Manufacturing Engineer II
Listed on 2026-07-04
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Manufacturing / Production
Quality Engineering, Manufacturing Engineer, Production QC/QA, Regulatory Compliance Specialist
Job Description
A healthy heart is essential to good health. That’s why we’re committed to accelerating treatments for people with cardiovascular disease. As a global leader in Cardiac Rhythm Technologies, our breakthroughs restore people’s health so they can live their best lives, faster. We focus on innovative technologies that improve the way doctors treat heart arrhythmias or irregular heartbeats.
Main Purpose of the RoleThis position will design and develop manufacturing processes, tooling, and fixtures to meet daily production schedules while enhancing productivity and product quality.
Main Responsibilities- Design and develop manufacturing processes, tooling, and fixtures to meet daily production schedules while enhancing productivity and product quality.
- Evaluate production equipment.
- Provide production support and process validation.
- Interface with vendors for incoming components.
- Troubleshoot manufacturing processes and equipment.
- Utilize tools like Gage R&R, Cp, Cpk, and SPC to improve processes.
- Apply manufacturing concepts such as Value Stream mapping, 5S, and Visual Workplace to improve quality, labor efficiency, and throughput.
- Write protocols and reports.
- Generate and modify manufacturing process documentation.
- Work with cross‑functional teams as required.
- Develop and implement process improvements.
- Support all company initiatives as identified by management in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
- Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments. Maintain positive and cooperative communications with all levels of employees, customers, contractors, and vendors.
- Perform other related duties and responsibilities as assigned.
Major/Field of Study:
Bachelor’s Degree (± 16 years)
Mechanical, Industrial, Chemical, Biomedical or related Engineering area or equivalent.
An equivalent combination of education and work experience.
Experience/BackgroundMinimum 3 years manufacturing engineering experience required. Previous medical device experience preferred.
Experience working in a broader enterprise/cross‑division business unit model preferred.
Ability to work in a highly matrixed and geographically diverse business environment.
Ability to work within a team and as an individual contributor in a fast‑paced, changing environment.
Ability to leverage and/or engage others to accomplish projects.
Strong verbal and written communication skills with the ability to effectively communicate at multiple levels in the organization.
Multitasks, prioritizes, and meets deadlines in a timely manner.
Strong organizational and follow‑up skills, as well as attention to detail.
Ability to travel approximately 25%, including internationally.
Base Pay$81,500.00 – $
In specific locations, the pay range may vary from the range posted.
Job FamilyManufacturing
DivisionCRM Cardiac Rhythm Management
LocationUnited States >
Sylmar: 15900 Valley View Court
Standard
TravelYes, 25 % of the Time
Medical SurveillanceYes
Significant Work ActivitiesAwkward/forceful/repetitive (arms above shoulder, bent wrists), continuous sitting for prolonged periods (more than 2 consecutive hours in an 8‑hour day), work in a clean room environment.
Equal Opportunity EmployerAbbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
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