Job Details

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.

The Operations Quality Manager is responsible for supporting and sustaining the Quality Management System and Quality initiatives. The role will ensure that procedures, analytics, and technology are being leveraged to maximize quality processes and compliance. 

Key Responsibilities

• Lead licensing compliance for distribution centers including reviewing and approving license requirements.
• Establish and lead QMR process.
• Develop quality scorecard and metrics to track DC performance and ensure compliance.
• Manage and support activities to ensure continuous improvement and compliance of our QMS.
• Support CAPA activities associated with continuous improvement, audit findings, QMS updates, etc.
• Support with updating SOPs and Work Instructions to ensure compliance with internal and external regulatory requirements.
• Support additional QMS activities as needed.
• Evaluate improvement opportunities from event resolution.

Minimum Requirement

Degree or equivalent and typically requires 7+ years of relevant experience.

Education

4-year degree in business, STEM, or related field or equivalent experience.

Critical Skills

• 7+ years of healthcare experience.
• Demonstrated experience managing complex business processes, technology and change programs across a matrixed organization.
• Knowledge of FDA, DEA, State BoP and other regulatory agencies.
• Knowledge of wholesale distribution and/or pharmaceutical manufacturing.
• Knowledge of wholesale and/or regulatory licensing requirements.
• Experience leading or participating in management reviews.
• Excellent written and verbal communication skills.
• Strong analytical skills.

Additional Knowledge & Skills

• Technical writing experience.
• Involvement with FDA or other regulatory body inspections.
• CAPA experience.
• Worked in a highly matrixed environment.

Working Conditions

• Able to travel 10% of the time.
• Remote work environment – Work from Home.
• Must be authorized to work in the US unrestricted – This position is not eligible for sponsorship.

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

McKesson is an Equal Opportunity Employer

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

Join us at McKesson!