VP Manufacturing Quality: Strategy, Compliance & Leadership

Medline Industries, LP; Northfield (MN); On-site; USD 234,000 - 351,000; Full time

Benefits offered by this job

Health insurance

Life and disability

401(k) contributions

Paid time off

Job summary

Medline Industries, LP is seeking a Director of Quality Assurance to oversee QA functions across divisions, ensuring proper controls, staffing, and regulatory compliance. The role involves directing QA for new product development and supplier qualification, mentoring staff, and coordinating with Corporate Quality and division leadership.

You will ensure alignment with FDA, EU MDR and cGMP standards, build cross-functional relationships, and maintain robust training programs.

Qualifications

• Bachelor’s degree required.
• 7+ years of QA related experience in a business environment.
• At least 5 years of experience managing people, including hiring, developing, motivating and directing staff.

Responsibilities

• Oversee, lead and set strategic direction for the assigned divisions’ QA functions.
• Coordinate with Corporate Quality and division leadership to ensure adherence to FDA, MDR and other applicable requirements/cGMP’s.
• Develop and mentor staff through onboarding, training and performance management; maintain morale and ensure staffing with required competencies.
• Facilitate communication between QA Directors, Managers and Specialists and their divisional teams.
• Direct quality efforts for new product development and supplier qualification.
• Ensure communication between related functions, and meet project timelines and objectives.
• Develop training programs and approve process and procedural changes.
• Ensure systems support a smooth process for new products and services and outstanding customer service.

Job description

Medline Industries, LP is seeking a Director of Quality Assurance to oversee QA functions across divisions, ensuring proper controls, staffing, and regulatory compliance. The role involves directing QA for new product development and supplier qualification, mentoring staff, and coordinating with Corporate Quality and division leadership.

You will ensure alignment with FDA, EU MDR and cGMP standards, build cross-functional relationships, and maintain robust training programs.