Associate Quality Engineer

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 Title Associate Quality Engineer 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. You’ll also have access to: Career development with an international company where you can grow the career of which you dream. 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 bachelor’s 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. A company recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists. The Opportunity This position works out of our Houston, TX location in the Abbott Vascular Division. Abbott Vascular provides innovative, minimally invasive, and cost‑effective products for the treatment of vascular disease. This Is An Onsite Daily Required Position. What You’ll Work On This position is responsible for developing and maintaining quality engineering methodologies and providing quality engineering support within manufacturing, or system/services support. Main Responsibilities Identify and implement effective process control systems to support the development, qualification, and ongoing manufacturing of products to meet or exceed internal and external requirements. Lead in the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements. Assist in the development and execution of streamlined business systems which effectively identify and resolve quality issues. Apply sound, systematic problem‑solving methodologies in identifying, prioritizing, communicating, and resolving quality issues. Design and conduct experiments for process optimization and/or improvement. Appropriately document experiment plans and results, including protocol writing and reports. Lead process control and monitoring of CTQ parameters and specifications. Lead and implement various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing). Lead the investigation, resolution and prevention of product and process non‑conformances. Participate in or lead teams in supporting quality disciplines, decisions, and practices (e.g., represent the Quality function as a Core Team Member). Lead in the completion and maintenance of risk analysis. Work with design engineering in the completion of product verification and validation. Work with microbiology to ensure appropriate environmental monitoring and that microbiology requirements are considered in product and process development activities. Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintain positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. Education Bachelor’s Degree in Engineering or a Technical Field, or equivalent experience, or an equivalent combination of education and work experience. Master’s Degree Preferred. Experience 0–2+ years of Engineering experience and demonstrated use of Quality tools/methodologies. Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971. Solid communication and interpersonal skills. Project management and leadership skills, including the demonstrated ability to lead multi‑departmental project teams and resolve quality‑related issues in a timely and effective manner. Advanced computer skills, including statistical/data analysis and report writing skills. Prior medical device experience preferred. Experience implementing various product and process improvement methodologies (e.g., Six Sigma and Lean Manufacturing). ASQ CQE or other certifications preferred. 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 a timely manner. Strong organizational and follow‑up skills, as well as attention to detail. Apply Now Abbott is an Equal Opportunity Employer, committed to employee diversity. The base pay for this position is $50,700.00 – $101,300.00. In specific locations, the pay range may vary from the range posted. #J-18808-Ljbffr