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Principal, Verification Engineer

3 months ago

Cleveland MS, United States BAXTER Full time

At Baxter, we are deeply connected by our mission. 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.

About Baxter’s Cleveland, MS Facility:
Cleveland’s technology and automation are innovative. S. source for plastic pour bottles, glass IV, and various reconstitution devices. This facility has several major product lines with a diverse array of automated manufacturing technologies including bottle solution filling, injection molding, and device assembly.

 
Our Cleveland plant has been an integral part of Baxter for over 70 years. The work is challenging and rewarding, as Baxter offers competitive compensation and benefits. Your Team: Within Quality, every role makes a difference. Products that Baxter makes are shipped worldwide for patients in need. Whether it's building a new process from scratch or facing a never-before-seen production hurdle, individuals within Quality are given the trust and opportunity to bring creativity to the table. Regardless of your specific role with a product, it is sure to touch a portion of our global operation.

 
This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality. The Quality function values both working together as a team and independently. We draw energy from working in a plant or an office where there are opportunities to collaborate. Must perform equipment qualification, test method and process validation activities, process capability and process control studies for assigned areas.
Must plan and implement software validation activities in manufacturing and support areas.
Must drive quality/manufacturing projects applying Lean, problem solving, process control, and project management tools to achieve and sustain operational excellence.
Must support Manufacturing, Engineering, and Quality Management departments with the development and implementation of new processes/technologies.
Must assist in the identification and development of process improvement projects including automation and computerization.
Must ensure computer systems and applications are aligned with regulatory quality standards through validation activities. Responsible for audits, creation, and implementation of Specifications/SOPs.
Responsible for ensuring the quality of facility systems (validation):
Writing and implementing protocols and test cases for validations.
Coordinating testing and documentation of projects.
Documenting/performing changes to applications.
Assisting/leading training for systems.
Diversified knowledge of applied Statistical Analysis techniques, procedures, and criteria to carry out measurements, process, and product capability studies for the development of new or refined equipment, materials, processes, instruments, and products.
Ability to plan and prioritize different projects to ensure completion within the target dates.
Must have knowledge of both plant and department environmental health and safety regulations and follow said regulations accordingly.
Must perform all other duties and responsibilities as determined by supervision/management.

Preference in Engineering, Computer Science or other core Science Field)
~Knowledge of applications such as Wonderware, Allen-Bradley PLC/HMI, Access, Microsoft Project preferred.
~ Basic knowledge of manufacturing processes and the ability to quickly learn and understand processes/applications.
~ Self-motivated and works well without direct supervision.
~ Quality Assurance or Pharmaceutical industry experience desired.
~ We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. The successful candidate for this job may be required to verify that he or she has been vaccinated against COVID-19, subject to reasonable accommodations for individuals with medical conditions or religious beliefs that prevent vaccination, and in accordance with applicable law.


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.


Pay Transparency Policy

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.


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