Are you looking for a career that matters?
We believe every person deserves a chance for a healthy life, free from illness and full of possibility. We see a world full of healing, with viable care options available to those with limited choices today.
We envision new ways of providing physicians, pharmacists and nurses with technologies that not only treat chronic diseases, but also work to prevent them.
We’re looking for team members who are motivated to learn, grow and innovate, while making a meaningful difference for millions of people around the world.
Learn more about how Baxter is .
Essential Duties and Responsibilities
Write / update the production processes and procedure according to the cGMP requirement and Baxter requirement.
As the key player to complete all the validation activities according to cGMP requirement and Baxter quality system.
Continuously optimize the operational and quality processes and equipment to achieve the company strategy target.
Participate and present documents / process as the key player in production area if the audit or inspection, ensure to pass the inspections or audit, take the effective actions if any findings related to production area.
Handle the non-conformity and CR cases for the validation and daily operation.
Train the future employees, e.g. operators, technicians and engineers
At least a bachelor in Pharmacy or Engineering.
More than 3 year of production experience in a manufacturing environment
preferably in the pharmaceutical, medical or similar industry.
Familiar with the processes of pharmaceutical manufacturing and GMP management.