This is where your work makes a difference.

At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond.

Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results.

Here, you will find more than just a job—you will find purpose and pride. 

We have an oustanding opportunity in our San Vittore plant!

We are looking for a QA Process Coordinator:

WHAT YOU'LL BE DOING:

·       Responsible for change control management

·       Develop Validation Master Plan, collaborating with manufacturing/engineering/subcontractors to perform respective all type of process and equipment qualification (e.g. process validation, computer system validation, cleaning validation, equipment qualification, facilities qualification, IT Qualification etc.)

·       Write, execute and review of qualification and validation protocol and report. Ensure timeliness and effectiveness of validation and qualification activities.

·       Collaborate with Engineering, EHS, IT department in managing critical systems validation and maintenance

·       Ensure strong knowledge of data Integrity as SME of the site

·       Ensure strong risk-based approach using dedicated tools and statistical techniques where applicable

·       Lead further implementation and integration of RBLCM and CPV project

·       Lead of risk management (e.g. assessment, periodic review)

·       Implement and support effective In-process control program

·       Ability to suggest other options to improve efficiency, reduce operating costs

·       Ability to identify the root cause and hence the possible corrective and/or preventive actions in case of manufacturing issues

·       Collaborate in cross functional project e.g. digitalization, automation, GMP improvement

·       Collaborating on the Environmental Control monitoring activities

·       Supervisor of equipment Calibration program

WHAT YOU'LL BRING:

·       Italian language: Fluent written and spoken

·       English Language: Fluent written and spoken

·       Good knowledge of Office Suite

·       Preferred good knowledge of Minitab software

·       Preferred good technical knowledge of extrusion process and critical systems

·       Strong analytical and problem-solving skills.

·       Good interpersonal/communication/influencing/negotiation skills.

·       Good project management skills

·       Optimum time management

Equal Employment Opportunity

Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

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.

Recruitment Fraud Notice

Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.