239 Qa Lead jobs in Ireland

We are seeking an experienced QA Lead with a robust background in Mechanical Engineering, and a proven track record in both the Pharmaceutical and Construction sectors. This is a unique cross-industry role requiring a deep understanding of GMP, GEP, and engineering best practices to oversee and enhance quality processes throughout the project lifecycle.

• Lead QA activities across pharma and construction projects, ensuring compliance with GMP, GEP, ISO standards, and other applicable regulations.
• Develop, implement, and maintain Quality Management Systems (QMS) to ensure adherence to project, client, and regulatory requirements.
• Oversee mechanical system installations (e.g., HVAC, piping, pressure vessels) with a focus on quality and compliance in both cleanroom and construction environments.
• Coordinate with multidisciplinary teams including engineering, validation, commissioning, construction, and operations to align quality standards.
• Perform supplier and contractor audits, review quality documentation, and ensure proper IQ/OQ/PQ protocols are followed (in pharma).
• Lead Non-Conformance (NC) investigations, CAPAs, and root cause analysis for deviations in construction or pharma environments.
• Ensure all materials, equipment, and systems used in construction or manufacturing are installed and qualified to meet regulatory expectations.
• Participate in project planning, risk assessments, and quality reviews from design through handover phases.
• Serve as the primary quality interface with regulatory bodies and client auditors.

• Bachelor's degree (or higher) in Mechanical Engineering.
• 7+ years of QA experience, with at least 3-5 years in Pharma (GMP environment) and 3+ years in Construction/Infrastructure.
• Solid understanding of mechanical systems within GMP manufacturing and industrial construction.
• Hands-on experience with validation, commissioning, and qualification processes.
• Strong familiarity with regulatory standards such as FDA, EMA, MHRA, and ISO 9001.
• Experience implementing or working with QMS platforms (e.g., TrackWise, MasterControl).
• Proven experience in managing teams and leading cross-functional quality initiatives.
• Excellent written and verbal communication, reporting, and stakeholder management skills.

If you are interested in this role, please apply directly or email your CV to

Date Opened

10/16/2025

Job Type

Full time

Industry

Construction

City

Dublin 15

State/Province

Dublin

Country

Ireland

Zip/Postal Code

D15

We're VOID Interactive
, the kickass team behind the best-selling FPS game,
Ready or Not
. We're made up of some seriously talented individuals who love games and creating awesome content together. We're seeking a dedicated and enthusiastic Videogame QA Lead to join us remotely and help us elevate
Ready or Not
to new heights.
Our goal is strong: to establish
Ready or Not
as the quintessential FPS of our time.

As the Videogame QA Lead you play a pivotal role in ensuring the seamless execution of our QA processes. You will collaborate with developers and project managers to guarantee project delivery with the highest standards of quality assurance, in addition to providing guidance, direction, and mentorship to the QA team.

In this role, you'll be in charge of:

• Management of the QA team, fostering a culture of excellence in testing practices.
• Ensuring thorough testing coverage for all aspects of the game, from functionality to performance and beyond.
• Understand project goals, scope, and deliverables, actively participating in the development process to embed quality assurance from the ground up, including creating relevant documentation for the QA process.
• Optimising workflow to meet project milestones and deadlines.
• Bridge the gap between QA and development teams, ensuring seamless information exchange and issue resolution.
• Implement effective solutions and contingency plans to mitigate risks.
• Keep the leadership team informed about project status, challenges, and achievements, actively seeking input and feedback.
• Ensure strict adherence to project specifications and standards, maintaining a keen eye for detail.
• Identify areas for optimisation and efficiency improvements.
• Ensure optimal test coverage, bug reporting, and a collaborative working environment.
• Share knowledge with the QA team to continually improve testing processes.

Of course, you won't be alone on this mission - you'll be collaborating with the entire team and outside vendors to ensure we're maximising our efforts and achieving our goals

Here's what you'll be bringing to the team:

• Minimum of 5 years of experience in a QA testing leadership position.
• Bachelor's degree in a relevant field or equivalent experience preferred.
• Demonstrated experience successfully managing QA processes for complex projects.
• Strong leadership skills, with the ability to inspire and motivate the QA team.
• In-depth understanding of the QA process and familiarity with testing tools and methodologies.
• Strong problem-solving and decision-making abilities, with a creative mindset.
• Passion for video games with a keen eye for detail.
• Highly proficient in utilising QA tools and documentation platforms.
• Ability to consolidate large amounts of information into clear, concise, and actionable items.
• Self-motivated, adaptable and a great team player.

