QC Chemist

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 detail-oriented and proactive QC Chemist to join our Quality Control team. The successful candidate will be responsible for performing chemical analyses, supporting product release, and ensuring compliance with GMP and regulatory requirements.

• Perform routine and non‑routine chemical testing of raw materials, intermediates, and finished products using analytical techniques (e.g., HPLC, GC, UV, FTIR).
• Prepare and review test documentation in compliance with GMP and internal SOPs.
• Support method development, validation, and transfer activities.
• Investigate out-of-specification (OOS) and out-of-trend (OOT) results, ensuring timely resolution.
• Maintain laboratory equipment and ensure calibration and qualification are up to date.
• Participate in continuous improvement initiatives within QC operations.
• Ensure compliance with health, safety, and environmental standards.

• Degree in Chemistry, Analytical Science, or related discipline.
• Experience in a GMP‑regulated environment (pharmaceutical or medical device preferred).
• Hands‑on experience with analytical techniques such as HPLC, GC, UV spectroscopy.
• Strong attention to detail and ability to work independently and in a team.
• Excellent documentation and communication skills.

• Knowledge of regulatory requirements (ICH, FDA, EU GMP).
• Experience with LIMS and electronic data systems.

• Opportunity to work in a world‑class healthcare organization.
• Professional development and training in advanced analytical techniques.
• Collaborative and supportive team environment.

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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