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Abbott Engineer Jobs (NOW HIRING)

Abbott

Validation Engineer III

Centre, AL · On-site

Abbott is looking for an outstanding Validation Engineer-Contractor who will effectively lead ... quality related validation activities to support the Quality Management System. The end goal is to ...

Abbott

Process Quality Engineer

Saint Paul, MN · On-site

$61K - $122K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Job Title Process Quality Engineer Working at Abbott At Abbott, you can do work that matters, grow ...

Abbott

Manufacturing Engineer

Minnetonka, MN · On-site

$34 - $37/hr

Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs. * Published on 30 Mar 2026, 8:43 PM

Abbott

Sr. Quality Engineer

Saint Paul, MN

$78K - $156K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Job Title Sr. Quality Engineer Working at Abbott At Abbott, you can do work that matters, grow, and ...

Abbott

Senior Manufacturing Engineer

Des Plaines, IL · On-site

$88K - $121K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Senior Manufacturing Engineer Working at Abbott At Abbott, you can do work that matters, grow, and ...

Abbott

Manufacturing Engineer II

Saint Paul, MN · On-site

$34 - $40/hr

Manufacturing Engineer II Location : Saint Paul, MN, 100% Onsite Duration : 6+ months ... into Abbott. * Support the maintenance of controlled process documentation, including work ...

Abbott

Quality Engineer II

Alameda, CA · On-site

$90K - $180K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... As the Quality Engineer II you will be responsible for activities related to design control ...

Abbott

Quality Engineer II

Alameda, CA · On-site

$90K - $180K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... As the Quality Engineer II you will be responsible for activities related to design control ...

Abbott

Process Development Engineer I

Plymouth, MN · On-site

$50K - $101K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Electrical or related ...

Abbott

Associate Design Quality Engineer

Temecula, CA · On-site

$50K - $101K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Job Title Associate Design Quality Engineer Working at Abbott At Abbott, you can do work that ...

Abbott

Associate Design Quality Engineer

Temecula, CA · On-site

$50K - $101K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Job Title Associate Design Quality Engineer Working at Abbott At Abbott, you can do work that ...

Abbott

Process Development Engineer I

Plymouth, MN · On-site

$50K - $101K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Electrical or related ...

Abbott

Cloud Software Engineer II

Los Angeles, CA

$81K - $141K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Cloud Software Engineer will contribute to the design and development of cloud service applications ...

Abbott

PCB Design Engineer

Saint Paul, MN · On-site

$50K - $101K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... As a PCB Design Engineer, you'll work within a team environment to maintain CAD component libraries ...

Abbott

Associate Design Quality Engineer

Temecula, CA · On-site

$50K - $101K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Job Title Associate Design Quality Engineer Working at Abbott At Abbott, you can do work that ...

Abbott

Lead AI Security Engineer

Waukegan, IL · On-site

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... The Opportunity The Lead AI Cybersecurity Engineer is responsible for developing the strategies ...

Abbott

Controls Calibration Engineer

Abbott, TX

$73K - $94K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... The Controls Calibration Engineer will be responsible for the installation, maintenance ...

Abbott

Process Quality Engineer

Saint Paul, MN

$61K - $122K/yr

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our ... Job Title Process Quality Engineer Working at Abbott At Abbott, you can do work that matters, grow ...

Abbott

$34 - $40/hr

Manufacturing Engineer II Location: Saint Paul, MN, 100% Onsite Duration: 6+ months ... into Abbott. Support the maintenance of controlled process documentation, including work ...

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Abbott Engineer information

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$37K

$87.2K

$136.5K

How much do abbott engineer jobs pay per year?

As of Jun 7, 2026, the average yearly pay for abbott engineer in the United States is $87,220.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,500.00 and $97,500.00 per year, depending on experience, location, and employer.

What is the difference between Abbott Engineer vs Abbott Technician?