If this sounds like you, please submit your resume, portfolio, and an optional, brief cover letter outlining your relevant experience and why you are excited about this opportunity. We look forward to hearing from you and discussing how you can contribute to our mission of delivering exceptional gameplay experiences

Please Note:

This position is a fully remote role based in Ireland.

You'll have the flexibility to work from anywhere within the country while remaining connected to a supportive and collaborative team.

Job description:

QA Lead Drug Substance (DS) Manufacturing

- Associate Director

A critical role within the QA organisation, the QA Drug Substance (DS) Manufacture Lead will lead the QA team. Responsible for ensuring that biologic drug substance manufacturing is performed in compliance to cGMP, site SOPs and controlled documents from end-to-end, covering warehouse and supply chain management operations, manufacturing operations, batch certification by QP, batch release and shipment for biologics drug substance manufactured in WuXi Biologics Ireland.

Organization Description

WuXi Biologics is a premier provider of biologics services (from discovery to commercialization) with global customers in the biopharmaceutical and healthcare industries. We´re one of the world's top three contract development and manufacturing companies for biopharmaceuticals, we provide our clients with a world-leading open access technology platform. We enable our clients to research, develop and manufacture drugs from the concept phase to commercial manufacturing.

Department Description

As QA DS Manufacture Lead, you'll be joining an organization where people of all backgrounds and experiences are respected, and where we work together focused on changing lives.  In this role you'll be reporting to the Director of Quality, WuXi Biologics.

Your Responsibilities

In this role, you will:

• Lead the QA teams responsible for 24/7 oversight of Warehouse and Supply Chain Management (SCM), Drug Substance Manufacturing Operations and the QA team responsible for batch disposition operations.
• Develop, implement, and monitor the quality systems relating to warehouse, SCM and manufacturing and batch disposition operations.
• Provide QA review and approval of SOPs, master batch records, quality risk assessments, change controls and other documentation, as applicable, associated with Manufacturing, Warehouse, SCM and batch disposition operations.
• Review and approve deviation reports, CAPAs, and technical documents to support GMP decisions and batch disposition.
• Ensure online QA presence in Warehouse and Manufacturing areas during operation, as required.
• Lead the GMP Release program.
• Liaise with internal and external teams, as appropriate, to ensure that all deviations, investigations, and batch record review comments are adequately addressed and closed out in a timely manner as defined in SOPs.
• Liaise with internal and external teams, as appropriate, to ensure that all CAPAs, change controls, internal audit observations are addressed and closed out in the required time frame.
• Ensure timely and efficient disposition of biologics drug substance batches.
• Supervise direct reports on a day-to-day basis, provide training and communications, assignment, and prioritisation of work.
• Manage performance, delivery of objectives and career development of direct reports.
• Ensure clear communication on issues and timely escalation as applicable.
• Support inspection/audit readiness activities, act as SME for QA DS function during regulatory inspections and Client audits, prepare responses to observations, monitor implementation of follow-up actions.
• Lead and/or represent QA on multidisciplinary teams including New Product Introduction (NPI), Technology Transfer and continual improvement projects.
• Perform internal and external audits, as required.
• Identify and drive opportunities for continuous improvement.
• Champion site metrics and KPIs to ensure targets are achieved, met and counter measures in place when applicable.
• Perform all duties in accordance with GMP requirements, SOPs and controlled documents.
• Flexibility to take on additional tasks and responsibilities at the discretion of the Senior Director of Quality.
• Will act as a role model for the QA function and also the wider organisation in adherence to the WuXi Biologics' corporate core values and PROUD culture.

Your Profile

The ideal candidate for this position, will have the following:

Education:

• A Bachelor's degree in a technical discipline (e.g., biochemistry, chemistry, engineering) would be an advantage.

