Sr. Quality Engineer - Cleveland, United States - Baxter Healthcare Corporation

Description

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.

About Baxter's Cleveland, MS Facility:
Cleveland's technology and automation are cutting edge. It is the U.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.

Baxter encourages and values every employee and believes that each person can contribute to advancing healthcare for patients; work to be proud of.

Your Role at Baxter
This is where your creativity addresses challenges
You are creative, thorough, and a heads-down do-er. You embrace a challenge and truly apply the collaborative powers of your team to produce great results. You are motivated by work that is never the same from one day to the next.

As a Quality Engineer, you are unafraid of navigating through necessary internal processes to facilitate a product you deeply believe in.

You can absorb and act on complex procedures and data and train your team or peers if needed. You take pride in getting things done quickly without sacrificing safety or quality.

Your Team at Baxter
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.

The mission of Baxter is to save and sustain lives. This mission is embedded into everything we do.

This means if there is a decision to be made where quantity and quality are at odds, we will always choose quality.

Our patients come first, always.

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. As the company evolves, so does the way our team approaches work as it strives to create top-of-the-line products.

We build relationships with each other to get work done. Building these relationships is easy because we all share common traits of being reliable, ethical, and caring. We lean on our colleagues for their expertise and hold each other accountable. We feel empowered to speak up when there's a new insight or opportunity to improve something. This open dialog builds trust within the team and helps create a better product for our customers.

What we offer from Day One
Medical, Dental and Vision coverage

160 hours of Paid Time Off and Paid Holidays

401K match

Employee Stock Purchase Program

Paid Parental Leave

Tuition Reimbursement


What you'll be doing:
Must perform equipment qualification, test method and process validation activities, process capability and process control studies for assigned areas.

Must plan and execute software validation activities in manufacturing and support areas.

Must drive quality/manufacturing projects utilizing 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 compliant with regulatory quality standards through validation activities. May serve as SME for Computerized System Validation processes.

Responsible for ensuring FDA regulations are met for system upgrades/replacements.

Responsible for audits, creation, and implementation of Specifications/SOPs.

Responsible for ensuring the quality of facility systems (validation):

Writing and executing protocols and test cases for validations.

Coordinating testing and documentation of projects.

Documenting/executing 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.

Must perform failure investigations and track follow-up corrective actions.

Ability to function effectively as a member of a team.

Ability to plan and prioritize multiple projects to ensure completion within the target dates.

Ability to communicate effectively in written and verbal form.

Must have knowledge of both plant and department environmental health and safety regulations and comply with said regulations accordingly.

Must perform all other duties and responsibilities as determined by supervision/management.


What you'll bring:

BS degree in Engineering, Computer Science or other core Science Discipline and 3-5 years minimum related experience (in house, co-op or acquired outside).

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.

ASQ Certification (CQE or CSQE) or equivalent desired.

Leadership skills.

Ability to work independently or with a diversified cross functional team across different locations.

Ability to mentor new Engineers to the Company.

Logical thought process.

Self-motivated and works well without direct supervision.

Quality Assurance or Pharmaceutical industry experience desired.

Ability to lift to 10 pounds, to sit, stand and/or walk for long periods of time.

Ability to reach above the shoulder, to bend/stoop.

We understand compensation is an important factor as you consider the next step in your career.

At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.

The estimated base salary for this position is $88,000 - $121,000 annually. The estimated range is meant to reflect an anticipated salary range for the position.

We may pay more or less than that of the anticipated range based upon market data and other factors, all of which are subject to change.

Individual pay is based on upon location, skills and expertise, experience, and other relevant factors.

For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.

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.

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.

EEO is the Law
EEO is the law - Poster Supplement
Pay Transparency Policy
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 .
N Davis|Cleveland, MS 38732|United States of America
#J-18808-Ljbffr