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Open nowPosted today

Senior Quality Specialist

McKesson695 open roles

Pay
$135,000 – $140,000 a year
Where
USA PA Remote
Work mode
Remote
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Your applicationOpen nowSenior Quality SpecialistMcKesson · USA PA Remote
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The clock on this job

Early applications get read.

14.0% of postings close within 7 days. Measured by our own scanner across the market. McKesson postings stay open a median of 20 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.7%3 days
  3. 14.0%7 days
  4. 22.5%14 days
  5. 38.3%30 days
  6. 59.0%60 days
This job: posted today

McKesson median: 20 days open

The posting

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 Senior Quality Specialist handles complex quality issues across US Pharmaceutical Distribution. The role leads investigations, temperature excursion reviews, and corrective and preventive actions (CAPA), and supports recalls and product disposition decisions. This person is expected to work independently, use sound judgment, and be a trusted resource for colleagues and business partners. The position also helps improve quality systems and maintain compliance across the distribution network.

Compensation: The target salary for this role is between $135,000 and $140,000 yearly with opportunity for an annual bonus.

Key Responsibilities

  • Leads complex product quality investigations, temperature excursion reviews, CAPAs, and critical-event activities. Determines the best approach, evaluates risk, identifies root cause, and documents clear, well-supported conclusions.
  • Looks for practical ways to improve quality processes and electronic quality management systems. Works with the appropriate teams to simplify processes, strengthen compliance, and improve the quality of data and documentation.
  • Provides technical guidance on investigations, recalls, CAPAs, quality risk assessments, and product disposition decisions. Helps colleagues work through difficult issues and serves as a resource when additional expertise is needed.
  • Leads cross-functional projects involving Operations, Compliance, distribution centers, Technology, and external partners. Keeps stakeholders informed, resolves issues, and makes sure agreed actions are completed.
  • Reviews investigation data, metrics, and trends to identify recurring problems or broader risks. Recommends corrective or preventive action and explains the findings to business and quality leaders.
  • Applies relevant FDA requirements, 21 CFR, the Drug Supply Chain Security Act, United States Pharmacopeia standards, Good Distribution Practice, current Good Manufacturing Practice, and internal procedures. Supports audits, inspections, and readiness activities.
  • Develops training, shares lessons learned, and provides mentoring and technical support to help others strengthen their investigation and quality-system skills.

Minimum Requirement

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

Education

Bachelor's degree in science, engineering, pharmacy, quality, or a related field, or equivalent experience.

Critical Skills

  • At least 7 years of experience in pharmaceutical quality, investigations, CAPA, recalls, regulated distribution, cold-chain operations, quality systems, or another regulated environment.
  • Experience independently handling complex quality or compliance issues and making risk-based decisions using sound technical judgment.
  • Experience leading projects and influencing decisions across teams without direct authority.
  • Strong knowledge of investigation methods, root cause analysis, CAPA, quality risk management, product disposition, data integrity, and audit or inspection readiness.
  • Working knowledge of applicable FDA regulations, 21 CFR, the Drug Supply Chain Security Act, Good Distribution Practice, current Good Manufacturing Practice, and relevant United States Pharmacopeia standards.
  • Experience using electronic quality management systems and working with quality data, technical documents, and process improvements.
  • Strong writing, communication, presentation, and organizational skills. Able to explain technical issues clearly and work effectively with different teams.
  • Ability to manage several priorities, recognize when an issue needs to be escalated, and work with limited supervision.
  • Ability to work primarily from a remote location and collaborate regularly with distribution centers, cross-functional teams, and corporate partners.
  • Ability to occasionally work in distribution center, operational, or warehouse environments to support investigations, audits, and quality initiatives.
  • Ability to travel domestically, including occasional overnight travel, up to 10%.
  • Ability to work for extended periods at a computer and review detailed electronic records, data, and quality documentation.

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

$103,500 - $172,500

McKesson has become aware of online recruiting-related scams in which individuals who are not affiliated with or authorized by McKesson are using McKesson’s (or affiliated entities, like CoverMyMeds or RxCrossroads) name in fraudulent emails, job postings or social media messages. In light of these scams, please bear the following in mind:

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

McKesson Talent Advisors do not communicate with candidates via online chatrooms or using email accounts such as Gmail or Hotmail. Note that McKesson does rely on a virtual assistant (Gia) for certain recruiting-related communications with candidates.

McKesson job postings are posted on our career site: careers.mckesson.com.

McKesson 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.

McKesson 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) [email protected] or (Canada) [email protected]. Resumes or CVs submitted to this email box will not be accepted.

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