Knowledge/Experience

Required:

• 8 plus years' experience in the biotechnology and/or pharmaceutical industries within a Quality role, preferably in QA or similar.
• Candidates from Warehouse, Distribution (GDP) or Manufacturing Operations disciplines within the biotechnology and/or pharmaceutical industry will be considered but knowledge of Quality Management System, pharmaceutical regulations and continuous/process improvement tools will be required to be demonstrated.
• Experience managing a QA operations team would be an advantage.
• Experience in performing internal audits would be an advantage.
• Experience interacting the regulatory Inspectors would be an advantage.
• Experience working in a CMO in Client-facing role would be an advantage.
• Demonstrated knowledge of Quality Management System and continuous/process improvement tools.

Personal skills

• Strong technical aptitude (i.e., able to read & comprehend technical documentation & execute procedures).
• Strong knowledge of cGxP requirements and regulations.
• Knowledge of trouble shooting and problem-solving skills, e.g., formal root cause analysis such as Ishikawa diagrams, FMEA etc.
• Demonstrated knowledge of Quality Management System and continuous/process improvement tools.
• Adaptable, able to multi-task and handle tasks with competing priorities effectively.
• Strong sense of urgency with a drive to close actions to closure on time and in full.
• Excellent interpersonal and communication skills.
• Excellent organisational skills.
• Proactive attitude.
• Excellent attention to detail.

Other Requirements

• There may be a requirement for occasional travel to locations within Ireland and overseas to support business needs. Must be willing to travel when required.
• There will be a requirement for direct reports to work shift pattern once the project phase is complete.

Delegation of Responsibilities

When absent from the site, duties and responsibilities (with exception of QP confirmation/ certification of biologics drug substance) will be delegated to the following designates:

• Job Title: Senior Director of Quality
• Job Title: QA Drug Substance Group Leader, QA for WH Group Lead

As we extend our global reach, we need colleagues interested in change, in challenge, and in building a new future together. Reach beyond yourself and discover your true potential

If you have the ability to thrive in a dynamic and fast-paced environment and feel that the moment has come for you to be part of such an exciting journey towards accomplishing our vision - Any drug can be made, and any disease can be treated - don't miss out on this opportunity to join us and reach beyond yourself and discover your true potential.   Apply now

Would you like to know more before you apply? Please visit us at or contact us via

WuXi Biologics is an equal opportunities employer.

Introduction & Company Overview
Catalyst is a leading technical advisory and construction technology SaaS company, operating

primarily in Ireland and the UK. Our purpose is to make the built environment safer and greener. We

also provide ESG services to funds, developers and corporations, supporting them in creating and

managing safer, more sustainable places to live and work.

We are seeking a dynamic and experienced senior QA Engineer with both manual and automation

expertise. The successful candidate will lead a small QA team and take full ownership of the QA

function within our company.

Role Overview

In this role you will manage and guide our two existing QA engineers while remaining hands-on when

required. We have an automation framework in use, which you will be expected to extend and

strengthen. This role is critical to our software development lifecycle. You will be responsible for

designing and executing tests to ensure our software runs smoothly, meets client needs, and is free of

defects. You will work closely with the development team to identify issues, suggest improvements, and

help deliver high-quality, reliable software. Our QA technology stack consists of:

• Unit, Selenium with .NET C#, Puppeteer, Swagger and Postman
• Azure DevOps for CI/CD, work tracking, and test management
• Documentation tools: Confluence, Azure DevOps & SharePoint

We are looking for an experienced senior QA Engineer to take ownership of the QA function within our

company. This is a hands-on leadership role where you will guide a small team, strengthen our

automation framework, and ensure the quality of our products in a fast-paced Agile environment. If you

are driven to improve quality, enjoy mentoring others, and thrive on delivering reliable software, we'd

love to hear from you.

Key Responsibilities

• Lead and mentor a small QA team while remaining hands-on in testing activities.
• Drive automation by extending and enhancing the existing framework.
• Design, execute, and maintain manual and automated test plans.
• Own testing end-to-end, from requirements through to production release.
• Collaborate with product and development teams to define objectives and ensure quality.
• Analyse results, manage defects, and ensure timely resolution.
• Actively contribute to Agile ceremonies and product releases.
• Promote QA best practices and continuous improvement.
• Take direct responsibility for all QA artefacts (e.g., test cases, processes, automation repositories,

documentation).

