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Avi Jobs (NOW HIRING)

Stellantis

ICT Launch AVI/Broadcast Lead

Auburn Hills, MI

$151K - $158K/yr

Serve as the technical SME for AVI, QAS, Broadcast, and PFS systems during launch activities. * Act as the design authority for launch‑related system configurations, integrations, and process ...

AVI-SPL

Project Manager

Englewood, CO · On-site

WHO WE ARE AVI-SPL is a digital enablement solutions provider who transforms how people and technology connect to elevate experiences, create new value, and enable organizations to thrive and grow.

AVI-SPL

Associate Project Manager

Woodinville, WA · On-site

AVI-SPL will help you acquire/develop skills over time to manage smaller complexity projects with the ultimate goal to progress into the Project Manager position. WHO WE ARE AVI-SPL is a digital ...

New

AVI-SPL

Associate Project Manager

Mesa, AZ · On-site

AVI-SPL will help you acquire/develop skills over time to manage smaller complexity projects with the ultimate goal to progress into the Project Manager position. WHO WE ARE AVI-SPL is a digital ...

AVI-SPL

Project Manager

Irvine, CA · On-site

WHO WE ARE AVI-SPL is a digital enablement solutions provider who transforms how people and technology connect to elevate experiences, create new value, and enable organizations to thrive and grow.

AVI-SPL

Project Manager

Richmond, VA · On-site

WHO WE ARE AVI-SPL is a digital enablement solutions provider who transforms how people and technology connect to elevate experiences, create new value, and enable organizations to thrive and grow.

AVI-SPL

Vice President - Strategic Accounts

Astoria, NY · On-site

$130K - $160K/yr

You will influence (and in some cases lead) major cross-functional projects affecting AVI-SPL business product and service leadership articulate product and services strategies. This position ...

AVI-SPL

Project Manager

Indianapolis, IN · On-site

WHO WE ARE AVI-SPL is a digital enablement solutions provider who transforms how people and technology connect to elevate experiences, create new value, and enable organizations to thrive and grow.

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Showing results 41-60

All JobsAvi Jobs

AVI information

See salary details

$10

$19

$32

How much do avi jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for avi in the United States is $19.73, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $22.36 per hour, depending on experience, location, and employer.

What is an avi?

Avi jobs typically refer to roles associated with the company Avi Networks, which specializes in application delivery services, such as load balancing, web application firewalls, and analytics. These jobs can include positions in software engineering, technical support, sales, and product management. Employees in Avi-related roles often work on developing, deploying, or supporting cloud-native application services for enterprise clients. The work environment is generally fast-paced and technical, focusing on innovation and customer satisfaction.

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

To thrive as an Aviation Mechanic, you need strong mechanical aptitude, technical troubleshooting abilities, and typically an FAA Airframe and Powerplant (A&P) certification or equivalent credentials. Familiarity with diagnostic tools, maintenance tracking software, and aircraft-specific systems is essential. Attention to detail, problem-solving skills, and effective communication help ensure tasks are completed accurately and safely. These skills and qualifications are vital for maintaining aircraft safety, regulatory compliance, and operational reliability.

What are some common challenges faced by aviation maintenance technicians, and how can they be managed effectively?

Aviation maintenance technicians often face challenges such as adhering to strict safety regulations, troubleshooting complex mechanical or electronic systems, and managing time-sensitive repairs to minimize aircraft downtime. Effective management of these challenges involves staying current with industry training, maintaining strong attention to detail, and collaborating closely with engineers and flight crews. Proactively communicating issues and documenting all maintenance tasks accurately are also essential to ensure safety and compliance in this high-responsibility role.

What is the difference between Avi vs Network Engineer?

AspectAviNetwork Engineer
Required CredentialsTypically Cisco, CCNP, or vendor-specific certificationsCCNA, CCNP, or equivalent networking certifications
Work EnvironmentData centers, cloud environments, and enterprise networksCorporate offices, data centers, and service providers
Industry UsagePrimarily in networking, cloud, and security sectorsBroadly in IT, telecommunications, and networking

While both Avi and Network Engineers work within networking environments, Avi specialists focus on application delivery and security solutions, often requiring specific vendor certifications. Network Engineers have a broader scope, managing overall network infrastructure. Understanding these differences helps in choosing the right career path or job focus.

More about AVI jobs

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What states have the most Avi jobs?

States with the most job openings for Avi jobs include:

What job categories do people searching Avi jobs look for?

The top searched job categories for Avi jobs are:

AVI jobs near you
Infographic showing various Avi job openings in the United States as of August 2026, with employment types broken down into 82% Full Time, 17% Part Time, and 1% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $41,029 per year, or $19.7 per hour.

