In this position you will report directly to the VP, QA/RA and be an integral part of our Organization.

Your responsibilities will include, but are not limited to:

• the assurance that our products are compliant with the FDA and ISO for safety and efficacy.
• Maintain company registrations in US, Europe, Canada and other countries worldwide.
• Write and submit 510(k), technical files, license submissions for Canada, export certificate requests, and other required registration documents.
• You will also assist in the company’s sterilization and microbiological program
• You will represent the regulatory function in design control and risk assessment activities.

REQUIRMENTS

To qualify for this position you will need:

• 5-10 years Regulatory/Quality/Assurance experience in a FDA regulated industry with most recent experience in medical devices.
• Undergraduate or Graduate degree in scientific discipline (preferably in life sciences) required.
• Familiarity with registration, listing, and product approval process both in the US and internationally.

Join the team where we offer a rewarding work experience, compensation and benefits package.  Salary is commensurate with professional experience.  For immediate consideration, please forward your resume, along with salary requirements, to: 
Vera MacElroy, Bovie Medical Corporation, 5115 Ulmerton Road, Clearwater, FL 33760-4004 or fax your resume to 727-803-8504 or e-mail HR@boviemed.com.
 

If you are interested in becoming a member of the Bovie Medical team, you may download our Employment Application PDF, fill it out, and send it along with your resume using any of the following methods:

• Email our Human Resources department at hr@boviemed.com
   
• Fax a copy to (727) 803-8504
   
• Mail a hard-copy to:

  Vera MacElroy
  c/o Bovie Medical Corporation
  5115 Ulmerton Road
  Clearwater, FL 33760-4004