AspectAbbott EngineerAbbott Technician
Required CredentialsBachelor's degree in engineering or related fieldAssociate degree or technical certification
Work EnvironmentDesign, development, and testing in labs or officesEquipment maintenance and troubleshooting on-site or in labs
Industry UsageUsed across R&D, manufacturing, and quality assurancePrimarily involved in operational support and equipment servicing

Abbott Engineers focus on designing and developing medical devices, requiring a bachelor's degree, while Abbott Technicians handle equipment maintenance and troubleshooting, often with technical certifications. Both roles are essential in Abbott's healthcare industry, but they differ in responsibilities and qualifications.

How does an Abbott Engineer typically collaborate with cross-functional teams during product development?

As an Abbott Engineer, you will frequently work with cross-functional teams that include regulatory, quality assurance, manufacturing, and research professionals. Collaboration often involves participating in regular meetings, sharing technical updates, and integrating feedback from various departments to ensure compliance and optimize product performance. This teamwork helps streamline the development process and ensures that products meet both regulatory standards and user needs. Strong communication and project management skills are essential for successfully navigating these collaborative efforts.

What are Abbott Engineers?

Abbott Engineers are professionals who work at Abbott, a global healthcare company, specializing in areas such as medical devices, diagnostics, nutrition, and branded generic medicines. They are responsible for designing, developing, testing, and maintaining products and systems that improve patient care and health outcomes. Abbott Engineers often collaborate with cross-functional teams to ensure products meet regulatory standards and customer needs. Their work can span research and development, manufacturing, quality assurance, and process improvement within the healthcare industry.

What are the key skills and qualifications needed to thrive as an Abbott Engineer, and why are they important?

To thrive as an Abbott Engineer, you need a strong background in engineering principles, problem-solving abilities, and a relevant engineering degree such as in biomedical, mechanical, or electrical engineering. Familiarity with industry-standard tools like CAD software, quality management systems, and sometimes Six Sigma or Lean certifications is often required. Strong teamwork, communication skills, and adaptability help you excel in cross-functional, fast-paced environments. These competencies ensure the successful development, manufacturing, and support of innovative healthcare technologies while meeting regulatory and quality standards.
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Abbott Engineer jobs near you

Validation Engineer III

Abbott

Centre, AL • On-site

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 11 days ago

Abbott rating

7.9

Company rating: 7.9 out of 10

Based on 131 frontline employees who took The Breakroom Quiz

146th of 516 rated manufacturers

Job description

Title: Validation Engineer III
Location: San Diego, CA
Duration: 7 Month Assignment
Validation Engineer- Contract
Abbott Rapid Diagnostics (formerly Alere) is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry-leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions. At Abbott, diverse ideas, perspectives, and expertise allow us to create life-changing solutions that help people live healthier lives. In 150 countries and with businesses spanning nutrition, diagnostics, medical devices, and branded generic pharmaceuticals, Abbott offers you enormous opportunities to explore your interests and help you achieve your career and personal goals.
Abbott is looking for an outstanding Validation Engineer-Contractor who will effectively lead quality related validation activities to support the Quality Management System. The end goal is to deliver consistent and high-quality validation and supporting documentation for design and development organization. This role requires strong technical, communication, interpersonal and organizational skills, and a solid understanding of the application of FDA, ISO 13485, ISO 14971 standards and company strategies.
This opportunity is available with Infectious Disease Developed Markets (IDDM) Business unit within Abbott, at our location in Towne Centre San Diego, CA.
This job description will be reviewed periodically and is subject to change by management.
Technical Writing
  • Write procedures, investigations, protocols, deviations, CAPA's, reports, change controls, etc. to support ARDx Towne Centre site departments.
  • Perform and document investigations related to validation activities and performs risk assessments of equipment, processes and systems to determine the scope of validation efforts.
  • Generates validation documentation as required (URS, FRS, DRS, FAT, DQ, engineering studies, IOQ, PQ, PV) for cleaning, shipping, sterilization, facilities,
  • utilities, systems, equipment qualification/requalification, computer system validation, spreadsheets, test method validation and process validation.
  • Writes and/or revises IQ, OQ, PQ related documents, including any or all of the following: SOP's, validation master plans, guidelines and execution plans, automation test plans and technical documents.
  • Responsible for writing Standard Operating Procedures related to Validations and responsible for training Quality Assurance and R&D personal in the validation processes.

