Specialist Quality Assurance

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

     

JOB DESCRIPTION:

Specialist Quality Assurance

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a high employer contribution
• Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position works out of our Third-Party Manufacturer (TPM) location in Austin, TX within the Diabetes Care division. We’re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology.

The Abbott Diabetes Team (ADC) team on-site at the TPM consists of a cohesive group of professionals, representing various functions such as Operations, Quality, Engineering (both Site and Global), Program Management, and Supply Chain. This collaborative environment offers a unique opportunity to gain valuable cross-functional insights and experience. Additionally, the Quality Assurance Specialist will play a crucial role in supporting ADC's ambitious business growth. More importantly, you will have a positive impact on the quality of life for the patients we serve, as we strive to deliver 65 million units annually.

As a Quality Assurance Specialist, in this role you will:

Develop Quality Experience:  Support high-volume automated manufacturing.

Review & Approve Quality Records:  Gain experience with a variety of key quality documents.

Enhance Quality Mindset:  Cultivate a strong focus on quality.

Sharpen Critical Thinking Skills:  Operate in a fast-past manufacturing environment.

Develop Leadership Skills:  Mentor and coach TPM staff.

Acquire Valuable Knowledge:  Gain unique insights and experience that can only be obtained in a TPM environment, working withing another company’s quality system in addition to ADC’s quality system.

What You’ll Work On

The primary function of the Quality Assurance Specialist is to assist in maintaining the quality system. The Quality Assurance Specialist will be an integral part of a team supporting a high-volume, fully automated, 24/7 TPM manufacturing operation. Working collaborative with TPM Quality and partnering with Operations & Engineering, this role will help ensure that the TPM meets Abbott's quality standards and expectations.

Main Responsibilities:

TPM Maturity:

• Develop models that empower the TPM to drive effective problem-solving strategies and investigations.
• Implement agreed-upon actions and target reductions with the TPM and execute the plan.

Compliance:

• Create sustainable models for the TPM to improve quality control, increase efficiency, enhance reporting, and ensure long-term sustainability in addressing non-conformance issues.
• Support and ensure compliance with Quality Management Systems, including nonconformances, document change control, batch release, investigations, and more.
• Actively monitor Third Party Manufacturers (TPM) data and support areas for compliance with internal Standard Operating Procedures (SOPs) and relevant regulatory (cGMP, ISO) regulations.
• Review and approve TPM GMP-related documentation for compliance, such as nonconformances, batch records, and as