Manufacturing Process Engineer - Medical Devices

Abbott Laboratories; Pleasanton (CA); On-site; USD 70,000 - 116,000; Full time

Job summary

Abbott Laboratories in Pleasanton, CA, is seeking a Manufacturing Process Engineer to join the Heart Failure Division. You will assist in developing and validating manufacturing processes and equipment for medical devices, supporting cross-functional teams, and contributing to design reviews.

Requirements include an Associate's degree in engineering/technical field and 1–3 years of related experience, with knowledge of process development and data analysis.

Qualifications

• Associate's degree in engineering/technical field or related field is required.
• 1-3 years of work experience in engineering or manufacturing is preferred.
• Knowledge of general engineering principles is expected.
• Technical experience in mechanical or chemical engineering with strong written and verbal communication skills.
• Knowledge of processes used in development and manufacturing of medical devices, especially diabetes strips, is a plus.
• Experience in engineering calculations, controlled tests and statistical analyses is desirable.

Responsibilities

• Assist in designing or developing new manufacturing processes and equipment; help in process verification and validation.
• Assist in optimizing manufacturing processes.
• Conduct tests, collect and format data, and assist in analysis of engineering studies (DOEs).
• Assist in startup of new equipment and execution of validation protocols.
• Communicate effectively and participate on cross-functional development teams.
• Participate in technical design reviews for process equipment and product design and requirements documents.

Skills

General engineering principles

Mechanical or chemical engineering

Communication skills

Education

Associate's degree in engineering/technical field

Job description

Abbott Laboratories in Pleasanton, CA, is seeking a Manufacturing Process Engineer to join the Heart Failure Division. You will assist in developing and validating manufacturing processes and equipment for medical devices, supporting cross-functional teams, and contributing to design reviews.

Requirements include an Associate's degree in engineering/technical field and 1–3 years of related experience, with knowledge of process development and data analysis.