Quality Engineer I

at  Abbott Laboratories

Alajuela, Provincia de Alajuela, Costa Rica -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate07 Feb, 2025Not Specified12 Nov, 20241 year(s) or aboveEnglish,ManufacturingNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

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