Quality Site Specialist
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.
Are you passionate about delivering top-tier quality standards? As a Quality Site Specialist, you’ll be at the forefront of ensuring operational excellence and regulatory compliance at our facility. Working within our dynamic Quality department, you’ll play a vital role in safeguarding product integrity and supporting continuous improvement initiatives.
Join a collaborative environment where your expertise directly impacts patient safety and product reliability. What You’ll Do (Responsibilities) Monitor site processes to ensure compliance with quality systems and regulatory requirements. Conduct audits, inspections, and risk assessments to identify opportunities for improvement.
Lead and support the investigation and resolution of quality issues, collaborating with cross-functional teams. Develop, implement, and maintain documentation related to quality procedures and corrective actions. Champion best practices and drive quality culture throughout the site.
Contribute to project teams focused on process optimization and new product introductions. Basic Requirements Degree or equivalent and typically requires 4+ years of relevant experience Strong knowledge of GMP, ISO, or similar quality standards.
Excellent problem-solving and analytical skills. Proven ability to work independently and as part of a team. Preferred Skills/Experience Master’s degree or relevant certifications (e.g., Six Sigma, CQE). 3+ years’ experience in quality assurance, quality control, or regulatory affairs within the pharmaceutical, biotech, or medical device industry.
Experience with electronic quality management systems (eQMS). Exceptional communication and stakeholder management abilities. Project leadership experience. Adaptability and a proactive mindset. Travel/In-Office/Physical Requirements This position requires onsite presence at our Dublin facility with limited travel to partner sites (up to 10%).
You’ll work in a state-of-the-art office and production environment, adhering to all safety protocols. Physical requirements are limited to routine office and inspection activities. 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 $81,500 - $108,600 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) Disability_Accommodation@McKesson.com or (Canada) Accessibility@mckesson.ca . Resumes or CVs submitted to this email box will not be accepted.
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