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Title

Regulatory Affairs QA Manager 

EOE Statement We are an equal employment opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status or any other characteristic protected by law.  
Description

Position Summary:

The regulatory affairs (RA) department at Sciton is responsible for obtaining approval for new medical device products and ensuring that approval is maintained for as long as the company wants to keep the product on the market.

The Regulatory Affairs QA Manager is a hands-on working manager that will lead the day-to-day operational activities of the department and ensure that the project/s, department milestones and goals are met. This position is based at Sciton's headquarters in Palo Alto, CA. But is intermittently remote until our offices are open.

In this role, you will:

  • Oversee the regulation process for products requiring governmental approval and handling all domestic and international government interactions.
  • Obtain regulatory approvals and certifications for the company as and when necessary; 510(k)'s, ISO 9001, ISO 13485, QSR, CE and foreign government regulatory approvals.
  • Facilitate external inspections, audits and investigations; FDA (Fed and State), KFDA, ANVISA, etc., as well as TUV, EHS, fire department, etc., to ensure regulatory compliance.
  • Perform internal audits annually and whenever necessary to ensure continued regulatory compliance.
  • Coordinate the inspection of the organization and contract facilities to ensure regulatory compliance.
  • Generate CHRH product reports and maintain CDRH annual reports and VA quarterly reports.
  • Process clinical complaints and maintain customer service and clinical complaints files for USFDA, EU-MDR, and regulatory reporting.
  • Generate regulatory procedures as necessary to efficiently operate the business.
  • Generate and maintain all DHF's, including facilitating risk management, design reviews and formal product transfer.
  • Has full authority for personnel actions.
  • R & D efforts and direct product transfer to manufacturing.
  • Able to work cross-functionally with other departments to understand the requirements that require support.
  • Improve manufacture of existing products by streamlining and automating processes where necessary.
  • Provide leadership to assure that products meet quantity, cost, quality and regulatory objectives.

 
Position Requirements

 

Essential requirements for the role:

  • Direct experience with 510(k)’s, De Novo, IDE, CE, ANVISA, COFIPRIS, TGA, HC, MFDS, NMPA, PMDA, TFDA, etc. highly desirable.
  • Requires ten years of experience in the related area as an individual contributor.
  • Requires a bachelor's degree in an area of specialty.
  • 2 to 4 years of supervisory experience is required.
  • A technical degree is preferred but not required.

 

Experience and Education:

  • Direct experience with 510(k)’s, De Novo, IDE, CE, ANVISA, COFIPRIS, TGA, HC, MFDS, NMPA, PMDA, TFDA, etc.
  • Requires ten years of experience in the related area as an individual contributor.
  • 1 to 3 years of supervisory experience is preferred.
  • Requires a bachelor's degree in the specialty; a technical degree is preferred.
  • Able to work cross-functionally with other departments to understand the requirements requiring support.
 
Full-Time/Part-Time Full-Time  
Position Regulatory Affairs Manager  
Location Palo Alto (HQ)  
About the Organization SCITON is an industry leader and manufacturer of medical aesthetic lasers and light source technologies. With a vision to improve people's lives, our top-tier devices are built to order with integrity by pioneering, customer-focused, and results-driven individuals.










At the heart of it, innovation is a fundamental cornerstone of our culture. We strongly believe that new ideas can come from anyone, anywhere, at any time and embrace an open-door culture that welcomes and fosters individuals who are creative, driven, passionate, and willing to take the lead with us. Join us for an opportunity to grow and make an impact.



Life at Sciton:



At Sciton, people matter. We are more than a company; we are a family, which is why we give all our employees:


• The support, recognition, and room to grow their careers within Sciton.


• Empowerment to develop their creative genius and encouragement to be lifelong learners.


• Incentives for creativity and innovation across the organization.







What Sciton offers you:


• Competitive health benefits


• Retirement


• 401(k)Employer Match


• Time off


• Professional Development


• Stock Options


• Employee Referral Bonus


 

This position is currently accepting applications.

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