Quality Supervisor

Abbott • Los Angeles, CA

2d • $81,500 - $141,300

About The Position

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: MAIN PURPOSE OF THE ROLE Provide leadership to inspectors and technicians that support receiving, in-process and final inspection, tool inspection/qualifications and first article inspections.

Requirements

• Associates Degree (± 13 years) or Bachelor's preferred or an equivalent combination of education and work experience.
• Minimum 5 years of Quality supervisory experience in medical industry and Quality systems auditing experience desired.
• Experience working in a broader enterprise/cross-division business unit model preferred.
• Ability to work in a highly matrixed and geographically diverse business environment.
• Ability to work within a team and as an individual contributor in a fast-paced, changing environment.
• Ability to leverage and/or engage others to accomplish projects.
• Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
• Multitasks, prioritizes and meets deadlines in timely manner.
• Strong organizational and follow-up skills, as well as attention to detail.
• Ability to travel approximately 15-25%, including internationally.

Nice To Haves

• ASQ certification in quality, six sigma, and/or lean manufacturing is desired.
• Experience working in a broader enterprise/cross-division business unit model preferred.

Responsibilities

• Assure timely inspections that support materials, product releases and in-process inspections.
• Maintain staff and equipment to assure appropriate technical capabilities.
• Monitor inspection procedures for effectiveness.
• Monitor compliance to appropriate regulatory standards.
• Effectively communicate with and provide support to other departments as necessary.
• Maintain a department culture of continuous improvement.
• Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
• Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments.
• Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree
• Number of Employees: 5,001-10,000 employees