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This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission.

Your role at Baxter

As a Manufacturing Technical Writer, you will play a pivotal role in ensuring our operations adhere to the highest standards of quality and compliance. This is where your expertise will drive flawless execution of regulatory requirements and contribute to our world-class manufacturing processes. Your success in this role will be measured by your ability to effectively manage non-conformance investigations and implement corrective actions that maintain our outstanding standards.

Your team

Our team is dedicated to Baxter's mission of saving and sustaining lives. We cultivate a collaborative culture where we support each other to achieve ambitious goals. Our worksite in Round Hill, VA, offers a dynamic environment with opportunities for growth and development. Baxter values its employees, offering benefits such as volunteer days, support for working parents, and matching contributions to your retirement plan.

What you'll be doing

• Perform non-conformance (NCR) investigations within the Track Wise 8 Management System.
• Complete implementation of CAPAs associated with NCR investigations.
• Maintain a high level of expertise in current regulatory requirements.
• Serve as a plant resource for compliance and maintain audit-ready status.
• Provide mentorship and support on DMAIC problem-solving and process improvement projects.
• Ensure compliance with local procedures, US & International Regulatory, and Baxter corporate quality requirements.

What you'll bring

• BS/BA in science, engineering, or related field.
• 2-4 years of relevant work experience in a cGMP-related industry or clinical setting.
• Strong problem-solving and analytical skills.
• Excellent written/verbal communication and organizational skills.
• Ability to make independent decisions with minimum oversight.
• Greenbelt certification or equivalent experience using Six Sigma or other Lean Manufacturing tools.
• Experienced user of TrackWise.
• Working knowledge of FDA Regulations and International Regulatory requirements.
• Understanding of risk management tools.
• Available to work during off-shift or weekends as needed.

Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.