Validation Engineer III - OSD/Packaging/AVI

Thermo Fisher Scientific

Greenville, NC • On-site

Full-time

Posted 12 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 428 frontline employees who took The Breakroom Quiz

175th of 543 rated manufacturers

Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner, and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe, and helping find cures for cancer.
At our Greenville, North Carolina site, you'll join a highly collaborative Validation Engineering team supporting pharmaceutical manufacturing operations. Our team plays a critical role in ensuring manufacturing processes are validated, compliant, and capable of consistently producing high-quality medicines that improve lives around the world.
Discover Impactful Work
As a Validation Engineer III, you will support manufacturing process validation activities focused primarily on Oral Solid Dose (OSD) continuous manufacturing and pharmaceutical packaging operations. You'll lead validation efforts from protocol development through execution and final reporting while partnering with Manufacturing, Engineering, Quality, and Technical Operations teams.
This role offers an excellent balance of technical documentation and hands-on manufacturing support, allowing you to contribute directly to product launches, process improvements, and regulatory compliance. In addition to OSD process and packaging validation, you'll have opportunities to support Automated Visual Inspection (AVI) validation activities as business needs require.
A Day in the Life
This position offers approximately:
  • 70% desk-based work
    • Write validation protocols and supporting documentation
    • Perform data analysis and calculations
    • Prepare validation summary reports
    • Conduct data review and documentation review
    • Support investigation and technical problem solving
  • 30% manufacturing floor execution
    • Execute manufacturing process validation protocols
    • Perform packaging process validation activities
    • Collect validation samples and process data
    • Partner with Manufacturing and Quality during validation campaigns
    • Support Automated Visual Inspection (AVI) validation activities when needed
Key Responsibilities
  • Lead manufacturing process validation activities for Oral Solid Dose (OSD) pharmaceutical products.
  • Develop, execute, and document validation protocols, including IQ, OQ, and PQ.
  • Perform packaging process validation for commercial pharmaceutical manufacturing.
  • Analyze validation data and prepare technical reports that support regulatory compliance.
  • Support cleaning validation activities as part of overall manufacturing process qualification.
  • Collaborate with Manufacturing, Engineering, Quality, and Technical Operations teams to execute validation projects.
  • Participate in peer review of validation documentation and data.
  • Support Automated Visual Inspection (AVI) validation activities as assigned.
  • Contribute to continuous improvement initiatives that enhance manufacturing performance and compliance.
  • Support internal audits, customer audits, and regulatory inspections.
Keys to Success
Education
  • Bachelor's degree in Engineering, Life Sciences, Chemistry, or another technical discipline.
  • Advanced degree preferred.
Experience
  • Bachelor's degree with 5+ years of validation experience, or an advanced degree with 3+ years of validation experience within pharmaceutical, biotechnology, or another regulated manufacturing environment.
  • Experience developing and executing validation protocols in GMP manufacturing.
  • Experience with IQ/OQ/PQ documentation and execution.
Preferred Experience
Candidates with the following experience will be especially successful in this role:
  • Oral Solid Dose (OSD) manufacturing process validation
  • Continuous Manufacturing (CM)
  • Packaging process validation (preferred over equipment-only validation)
  • Automated Visual Inspection (AVI)
  • Sterile packaging validation
  • Cross-functional collaboration within pharmaceutical manufacturing
Knowledge, Skills & Abilities
  • Strong knowledge of FDA cGMP regulations and pharmaceutical manufacturing practices.
  • Experience with manufacturing process validation, equipment qualification, utilities, cleaning processes, and computer systems.
  • Strong technical writing and documentation skills.
  • Experience performing validation data analysis and interpretation.
  • Excellent analytical and problem-solving skills.
  • Strong communication and collaboration skills with cross-functional teams.
  • Proficiency with Microsoft Office and validation documentation systems.
  • Experience supporting regulatory inspections and customer audits is preferred.
  • Knowledge of Lean Manufacturing or continuous improvement methodologies is a plus.
  • Ability to work in cleanroom and manufacturing environments.
  • Flexibility to occasionally support extended hours during validation campaigns.
  • Occasional travel (up to 25%) may be required to support Factory Acceptance Testing (FAT) or other business needs.
Why Join Us?
At Thermo Fisher Scientific, your work directly impacts patients around the world. You'll collaborate with talented colleagues, work on cutting-edge pharmaceutical manufacturing technologies, and gain experience supporting innovative Oral Solid Dose manufacturing, packaging, and validation programs. We invest in our people through professional development, challenging projects, and opportunities to grow your career while making a meaningful difference.

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