Quality Engineer II (2nd Shift)

• 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

• A company that is 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.

• Follows all regulations and standards for quality, Environmental, Health, Safety, and Energy (EHS&E) Global Policies, Abbott engineering standards, and other governance areas as applicable.
• Implements and maintains the effectiveness of the Quality System.
• Identifies areas of risk with respect to compliance to internal and external requirements.
• Completes Non-conformance, CAPA, and complaint investigations and offers multiple solutions to issues with clear advantages and disadvantages.
• Influences key partners to develop and maintain QA procedures, forms, and systems.
• Leads meetings and communications for QA system information, concerns, and updates.
• Help drive standard methodologies for data trending and tracking and identification of manufacturing related complaints in alignment with Abbott goals.
• Follows 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.
• Performs other related duties and responsibilities, on occasion, as assigned.

• Bachelor level degree in Engineering, Technical Field, or equivalent (advanced degree preferred)
• 2-5 years technical experience
• Previous Quality assurance/engineering experience and use of Quality tools/methodologies
• Good communication and interpersonal skills
• Advanced computer skills, including statistical/data analysis and report writing skills
• Ability to work within a team and as an individual contributor in a dynamic, changing environment.
• Strong verbal and written communication skills with ability to effectively communicate at multiple levels in the organization.
• Multitasks, prioritizes and meets deadlines in timely manner.
• Excellent organizational and follow-up skills, as well as attention to detail.

• Detailed knowledge of FDA, GMP, and ISO 13485
• ASQ CQT, CQE, CQA certification
• Six Sigma root cause analysis/problem solving training and experience

Abbott