Biomed Quality Specialist

McKesson•Jacksonville, FL

1d•Hybrid

About The Position

McKesson is an impact-driven, Fortune 10 company that touches virtually every aspect of healthcare. We are known for delivering insights, products, and services that make quality care more accessible and affordable. Here, we focus on the health, happiness, and well-being of you and those we serve – we care. What you do at McKesson matters. We foster a culture where you can grow, make an impact, and are empowered to bring new ideas. Together, we thrive as we shape the future of health for patients, our communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you. Biomed Quality Specialist Why This Role Matters This is a unique opportunity to step into a high‑impact role at a pivotal moment for McKesson BioMed. As our organization continues to expand the scope of medical devices we support, we’re looking for a seasoned biomedical professional who is excited to help shape the future of our training, quality, and technical standards —not just maintain what already exists. Job Summary In this role, the Quality Specialist will drive regulatory and ISO compliance across the Biomed Solutions business. This individual will conduct both on‑site and virtual assessments to identify improvement opportunities that may require intervention and remediation planning, ensuring successful outcomes during ISO, FDA, or external audits. We are specifically seeking an experienced Biomedical Technician who brings broad medical device experience and can provide mentorship and leadership in the development of our internal technical training program as the organization expands beyond its current device portfolio. McKesson BioMed currently supports a core portfolio of medical devices, including infusion pumps, feeding pumps, and ventilators. While experience with these devices is important, preferred candidates will bring broader medical device experience and be able to help expand the organization’s device footprint by establishing training, competencies, and quality standards that support growth into additional medical technologies. In addition, this role supports the McKesson BioMed business through ongoing mentorship and engagement, helping Biomed Depots and Field Service teams consistently operate within McKesson standards for compliance and quality service delivery. This work is critical to enabling continued growth and expansion of services . Growth, Development & Career Path We’re seeking someone who is invested in this role and also excited about long‑term growth. This position offers exposure across BioMed operations, quality systems, and enterprise initiatives, opening pathways toward leadership roles within BioMed, broader Quality organizations, or other areas across NewCo/McKesson. This is a role where your experience will be valued today—and your potential supported tomorrow. Travel Up to 50% travel to Biomed Center locations and customer sites. Traditional home office environment. Preference for proximity to an existing Biomed Center in Jacksonville, FL; Los Angeles, CA; Chicago, IL; or Pittsburgh, PA .

Requirements

4+ years of relevant experience
Ability to travel up to 50% to Biomed Center locations and customer sites
4+ years of experience in the medical device service industry related to preventive maintenance, calibrations, and repair of biomedical equipment.
Working knowledge of accreditation and regulatory agencies, including The Joint Commission (TJC), Accreditation Commission for Health Care (ACHC), FDA, Centers for Medicare & Medicaid Services (CMS), and ISO 13485:2016 .
Proven ability to manage multiple projects and competing deadlines within a fast‑paced environment.
Excellent verbal, written, and presentation skills, with the ability to communicate clearly and tailor messaging to diverse audiences.
Self‑starter capable of working independently, exercising sound judgment, and proactively engaging support as needed.
Strong service mindset with a passion for helping Biomed teams succeed by removing barriers, providing guidance, and setting high performance standards.
Ability to collaborate effectively across functional teams within a matrixed organization.
Proficiency in Microsoft Office applications, including Excel, PowerPoint, Word, and related tools.

Nice To Haves

Preferred experience supporting a broad range of medical devices beyond infusion pumps, feeding pumps, and ventilators , with the ability to translate that experience into scalable training programs, competency frameworks, and quality standards that support expansion into additional medical technologies.
Direct experience training other technicians, along with demonstrated knowledge of quality‑related areas such as good documentation practices and process improvement strongly preferred.

Responsibilities

Participate in and take ownership of executing and monitoring the Quality Management System (QMS) , including CAPA, complaints, document control, training, ISO internal audits, recalls, and all other components of an ISO 13485 Quality System.
Conduct on‑site and virtual assessments to identify compliance gaps and improvement opportunities that may require intervention and remediation planning to support successful ISO, FDA, or external audit outcomes.
Ensure compliance with all applicable regulatory requirements and McKesson Quality Management System standards.
Mentor Biomed and Field Service teams to drive rapid transformation toward meeting and exceeding established McKesson performance and quality metrics.
Deliver on‑site and virtual QMS training to Biomed and Field Service employees.
Partner closely with the management team to foster a strong quality‑driven culture, ensuring employees understand the importance of quality in their daily work.

Stand Out From the Crowd

Upload your resume and get instant feedback on how well it matches this job.

Upload and Match Resume