Sr Quality Technician

Baxter•Batesville, IN

23h

About The Position

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. Your Role at Baxter This is where your creativity addresses challenges! As a Senior Quality Technician , you will play a critical role in ensuring the accuracy, integrity, and compliance of quality documentation and records. You will apply deep knowledge of quality systems and document control processes to support manufacturing operations, audits, and continuous improvement initiatives. 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.

Requirements

High school diploma or GED
Strong organizational/documentation skills.
Microsoft Excel experience
Demonstrated high attention to detail

Nice To Haves

4-year technical degree or equivalent work experience preferred
Agile and or JD Edwards experience is preferred

Responsibilities

Ensure the Device History Records (DHRs) are properly and accurately completed.
Verify required documentation for entering DHRs into the Document Control System.
Respond to and fulfill internal and external DHR requests, ensuring accuracy, completeness, and timely turnaround.
Maintain accurate document control practices in accordance with internal quality system requirements.
Manage document retention activities, ensuring controlled records are stored, archived, and retrievable per regulatory and company standards.
Act as a liaison to offsite document control storage sites, coordinating transfers, retrievals, and audits.
Perform Periodic Document Reviews (PDRs) for Job Instructions (JIs), ensuring documents remain current and compliant.
Execute responsibilities as a Document Control Change Analyst, including review, routing, and processing of document change requests (DCRs).
Support internal and external audit activities by providing accurate documentation and records.
Collaborate cross-functionally with manufacturing, engineering, and quality teams to resolve issues and support continuous improvement.
Train peers or team members as needed on procedures or documentation processes.
Lead and participate in cross-training initiatives to build team capability and ensure coverage across all Quality functions.

Benefits

medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and 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
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