- Quality Assurance
- Six Sigma
- Process Improvement
- Microsoft Word
Around the world, our employees are united by our mission to save and sustain lives. Together, we create a culture that encourages colleagues to pursue rewarding careers - where everyone has the opportunity to do meaningful work as a part of a team they respect, in an environment that values each person’s contributions. We’re happy you’re interested in continuing your career journey with Baxter.
Essential Duties & Responsibilities
Ability to perform standalone repeat and/or routine validations with little or no guidance.
Ability to provide requirements for change control based on procedural requirements
Be able to assist, present, defend and communicate with external auditors and others validations or projects in which you lead or participated.
Assist or lead process improvement projects (scrap reduction, defect reduction, etc.) with little or no guidance.
Can work with other support groups (production, quality, laboratory, etc.) in a collaborative manner.
Display a solid technical understanding of engineering principles and procedures (e.g. CAD and its application or scheduling a series of technical tasks utilizing software-based tools and/or specialties such and chemical, industrial or biological).
Assists in the preparation and participation in technical reviews and responsible for organizing data and preparing appropriate documentation for assigned projects.
Provide assistance to management or other engineers during design, installation, qualification and/or process monitoring.
Provide technical reports and/or data driven analysis after training.
Qualifications for this role
B.S. in technical area (mechanical, electrical, chemical, biological, etc.)
0 - 2 year related process validation experience. (In-house, co-op or acquired outside).
Prefer experience and/ or training with process improvement methods (e.g. six sigma, lean)
Ability to discuss normally encountered technical or project management issues, both verbally and in written form.
Ability to work as a collaborative team member.
Ability to solve routine design, engineering problems with little assistance.
Basic understanding of validation guidelines, cGMPs Regulations and Good Manufacturing Practices
Support plant initiatives with the development and implementation of new process/technology
Skilled in Microsoft Excel, Microsoft Word, Microsoft PowerPoint or equivalents.
Education & Experience
Bachelor's degree in Engineering,
0-2 years’ experience in Quality Assurance
Validation in regulatory industry is desired
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
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to Americas_TTA@baxter.com and let us know the nature of your request along with your contact information.