Quality Engineer I
at Abbott Laboratories
Alajuela, Provincia de Alajuela, Costa Rica -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 07 Feb, 2025 | Not Specified | 12 Nov, 2024 | 1 year(s) or above | English,Manufacturing | No | No |
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Citizen | GC |
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Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
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Description:
ABOUT ABBOTT
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
REQUIRED 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.
- 1 year of experience in medical device or related industries
- Intermediate commands of English / Required
Responsibilities:
- Apply quality principles, analyze quality records, prepares reports and recommend 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.
- 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, maintains FMEAs.
- Resolves problems, such as production process deviations, and 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 and product/Mfg. performance, Develops procedures, and maintains FMEAs.
REQUIREMENT SUMMARY
Min:1.0Max:6.0 year(s)
Information Technology/IT
Production / Maintenance / Quality
Software Testing
Graduate
The medical device industry
Proficient
1
Alajuela, Provincia de Alajuela, Costa Rica