Quality Control Manager

Logistics done differently.

You know how to bring out the best in your team. Youre ready to grow as a professionalto go bigger and better. As the Quality Control Manager at XPO Logistics, you will be responsible for providing leadership and oversight for the facility (a Medical Device site), leading and participating in all facility audits, and developing, implementing, and maintaining quality systems to ensure FDA and ISO compliance. If youre looking for a growth opportunity and a better lifestyle, join us at XPO.

Pay, benefits and more.

We are eager to attract the best, so we offer competitive compensation and a generous benefits package, including full health insurance (medical, dental and vision), 401(k), life insurance, disability and more.

What youll do on a typical day:

  • Develop the vision for the Medical Device organization and deploy processes to enable rapid targeted growth
  • Plan, develop, and monitor the Quality Management System (QMS) for all business clients/customers
  • Manage Corrective and Preventive Action (CAPA) teams to provide 8D documentation, which delivers accurate, thorough, and timely problem resolution for customers
  • Verify that quality, operational, and process improvement projects are efficiently and effectively implemented; optimize quality systems to effectively identify, measure, and reduce costs of quality activities
  • Communicate with operations team and customers to resolve any quality incidents
  • Effectively maintain all QMS documentation including the annual document review process; administer associate QMS training programs
  • Provide leadership in the execution of Quality Systems activities related to CAPA, internal/external audits, management review, nonconforming product, QMS training activities, validations, root cause analysis, etc.

What you need to succeed at XPO:

At a minimum, youll need:

  • 7 years of experience in the Medical Device industry with strong quality system oversight as it relates to ISO 13485:2016 and FDA Regulation 21 CFR 820
  • Extensive, hands-on experience with QMS, performing CAPA, FMEA, control plans, and required cGMP compliance
  • Proficiency in Microsoft Office

Itd be great if you also have:

  • ASQ certification as a Certified Quality Auditor (CQA) and Certified Quality Engineer (CQE)
  • Ability to lead teams to resolve quality/technical issues
  • Strong aptitude for understanding and analyzing large amounts of data from multiple sources
  • Excellent verbal and written communication skills

Be part of something big.

XPO provides cutting-edge supply chain solutions to the world's most successful companies, including Disney, Pepsi, L'Oral, Toyota and many others. Were the fastest-growing transportation company on the Fortune 500 list and were just getting started.

We are proud to be an Equal Opportunity/Affirmative Action employer. Qualified applicants will receive consideration for employment without regard to race, sex, disability, veteran, or other protected status.

The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All employees may be required to perform duties outside of their normal responsibilities from time to time, as needed.

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