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.