QA Officer

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

An exciting opportunity for an individual with an established background in quality and proven ability to drive and develop quality system requirements. The successful candidate will be responsible for ensuring the delivery of Batch release and that all quality system procedures and processes are effectively implemented.

Working hours are Monday to Friday, 9am - 5pm (with some flexibility).

Essential Duties & Responsibilities

• Co-ordinate the completion of Quality System requirements.
• Be part of investigating events using root cause analysis tools and assisting in driving change through recommendations to correct the event and prevent recurrences.
• Work with other departments to assure timely completion of CAPA's, Change Controls and ensure site KPIs are met.
• Drive a right first-time culture across all departments, working with cross functional teams to drive compliance through the correct implementation of policies, procedures, and practices.
• Participate in scheduled internal and Global Compliance audits.
• To be familiar with GMP, CAPA, Change Control and Training Management Systems and to deliver associated training.
• Actively working on Batch Release workload.
• Proactively identify and support implementation of continuous improvement.
• Maintain and organise the Archive of GMP documentation on and off site.
• Perform other reasonable duties as required for the efficient operation of the QA function.

Education and Experience

• Science based education.
• Ideally a minimum of 2 years’ experience in a GMP manufacturing environment as QA.
• Demonstrated use of lean management tools.
• Knowledge and application of root cause investigation techniques.
• Experience of leading change in own area of expertise and cross functionally.
• Experience in training delivery and training processes.

What are some of the benefits of working at Baxter?

• Competitive total compensation package.
• Professional development opportunities.
• High importance placed on work life balance.
• Commitment to growing and developing an inclusive and diverse workforce.

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.