Quality Manager

job
  • Jobot
Job Summary
Location
Miami ,FL 33222
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
16 Mar 2025
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Job Description

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This range is provided by Jobot. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$100,000.00/yr - $130,000.00/yr

Job Details

Full-Time & Direct Hire Quality Manager needed for robotics-driven dental innovation!

This Jobot Job is hosted by James Thai. Are you a fit? Easy Apply now by clicking the "Easy Apply" button and sending us your resume.

A Bit About Us

Based in Miami, FL, we are pioneering the next wave of robotic-assisted surgery, revolutionizing the dental industry with cutting-edge innovation. Our technology empowers surgeons with precision, efficiency, and groundbreaking advancements in patient care. In this role, you will lead quality management initiatives to ensure our medical devices meet the highest industry standards.

Title

Quality Manager

Location

Miami, FL 33127

Salary

$100,000 - $130,000

Why join us?

  • Competitive base salary $100,000 - $130,000
  • Full benefits Medical, Dental, Vision
  • 401 (K) with generous company match
  • Generous Paid time off (PTO)
  • Vacation, sick, and paid holidays
  • Life Insurance coverage

Job Responsibilities

  • Oversee and enhance Quality Management Systems (QMS) and Design Control processes.
  • Ensure compliance with FDA, ISO 13485, ISO 14971, MDSAP, and EU MDR regulations.
  • Lead risk management, design transfer, and verification & validation (V&V) initiatives.
  • Conduct internal & supplier audits, manage CAPA processes, and drive quality improvements.
  • Collaborate cross-functionally with R&D, Engineering, and Manufacturing teams to maintain top-tier product standards.
  • Serve as the Management Representative for QMS compliance and reporting.

Qualifications

  • Bachelor’s degree (Engineering, Science, or related) with 4+ years in Quality Management (Medical Devices preferred).
  • In-depth knowledge of FDA regulations (21 CFR 820, 21 CFR 807) and ISO 13485, EU MDR, and MDSAP.
  • Expertise in design control, risk management (ISO 14971), software validation, and statistical analysis.
  • Experience in medical device software, electronics, or manufacturing is a plus.
  • Lean Six Sigma & ASQ certifications are highly desirable.

Interested in hearing more? Easy Apply now by clicking the "Easy Apply" button.

Seniority level

Not Applicable

Employment type

Full-time

Job function

Quality Assurance

Industries

Construction, Civil Engineering, and Industrial Machinery Manufacturing

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