Salary: Open
Location: Camarillo, California
Employer: Kinamed Inc
Type: Full Time — Experienced
Sector: Private Industry
Discipline: Regulatory/Quality
Required Education: 4 Year Degree

Employer Information

About Kinamed Inc

Kinamed is a small, privately-held medical device company with a seasoned management team and an experienced workforce. We are fully integrated, focusing on implantables and instruments for orthopaedics and neurosurgery, including sterile-packed implants, instruments, and disposables. Our devices are sold in over 20 countries throughout the world.

Job Description

The position is primarily responsible for managing regulatory submissions and certifications for regulatory jurisdictions outside the United States. It requires the application of practical experience and a technical knowledge base for preparing and managing submission dossiers in conjunction with in-country regulatory experts. It requires both attention to detail and process considerations in execution of responsibilities. This position reports directly to the Company’s Senior Director of Regulatory Affairs and Quality Assurance.

Requirements

• A bachelor’s degree in a scientific or technical discipline with 3 years of related industry experience in quality or regulatory affairs;
• Self-motivated, self-directing, strong attention to detail; excellent organizational and time management skills;
• Strong interpersonal and project management skills with the ability to communicate well, verbally and in writing;
• Multi-lingual skills are beneficial;
• RAC certification is beneficial.

Please submit cover letter and resume

• Location: Camarillo, CA
• Principals only. Recruiters, please don’t contact this job poster.
• Please, no phone calls about this job!
• Please do not contact job poster about other services, products or commercial interests.