Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

We are seeking a Process Validations Engineer to join our growing team of talented and passionate people at our Castlebar, Co. Mayo site. Across our Castlebar and Swinford facilities, more than 1,300 colleagues work together in a 24/7 operation dedicated to extending lives and expanding possibilities.

In this role, you will play a key part in ensuring the robustness, compliance, and continuous improvement of our manufacturing processes and support equipment. You will join a supportive Process Validation Department.

Duties and responsibilities:

• Author validation protocols, reports, and risk assessments that ensure compliance and process reliability.

• Review engineering trials and product development documentation to support new and existing processes.

• Complete validation and risk assessments within TrackWise 8.

• Provide technical approval of validation documentation.

• Lead validation projects, ensuring they are executed in a controlled, compliant, and timely manner.

• Deliver clear project updates to stakeholders.

• Prepare and deliver presentations, contributing to effective project communication and management.

Education and experience required:

• A degree in Science, Engineering, or a related discipline (or equivalent experience).

• Experience in process validation is desirable, but not essential—training will be provided.

• Knowledge of EU GMP and FDA regulatory requirements.

• Strong critical thinking, analytical, and problem‑solving skills.

• Ability to make sound decisions and work through complex technical challenges.

• A collaborative mindset and the ability to work effectively within a team environment.

What Vantive can offer to you:

• A permanent contract with a stable and secure work environment.
• A comprehensive benefits package, including private medical insurance, company pension scheme, and annual bonus scheme.
• A collaborative and dynamic work environment.
• Access to state-of-the-art equipment and technology.
• Recognition and reward for outstanding performance.

Reasonable Accommodation

Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link

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