• Ensure QA activities support product and business objectives, demonstrating an understanding of and

commitment to the overall business plan.

• Maintain scalable test environments and comprehensive documentation.

Essential Requirements

• Eligible to work in the Republic of Ireland.
• 10+ years of professional QA experience, including at least 3 years in an Agile environment.
• Access to high-speed broadband (>100Mb download, >20Mb upload). This is a hybrid role.
• Extensive experience in web-based testing and browser developer tools.
• Strong background in continuous integration and delivery processes/tools.
• Proven expertise in test automation with Selenium (.NET C#) and Playwright.
• Experience with API testing (manual and automated, e.g., Postman/Swagger).
• Ability to improve test coverage and define the technical QA roadmap.
• Experience developing and maintaining test plans, test cases, and automation best practices.
• Experience with Jira, Confluence, or Azure DevOps for Agile project management.
• Excellent written and verbal communication skills.
• Strong analytical, planning, and organisational ability.
• Broad IT knowledge with the ability to adapt in a dynamic, fast-changing environment.
• Bachelor's degree in a relevant technical field, or equivalent experience.

Good to Have (Not Mandatory)

• Familiarity with SQL and databases
• Mobile app testing (Android/iOS).
• Experience with CI/CD pipelines, scripting, and build maintenance.
• ISTQB or other software testing certifications.

Job Description
Are you passionate about Quality Assurance and have a strong background in Drug Product & Drug Substance GMP manufacturing? In this role, you will be pivotal in ensuring GMP manufacturing meets all regulatory, cGMP, and company requirements. Your expertise will uphold our high standards of quality and contribute to the success of our programs. If you are dedicated to excellence in quality assurance, we welcome your application to be part of our innovative team.

Your Core Responsibilities

• Act as site QA responsible for onsite quality monitoring of DP/DS manufacturing and participate in GMP production activities.
• Support Technology Transfer, PPQ activities and monitor the quality of GMP production.
• Create, Review/ Approve department SOPs in collaboration with functional departments, ensuring alignment with corporate policies.
• Audit quality documents to ensure data integrity and provide QA guidance.
• Support site GMP Readiness activities
• Support self-inspection program and Health Authority Inspections as required
• Establish and manage the DP & DS QA Operations team, providing support and ensuring performance management requirements are met.
• Review and approve manufacturing-generated documents, ensuring compliance with regulatory standards.

Who You Are
You are ready if you have

• Qualification Degree in Biopharmaceutical Science or other related science discipline.
• Knowledge of legislative, regulatory, market and data integrity requirements.
• Minimum of 8 years experience in vaccine/biopharma DP/DS Manufacturing. Desirable to have sterile DP filling experience.
• Proven track record in people management, problem-solving, with strong interpersonal skills.
• Proven ability to lead continuous improvement initiatives to enhance quality standards and operational efficiency within the QA team.
• Exceptional skills in collaborating with cross-functional teams to integrate QA processes and address issues promptly.
• Strong leadership skills, including strategic planning, innovation, and talent development, with a commitment to diversity, equity, and inclusion.
• Strong communication skills with the ability to work in a matrix environment.

Current Employees apply HERE

Current Contingent Workers apply HERE

Secondary Language(s) Job Description
As a company, we are committed to keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world's most challenging healthcare needs.

As an equal opportunity employer, we are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. Please don't hesitate to contact the Talent Acquisition Advisor assigned to this role should you need any support during our recruitment process.

So, if you are ready to
Invent solutions to meet unmet healthcare needs,
please apply today.
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status
Regular

Relocation
VISA Sponsorship
Travel Requirements
Flexible Work Arrangements
Not Applicable

Shift
Valid Driving License
Hazardous Material(s)
Required Skills
Preferred Skills
Job Posting End Date
09/19/2025

• A job posting is effective until PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID
R

QA Operations Lead

Setting the Quality Standard for the site, providing site QA support and management of the Systems & Compliance group.

