Quality Assurance Specialist, Medical Devices Position Available In Palm Beach, Florida
Tallo's Job Summary: The Quality Assurance Compliance Specialist position for Medical Devices in Riviera Beach, Florida offers a salary of up to $95,000 per year. This role involves leading audit teams, maintaining quality documentation, and ensuring compliance with ISO 13485, MDD/MDR, CE, and CSA standards. Ideal candidates have experience in regulated manufacturing environments and strong communication skills.
Job Description
Quality Assurance Compliance Specialist –
Medical Devices Location:
Onsite in
Riviera Beach, Florida Salary:
Up to $95,000 per year
Employment Type:
Full-time, 40 hours per week We are supporting a U.S.-based medical device manufacturer that designs and builds high-specification Class II medical devices within Respiratory for hospital and clinical environments. Known for engineering excellence and a strong commitment to regulatory compliance, the company has a long-standing reputation for delivering safe, effective, and durable systems that support patient care in critical settings. As part of their ongoing growth, the company is seeking a Quality Assurance Compliance Specialist to join their onsite team in Riviera Beach, Florida. This role is ideal for someone who thrives in a regulated manufacturing environment and has the confidence to lead audits, maintain compliance systems, and contribute to continuous quality improvement.
Key Responsibilities:
Lead and coordinate internal and external audit teams Develop, review, and maintain quality and compliance documentation Ensure ongoing compliance with
ISO 13485, MDD/MDR, CE
marking, and CSA standards Work closely with engineering, manufacturing, and leadership to support quality and regulatory goals Identify and implement opportunities for continuous improvement within the quality system
Requirements:
Strong experience working with
ISO 13485
quality systems In-depth knowledge of
MDD/MDR, CE/CSA
standards Proven experience leading audit teams and managing audit activities Excellent documentation and communication skills Must be able to work onsite 40 hours per week in Riviera Beach, FL Nice to
Have:
Experience in a regulated manufacturing setting, ideally within medical devices Familiarity with FDA regulations and other international standards This is an exciting opportunity to join a company that manufactures life-enhancing technology and takes pride in producing high-performance, compliant medical systems that make a difference in patient care. If you’re ready for a role where your expertise will be valued and your contributions will have real impact, we’d love to hear from you.
