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Senior Technologist, Maintenance & Manufacturing Support


Job Location:

Irvine, CA - USA

Monthly Salary: Not provided by the employer
Posted: 8 August 2026 (29 days ago)
Application Deadline: 5 November 2026
Vacancies: 1 Vacancy

Job Summary

Imagine how your ideas andexpertisecan change a patients life. Our GlobalOperations &Qualityteam plays a central part in ensuring our products are delivered to patients with cardiovascular disease.Youllpartner cross-functionally with manufacturing operations and sales teams delivering thoughtful solutions to complex challenges all while developing your knowledge of the medical device industry. Whether your work includes strategic inventory planning labeling warehouse management material handling or any of our other supply chain opportunities you will be making a meaningful contribution to our team and to patients all over the world.

The Senior Technologist Maintenance and Manufacturing Support role provides technical manufacturing support to Operations and Engineering.

The standard hours for this role are Monday-Friday 8:30am-5pm.

How youll make an impact:
SME (Subject Matter Expert) with in-depth knowledge and technical proficiency in asset management equipment maintenance and manufacturing support activities.
Design set-up and execute complex feasibility studies experiments and tests - both creating and following established protocols - to develop findings for the validation and improvement of equipment and manufacturing processes/methods based on engineering principles; analyze results make recommendations and develop reports for Engineering review.
Lead and manage projects related to new equipment validation equipment investigations testing objective evidence of product dispositions and rework.
Review documentation and take appropriate actions to ensure that information is appropriately catalogued and follow through to validation and qualification of equipment including transferring information to appropriate locations e.g. ECRs SOPs drawings and tooling for Engineering approval.

Troubleshoot maintain and optimize PLC HMI and automated control systems to improve equipment reliability and minimize production downtime.
Collaborate with Engineering and CAD/Designers to develop new complex tools/equipment.
Perform primarily unscheduled preventive maintenance routines on a wider range of complex equipment to validate user operation and avoid program down time including providing expertise and guidance in resolving complex failures.
Check for failures in equipment and perform corrective actions to affected areas that have down time including conducting and writing impact assessment reports of incidents exception work orders (EWOs) Equipment Non-conformance Reports (ENCRs) and Out of Tolerance (OOTs).

What youll need:
H.S. Diploma or equivalent with 10 years related experience required or
Associates Degree or equivalent 8 Years years experience related experience required
Previous experience in manufacturing and/or medical device experience required

What else we look for:
Excellent written and verbal communication interpersonal and relationship building skills with focus on influencing and conveying recommendations.
Problem solving methodology root cause analysis and GDP (Good Documentation Practices).
Strong computer skills including usage of MS Office Suite utilizing manufacturing software (e.g. JDE QMS PLM) to update documentation in systems (e.g. ECRs Blue Mountain); and CAD if applicable.
Extensive knowledge of routine preventive maintenance of production equipment validation and improvement of automated equipment electrical/mechanical/pneumatic controls and troubleshooting equipment.

Working knowledge of industrial control systems including PLC programming troubleshooting and diagnostics.

Experience supporting and modifying Human Machine Interface (HMI) applications used in manufacturing environments.

Familiarity with industrial communication protocols and networked automation systems.

Ability to interpret and troubleshoot control system architectures electrical schematics and I/O configurations.
Knowledge of Good Manufacturing and Good Documentation Practices supporting a medical device environment.
Must be able to work independently in completing assigned projects developing work instructions and advancing the competency of other technicians.
Adhere to all company rules and requirements (e.g. pandemic protocols Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control.

Aligning our overall business objectives with performance we offer competitive salaries performance-based incentives and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California the base pay range for this position is $70000 to $99000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g. qualifications education prior experience). Applications will be accepted while this position is posted on our Careers website.






Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.


Required Experience:

Senior IC


About Company

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Edwards Lifesciences (NYSE: EW), is the global leader of patient-focused medical innovations for structural heart disease and critical care monitoring. We are driven by a passion for patients, dedicated to improving and enhancing lives through partnerships with clinicians and stakehol ... View more

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