Responsibilities
:

• Ensure that the site quality standards are embedded, measured and sustained in line with Regulatory and Global requirements.
• Preparation and management of the Annual Site Quality Management Plan.
• Providing Overview to site leadership team on the status of the site's quality system through Site Quality Governance Board and Annual Quality Management Review.
• Ensure Global and Local QA Projects and Initiatives are resourced as required.
• Support Quality Culture and Data Integrity on site.

Requirements
:

• Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent.
• At least 8 years' experience working on a manufacturing site (e.g. QA and/or Production) or equivalent experience from external company or other line function. 4 years' experience leading a team.
• Good working knowledge GMP regulations required within the pharmaceutical industry.

We are seeking an experienced QA Lead with a robust background in Mechanical Engineering, and a proven track record in both the Pharmaceutical and Construction sectors. This is a unique cross-industry role requiring a deep understanding of GMP, GEP, and engineering best practices to oversee and enhance quality processes throughout the project lifecycle.

• Lead QA activities across pharma and construction projects, ensuring compliance with GMP, GEP, ISO standards, and other applicable regulations.
• Develop, implement, and maintain Quality Management Systems (QMS) to ensure adherence to project, client, and regulatory requirements.
• Oversee mechanical system installations (e.g., HVAC, piping, pressure vessels) with a focus on quality and compliance in both cleanroom and construction environments.
• Coordinate with multidisciplinary teams including engineering, validation, commissioning, construction, and operations to align quality standards.
• Perform supplier and contractor audits, review quality documentation, and ensure proper IQ/OQ/PQ protocols are followed (in pharma).
• Lead Non-Conformance (NC) investigations, CAPAs, and root cause analysis for deviations in construction or pharma environments.
• Ensure all materials, equipment, and systems used in construction or manufacturing are installed and qualified to meet regulatory expectations.
• Participate in project planning, risk assessments, and quality reviews from design through handover phases.
• Serve as the primary quality interface with regulatory bodies and client auditors.

• Bachelor's degree (or higher) in Mechanical Engineering.
• 7+ years of QA experience, with at least 3-5 years in Pharma (GMP environment) and 3+ years in Construction/Infrastructure.
• Solid understanding of mechanical systems within GMP manufacturing and industrial construction.
• Hands-on experience with validation, commissioning, and qualification processes.
• Strong familiarity with regulatory standards such as FDA, EMA, MHRA, and ISO 9001.
• Experience implementing or working with QMS platforms (e.g., TrackWise, MasterControl).
• Proven experience in managing teams and leading cross-functional quality initiatives.
• Excellent written and verbal communication, reporting, and stakeholder management skills.

If you are interested in this role, please apply directly or email your CV to

Date Opened

10/17/2025

Job Type

Full time

Industry

Construction

City

Dublin 15

State/Province

Dublin

Country

Ireland

Zip/Postal Code

D15

We are seeking an experienced Mechanical QA/QC Lead to support a large-scale pharmaceutical construction project in Limerick.

The successful candidate will oversee all QA/QC activities related to mechanical systems and ensure that construction works are executed to the highest standards of quality, compliance, and safety.

You will play a key role in ensuring adherence to project specifications, GMP requirements, regulatory codes, and client expectations. Prior experience in pharmaceutical construction projects is essential.

Key Responsibilities:

• Lead mechanical QA/QC efforts across all phases of construction on a live pharmaceutical project.
• Develop and maintain Mechanical Quality Plans, Inspection & Test Plans (ITPs), and commissioning checklists.
• Coordinate and supervise inspections and testing of mechanical systems, including piping, HVAC, process equipment, and utilities.
• Review and verify that mechanical installations comply with cGMP standards, project specifications, and relevant codes.
• Manage and mentor a team of Mechanical QA/QC Inspectors on-site.
• Review vendor/supplier quality documentation, welding procedures, and materials certifications.
• Oversee pressure testing, flushing, cleaning, and pre-commissioning activities.
• Ensure NCRs (Non-Conformance Reports) are managed, investigated, and closed out appropriately.
• Interface with client representatives, construction teams, and validation personnel to support seamless handover and system turnover.
• Support audits, walkdowns, and quality punch list resolution.
• Prepare and compile turnover packages, quality dossiers, and final documentation for CQV and handover.

