In September 2024, Morgan Scientific Incorporated (MSI) joined the Vitalograph group of companies as a wholly owned subsidiary. Vitalograph - a global leader in respiratory diagnostics - has had a long and enduring relationship with Morgan Scientific. For both companies, the decision is a natural progression as the combined expertise allows the enlarged organisation to focus on delivering the best possible diagnostic solutions that can enable a better understanding of lung health.
The acquisition of Morgan Scientific is a key milestone in Vitalograph's plan to develop its respiratory diagnostics business globally, furthering its goal of providing comprehensive testing solutions that enable the best possible respiratory healthcare. Vitalograph is implementing an ambitious growth strategy and is on track to treble its respiratory diagnostics business in the four years leading to 2026.
Benefits:
- 401(k)
- Health insurance
- Paid time off
- Professional development assistance
- Tuition reimbursement
Job Summary:
As a
Principal Inbound/Outbound QC Testing Support, you will oversee quality assurance testing for both inbound and outbound shipments of our respiratory diagnostic products. This role is responsible for developing and implementing quality protocols to ensure that all equipment and components meet stringent industry standards before distribution to healthcare providers. Your expertise in quality assurance, testing, and compliance will be essential in maintaining our commitment to high-quality diagnostics that enable effective patient care.
Key Responsibilities:
- Quality Assurance Testing: Conduct and oversee QC testing for all incoming and outgoing respiratory diagnostic equipment, ensuring compliance with quality standards and regulatory requirements.
- Inspection Protocols: Develop, implement, and maintain inspection and testing protocols for both inbound supplies and outbound shipments to ensure product integrity and functionality.
- Documentation and Reporting: Accurately document test results, quality checks, and any issues encountered during testing. Report findings to relevant departments and provide recommendations for corrective actions.
- Cross-Functional Collaboration: Work closely with warehouse, logistics, procurement, and customer service teams to resolve quality issues quickly and prevent recurrence.
- Compliance Management: Ensure that all QC procedures align with industry regulations (such as FDA, ISO standards) and internal compliance guidelines for medical devices and respiratory diagnostics.
- Process Improvement: Identify areas for improvement in the QC process and lead initiatives to enhance testing efficiency, product quality, and supply chain reliability.
- Training and Mentorship: Train and mentor junior QC staff and testing support personnel, ensuring adherence to quality standards and fostering a culture of quality across the team.
Role Requirements:
- Education: Bachelor's degree in quality assurance, engineering, life sciences, or a related field; advanced certifications in quality management (e.g., Six Sigma, CQE) are a plus.
- Experience:
- 8+ years of experience in quality assurance or testing within the medical device, healthcare, or diagnostics industry.
- Strong background in QC protocols, equipment testing, and regulatory compliance.
- Technical Skills:
- Proficient in QC software and tools for testing, inspection, and data management.
- Familiarity with healthcare regulations and quality standards, including ISO 13485, FDA QSR, and other relevant guidelines.
- Analytical and Problem-Solving Skills: Strong ability to analyze test data, detect quality trends, and implement corrective actions to improve product quality.
- Communication and Leadership: Excellent written and verbal communication skills, with the ability to present findings and recommendations to senior leadership and mentor team members.