Quality Manager Position Available In Miami-Dade, Florida

Tallo's Job Summary: Full-time Quality Manager needed in Miami, FL, with a salary range of $100,000 - $130,000 per year. Lead quality management initiatives to ensure medical devices meet industry standards. Oversee Quality Management Systems, FDA compliance, and cross-functional collaboration with R&D and Manufacturing teams. Bachelor's degree required, with 4 years of Quality Management experience in Medical Devices. Apply now for this exciting opportunity.

Company:
Unclassified
Salary:
$115000
JobFull-timeOnsite

Job Description

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 “Apply Now” button and sending us your resume.

Salary:

$100,000 – $130,000 per year 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 Details 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 ). 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 “Apply Now” button. Jobot is an Equal Opportunity Employer. We provide an inclusive work environment that celebrates and all qualified candidates receive consideration for employment without regard to , , , , , , status, genetics, protected veteran status, , or expression, or any other characteristic protected by federal, state or local laws. Sometimes Jobot is required to perform background checks with your authorization. Jobot will consider qualified candidates with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.

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