• Friday, October 07th, 2011

Regulatory Affairs Specialist

Location: Danvers, MA           

Salary: Commensurate with experience

>> Click here to apply online <<

Position Requirements Include:

  • 3-5 years of experience in Regulatory Affairs of Spinal medical device products
  • B.Sc. in Engineering or related fields
  • Experience in regulatory submissions, including 510(k), IDE, PMA
  • Strong knowledge of the CFR 21 QSR, ISO 13485, and MDD regulations
  • Strong successful history as RA specialist on product development teams
  • Ability to work in fast paced and dynamic environment

>> Click here to apply online <<

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About us:

Arkay Career Services is an executive recruiting firm specializing exclusively in the nationwide recruitment of medical professionals in the areas of Medical Devices, Biotechnology, and Bio-Pharma within the country. Our success can be attributed to our commitment to find Top Tier Candidates for our clients making a difference in the healthcare industry.

Within our primary niche market, our search expertise include the following positions: C-level executives, VP, senior level managers and directors, operations, sales, business development, marketing, product management, engineering, quality assurance and regulatory affairs (QA/RA), clinical, and more…

 

Specialties:

Medical Devices, Medical Device Recruiters, Medical IT, Cardiovascular, Stents, LVAD, DES, Orthopaedic, Joint Replacement, Cartilage Repair, Imaging, CT, MR, PET, Ultrasound, HIFU, PACS, Navigation, IGS, CAS, Robotics, Wound Care, Dental, Biotechnology, Tissue Engineering, Bio-Pharma, Drug Delivery, Neurology, and Nanotechnology…

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