementation
Health Economics Health Economics
Quality Systems & Compliance Quality Systems & Compliance
Biostatistics Biostatistics
Venture Capital Due Diligence Venture Capital Due Diligence

 

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Quality Systems Project Manager

RCRI, a provider of integrated services to the medical device and biosciences industries, is seeking a Quality Systems Project Manager.

Responsibilities include managing RCRI's internal Quality System and providing consulting services to clients relative to their quality systems and compliance activities regarding applicable regulations and standards (US and International). Duties include maintaining RCRI's internal quality system, advising clients on quality system functions and structure, ensuring compliance with applicable national and international regulations, and contributing to the development of products and manufacturing design/development, as well as coordinating with clinical affairs and biostatistics for support in comprehensive projects. Qualified applicants will have a degree in a scientific or technical field, Quality Auditor Certification, a minimum of five years quality systems experience in medical device industry, preferably with Class II or Class III devices, excellent analytical and qualitative skills, and a strong understanding of project management. RCRI offers a progressive work environment including flexibility and comprehensive medical, dental, retirement and profit-sharing benefits. Forward resume with salary requirements to: hr@rcri-inc.com RCRI, Inc. 5353 Wayzata Blvd., Suite 505, Minneapolis, MN 55416. No phone calls, no agencies please. EOE





















 

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