JOB DESCRIPTION : MAIN PURPOSE OF ROLE
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.
Apply quality principles, analyzes quality records, prepares reports and recommends improvements.
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.
Bachelor Degree in engineering, science or closely related discipline
3 years of experience in medical device or related industries.
Intermediate commands of English (B1) / Required