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Biomed Quality Specialist

Why This Role Matters

This is a unique opportunity to step into a high‑impact role at a pivotal moment for Mc Kesson Bio Med. 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.

Mc Kesson Bio Med 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 Mc Kesson Bio Med business through ongoing mentorship and engagement, helping Biomed Depots and Field Service teams consistently operate within Mc Kesson 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 Bio Med operations, quality systems, and enterprise initiatives, opening pathways toward leadership roles within Bio Med, broader Quality organizations, or other areas across New Co/Mc Kesson.
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.

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 Mc Kesson Quality Management System standards.

• Mentor Biomed and Field Service teams to drive rapid transformation toward meeting and exceeding established Mc Kesson 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.

Minimum Requirements

• 4+ years of relevant experience

• Ability to travel up to 50% to Biomed Center locations and customer sites

Critical Specialized Skills

• 4+ years of experience in the medical device service industry related to preventive maintenance, calibrations, and repair of biomedical equipment.

• 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.

• 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.

Additional Knowledge & Skills

• 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.

Working Conditions

• Up to 50% travel to Biomed Center locations and customer sites where walking throughout those facilities and extended periods of standing will be needed

• Remaining time spent working from home-based office at a computer

We are proud to offer a competitive compensation package at McKesson as part of our Total Rewards. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. The pay range shown below is aligned with McKesson's pay philosophy, and pay will always be compliant with any applicable regulations. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered. For more information regarding benefits at McKesson, please click here.

Our Base Pay Range for this position

$79,100 - $131,900

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Mc Kesson Talent Advisors will never solicit money or credit card information in connection with a Mc Kesson job application.

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Mc Kesson is an Equal Opportunity Employer

McKesson provides equal employment opportunities to applicants and employees, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, age, genetic information, or any other legally protected category. For additional information on McKesson’s full Equal Employment Opportunity policies, visit our Equal Employment Opportunity page.

Mc Kesson is committed to being an Equal Employment Opportunity Employer and offers opportunities to all job seekers including job seekers with disabilities. If you need a reasonable accommodation to assist with your job search or application for employment, please contact us by sending an email to (United States) [Disability_Accommodation@Mc Kesson.com](mailto:Disability_Accommodation@Mc Kesson.com) or (Canada) Accessibility@mckesson.ca. Resumes or CVs submitted to this email box will not be accepted.

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