Service Delivery
  • Performs on site or support work, including but not limited to:
  • Validation protocol executions for FAT/SAT/IQ/OQ/PQ/PV.
  • Equipment Qualification test execution.
  • Investigations and deviations.
  • Provides gap analysis, risk management, risk assessment, risk analysis and validation strategy.
  • Data integrity assessments and review of client data
  • Executes protocols and resolves deviations/discrepancies, analyzes data and writes reports.
  • Performing and supervising thermal mapping of temperature-controlled units, Laboratories, warehouses, etc.
  • Ensures that validations are documented using Good Documentation Practices and are in compliance to FDA, ISO 13485, and Abbott Policies and Procedures.
  • Evaluate impact on legacy qualifications/validations and determines the scope of re-validation.
  • Support the continuous improvement to the Quality Management System, with a specialty focus on validation processes.
  • Responsible for maintaining a Site Master Validation Plan and ensuring that critical Performance Qualification and/or Process Validations are performed per established schedule.
  • Identify and propose remediation for existing and potential validation issues; provide technical expertise and provide solutions to maintain compliance.
  • Assist with internal and external audits.
  • Manages validation metrics.
  • Manages change control for validation deliverables in the electronic documentation management system.
  • Participate in multiple, concurrent projects.
  • Develops timelines and tracks project status on assigned projects.
  • Keeps stakeholders informed on the status of important projects.
  • Performs other duties as assigned by Management.

BASIC QUALIFICATIONS | EDUCATION:
  • Bachelors' degree (B.S.) in a Science related field (Engineering, Biology, Chemistry or equivalent)
  • 5+ years of related work experience in a medical device industry with strong technical competency in performing equipment qualification (IQ/OQ/PQ), facility/lab qualification, process validations and excel spreadsheet validations.
  • Proficient understanding of Design Control, Good Documentation Practices (GDP), and current Good Manufacturing Practices (cGMP)
  • Significant experience with application of the FDA regulations and recognized standards (e.g., FDA 21 CFR 820.30, FDA 21 CFR 820.70, FDA 21 CFR Part 11, ISO 13485, ISO 14971, cybersecurity)

PREFERRED QUALIFICATIONS:
  • Experience in validation of In Vitro Diagnostic Lab equipment (e.g., Real- Time PCR System, Freezers, Refrigerators, Environmental Chambers, Incubators) and Thermal Mapping, Computerized System Validation.
  • Experience supporting ISO 13485 inspections and FDA inspections.• Experience in a multi-site development environment.
  • Experience in compliance management within a rapid-growth, dynamic organization.
  • Statistical or Lean Six Sigma background
  • Working experience with GAMP5 and FDA's Computer Software Assurance initiatives
  • Working experience with Agile, Maximo and ViewLinc.

COMPETENCIES:
  • Good working knowledge of Excel and Microsoft Word software
  • Working knowledge of quality techniques such as root cause analysis, 5 why's, and Ishikawa diagrams.
  • Excellent problem solving and decision-making skills.
  • Self-starting, detail oriented, and ability to focus on task at hand
  • Initiative to work towards goals with minimal supervision
  • Ability to work independently with multiple departments to resolve Validation issues
  • Must be able to work effectively in a fast paced, cross-functional team-oriented environment
  • Well-developed English written and verbal communication skills

An equal opportunity employer, Abbott welcomes and encourages diversity in our workforce.We provide reasonable accommodation to qualified individuals with disabilities.
Consultants Eligible Benefits Upon Waiting Period:
  • Medical and Prescription Drug Plans
  • Dental Plan
  • Vision Plan
  • Health Savings Account (for High-Deductible Health Plans)
  • Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
  • Supplemental Life Insurance
  • Short Term Disability (coverage varies by state)
  • Long Term Disability
  • Critical Illness, Hospital coverage, Accident Insurance
  • MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
  • 401(k)

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, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.
  • Published on 27 May 2026, 1:56 PM

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