Senior RA Specialist- Great Company- New Product Development!

PLEASE NOTE:  To properly respond, you should format your resume in MS Word or Corel WordPerfect and send it to lar3916@jobquestsite.com . Visit our website at http://www.jobquestsite.com for other career opportunities. If your qualifications are not a perfect match- send your resume anyway. Opportunities for all levels of quality and regulatory as well as engineering and operations professionals available.. IMPORTANT! No resume will be sent to Client without your consent. To be considered for this job you must have: Med Device Background in Regulatory Affairs with Class III implantable devices Must have a comprehensive knowledge of FDA regulations Must have a Bachelor of Science degree or a related field. Positive relationship with FDA and experience with audits. Preparation of 510ks, PMAs and IDEs submissions. Ability to interface with Design Team in areas of compliance/regulationDESCRIPTION: Exciting New product development in Neuro Modualtion devices, cutting edge technology, great advancement opportunity with one of the leaders in implantable device manufacturing. KEYWORDS:   regulatory affairs, compliance, quality, FDA,, 510k submissions, orthopedic, implantable devices, Class III Compensation:   High: $110,000.00 plus Great Incentives & Relocation & BenefitsLow:  $80,000.00  MRINetwork is the largest and most successful search organization in the world. Each MRINetwork office is a single point of contact to over 1,100 offices in more than 37 countries, our candidates have access to the right jobs virtually anywhere in the world. LOCATION: Kalamazoo, MI JOB CATEGORY: Legal TYPE: Full Time, Employee JOB REFCODE: LAR3916 COMPANY: Management Recruiters of Myrtle Beach, Inc. CONTACT NAME: Lori Rowe, Account Executive EMAIL: Apply by Email