Senior Technical Quality Supervisor

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 115,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: Abbott is a global healthcare leader, creating breakthrough science to improve peoples health. Were always looking towards the future, anticipating changes in medical science and technology. Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. Youll also have access to: Career development with an international company where you can grow the career you dream of . Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year An excellent retirement savings plan with high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelors degree. A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune. MAIN PURPOSE OF THE ROLE This individual will be responsible for leading and overseeing the daily operations of Receiving Inspection and Supplier Quality, while providing leadership, direction, and support to engineers, technicians, and inspectors. This role is based out of Minnetonka, MN and is an ONSITE role. MAIN RESPONSIBILITIES Provide daily leadership, supervision, work direction, and on-the-job training to engineers, technicians, and inspectors, fostering a high-performing and engaged team environment. Develop and maintain a competent workforce through effective recruitment, coaching, communication, recognition, performance management and employee development. Monitor, prioritize, and allocate departmental resources and workloads to ensure internal customer requirements, schedules, and business objectives are achieved. Lead department operations while driving collaboration across cross-functional teams, including Quality, Manufacturing, Supply Chain, Engineering, and Regulatory Affairs, to support organizational goals. Build and maintain effective working relationships with external stakeholders, including suppliers, contract laboratories, auditors, and regulatory agencies, to ensure alignment with quality and compliance requirements. Ensure adherence to company policies, quality systems, and applicable regulatory standards, while monitoring compliance and driving continuous improvement initiatives. Contributes to establishing department goals, objectives and accountabilities. Recommends, justifies and acquires measurement equipment and supplies to meet department objectives. Monitor and improve the effectiveness of inspection and testing processes through data-driven decision-making and continuous improvement methodologies. Oversees and evaluates the effectiveness of inspection and testing procedures, driving enhancements to ensure quality, efficiency, and compliance. Leads, coaches, and motivates team members to achieve performance objectives while fostering a culture of accountability, engagement, and high performance. Promotes and sustains a department culture focused on continuous improvement, operational excellence, and customer satisfaction. Effectively communicate and collaborate with internal and external partners to resolve issues, manage risks, and achieve business objectives. Department's technical lead during audits, inspections, and quality system inquiries, providing expert guidance and support to ensure compliance and successful outcomes. 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 communication and collaboration with all levels of employees, customers, contractors, and vendors. QUALIFICATIONS Education Bachelors Degree (± 16 years) in Business or related field or an equivalent combination of education and work experience. Experience/Background Minimum 5 years experience in related experience, including supervision. Previous Quality inspection, technician or engineering experience required. Knowledge of FDA, GMP, and ISO 13485. Strong communication and leadership skills. Prior medical device experience preferred. ASQ certification or equivalent preferred. Ability to work in a highly matrixed and geographically diverse business environment. Strong leadership skills, including the ability to set goals and provide positive and constructive feedback respectfully to build positive relationships and improve business results. Ability to work effectively within a team in a fast-paced changing environment. Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. Multi-tasks, prioritizes and meets deadlines in timely manner. Strong organizational, planning, and follow-up skills and ability to hold others accountable. Ability to travel approximately 25%, including internationally. Apply Now Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $78,000.00 $156,000.00 In specific locations, the pay range may vary from the range posted. JOB FAMILY: Operations Quality DIVISION: CRM Cardiac Rhythm Management LOCATION: United States > Minnesota > Minnetonka : 14900 Minnetonka Industrial Road ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 25 % of the Time MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday) Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans. EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf Abbott is about the power of health. For more than 135 years, Abbott has been helping people reach their potential because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions across the spectrum of health, around the world, for all stages of life. Whether its next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health. The people of Abbott come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well-being of millions of people. They push the boundaries to help manage and treat some of lifes greatest health challenges. We invite you to explore opportunities at Abbott, to see if your talents and career aspirations may fit with our openings. An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce. Follow Us: Facebook LinkedIn YouTube Twitter