Bentec is a worldwide leader in the development, manufacture and distribution of devices for the medical and microelectronic industries. We offer competitive salary and benefits package. Below is a list of our current openings:

Regulatory Affairs Manager

• Develops, implements, regulatory strategies and processes to assure timely domestic and international commercialization of Class II and III medical device products in compliance with applicable regulations and standards.
  
• Develop IDE/510K/and PMA submissions for Class II and III medical devices.  Prepare new product technical files for CE Mark approval.
  
• Instill and drive a regulatory culture.  Establish and support policies and standards for measurement of new products compliance with the FDA QSR, ISO 9001, ISO 13485.
  
• BS degree required in Engineering, Physical or Biological Science with 5-7 years experience in medical device industry with at least 5 years in Regulatory Affairs of medical devices. MS degree preferred.

Bentec is always looking for talented individuals to join our team. Please feel free to submit your resume, if a position becomes available you will be notified.

Please fax resumes to (530) 406-3306
or e-mail resumes to HR@bentecmed.com
Questions please call (530) 406-3333.