Senior Quality Control Specialist

Probo Medical; Fort Lauderdale (FL); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player in healthcare is seeking a Senior Quality Control Specialist to ensure high standards in diagnostic imaging products. This role involves executing quality activities, approving repairs, and maintaining compliance with ISO and FDA regulations. If you are detail-oriented and passionate about enhancing patient access to quality healthcare, this position offers a chance to make a significant impact. Join a team that values integrity and teamwork while contributing to the mission of improving healthcare quality and affordability.

Qualifications

• 5+ years of quality control experience with medical devices.
• Knowledge of ISO 13485:2016 and FDA regulations preferred.

Responsibilities

• Approve incoming equipment and finished products through tests.
• Document inspection results and maintain quality documentation.
• Promote safety, quality, and productivity standards.

Skills

Attention to detail

Analytical problem-solving

Communication skills

Self-motivated

Education

High School Diploma

Tools

MS Office

Job description

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Description

Probo Medical is a diagnostic imaging sales and service provider dedicated to delivering high-quality, affordable healthcare products and services worldwide. With locations across the US, Canada, the UK, and parts of Europe, our mission is to increase access to healthcare by reducing costs and empowering medical professionals to make informed decisions. We focus on building strong relationships with customers through teamwork and problem-solving. If you are passionate about healthcare and committed to expanding patient access to quality products and services, we encourage you to apply.

Position Overview

The Senior Quality Control Specialist is responsible for executing daily quality activities in a depot repair environment. This includes approving incoming repairs, in-process work, and finished equipment, as well as maintaining quality documentation in compliance with internal standards, ISO 13485, and FDA requirements. The role also involves guiding and training Quality Control specialists.

Essential Duties and Responsibilities

1. Approve incoming equipment by verifying specifications, conducting visual and measurement tests, and assessing damages.
2. Approve finished products by confirming specifications, conducting tests, and managing re-work if necessary.
3. Document inspection results through reports and logs, and summarize re-work activities.
4. Maintain a safe and healthy work environment by adhering to standards and legal regulations.
5. Update knowledge through educational opportunities and technical publications.
6. Support document control and retention processes.
7. Follow established procedures to support quality system requirements.
8. Promote company standards on safety, quality, and productivity.
9. Contribute to the organization's quality and mission objectives.

The above list describes the core functions of the position and is not exhaustive.

Requirements

Education and Experience

• High School Diploma or equivalent required.
• At least 5 years of quality control or technician experience working with medical devices or related mechanical/electronic devices.
• Experience working in environments regulated by ISO 13485:2016, FDA QSR (21 CFR Part 820), and related standards preferred.

Knowledge, Skills, and Competencies

• Attention to detail and analytical problem-solving skills.
• High ethical standards and integrity.
• Proficiency in MS Office (Word, Excel, Outlook).
• Excellent communication skills, both verbal and written.
• Self-motivated and able to work independently.

Supervisory Responsibilities

This position does not have supervisory responsibilities.

Work Environment and Physical Demands

The role is performed in a depot repair environment, working at a bench station. The environment is generally quiet but active, with moving inventory. Reasonable accommodations are available for individuals with disabilities.

Physical requirements include lifting up to 20 pounds, sitting, handling, speaking, hearing, and occasional bending or reaching. Visual acuity for close work is necessary.

Travel

Less than 10% travel required.

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