MAIN JOB RESPONSIBILITIES / COMPETENCIES
1. Provide administrative support for Quality Department Activities, as required, including but not limited to activities associated with:
a. Document Control
b. Post-Market Surveillance
c. Medical Affairs
d. Submissions
e. External audits and inspections
f. Quality Assurance
g. Quality Control
h. Complaints
2. Other duties as assigned.
REQUIREMENTS
EDUCATION & TRAINING
• High school diploma or equivalency required.
EXPERIENCE
• 1-3 years of experience in the medical device industry, preferred.
SKILLS
• Solid interpersonal and communication skills.
• Knowledge of GCP and medical device regulatory requirements and terminologies.
• Excellent verbal and written communication skills.
• Excellent organizational skills.
• Proficient with Microsoft Office.
• Ability to follow written and verbal directions with a high level of accuracy.
• Extreme attention to detail.
• Ability to work in a team setting.
STAAR, which has been dedicated solely to ophthalmic surgery for over 40 years, designs, develops, manufactures and markets implantable lenses for the eye. These lenses are intended to provide visual freedom for patients, lessening or eliminating the reliance on glasses or contact lenses. All of these lenses are foldable, which permits the surgeon to insert them through a small incision. STAAR’s lens used in refractive surgery is called an Implantable Collamer® Lens or “ICL,” which includes the EVO ICL™ product line. More than 3,000,000 ICLs have been sold to date and STAAR markets these lenses in over 75 countries. To learn more about the ICL go to: EVOICL.com. Headquartered in Lake Forest, CA, the company operates manufacturing and packaging facilities in Aliso Viejo, CA, Monrovia, CA and Nidau, Switzerland. For more information, please visit the Company’s website at www.staar.com.
