Baxter International Inc. develops, manufactures and markets products that save and sustain the lives of people with hemophilia, immune disorders, infectious diseases, kidney disease, trauma, and other chronic and acute medical conditions. As a global, diversified healthcare company, Baxter applies a unique combination of expertise in medical devices, pharmaceuticals and biotechnology to create products that advance patient care worldwide.
- Perform batch record review on the manufacturing floor as processes are completed.
- Review charts and documentation produced by manufacturing operations including reconciliation of any documentation errors.
- Provide cGMP/SOP support and guidance to manufacturing personnel.
- Issue, monitor and assist in the reconciliation of any process or product exceptions resulting from the manufacturing process.
- Able to occasionally work long hours and off-shifts.
- Able to occasionally be on-call for weekend support of production.
- Stay at work until assigned tasks and associated documentation is completed.
- Maintains an accurate and up-to-date training history.
- Strong team player and willingness to help others when needed.
- Proper use of safety procedures.
- Participate in continuous improvement functions involving teams, which increase efficiency, solve problems, generate cost savings and improve quality.
- A BA or BS in a science related field.
- Prefer manufacturing experience in a quality (ISO, cGMP) environment.
- Excellent interpersonal and technical skills.
- Communicates Effectively
- Openly shares information, listens to and values feedback, shares opinions and feedback directly
- Good documentation skills
- Computer skills
Baxter provides its employees with comprehensive compensation and benefits.To view other opportunities at Baxter and to learn more about the company, please visit our Web site at http://www.baxter.com/about_baxter/careers . EOE M/F/D/V.
