Validation Specialist

Vantive: A New Company Built on Our Legacy

Since last year, Baxter has been on a journey to separate our Kidney Care segment into a standalone company. Vantive* will build on our nearly 70-year legacy in acute therapies and home and in-center dialysis to provide best-in-class care to the people we serve. 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 are driven to help improve patients’ lives worldwide. Join us as we revolutionize kidney care and other vital organ support.

*Completion of the proposed sale of Vantive to funds managed by the Carlyle Group is subject to receipt of customary regulatory approvals and satisfaction of other closing conditions.

Summary

Join Baxtern Validation Specialist and become an integral part of our bold Validation team. Reporting directly to the Validation Supervisor, you will play a key role in ensuring our processes and equipment meet the highest standards of quality and compliance. This outstanding opportunity allows you to contribute to world-class healthcare solutions while working within an encouraging and dynamic environment.

What you'll be doing

• Drafting equipment qualification and process validation protocols and reports (OQ / PQ) to ensure optimal performance and compliance.
• Developing comprehensive cleaning validation protocols and reports to uphold our exceptionally high standards.
• Driving tests to support validations, including statistical analysis of data, ensuring accuracy and reliability.
• Actively participating in departmental investigations for A3, CAPA, or Non-compliance projects to successfully implement corrective actions and improvements.
• Conducting periodic re-evaluations of the validation status of processes and equipment to maintain continuous compliance and quality.

Qualifications

• Degree in Engineering, Pharmacy, Biology, or similar disciplines.
• Experience in Validation activities or within a Quality Assurance department, preferably in a pharmaceutical company is a plus
• Outstanding interpersonal, organizational, and team-building skills that foster a collaborative and inclusive work environment.
• Strong command of English, both written and spoken.
• Basic knowledge of statistical concepts and their applications.
• Availability to work on weekends when necessary to meet project deadlines.

Reasonable Accommodations

Baxter 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.

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