**_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)