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Abbott Sylmar Jobs (NOW HIRING)

Regulatory Affairs Coordinator

Los Angeles, CA · On-site

$24.65 - $49.35/hr

  • Medical

  • Retirement

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... This Regulatory Affairs Coordinator will work on-site at our Sylmar, CA location in the Cardiac ...

Cloud Software Engineer II

Sylmar, CA · On-site

$81K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Our location in Sylmar, CA currently has an opportunity for a Cloud Software Engineer . Cloud ...

Cloud Software Engineer II

Los Angeles, CA

$81K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Our location in Sylmar, CA currently has an opportunity for a Cloud Software Engineer . Cloud ...

Cloud Software Engineer II

Los Angeles, CA · On-site

$81K - $141K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Our location in Sylmar, CA currently has an opportunity for a Cloud Software Engineer . Cloud ...

Manager, Business HR

Los Angeles, CA · On-site

$114K - $228K/yr

  • Medical

  • Retirement

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... The role will be based out of Sylmar, CA. This is an on-site role requiring occasional travel. What ...

Regulatory Affairs Coordinator

Los Angeles, CA

$24.65 - $49.35/hr

  • Medical

  • Retirement

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... This Regulatory Affairs Coordinator will work on-site at our Sylmar, CA location in the Cardiac ...

Manager, Business HR

Sylmar, CA · On-site

$114K - $228K/yr

  • Medical

  • Retirement

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... The role will be based out of Sylmar, CA. This is an on-site role requiring occasional travel. What ...

Regulatory Affairs Coordinator

Sylmar, CA · On-site

$24.65 - $49.35/hr

  • Medical

  • Retirement

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... This Regulatory Affairs Coordinator will work on-site at our Sylmar, CA location in the Cardiac ...

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Our location in Sylmar, CA currently has an opportunity for a Staff Facilities Engineer . MAIN ...

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Abbott Sylmar information

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How much do abbott sylmar jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for abbott sylmar in the United States is $14.99, according to ZipRecruiter salary data. Most workers in this role earn between $12.98 and $16.35 per hour, depending on experience, location, and employer.

What is Abbott Sylmar?

Abbott Sylmar refers to the Abbott facility located in Sylmar, California, which specializes in the development and manufacturing of medical devices, particularly those related to cardiac rhythm management such as pacemakers and implantable cardioverter defibrillators (ICDs). This location is a hub for innovation within Abbott’s medical device division, contributing to advancements in heart health technology. Employees at Abbott Sylmar work in various roles including engineering, research and development, manufacturing, and quality assurance. The site is known for its high standards in patient safety and product reliability.

What are the key skills and qualifications needed to thrive as an employee at Abbott's Sylmar facility?

To thrive at Abbott Sylmar, especially in roles related to medical device manufacturing or engineering, you need a solid background in biomedical engineering, quality assurance, or related scientific fields, often with a relevant degree. Familiarity with FDA regulations, Good Manufacturing Practices (GMP), and tools like SAP or quality management systems is typically required. Strong problem-solving abilities, attention to detail, and effective teamwork are essential soft skills for success. These skills and qualifications ensure product safety, regulatory compliance, and high standards in the production of life-saving medical devices.

What can I expect from the work environment and team structure at Abbott's Sylmar facility?

At Abbott's Sylmar facility, team members typically work in a collaborative, cross-functional environment focused on medical device development and manufacturing. You can expect to interact regularly with colleagues from engineering, quality assurance, regulatory, and manufacturing departments. The facility values innovation, continuous improvement, and adherence to strict regulatory standards, which means teamwork and clear communication are essential. New hires often benefit from mentorship programs and have opportunities to participate in ongoing training and professional development. The dynamic pace and supportive work culture make it an excellent place for those seeking to contribute to life-changing healthcare solutions.
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Infographic showing various Abbott Sylmar job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, 4% Contract, and 1% Nights. Highlights an 93% Physical, and 7% Remote job distribution, with an average salary of $31,171 per year, or $15 per hour.

Regulatory Affairs Coordinator

Abbott

Los Angeles, CA • On-site

$24.65 - $49.35/hr

Full-time

Medical, Retirement

Posted 29 days ago


Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

178th of 540 rated manufacturers


Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:

Job Description

About Abbott

Abbott is a global healthcare leader, creating breakthrough science to improve people's health.We'realways looking towards the future,anticipatingchanges in medical science and technology.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life.You'llalso have access to:

  • Career development with an international company where you can grow the career you dream of.

  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

  • An excellent retirement savings plan with high employer contribution

  • Tuition reimbursement, theFreedom 2 Savestudent debtprogramandFreeUeducation benefit - an affordable and convenient path to getting a bachelor's degree.

  • A company recognized asa great placeto work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.

  • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

As a global leader in Cardiac Rhythm Technologies, we focus on innovative technologies that can improve the way doctors treat people with heart arrhythmias, or irregular heartbeats.

ThisRegulatory Affairs Coordinatorwill work on-site at our Sylmar, CA location in the Cardiac Rhythm Management Division. This new team member will provide administrative support for regulatory processes and procedures. The individual may coordinate and support technical and scientific regulatory activities, researchregulationsand guidance, and organize andmaintainkey information sources.

WhatYou'llWork On

Responsible for compliance with applicable Corporate and Divisional Policies and procedures.

Strategic Planning:

  • Execute global regulatory assessment

  • Analyze, plan, execute and track Product Release Authorizations

  • Develop,analyzeand execute on improvements to regulatory processes

  • Collaborate cross functionally for inputs to regulatory processes

  • SOP and other document maintenance

  • Maintain records on legislation,regulationsand guidelines

  • Assistin monitoring and reporting project timelines

Premarket:

  • Secure global regulatory assessments for input into global regulatory strategy

  • Assistin the releasing of product to market

  • Assistin the compilation and organization of materials forpresubmissionreports

  • Assistin the preparation of submission/registration packages

  • Assistin the organization of materials from preclinical and clinical studies for review

  • Assistin notarization of documents

Postmarket:

  • Update andmaintainpaper/electronic document regulatory files and archival systems

  • Assistin the preparation of routine reports and regulatory agency communications

  • Assistwith internal audits and inspections

  • Assistin the preparation ofpostmarketreports and submissions

  • Update andmaintainglobal product listings, facility registrations, licenses/approvals, and annual registrations.

Required Qualifications

  • Technical Diploma ( 12 years)

  • Minimum1 yearrelated experience

Preferred Qualifications

  • Associate's or Bachelor'sdegree in a technical area (such as biology, chemistry, engineering, microbiology, immunology, medical technology, pharmacy)

  • Experience in a regulated business environment (e.g., legal office, regulated industry).

  • Project Management skills

  • Experience with Windchill or other PLM system

The base pay for this position is

$24.65 - $49.35/hour

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:Regulatory OperationsDIVISION:CRM Cardiac Rhythm ManagementLOCATION:United States > Sylmar : 15900 Valley View CourtADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:NoMEDICAL SURVEILLANCE:NoSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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