Quality Technician

Baxter Healthcare; Batesville (IN); On-site; USD 43,000 - 59,000; Full time

Benefits offered by this job

Medical and dental coverage

ESPP (Employee Stock Purchase Plan)

401(k) with company matching

Paid time off 20–35 days

Family and medical leaves of absence

Parental leave

Job summary

As a Quality Assurance (QA) Technician at Baxter’s Batesville site, you will support quality and regulatory work behind medical bed devices. You’ll collaborate with Manufacturing and Document Control to ensure products meet quality standards and FDA requirements, while maintaining accurate quality records in a patient-focused, regulated environment.

You will join a Quality Assurance and Regulatory Affairs team, providing hands-on quality support throughout production and contributing to

Qualifications

• Knowledge of FDA and ISO standards.
• Strong organizational/documentation skills.
• Demonstrated high attention to detail.

Responsibilities

• Ensure the Device History Records (DHR) are properly and accurately completed.
• Serve as a primary point of contact for rapid and effective corrections of quality issues identified with the Device History Records.
• Provide training to ensure proper completion and accurate GDP used with the Device History Records.
• Ensure the NCMR’s have been properly documented prior to release of the product for distribution.
• Release the product for distribution by properly signing the Device History Record.
• Complete the required documentation for properly entering the Device History Records in the Document Control System.
• Perform audits to include testing and visual inspection of products.
• Capable of performing non-routine or complex tasks.
• Observes, records, and analyzes data to maintain daily audit reports.
• May require developing new procedures.

Skills

Attention to detail

Organizational skills

Documentation skills

Computer skills

FDA/ISO knowledge

Education

High school diploma or GED

2-year technical degree or equivalent

Job description

This is whereyour 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.

Your Role at Baxter

This is where your creativity addresses challenges!

As a Quality Assurance (QA) Technician, you’ll help support the quality and regulatory work behind medical bed devices made at Baxter’s Batesville site. You’ll work closely with manufacturing and other teams to make sure products are built to quality standards, meet FDA requirements, and follow Baxter policies. Part of your role includes keeping quality records accurate and up to date, all while contributing to a positive, team‑oriented work environment.

Your Team

You’ll be part of a supportive Quality Assurance and Regulatory Affairs team focused on making sure Baxter products are safe, reliable, and compliant. In this role, you’ll collaborate with Manufacturing, Engineering, and Document Control teams and provide hands‑on quality support throughout the production process. It’s a patient‑focused, regulated environment where teamwork, attention to detail, and continuous improvement are truly valued.

What You'll Be Doing

• Ensure the Device History Records (DHR) are properly and accurately completed.
• Serve as a primary point of contact for rapid and effective corrections of quality issues identified with the Device History Records.
• Provide training to ensure proper completion and accurate GDP used with the Device History Records.
• Ensure the NCMR’s have been properly documented prior to release of the product for distribution.
• Release the product for distribution by properly signing the Device History Record.
• Complete the required documentation for properly entering the Device History Records in the Document Control System.
• Perform audits to include testing and visual inspection of products.
• Capable of performing non‑routine or complex tasks.
• Observes, records, and analyzes data to maintain daily audit reports.
• May require developing new procedures.

What You'll Bring

• High school diploma or GED or above
• 2-year technical degree or equivalent work experience preferred
• Knowledge of FDA and ISO standards.
• Strong organizational/documentation skills.
• Strong Computer skills.
• Demonstrated high attention to detail

Applicants must be authorized to work for an employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.

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 $43,200 - $59,400 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than or of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based 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.

US Benefits at Baxter (except for Puerto Rico)

• medical and dental coverage that start on day one
• basic life, accident, short‑term and long‑term disability
• business travel accident insurance
• Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
• 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
• Flexible Spending Accounts
• educational assistance programs
• time‑off benefits such as paid holidays
• paid time off ranging from 20 to 35 days based on length of service
• family and medical leaves of absence
• paid parental leave
• commuting benefits
• Employee Discount Program
• Employee Assistance Program (EAP)
• childcare benefits
• Join us and enjoy the competitive compensation and benefits we offer to our employees.

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.

Know Your Rights: Workplace Discrimination is Illegal

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.

1125 East Pearl Street|Batesville, IN 47006|United States of America