Qualifications:

• Bachelor's Degree in Mechanical Engineering or related discipline.
• Minimum 5 years of mechanical QA/QC experience, with at least 2 years in pharmaceutical construction.
• Strong knowledge of GMP, GEP, ISPE Baseline Guides, and EU/US regulatory expectations.
• Familiarity with piping codes and standards (e.g., ASME B31.3, ASTM, EN standards).
• Certified Welding Inspector (CWI), CSWIP, or equivalent desirable.
• Proficient in interpreting P&IDs, isometrics, HVAC schematics, and installation drawings.

Skills and Competencies:

• Proven ability to lead QA/QC teams on complex, fast-paced construction projects.
• Excellent communication, documentation, and stakeholder management skills.
• Strong attention to detail and understanding of documentation and compliance in a regulated industry.

Next Steps

If you are interested in this role, please apply directly or email your CV to

Date Opened

08/29/2025

Job Type

Full time

Industry

Construction

City

Limerick

State/Province

Limerick

Country

Ireland

Zip/Postal Code

V94

Kaseya is the leading provider of complete IT infrastructure and security management solutions for Managed Service Providers (MSPs) and internal IT organizations worldwide powered by AI. Kaseya's best-in-breed technologies allow organizations to efficiently manage and secure IT to drive sustained business success. Kaseya has achieved sustained, strong double-digit growth over the past several years and is backed by Insight Venture Partners ), a leading global private equity firm investing in high-growth technology and software companies that drive transformative change in the industries they serve.

Founded in 2000, Kaseya currently serves customers in over 20 countries across a wide variety of industries and manages over 15 million endpoints worldwide. To learn more about our company and our award-winning solutions, go to and for more information on Kaseya's culture.

Kaseya is not your typical company. We are not afraid to tell you exactly who we are and our expectations. The thousands of people that succeed at Kaseya are prepared to go above and beyond for the betterment of our customers.

Senior Automation QA Engineer – Playwright Focused
What We Are Looking For
We are seeking an
Automation QA Engineer
with a passion for modern web automation and software quality. The ideal candidate has strong experience in Playwright, a solid understanding of automated testing strategies, and a continuous improvement mindset.

What You'll Do

• Design, develop, and maintain automated test scripts using Playwright (Typescript) and other modern automation tools
• Execute automated test cases to validate web application functionality, performance, and security
• Collaborate with developers and product teams to define test requirements and create effective, scalable test plans
• Analyze test results, log and track defects, and partner with engineering teams to ensure timely resolution
• Enhance and optimize existing Playwright-based automation frameworks to ensure coverage, reliability, and scalability
• Conduct regression testing to verify that new releases do not impact existing functionality
• Integrate automated testing into CI/CD pipelines (e.g., GitHub Actions, Jenkins, GitLab CI)
• Stay informed of emerging test automation trends and contribute ideas to improve QA practices
• Implement automation strategies across functional, regression, and smoke testing suites
• Continuously review and improve test coverage and test case efficiency
• Assist with manual testing of new features
• Mentor and guide Manual QA engineers through onboarding and upskilling in automation

What You'll Bring
Education & Experience

• Bachelor's degree in Computer Science, Engineering, or a related field
• 3+ years of experience in test automation for web applications

Technical Skills

• Hands-on experience with Playwright (JavaScript or TypeScript preferred)
• Proficiency in at least one modern programming language: JavaScript, TypeScript, Python, or Java
• Familiarity with other automation tools (e.g., Selenium, Cypress) is a plus
• Knowledge of CI/CD systems such as GitHub Actions, Jenkins, or GitLab CI
• API testing experience using Postman, RestAssured, or similar tools
• Solid understanding of software testing methodologies and Agile/Scrum practices

Soft Skills

• Analytical thinker with excellent problem-solving abilities
• Strong communication and cross-team collaboration skills
• Self-driven and able to manage priorities in a dynamic environment

Why Join Us?
If you're excited about quality and automation, passionate about Playwright, and eager to build high-quality software at scale, we'd love to hear from you

Join the Kaseya growth rocket ship and see how we are #ChangingLives

Additional Information
Kaseya provides equal employment opportunity to all employees and applicants without regard to race, religion, age, ancestry, gender, sex, sexual orientation, national origin, citizenship status, physical or mental disability, veteran status, marital status, or any other characteristic protected by applicable law.