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Sr Manufacturing Engineer
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Sr Project Engineer
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Added 20 mins ago
Senior Functional Safety Engineer
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…ensuring a robust autonomous vehicle platform. We are seeking a Senior Systems Engineer who is deeply experienced with Functional Safety and familiar with SOTIF and passionate about…
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Senior Mechanical Design Engineer
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Engineer II (US)
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Senior Application Engineer
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Senior R&D Metallurgist (Alloy & Process Development)
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Senior Engineer, Manufacturing Engineering
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…in Colorado Springs. We are looking for a dynamic, versatile Senior Equipment Engineer who will be responsible for acquiring custom equipment needed to support our production for…
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Senior SATCOM Lab Engineer
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Support the integration of RF components, networking equipment, power systems, and computers
Added 51 mins ago
Senior Mining Engineer (Estimating Services)
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As a Senior Mine Engineer (Estimating Services), you will support Thiess throughout North America. This position reviews planning and operational parameters, performs fundamental quantity…
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Senior Project Manager (Steel or Mechanical Piping)
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Looking to lead high-impact projects with a top-tier Steel team? We're hiring a Senior Project Manager to drive complex structural steel builds, sophisticated skidded systems, modular…
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Program Management Engineer
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…converters, controller and emerging areas such as 100V GaN process, package, IP and test for industry leading automotive, industrial, Functional Safety and Datacenter customers. On this…
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Facilities Engineer
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This position is responsible for maintaining the production machinery equipment and operating press stamping tools.
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Data Solutions Architect - Data Platform, Data Products & AI-Ready Data
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As a Software Engineer at Applied Materials, you’ll dive deep into ground-breaking technologies - like machine learning and AI - to craft novel software solutions that solve our customers’…
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Software Dev Engineer-II, Route 53 Resolver
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…all of the servers, storage, networking, power, and cooling equipment that ensure our customers have continual access to the innovation they rely on. We work on the most challenging…
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Principal/Sr. Principal Engineer, Automation Engineering, Controls System Hardware - Lilly Medicine Foundry
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Added 1 hour ago
Senior Development Test Engineer
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We are looking for a Senior Development Test Engineer to join our rapidly growing team in Costa Mesa, CA. In this role, you will be responsible performing hardware testing on a variety of…
Added 1 hour ago
Senior Product Development Engineer
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…electronics, semiconductor packaging, and optical systems. The engineer must be comfortable debugging hardware and working across disciplines, rather than owning only one…
Added 1 hour ago
A
QA Validation Engineer
AbbVie
Irvine, CA
- $65,500 to $125,500 USD / year
The Validation Engineer supports the development and maintenance of validation activities for facilities, utilities, equipment, systems, processes, cleaning processes, and laboratory…
Added 1 hour ago
Sr. Project Engineer
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The Senior Project Engineer works collaboratively with fast-paced cross-functional teams to solve complex issues, set goals, track deliverables, and report out. The Senior Project Engineer…

AbbVie

QA Validation Engineer

Irvine, CA, United States

$65,500 to $125,500 USD / year

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Job details

Pay: $65,500 to $125,500 USD / year
Posting language: English
Posted: Nov 9, 2026

Original job description

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

Purpose:

The Validation Engineer supports the development and maintenance of validation activities for facilities, utilities, equipment, systems, processes, cleaning processes, and laboratory instruments in accordance with company standards, health authority regulations, cGMP, and site procedures. Under the direction of the Validation Section Manager and guidance from senior validation personnel, this individual executes assigned validation activities, prepares and reviews validation documentation, supports routine requalification activities, and helps maintain the validated state of systems at the plant. This role applies established procedures, escalates issues appropriately, and develops validation knowledge while contributing to the effectiveness of the Quality System.

Responsibilities

Main responsibilities for this role include assigned execution, documentation, and support activities, with guidance from management or senior validation personnel as needed.

Participate in the implementation and maintenance of validation programs and Quality System requirements to meet applicable regulatory and company standards.
Follow approved practices and procedures to help ensure compliance with company policies, cGMP, and applicable regulations for assigned validation activities.
Execute assigned tasks that support the Validation Master Plan and help maintain the validated state of equipment, utilities, facilities, automated process controllers, information systems, cleaning processes, sterilization processes, and laboratory instruments.
Support investigations of validation discrepancies or failures by gathering information, documenting results accurately, and assisting with corrective and preventive actions under supervision.
Participate with plant, engineering, quality, laboratory, and external resources on new installations or system changes to help ensure commissioning and qualification documentation supports cGMP expectations.
Support routine qualifications and requalifications by preparing materials, coordinating assigned activities, executing protocols, and helping ensure completion in a timely manner.
Draft and revise validation-related documents such as protocols, reports, lifecycle documents, user requirements, system classifications, risk assessments, and procedures for review and approval by senior staff or management.

Qualifications

Required and preferred qualifications for this role include education, foundational technical skills, and relevant early-career experience.

Bachelor's degree, preferably in Biology, Chemistry, Engineering, or a related scientific discipline; equivalent relevant experience may be considered where appropriate.
2+ years of overall experience in Manufacturing, Quality, Engineering, Validation, or a related regulated environment preferred.
Good verbal and written communication skills, with the ability to document work clearly and accurately.
Good problem-solving and analytical skills, with the ability to escalate issues and seek guidance when needed.
Good interpersonal and cross-functional communication skills.
Basic knowledge of quality systems, compliance expectations, cGMP, data integrity, and regulations or standards affecting API, bulk drug, or finished goods manufacturing preferred.
Familiarity with cGMP systems such as RAM, Maximo, KNEAT, TrackWise, and Veeva Vault is a plus.
Experience with Temperature mapping devices, such as Kaye, Ellab, and Temptales preferred.

Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html

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More about this job

Skills

Cleaning
Documentation
Regulatory compliance
Communication skills
Problem solving
Analytical skills
Quality control systems
Maximo
Compensation and benefits

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