Senior Scientist, Pharmacy I

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

The Parenteral and Eyecare Operations S&T organization is responsible for the technical transfer and support of marketed and pipeline injectable products. This person will support the AbbVie Technical Operation functions and the AbbVie Technical Centers worldwide. Identify and resolve manufacturing issues for commercial and Research and Development products. Provides technical support to cross-functional teams during development, commercial launch or problem solving for a given drug product through investigational experimental approach, and optimization. The work would include support of both drug product process, analytical testing, and test method development activities. This person will also support process development lab management in partial capacity. The person is expected to demonstrate experimental precision and should possess general understanding of core disciplines supporting parenteral processes. 

Responsibilities: 

• Highly autonomous and productive in performing laboratory research and/or method development. 

• Liaison between functional groups as well as sister divisions (ie Operations, Quality, Regulatory, Validation, Materials Management, R&D, Analytical Test Labs, Stability and API) 

• Capable of working totally independently and providing technical support to a project team. 

• Provide individual technical support of all scale-up activities and maintain timelines for on-going projects. 

• Write/co-author process memos and scientific reports in support of Regulatory Submissions, Regulatory Field Alerts and supportive quality control and manufacturing documents. 

• Responsibility of writ