MAIN PURPOSE OF ROLEAn 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 wih 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.- Interfaces primarily with internal company contacts.- Plans and conducts small size assigned projects within engineering specialty requiring conventional types of plans, investigations, and/or equipment.- Investigates, conducts tests or experiments, gathers data, and performs preliminary analysis. Reports findings. Prepares and communicates recommendations.- 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).- 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.- Identifies and Evaluates areas of risk with respect to compliance, Product/Mfg performance, Develops procedures, maintain FMEAs.QUALIFICATIONS- Bachelor's degree- Engineering, science or closely related discipline is desired, or equivalent technical.- Minimum 80% of bachelor's degree completed and at least 1 year of experience in manufacturing or quality in the medical device industry.Experience/Background- 1 year of experience in medical device or related industries- Intermediate commands of English / RequiredPreferred Qualifications & Education- Quality Background desired.- FDA/ISO regulation knowledge desired.- Statistic knowledge desired.- Personal skills needed include Accountability, nimble learning, diligence, Resourcefulness, and customer focus. Effective communication skills.
