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.

Vantive is seeking a proactive and solutions‑driven QA In‑Process Engineer to join our high‑performing team in Swinford. This is a fantastic opportunity to contribute directly to quality performance, compliance excellence, and continuous improvement within a world‑class manufacturing environment.

In this role, you will support the achievement of department KPIs, drive quality investigations, collaborate cross‑functionally, and ensure the highest standards of compliance and operational effectiveness.

What You Will Be Doing

Achieve and improve department KPIs while supporting broader plant goals with limited supervision.
Review executed production batch records and provide deviation/batch dispositions.
Investigate customer complaints, ensuring timely and effective closure of each case.
Ensure all NCRs/deviations are fully investigated and documented, with appropriate corrective actions implemented.
Support ongoing process improvement initiatives across the plant.
Make regular decisions that impact product quality, timelines, and/or cost.
Review, create, and update SOPs, work instructions, and other GMP documentation.
Work proactively within cross‑functional teams to resolve quality issues.
Manage assigned projects and collaborate cross‑functionally to deliver results.
Provide support during regulatory and compliance audits.
Prepare and present quality management reports to key stakeholders.

What We’re Looking For

Someone who embodies Vantive’s values and is ready to contribute to a culture of quality, accountability, and innovation.

Key Competencies & Attributes

Takes accountability for delivering results.
Innovative mindset with a drive to find effective solutions.
Comfortable working with ambiguity while maintaining sound judgement.
Strong critical thinking and problem‑solving skills.
Team‑oriented with a strong customer and results focus.
Able to manage deadlines and handle workload effectively in a fast‑paced environment.
Excellent communication skills with the ability to convey ideas, data, and technical information clearly and accurately.

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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QA in Process Engineer

Benefits

Job Description