Associate Quality Engineer — MedTech (Second Shift)

Abbott Laboratories; Barceloneta (PR); On-site; USD 45,000 - 90,000; Full time

Benefits offered by this job

Health Insurance

401K Savings Plan with company match

Life insurance for you and your spouse

Short Term Disability

Long Term Disability

Education Assistance

Employee Assistance Program

Vacation

Sick Days

Personal Days

Job summary

Abbott Laboratories in Barceloneta, PR, is seeking an Associate Quality Engineer to support the AV division on second shift. You will help ensure the delivery of the highest quality medical devices by applying quality engineering principles across manufacturing processes.

The role requires a bachelor degree in engineering and at least 2 years of quality/compliance experience in medical devices, plus fluency in English and Spanish.

Qualifications

• Bachelor degree in Engineering.
• Minimum 2 years of related work experience in Quality and/or Compliance, preferably in medical device industry.
• Ability to effectively communicate cross-functionally to assist with resolving Quality issues.
• Excellent written, verbal and interpersonal communication skills in both English and Spanish.

Responsibilities

• Ensure compliance with applicable Corporate and Divisional Policies and procedures.
• Identify Manufacturing process defects and root causes and support CAPA.
• Assist in development of product quality plans, documents and systems including risk analyses and FMEAs.
• Learn Process Monitoring Systems and quality tools used in production.
• Support product/process improvement initiatives and data-driven quality metrics.

Skills

Quality engineering

Cross-functional communication

Bilingual English/Spanish

Interpersonal communication

Process improvement

Education

Bachelor degree in Engineering

Job description

Abbott Laboratories in Barceloneta, PR, is seeking an Associate Quality Engineer to support the AV division on second shift. You will help ensure the delivery of the highest quality medical devices by applying quality engineering principles across manufacturing processes.

The role requires a bachelor degree in engineering and at least 2 years of quality/compliance experience in medical devices, plus fluency in English and Spanish.