**_MAIN PURPOSE OF ROLE_**An engineering professional who applies scientific knowledge, engineering knowledge, mathematics, and ingenuity to complete assignments related to a specific technical field or discipline.Provide Quality support to manufacturing, helping to ensure delivery of the highest quality product to the customer. Provide support to Development /Improvement teams for new or existing products.Ensure that activities are performed and documented per systems and procedure in accordance with Abbott Policies and applicable Quality And Regulatory Requirements.**_ MAIN RESPONSIBILITIES_**- Conduct inspection, verification and validation of components or materials used in development processes.- Identify and address recurring problems either with the quality of the product or the reliability of testing procedures.- Document quality issues and performance measures for management review.- Interfaces primarily with internal company contacts and begins an extensive external network.- Plans and conducts small- to medium-size assigned projects within engineering specialty requiring conventional types of plans, investigations, and/or equipment.- Anticipates future directions. Benchmarks internally and externally.- Independently investigates, conducts tests or experiments, gathers data, and performs preliminary analysis. Reports findings. Prepares and communicates recommendations and respective action plans.- Builds relationships. Initiates and cultivates open, honest relationships with colleagues, developing an understanding of others' needs.- Identifies and Evaluates areas of risk with respect to compliance, Product/Mfg performance, Develops procedures, maintain FMEAs.- Resolves problems, such as production process deviations, non-conformances (CAPA), field product performance, urgent out-of-stock replacements, and crisis situations requiring fast, astute decisions with rapid implementation by utilizing technical training and experience.- May work in combination with SQE and Receiving Inspectors focused on driving improvements and CAPA in the quality of components sourced from outside suppliers.- Provides technical support in the supplier corrective action, manufacturing yield and field failures.**_ QUALIFICATIONS_**- Bachelor Degree in Engineering, science or closely related discipline- 3 years of experience in medical device or related industries.- Intermediate commands of English (B1)
