Associate Scientist II, Pharmacy

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Purpose:

Independently generate precise, reliable and reproducible data in a timely manner. Demonstrate experimental precision and strong data interpretation skills and should possess understanding of core discipline.

Responsibilities:

• Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, GxP compliance, etc. where applicable.
• Participate in projects impacting manufacturing to achieve process efficiencies, such as, increase in process yield, quality improvements, cycle time/throughput, and cost reduction initiatives.
• Gather and analyze process data using statistical process control methodology for the purpose of monitoring process performance.
• Responsible for providing technical support in the resolution of manufacturing investigations and executing assigned tasks as required, such as, laboratory experiments.
• Member of a cross-functional team responsible for implementation of site projects/initiatives (continuous improvement, cost reduction, capacity increase, etc.) that lead to process remediation.
• Member of cross functional team in the implementation of process validation for technology transfers, operational changes, new raw materials, and introduction of new process/technology.
• Generate technical justification determining impact of change and protocols/reports/manufacturing documents that support its execution. Assist the execution of experimental, demonstration, and validation lots.
• Maintain up-to-date product and process documentation and assure they are in compliance with applicable procedures and regulations. Writes justification memos and scientific reports supporting quality controls