Sr Associate Quality Engineer

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.

• Oversight of the Corrective Action/Preventive Action (CAPA) program for their area of responsibility, including review of all non-conformances, corrective/preventive actions for completeness, and execution of effectiveness checks when required.
• Assist with non-conformance investigations assigned to Quality Assurance and ensure timely closure of CAPA records.
• Generate status reports from applicable QMS applications, analyze data to identify potential trends and areas for improvement, and maintain related company measurements.
• Repackage and relabel projects in support of client requests as Project Leader, including communication with client and Program Manager, pricing proposals, creation of the project protocol, inspection of the project as required by protocol, and filing necessary paperwork with client, Program Manager, and/or regulators.
• Manage all special client project requests, client complaint memos, and other relevant client memos.
• Serve as a backup for the Associate Quality Engineer to perform inspection and release processes for incoming and returned products, including downloading and reviewing temperature device data, communicating results to clients, obtaining proper client approval, electronic storage of inspection records, and product retains.
• Assist with client and regulatory activities, quality-related training, validation of storage areas/systems/equipment where required, and other duties as assigned by manager.

11:00 AM – 7:30 PM. This role requires you to be on site 5 days a week.

Degree or equivalent and typically requires 2+ years of relevant experience.

• 3-5 years in a pharmaceutical quality/regulatory environment, preferred.
• Quality Management System and/or Document control management experience, preferred.
• Knowledge of pharmaceutical regulations, including FDA requirements, preferred.

• Ability to express ideas clearly both in written and oral communications.
• Ability to enter data accurately.
• Ability to handle multiple tasks well.
• Detail-oriented knowledge of word processing, database, and spreadsheet programs (preferably MS Office).
• Ability to work with internal departments to accomplish objectives and meet established deadlines.
• Personable, self-starter with a good attitude, and enjoy external and internal contact on the phone and in person with supervisors, co-workers, customers, and potential clients.

Our Base Pay Range for this position: $65,600 – $109,300.

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.