Process Engineer I, Medical Device Manufacturing

Abbott Laboratories; Pleasanton (CA); On-site; USD 74,000 - 116,000; Full time

Benefits offered by this job

HIP PPO medical plan

Retirement plan

Tuition reimbursement

FreeU education benefit

Job summary

Abbott in Pleasanton, CA, is seeking a process engineer to assist in developing manufacturing processes and equipment for medical devices. You will work on improving processes, perform tests, and support multidisciplinary teams to bring new products to production.

The role requires an associate degree in engineering, at least 3 years of technical experience, and strong communication. Familiarity with FDA Design Controls and quality systems is preferred; travel up to 10% may be needed.

Qualifications

• Associate degree in engineering or technical discipline required.
• Minimum 3 years technical or relevant experience.
• Knowledge of general engineering principles.
• Technical experience in mechanical or chemical engineering with strong communication.
• Knowledge of processes in development and manufacturing of medical devices, diabetes strips.
• Experience in engineering calculations, controlled tests, statistical analyses.

Responsibilities

• Design or develop new manufacturing processes and equipment.
• Assist in process verification and validation.
• Optimize manufacturing processes.
• Conduct tests, collect data, and analyze engineering studies.
• Assist in startup of new equipment and validation protocols.
• Communicate effectively and participate on cross functional development teams.
• Follow FDA Design Control procedures for process development.

Skills

Engineering knowledge

Written communication

Statistical analysis

DOE understanding

Education

Associate degree in engineering

Job description

Abbott in Pleasanton, CA, is seeking a process engineer to assist in developing manufacturing processes and equipment for medical devices. You will work on improving processes, perform tests, and support multidisciplinary teams to bring new products to production.

The role requires an associate degree in engineering, at least 3 years of technical experience, and strong communication. Familiarity with FDA Design Controls and quality systems is preferred; travel up to 10% may be needed.