Quality Assurance Associate I — Impact Patient Care

Baxter International Inc.; Marion (NC); On-site; USD 68,000 - 94,000; Full time

Benefits offered by this job

Medical, Dental and Vision coverage

Paid Time Off and Holidays

401K match

Employee Stock Purchase Program

Paid Parental Leave

Tuition Reimbursement

Job summary

Baxter International Inc. is seeking a Quality professional to provide oversight and regulatory/compliance support. The role focuses on risk assessment, process improvement, and ensuring adherence to cGMP and FDA guidelines.

You will lead daily quality operations, supervise staff, and contribute to writing and revising SOPs while supporting internal and external audits. Competitive benefits begin on day one, with opportunities for growth and impact.

Qualifications

• Bachelor's degree strongly preferred. Degree in engineering or science preferred.
• Knowledge of FDA Regulations, Good Laboratory Practices, and Good Manufacturing Practices as applicable.
• Strong interpersonal skills and excellent verbal and written communication.
• Ability to manage people, encourage teamwork and drive decisions.

Responsibilities

• Identify and assess regulatory and quality risks per agency rules and Baxter practices.
• Leads ongoing daily departmental operations.
• May supervise assigned personnel to achieve quality goals; interview/hire, evaluate, train and develop reports.
• Perform in-depth assessments by collecting and analyzing evidence on risks and magnitude.
• Determine logic, adequacy and effectiveness of processes and systems.
• Develop plans to correct identified risks and implement approved actions.
• Write, review, and revise SOPs to meet corporate and regulatory requirements.
• Support external audits and assist with audit reports.

Skills

Quality oversight

Regulatory knowledge

Team supervision

Process improvement

Attention to detail

Education

Bachelor's degree in engineering or science

Job description

Baxter International Inc. is seeking a Quality professional to provide oversight and regulatory/compliance support. The role focuses on risk assessment, process improvement, and ensuring adherence to cGMP and FDA guidelines.

You will lead daily quality operations, supervise staff, and contribute to writing and revising SOPs while supporting internal and external audits. Competitive benefits begin on day one, with opportunities for growth and impact.